Knize number tables

Image

KK242

KK242: Seed-grown on left; Live cutting from Knize on right

Some of the many collection numbers from Karel Knize

 

I’ve omitted some of the known problems in horticulture from this table; including commercial seedlots of KK242 being misidentified and producing what is clearly Trichocereus bridgesii and also Trichocereus cuzcoensis. Due to how MANY individuals now exist, KK242 can actually now be found equated with T. cuzcoensis but this is not any more accurate than Knize’s plant identifications (a lot of the time they are accurate). There is little doubt that Knize has in fact sold many thousands of Trichocereus cuzcoensis seeds through the world’s major cactus seed houses that were mislabeled as Trichocereus peruvianus KK242 (Knize has been a major supplier for their seeds beginning in the late 1960s) but KK242 can also be other quite different plants.
According to personal communication with Karel Knize, KK242 is a locality number rather than a collection number. Knize commented that, in his view, it represents up to 9 different populations “above Matucana”, 6 of which are short spined and all of which fall within the spectrum of pachanoi-peruvianus.
Any accurate definition of what KK242 represents needs to incorporate all of those AND the KK242 seed-grown T. cuzcoensis AND the KK242 seed-grown T. bridgesii.
Every example in the cactus images above was sold as a KK242 by Karel Knize.

While Knize certainly has introduced a bewildering wealth of confusing names and plants it was in the process of bringing an incredible number of cacti and succulents into the hands of horticulturalists world-wide. As is also true for northern hemisphere seeds collected by Horst Kunzler I suspect relatively few people realize how many of the plants they grow actually came from Knize seeds that were distributed through the major cactus houses.

 

Knize-1

Knize-2

Knize-3

Knize-4

 

Knize-5

 

Knize-6

Knize-7

 

Knize-8

Knize-9

 

 

 

 

 

 

Ritter

Some Friedrich Ritter field collection numbers of potential interest to readers

FR 17 Trichocereus terscheckioides (Famatina, La Rioja?, Argentina)
FR 17 Trichocereus terscheckioides  (31 km North of Tucumán, Argentina)
FR 17 Trichocereus terscheckioides (Famatina, La Rioja, Argentina)
FR 26  Trichocereus terscheckii (Betania, Salta, Argentina)
FR 26  Trichocereus terscheckii (Tacuarandi, Tarija, Bolivia;  1958/04)
FR 26  Trichocereus terscheckii (60 km South of Salta, Salta, Argentina)
FR 70  Trichocereus werdermannianus (Chuquisaca, Bolivia)
FR 70  Trichocereus werdermannianus (Tupiza, Potosí, Bolivia)
FR 70  Trichocereus werdermannianus (Near Cieneguillas, Tarija, Bolivia;  1958/04)
FR 72 Trichocereus tacaquirensis (Bolivia 1955)
FR 72 Trichocereus tacaquirensis (Tupiza, East of river, Potosí, Bolivia)
FR 72 Trichocereus tacaquirensis (Tupiza, Potosí, Bolivia)
FR 72  Trichocereus tacaquirensis (Curque, Tarija, Bolivia 1953)
FR 72 Trichocereus tacaquirensis (Tupiza, Potosí, Bolivia 1962)
FR 72 Trichocereus tacaquirensis (Cieneguillas, Tarija, Bolivia 1962)
FR 101  Trichocereus bridgesii  (Mecapaca, La Paz, Bolivia)
FR 101  Trichocereus bridgesii (Near La Paz, Abrajes, La Paz, Bolivia  03/1953)
FR 155 Trichocereus peruvianus
FR 155a  Trichocereus tacnaensis (var Estique)
FR 156 Trichocereus knuthianus
FR 270  Trichocereus glaucus
FR 270a  Trichocereus glaucus (Camaraca, Tarapacá, Chile) (forma pendens)
FR 567 Trichocereus pachanoi
FR 567a  Trichocereus santaensis
FR 615  Trichocereus crassicostatus  (Bolivia)
FR 676 Trichocereus pallarensis
FR 677 Trichocereus knuthianus
FR 677a  Trichocereus cuzcoensis
FR 853  Trichocereus crassicostatus  (Río Cajas, Tarija, Bolivia)
FR 853  Trichocereus crassicostatus  (La Merced – Río Negro, Tarija, Bolivia)
FR 853  Trichocereus crassicostatus  (Below Tarija city, on Río Tarija, Tarija, Bolivia)
FR 853  Trichocereus crassicostatus  (Angosto, Tarija, Bolivia)
FR 856 Trichocereus riomizquiensis
FR 991  Trichocereus scopulicola (Tapecua, Tarija, Bolivia 1000-1500m)
FR 991  Trichocereus scopulicola (Cañada – Palos Blancos, 24 km West of Palos Blancos, Tarija, Bolivia 1000-1500m)
FR 993 Trichocereus terscheckioides (Cafayate, Salta,  Argentina)
FR 993 Trichocereus terscheckioides (Famatina, La Rioja, Argentina)
FR 993 Trichocereus terscheckioides (54 km West of Belén, Catamarca,  Argentina)
FR 994  Trichocereus tacnaensis
FR 1467  Trichocereus torataensis
FR 1468  Trichocereus pallarensis (forma Machac)


Be aware that there are many databases which list Knize numbers but omit many of Knize’s actual applications of those numbers.  Confusion is prevented by their recognition not their avoidance.


A great collection of collection numbers can be found at Ralph Martin website (the above list was assembled using data from there and from Ritter’s Kakteen in Sudamerika)

  By number: http://ralph.cs.cf.ac.uk/Cacti/fieldno.html

  By name: http://ralph.cs.cf.ac.uk/Cacti/finder.html

Suggested reading: entoptic imagery

Suggested reading concerning phosphenes, drug or mind interactions with rhythmic stimuli (entrainment), and entoptic imagery in rock & other shamanic art

This is an incomplete list (also consult the references in the listed articles).

Adrian & Matthews 1934
Ardi & McKellar 1956
Bradley 1989 [Nice depictions of entoptic elements taken from Brittany & Ireland.]
Davis et al. 1970
Devereux 1997
Dowson 1992
Dronfield 1995a & 1995b
Eger 1978
Elgar 1963
Grant 1965
Halstead et al. 1942a & 1942b
Jones 1954
Kellog et al. 1965
Knoll 1958 & 1967 [See also contained references.]
Knoll & Kügler 1959
Knoll et al. 1962a, 1962b & 1963
Lewin 1991
Lewis-Williams 1981
Lewis-Williams & Dowson 1988, 1989, 1992 & 1993 [1988 has a great reference section with many interesting entries]
Livanov & Poliakov 1945
Marshall 1935
Neher 1961 & 1962
Patterson 1992
Patton 1990 & 1993
Reichel-Dolmatoff 1978a & 1978b
Rudgley 1995
Schaafsma 1980
Sherratt 1995
Siegel 1986 (1977),
Siegel & Jarvik 1975; See also Horowitz p. 178.,
Siegel & West (eds) 1975
Shirokogoroff 1935
Stone-Miller 1995
Syal 1996
Ulett 1953
Walter 1946 & 1953,
Walter & Walter 1949
Wellman 1978
Wheatley & Schueler 1950
Whitley 1994a & 1994b

Wheatley & Schueler 1950 reported that low doses of mescaline, too low to produce visual effects, were “adequate for the production of striking visual effects when these subjects were placed, with eyes closed, in front of a flashing light of frequency approximating that of the normal alpha rhythm.” It was not described how this compares with the striking visutal effects that same stimuli would produce in a normal person. Knoll et al. 1963 commented that electrical stimulation increased the intensity of images seen under the influence of mescaline but added that this effect was not noticeable during the peak of mescaline’s activity.]

1930_Szuman_fig8

Szuman 1930 figure 8 (sketched while under the influence of 400 mg)

Of particular interest is W. Gray Walker’s discovery in the 1940’s that brainwave activity tends to follow the frequency of flickering light [this phenomenon was first noticed by Adrian & Matthews in 1934], particularly if the frequency is in the alpha or theta range. (Flickering lights in the frequency ranges that are also seen in fire and in the ritual movement of dancers rhythmically dividing the image of a fire behind them.)

It has also been found that a similar effect can occur with repetitive sound, if it is of a complex frequency such as is produced by drums or other musical instruments.
Increased intensity enhances effects.
Low frequencies are apparently most effective since the corresponding sensory structures are not as susceptible to damage from high intensity as are those used for perceiving high frequencies.

Harner describes drumming viewed as a horse or canoe used to carry the shaman into the altered state known as a “shamanic state of consciousness”.
The phenomenon became known as “flicker phenomenon”, “the frequency following effect”, “entrainment”, “auditory driving”, “photic stimulation”, “photic driving” or “brainwave driving” depending on the source of reference.  The perceived colored moving images and geometric shapes variously being called phosphenes, entoptic imagery, entopic [sic] imagery, more simply (and improperly) hallucinations or in common street parlance ‘patterns-and-colors’.
Especially interesting is Walker’s observation that the effects induced in the brain (as followed via EEG) are not limited to the visual imaging areas but spill over into apparently unconnected areas of thought and perception.

Also worth mention is S. Williamson & L. Kauffman’s work with magnetic brain-mapping at NYU indicating that different areas of the brain are stimulated by different sound frequencies (tones).

Another line of interesting work is Dr. S. Cohen’s attempts to directly correlate brain structures and visual imaging apparatus physiology with the details and geometries observed in phosphenes; whether generated physically or chemically.
Interestingly, this entire area is seemingly dismissed as trivial distractions, or at best unimportant components of the experience, by MOST writers.

1930_Szuman_fig3

Szuman 1930 figure 3 (sketched while under the influence of 400 mg)

Historically, most frequent proposal concerning the generation of colored images and geometric patterns has been that they arise in the eye and involve retinal structures and floaters in the vitreous humors. This view and the thinking which was used to support it is nicely discussed and summarized in Lyttle & Smith 1990
In light of the work involving phosphene generation, and their deliberate, frequency-dependent manipulation, this must be considered to at least partially miss the point.  Careful study of these images shows that some elements of what is perceived does indeed arise from structures within the eye itself, even from reflections of light on the surface of the cornea and even its scintillating interplay with tears & eyelashes. These however are minor components of what is perceived.
Most serious researchers now believe that the bulk of images arise during visual processing in the brain and are directly related to brain structure itself. This is further supported by the fact that even patients with enucleated eyeballs can perceive these images if stimulation is applied.
It is now thought that at least part of what is seen may relate to the actual firing of neurons in the visual cortex, as visualized by reverse projection, but there is some suggestion that other areas in the brain may also be observed. [The visual elements, that the patterns
get interpreted as, being assigned by the brain itself.]

In attempting to sketch distinct and recurrent components of the visions I found them to curiously resemble glandular structures in the midbrain (such as the pituitary, hypothalamus and amygdala) and other macroscopic features of the brain.

Lophophora williamsii: music

References concerning peyote music and Icaros, magic melodies among Ayahuasceros:

This fascinating area deserves a work unto itself. This is an incomplete list. Many of the peyote music references were included by LaBarre and I have been unable to obtain copies. 

Densmore, Frances (nd) “Winnebago Songs.” (Bureau of American Ethnology, Manuscript no. 1971)

Densmore, Frances (1932) “Winnebago Songs of the Peyote Ceremony.” (Bureau of American Ethnology, Manuscript 3261)

Densmore, Frances (1936) Southwest Museum Papers 10: 15-23, 82-93. “Cheyenne and Arapahoe Music.”

Densmore, Frances (1938) American Anthropologist 40: 175-177. “The influence of hymns on the form of Indian songs.”

Densmore, Frances (1941) American Anthropologist 43: 77-82. “Native songs of two hybrid ceremonies among the American Indians.”

Kurath, Gertrude (1953) American Anthropologist 55: 113 Review of: Cantos indigenas de Mexico, by Concha Michel (Mexico, D.F.)

Luna, Luis Eduardo (1984)b Journal of Ethnopharmacology 11 (2): 135-156. “The Concept of Plants as Teachers Among Four Mestizo Shamans of Iquitos, Northeastern Peru.” [includes scored icaros]

Luna, Luis Eduardo (1992) “Icaros. Magic Melodies Among the Mestizo Shamans of the Peruvian Amazon.” pp. 231-253 (Chapter 10) in: E. Jean Matteson Langdon and Gerhard Baer (Eds.) “Portals of Power. Shamanism in South America.” University of New Mexico Press, Albuquerque [includes several scored icaros]

McAllester, David P. (1949) “Peyote Music” Viking Fund Publications in Anthropology No. 13.

McAllester, David P. (1951) American Journal of Sociology (January) “Peyote Music”

McAllester, David P. (1952) in J.S. Slotkin’s “Menomini Peyotism” (Transactions of the American Philosophical Society 42, pt. 4.) pp. 681-700. “Menomini peyote music.”

McAllester, David P. (1954) “Enemy way music: A study of social and esthetic values as seen in Navaho music.” (Reports of the Rimrock Project, Values Series No. 3, Papers of the Peabody Museum of American Archaeology and Ethnology.)

Merriam, Alan P. and D’Azevedo, Warren L. (1957) American Anthropologist 59: 615-641. “Washo peyote songs.”

Moore, Harvey C. (1956) American Anthropologist 58: 220. Review of: Enemy way music: A study of social and esthetic values as seen in Navaho music, by David P. McAllester.

Nettl, Bruno (1953) Journal of American Folklore 66 (260): 161-164. “Observations on meaningless peyote song texts.”

Nettl, Bruno (1954) Journal of American Folklore 67: 305-307. “North American Indian Musical Styles.”

Nettl, Bruno (1958) American Anthropologist 60 (3): 518-532. “Historical aspects of ethnomusicology.”

Rhodes, Willard (1958) Journal of the International Folk Music Council 10: 42-49. “A study of musical diffusion based on the wandering of the opening peyote song.”

The Library of Congress offers several Native American music assemblages that each contain one peyote song (along with other songs): Tape and booklet; $8.95 ea. plus p & h. [Check for current pricing]

    AFS L 35 Kiowa

    AFS L 40 Sioux

    AFS L 41 Navajo

Woodward, Hope Draper (1991) M.A. Thesis University of Texas at Austin. “Ashaninca Shamanic Healing Ritual and Song.”

Peyote Music

Available on Audio Tapes or on LPs (A partial listing) 

The following recordings are what has been encountered in print.
Inclusion here does not necessarily mean that they are still available or that the current offerings are necessarily limited to these; please inquire before ordering. Some are available on CD.

All record labels are from Rätsch 1998.

Cheyenne Peyote Songs. Volumes 1 and 2. (Rätsch lists Indian House, 1975 for a single entry) [C, D]

Crow Dog’s Paradise. Songs of the Sioux. (Richard Erdoes) Album EKS-74091; Elektra: New York.

Comanche Peyote Songs. Volumes 1 and 2. [D]

Guy and Allen. Volumes 2 through 4. [D]

Healing and Peyote Songs in Sioux and Navajo. [Primeaux, Mike and Attson] (Canyon Records, 1994) [C]

Healing Songs in Navajo (by Jimmy Knight) [B]

Huichol Sacred Music/Musica y Canto Ceremonial Huichol [Mother Eagle Kaili] (Paraiso, 1995) [C]

Indiens Yaquis: Musique et dances rituelles. (Arion, 1978) [C]

Intertribal Morning Peyote Songs. Volumes 1 and 2. [D]

Intertribal Peyote Chants. Volumes 1 through 6. [Bill Denny Jr.] (Rätsch lists 1984 Canyon Records) [D, C, D]

The Kiowa Peyote Meeting. (Ethnic Folkways Records, 1973) [C]

Kiowa Peyote Songs. [Kaulaity, D. Kozd, J. Kozd] (also offered by B; artists given as Kaulaity & Cozad) [B, D]

Lord’s Prayer Songs. [Alfred Armstrong] [D]

Musical atlas: Mexico (EMI Records, 1982) [C]

Music of the plains: Apache (Asch Records, 1969) [C]

Musiques Mexicaines (Ocora Disques. o.J.) [C]

Old Peyote Songs (by various artists) [B]

Navajo Peyote Ceremonial Songs. Volumes 1 through 4. (Rätsch gives Indian House 1981 for Vol. 1) [B, C, D]

Navajo Peyote Songs. [Kevin Lewis.] [D]

Navajo Peyote Songs. Volume 2. [Kevin Lewis] [D]

Navajo Wildcat Peak. Volumes 1 through 5. [Vols. 1, 3 and 4 are morning songs.] [D]

Navajo Wildcat Peak Youth. [D]

Peyote – A Collection. [D]

Peyote Brothers. [Guy & Allen] (Soar Sound of America Records, 1993) [C]

Peyote Canyon. [Guy & Allen] (Soar Sound of Records, 1991) [A, C, D]

Peyote early Morning Chants (by Daukei & Chester) [B]

Peyote Prayer Songs. Volumes 1 and 2. [W. Van Horn, E. Barker, A.C. Clark] [D]

Peyote Songs from Navaholand [Billie Nez] (Soar Sound of America Records, 1992; Spalax Music, 1993) [C]

Peyote Strength. [Guy & Allen] (Soar Sound of America Records, 1994) [C]

Peyote Songs from Rocky Boy. Volumes 1 through 3. [The Parker Singers] (Canyon Records, 1978) [B, C, D]

Peyote Songs. Volume 2. [Everette Barker] [D]

Ponca Peyote Songs. Volumes 1 through 3. [D]

Primeaux & Mike. [Peyote songs in Sioux and Navajo] (B offers Primeaux & Mike Volumes 1-7) [B, D]

Primeaux, Mike and Attson. Volumes 2 and 3. [D]

Songs of the Native American Church. Volumes 1 and 2. [Volume 2; Billy McClellan Sr.] [D]

32 Cheyenne Peyote Songs [Grover Turtle and Sam Sweezy] (Indian Records, 1979) [C]

Walk in Beauty: Healing Songs of the Native American Church. [Primeaux and Mike] (Canyon Records, 1995) [C]

Yankton Sioux Peyote Songs. Volumes 1 through 8. (Rätsch list Indian House, 1976 for a single entry) [A, B, C]

[Sources:]

A: The Basement Shaman, P.O. Box 1255, Elgin, IL, 60121. [tape & CD]

B: The Peyote Foundation, POBox 778, Kearny, AZ 85237.

C: Listed by Rätsch 1998

D: Listed in October 1995 by Richard Wood’s: Wooden Penny Trading Post; 409-297-8953, FAX 409-265-6813. [Literature obtained at an Intertribal Pow-wow in Austin, Texas.]

Ayahuasca Music available on Audio Tapes

Luna, Luis Eduardo (ed.) (199?) “Music the Plants Taught Us.” (Audio tape of ayahuasca icaros; offered through many sources including the Basement Shaman.)

Rivas, Augustin. “Canto Musica Ayahuasca en la Silva de Peru: Agustin Rivas.” (Tape available through the Basement Shaman.)

Vasquez, Luis Panduro (2000) Ayahuasca Songs from the Peruvian Amazon. Colibri Publishing. (70 minute CD.)

See Rätsch 1998 for more.

Suggestions for readers

 Literature about peyote that may be of potential interest to readers

 

 

Aberle, David F. (1966) & (1982) (second edition)

Peyote Religion among the Navaho.

    A classical treatment with an excellent public health assessment.

Anderson, Edward F. (1980) & (1997) (second edition)

Peyote the Divine Cactus

    Slightly dated but still the most comprehensive work ever done on the Peyote plant. The second edition was primarily updated in the legal discussion.

Anderson, Edward F. (1995) Cactus and Succulent Journal 67: 67-73

“The “Peyote Gardens” of South Texas: A Conservation Crisis.”

    An important work on the state and future of this plant in Texas.

Backeberg, Curt (1961)

Die Cactaceae. Handbuch der Kakteenkunde. Vol. V. “Cereoideae (Boreocactinae).” page 2893-2903.

Many pictures: including a crested example on page 2904.

Benitez, Fernando (1975)

In the Magic Land of Peyote.

    A Westerner’s tale of a pilgrimage with the Huichols.

Bohata, Mysak & Snicer (2005)

Kaktusy’s Special Lophophora Issue.

This is easily the best work in existence concerning the Lophophora species.

Nathaniel Lord Britton & J.N. Rose (1922)

The Cactaceae. Descriptions and Illustrations of Plants of the Cactus Family. Volume 3: 83-85.

Byarlay, Patricia (ed.) The Peyote Awareness Journal later as “Peyote: A Medicine Journal.”

    Short but valuable periodical publication of the Peyote Foundation.

Collier, Donald (1929) (US Congress) Senate Committe on Indian Affairs 34: 18234-18255.

“Peyote, A General Study of the Plant, the Cult and the Drug.”

    An interesting account considering the time frame.

Dogin (1976) Federal Register, 41: 4015

“Peyote”

    FYI

Gottlieb, Otto (1997)

Peyote and Other Psychoactive Cacti.

    Nice popular work aimed at a general audience of readers.
Some outright errors overall, including an unfortunate perpetuation of MANY myths, but Derek Westlund’s cultivation material is excellent.

 Gottlieb’s suggestion that dopamine be injected into the plants as a mescaline precursor would result in only trivial increases in mescaline content but could lead to toxic results if said cacti were consumed due to the accumulated dopamine.

Grym, Rudolph (1997) Also revised in 2014.

Rod/ Die Gattung Lophophora

    A new classic (in Czech & German). Lavishly illustrated.

LaBarre, Weston (1964) (1969) (1975) (1989)

The Peyote Cult.

    The classic work. Considered, by scholars and peyote-ists alike, to be the authoritative work on the peyote religion. Meticulous work documenting the religion from a Western framework of analysis.

  First published in 1938. Original written as his doctoral dissertation, LaBarre was disturbed when it became used by the NAC as a guidebook for new chapters.

LaBarre, Weston (1960) Current Anthropology 1: 45-60

“Twenty Years of Peyote Study.”

    Good overview.

McLaughlin, Jerry L. (1973) Lloydia 36 (1): 1-8.

“Peyote: an introduction.”

    A good intro and overview for the naive.

Mercado, Leo (ed.) The Peyote Foundation Journal

Publication of the Peyote Foundation, POBox 778, Kearny, Arizona 85237. [http://www.peyote.net]

Morgan, George R. (1983) Botanical Museum Leaflets. Harvard
University 29 (2): 73-86

“The Biogeography of Peyote in South Texas.”

    An intimate look at peyote and its home in Texas.

Mount, Guy (1990)

The Peyote Book: A Study of Native Medicine.

    Even handed popular work. Nice overview and account of modern day peyoteists.

Opler, Marvin K. (1940) American Anthropologist 43 (3) part 1:
463-474.

“The Characteristics and History of the Southern Ute Peyote Rite.”

    Very standard approach but interesting comparative reading.

Ott, Jonathan (1993) [Second edition densified 1996]

Pharmacotheon

    Excellent summary of peyote’s history.

Petrullo, Vincenzo (1934)

The Diabolic Root. A study of Peyotism, the New Indian Religion Among the Delaware.

A good discussion of the peyote faith from its early founding through its spread across the United States and Canada. A nice early viewpoint on the origins of its unjustifiable religious persecution.

Roseman, Bernard (1968)

The Peyote Story. The Indian Mind Drug.

    An interesting view of the Native American Church by a white who was allowed to participate.

Schultes, Richard Evans (1936) Thesis, Harvard University.

Peyote Intoxication, A Review of the Literature on the Chemistry, Physiology and Psychological Effects of Peyotl.

    Have not yet obtained a copy but certainly sounds interesting.

Schultes, Richard Evans & Albert Hofmann (1980)

Botany and Chemistry of the Hallucinogens. 2nd Ed.

Schultes, Richard Evans & Albert Hofmann (1992)

Plants of the Gods

History, sacramental use, ethnopharmacology, botany and chemistry. Wonderful pictures.
Both are classic works. 

Slotkin, J.S. (1952) Transactions of the American Philosophical Society, 42 (pt. 4): 565-700. “Menomimi Peyotism. A study of individual variation in a primary group with a homogenous culture.”

Stewart, Omer C. (1956) Colorado Quarterly 5: 79-90.

“Peyote and Colorado’s Inquisition Law.”

Nice piece on the history (up to the time this article was written) of anti-peyote activity and legislation as a religiously sponsored agenda coexisting with abundant available evidence indicating they were in error as to their assertions and prejudicial activities.

Stewart, Omer C. (1987)

Peyote Religion. A History

    [Civilization of the American Indian Series. Vol. 181]

    A definitive study that complements LaBarre very well.

also Stewart, Omer C. (1993) “Peyote Religion. A History.” [Have not seen the latter. From Books-in-Print]

Stewart, Omer C. (1993)

Peyotism in the West: A Historical and Cultural Perspective. [Anthropological Papers: No. 108]

Another interesting short piece that readers might enjoy:

James H. Howard (1962) Journal of American Folklore, 75 (296): 10-14. “Peyote jokes.”

Addition titles encountered in various sources

(including but not limited to Book-In-Print, Samorini 1998, Rätsch 1998, Mind Books’ catalog and Ott’s column in MAPS) See full citations in the reference section. I did not use or in some cases have not yet obtained copies of these articles or books but wanted to list them for the reader’s convenience:

No author listed (1991) Peyote: A Source Book of the Ritual Drug. Gordon Press. 0-8490-4656-4. If not for the $79.95 price tag this would have been ordered just to find out what it is. (Listed in Books-In-Print on CD-ROM simply as “Peyote.” Unable to directly contact the publisher. The voice mail for the listed phone number has been “full” for a surprising number of years now.

B.J. Albaugh & P.O. Anderson 1974

Gunter Ammon & Jorgen Gotte 1971 & 1974a & 1974b

Edward F. Anderson 1996

Antonin Artaud 1966 & 1975

L. Warren Azevedo 1995

L. Beltrami 1941

Fernando Benitez 1972

Mario Benzi 1969, 1972 & 1998

Kathleen Berrin 1978

Victor Blanco Labra 1992

Thomas Benno Bollhart 1985

Charles S. Brant 1950

Silvester J. Brito 1989

Ronald K. Bullis 1990

Alejandro Camino 1992

D. Canestrini 1993

Armando Casillas Romo 1990

Luigi Ceroni 1932

Warren d’Azevedo 1978

Calus Deimel 1980, 1985, 1986 & 1996

L. Diguet 1907

Allen T. Dittman & Harvey C. Moore 1957

C. Burton Dustin 1962

Havelock Ellis 1897 & 1971

A. Don Evans 1989

Irwin Feinberg 1965

Jay Courtney Fikes 1993

D. Flattery & J. Pierce 1965 (1992)

Bianca Maria Frigerio 1974-1975

Peter T. Furst 1965, 1969 & 1981

Peter T. Furst & M. Anguino 1977

Peter T. Furst & Salomón Nahmed 1972

Jochen Gartz 1995

Peter Gerber 1980

John M. Goggin 1938

A. Gottlieb 1998

Martin Gusinde 1939

Carl Hammerschlag 1988

Alden Hayes 1940

Christina Hell 1988

Jennifer James 1996 [This is an informational brochure]

Joyce James 1964

M. Kan et al. 1989

Weston LaBarre 1981

Lame Deer & Richard Erdoes 1979

Vittoria Lanternari 1974 (1960)

James H. Leuba 1960

Lumholtz, Carl 1902 & 1989

Alice Marriott & Carol K. Rachlin 1972 & 1988

Chase Mellen III 1963

Henri Michaux 1967, 1968 & 1986

Laurenchich Minelli 1977

Laurenchich Minelli & Bianca Maria Frigerio 1976

Claudia Müller-Ebeling & Christian Rätsch 19??

Barbara G. Myerhoff 1973, 1975, 1976 & 1980

S. Nahmed Sittri et al. 1972

Marvin K. Opler 1940

Morris E. Opler 1938 & 1940

V.M. Palmieri 1942

Paul Pascarosa & Sanford Futterman 1976

Torsen Passie 1994

Tom Soloway Pinkson 1995

Alexandre Rouhier 1988 & 1996

Victor Sanchez 1996

Stacy Schaefer 1989, 1993a, 1993b, 1995, 1996, 1997, 1998a, 1998b & 1998c

Stacy Schaefer & Peter T. Furst (eds.) 1996

George Schäfer & Nan Cuz 1968

J.S. Slotkin 1956

J.S. Slotkin & D.B. McAllester 1952

Weston LaBarre 1957

Huston Smith & Reuben Snake (eds.) 1996

J.R. Smythies 1963

G. Sogliani & P. Sagripanti 1957

Paul Steimetz 1990

Omer C. Stewart 1944

Silke Straatman 1988

Mariano Valadez & Susana Valadez 1992

Christopher Vecsey (ed.) 1991

Günter Wagner 1932

Günter Wallraff 1968

Dennis Wiedman 1985

Dennis Wiedman & Candace Green 1985

Jon Wright 1994

R.M. Zingg 1938 & 1982

 

There are several bibliographies focusing on hallucinogen research in the works or completed that should be available, reportedly on-line, according to MAPS.

An excellent bibliographic database for peyote and mescaline could be assembled by merging the appropriate references in those bibliographies with those included by Abramson 1956, Anderson 1980 (1997), Beringer 1927, Bruhn & Holmstedt 1974, Cholden 1956, Janiger & Paltin 1971, Kapadia & Fayez 1970 & 1973, Kline 1956, LaBarre 1975 (1989), Ott 1993 (1996) & 1997, Patel 1968, Reti 1950, Safford 1915 Journal of Heredity and 1921 JAMA, Samorini 1998 Allucinogeni, empatogeni, cannabis. Bibliografia italiana commentata, Schultes 1937 & 1940, Schultes & Hofmann 1980, Slotkin 1951, 1955 & 1956a, the SISSC (Società Italiana per lo Studio degli Stati di Cosienza 1994 “Bibliografia Italiana su Allucinogenie Cannabis”, Stewart 1989 and 1994, Wikler 1957 [summary of psychiatric and pharmacological work on mescaline.] Also the bibliographies on use of mescaline and other hallucinogens in psychotherapy by Unger 1963a LSD, Mescaline, Psilocybin and Psychotherapy: An Annotated Chronology.” and Unger 1963b Psychiatry 26 (2): 111-125. “Mescaline, LSD, Psilocybin, and Personality Change: A Review.” and Unger 1965 “LSD and Psychotherapy: A Bibliography of the English-Language Literature” pp. 241-248 in The Psychedelic Reader (Weil, G.M. et al. Editors). The NIH is also said to have a bibliographic listing on the subject.

Good sources for on-line sites and a wealth of information and data bases are the Erowid website [http://www.erowid.org], Will Beifus 1996 Psychedelic Sourcebook, Jon Hanna 1996 Psychedelic Resource List and MAPS [Multidisciplinary Association for Psychedelic Studies] 2105 Robinson Avenue / Sarasota, Florida 34232 (http://www.maps.org).

Also keep an open eye for the completion of the Albert Hofmann Foundation archives some day in the future.

Krebs & other cactus compounds

Mescaline’s Krebs acid conjugates & many other compounds have been reported from Lophophora williamsii and/or the other cacti discussed in this work.

A partial view of some of those compounds is below and a far more detailed look can be found in the books:
Cactus Chemistry By Species
(illustrated PDF)
(“light” PDF)
&
The Cactus Alkaloids
(PDF)

Krebbs

Lemairin

Lemairin

compounds-2

betanins

the Peyote Crisis and some Suggestions – Revisited

It appears to be a ripe time for reevaluating the article entitled “the Peyote crisis & some suggestions“.
This was variously positioned as Chapter 2 or Chapter 3 in the revisions of the book Sacred Cacti.
That chapter, as written, is greatly in need of revision & updating; and some additional questions being asked about *its* suggestions. Our use of the word “I” in this article simply means we want to say this with one voice. Use of the word “we” refers to the reader and ourselves.
This commentary, as written, is meant to serve the great need for better accurate public education and has been constructed primarily for clarity of presentation of the contained material. It has not been created with the same density of in-line references such as would be the case for a work that was intended for print publication in a peer reviewed journal. It is hoped that adequate documentation and references are included for the benefit of people wanting to learn more but if YOU want to learn more or need any additional clarification or supportive documentation please drop an email to keepertrout at gmail and ask.
Accompanying this information is the feeling that there is some urgency in it being released. It is therefore being made available for public inspection and comment without further delay.
The plants of tomorrow begin with the seeds that are planted today.

Commentary & thoughts
by Keeper Trout, Blake Edwards & Martin Terry

I also went to survey the gardens in February [1998]. The situation is sad, intolerable, several parcels hunted completely clean. On inquiring with the dealers, I was able to hand sort well over 10,000 dime sizers, most w/roots. They are picked that way because the payment is per unit. […] those 10,000 plus babies are now growing. My idea is to purchase all the babies we can for their eventual re-planting in Texas.”
Leo Mercado 6 July 1998 (personal communication).

Those same plants were later seized (as part of a dump-truck load containing more than 11,230 living peyote plants) and destroyed by a “multijurisdictional task-force” of law enforcement officials despite Leo at that time having been found in court to be in compliance with Arizona state law permitting the sincere religious use of peyote. In the aftermath of what can only legitimately be described as a terroristic home invasion, Leo posted a notice online that he had replanted the 200 or so peyote plants that had been missed or dropped during the raid.
No charges were filed, which fact was likely to prevent a return of his peyote as had occurred after the first time that they seized Leo’s peyote. Instead Leo’s landlord found himself being threatened with the seizure and forfeiture of his property if he did not evict Leo and his family. The basis of that threat was his supposedly renting to a “known illegal drug dealer”, namely Leo!
Apparently Leo’s living example as a human of only modest means successfully propagating and cultivating large numbers of peyote plants outside of Texas was too powerful of an example to be allowed to exist. At the very least, his Kearny, Arizona shade-house and gardens had to be seen as an awkward truth running counter to the lies actively being propagated about it being impossible to grow peyote outside of its native habitat.
From Ch. 3 in Sacred Cacti 3rd edition (with some edits).

 

Lophophora-williamsii-threatened-by-knife

Cutting crowns flush at the level of the ground has been established to be the best known harvesting technique for peyote. This approach to enable sustainable harvesting has been known of and employed by peyote consumers in Mexico for millenia. The archaeological peyote specimens discovered strung on a cord at Cuatro Cienegas are more than a thousand years old; the Shumla peyote effigies are over six thousand years old.

 

First, concerning the “crisis”….

One suggestion, really, is all that is required; assuming that it can be heard, without prejudice, where it matters.

Cultivate the Medicine.

It is really simple yet that simple truth of the matter has been almost completely buried, if not forgotten or deliberately obscured, in rhetoric that has at times variously been self-serving, manipulative, deceptive, disingenuous, confused, based on misunderstandings, culturally bigoted, or sometimes even entirely delusional. There really was not any delicate way to put that so I apologize for trodding on anyone’s conceptual toes.

Some people might ask:
If peyote is a pressured species, why isn’t it cultivated?

The question, “why isn’t it cultivated?” is a really good one. You and I will be exploring its answers in some detail.

We should start by clarifying some things and being certain that we all have a good grasp of an unnecessarily convoluted story.

 

The conservation status of peyote

Peyote is most certainly not extinct as some people strangely seem to believe and are even willing to say openly as if it were a fact. It is not yet really even an endangered species as more than a million living peyote crowns were no doubt harvested in South Texas again this past year by the licensed peyote distributors (I have to say probably as the numbers are not yet available).

A perception that the pressure from peyote harvesting is endangering the species is nothing new. While it does not appear on any federal listing of endangered species, peyote WAS declared an endangered species by the Texas Organization of Endangered Species (TOES) according to Morgan 1983: 83-84. Despite having a long history of cost sharing with land owners for brush removal and clearing of land, since the late 1970’s the U.S. Soil Conservation Service has refused to do so in any area containing peyote, as the SCS recognizes it to be a potentially endangered member of Texas flora (Morgan 1984: 292). Their lack of financial contribution has not slowed the clearing of land in the development of South Texas.

Only recently was peyote actually finally recognized as having adequately dwindling numbers to merit being assigned a status of “vulnerable” and being placed on the IUCN Red List of Threatened Species. Version 2013.2. [http://www.iucnredlist.org/details/151962/0].

Debates as to whether it should or should not be placed on the Red List had been going back and forth for some years, Oddly, what seems to have tipped the balance of opinion was the appearance of cosmetic/pharmaceutical industry products known as Pomada de Peyote. [Link 1] [Link 2] [Link 3] [Link 4] [Link 5].
I’m not including these links to suggest that any should be patronized but simply to note what came up in a Google search for “pomada de peyote” on 1 November, 2014.
Here are images of five of the products that were found to be offered on the first search results page.

 

Pomada-de-Peyote

 

It is certain that as both a liniment and an ointment, similar formulations have existed for a very long time at the folk level, and more recently as products of a local cottage industry. These products have likely achieved visibility only when the distribution venue was moved from local yerbarias to online marketing.

The use of peyote is traditional among some Hispanics in South Texas, too.
“When I was younger, you could buy it at the market in Nuevo Laredo, or at any of the local yerberias (herb shops),” [Salvador] Johnson said.
His wife, Vicenta, said that elderly Hispanics still use the drug as a cure for a variety of ailments, including as a rubbing lotion to treat arthritis when it is mixed with alcohol.
Grant 2000 Ft. Worth Star-Telegram, Sunday, 23 January.

One of the companies now producing pomada de peyote is an established business that is substantial in size and has previously developed other successful product lines. The future development of this product will be interesting to watch. It may be noteworthy that the number of different producers showing up as hits on the first Google search result page went from two to five within the past year.

Peyote is not endangered as a species for a variety of reasons. The most notable being that there are large expanses of the Mexican peyote populations left. The secondary reason is that not all peyote is accessible for harvest. In some cases, harvests are deterred by a lack of road access but in at least one instance a local population (in Mexico) is protected by the resident humans who interestingly do not use their local peyote for any purposes other than as an external analgesic applied to burns, bruises and aching muscles & joints.

In Texas it is a different story. The vast majority of its peyote populations have long since been removed during the course of the modern-day occupation/development of South Texas real estate and the collateral development of its assorted resources. Some peyote finds protection on large ranches with tall fences designed to retain game animals that are hunted for a hefty fee. When the owners of such large tracts of brush also do not permit peyote harvesters to access their land those properties form unintentional peyote reserves. The land that is left as accessible is heavily impacted by the existing peyote trade. In addition, the commercial peyote harvest has been insufficient for meeting NAC needs for some time.

There are two distinct but inseparable subtopics within this main topic of the threats to peyote, whether those threats are due to habitat loss or over-harvesting or any of the other known challenges that peyote faces.

One is the future of peyote as a species and the other is the future of the NAC as a Medicine-based spiritual organization that has both adequate and uninterrupted access to its Medicine.
We will examine both of those subtopics separately as this overview unfolds.

 

What has happened to create dwindling peyote populations?

Reading the popular press or listening to people talk, one would think that overharvesting by Native Americans or “hippies” is the cause. One or the other or both typically gets the most common and most vocal blame. This is true, despite it being absolutely clear that the vast majority of peyote’s obliteration, both in terms of absolute numbers and in total acreage, has actually been the incidental destruction of populations during the process of land conversion. All other factors combined pale by comparison.

There have been many reasons for this; the development of land for various projects, such as construction projects, shipping centers, parking lots and tract communities, or as a result of the brush suppression methods that enable ranchers to use their land for agriculture or ranching. Once a piece of land has been converted, peyote does not return.

 

peyote gardens today

Aerial view of a portion of the Peyote Gardens in Starr County showing extent of the land use and clearing. Photo clipping came from a topographic map from the US Geological Survey (USGS).

Most of peyote’s habitat in South Texas is covered with a tangle of dense thorny brush. To make their land available for agriculture or cattle, it was once a common practice for landowners to root-plow the soil due to the tendency of the thorny brush to come back with an aggressive vigor after being cleared.
Root-plowing severs the roots below the soil surface thereby weakening whatever of the roots can’t be uprooted and suppressing their ability for good regrowth. Or at least suppressing it for longer than might be the case without it. Repeating the process a few times does help but it is noteworthy that what actually becomes most suppressed is the diversity of life while the actual species that were attempted to be eradicated often go on to become the predominate vegetation.

 

rootplowed land

rootplowed land

Land in Maverick County that was root plowed several decades ago. The ranch foreman claimed that peyote was here before that occurred.
Their most likely intended target for eradication was the Acacia rigidula which comprises about a third of the plants seen in the lower image above.

 

Root-plowing has been determined to have lasting adverse impacts when used in dry regions. In arid environments with abundant limestone, in this case it is present as a calcareous gravel, rainwater dissolves the carbonates and other soluble ions but there is insufficient volume of water to carry what is dissolved more than a fairly short distance into the earth, accumulating and eventually creating a bed of ‘caliche’ at the depth of maximum moisture penetration. Due to rainfall being variable in the total amounts delivered per storm, this eventually forms an irregular gradient of alkali concentrations existing between the caliche and the surface ; with the surface obviously being the most life friendly. The layer of decomposing organic materials at or near the surface adds to the ability of the soil to support life.
This natural zoning develops over long periods of time with whatever level of moisture they DO have accessible. As it becomes increasingly basic with increasing depth this also means that that the surface is most amenable to supporting life. Accompanying that is the observation that, as rains moved part of the soluble alkali into the earth, that action helps make the surface more life friendly.
This fragile balance becomes completely undone with the mixing of the top half meter of soil during root plowing.
In this process, the more basic material that has been migrating away from the surface is partially returned to the surface during the mixing process. Recovery is typically slow since the reduction of the alkalinity at the surface level relies on repeated water percolation over time. The resulting increase of surface alkalinity leads to a die-off of small cover plants following seed germination and adds prolonged difficulty in reestablishing the normal flora. In adjacent areas that are used for agriculture due to being more sandy loamy than gravelly, and additionally due to the topography of the land being flatter & less sloping, this creates problems with blowing dust.

As a result root-plowing is now discouraged for those soil types and when it becomes needed specialized implements are used to selectively remove single plants.
The important thing to understand about root-plowing is that unlike the thorny brush that the root-plowing is intended to eradicate, a single thorough root-plowing will generally permanently exterminate all of the existing peyote on that a given piece of land.
If you want to gain a really solid grasp of this technology and a better understanding about why it would impact peyote so adversely, visit http://YouTube.com and search for “root plow” or “rootplowing“. Nothing describes the process better than watching a root-plow in action.

Other brush-clearing methods are not less destructive to peyote but they do impact the soil and ability of the land to recover less than root-plowing. YouTube can provide looks at modern techniques of “brush clearing in South Texas” as well.

 

root plow

 

Root plow Those fins are designed to force the severed roots to the soil surface and into the sun to dry and die.

 

The root plow is a tool for removing vegetation by cutting it below the soil surface […] killing brush and light vegetation by undercutting it […] at depth from 20 to 50 centimeters (8-20 inches). […] The advantage of the root plow is that it cuts the vegetation below the bud ring, killing brush that would normally resprout if cut at ground level.
US Army 1974 Tactical Land Clearing, p. 3-6

 

root plowing

Trunnion-mounted root-plow in action.
Both scanned photos came from a 1974 US Army
training manual entitled “Tactical Land Clearing”.

A new threat to peyote in South Texas are windfarms which choose the highest points in the Bordas Escarpment for their placement. These of course need an access road permitting both construction and maintenance. Those roads potentially carve through some of what few undisturbed peyote populations still remain in South Texas.

 

What do we actually know about the harvesting of peyote?

Surprisingly little study has been done on the impact of harvesting itself. As far as I am aware, only one organization, a nonprofit group named the Cactus Conservation Institute, has taken the time to learn more despite the immense need for this information as regards both the NAC and peyote conservation. It is clear that the peyote plant is a resilient species or it never could have permitted mass harvests to continue for so many years in the face of diminishing habitat. There are many articles that are available concerning the harvesting of the peyote plant and about its habits and habitat.

It IS known that the best way to cut peyote is at ground level. Cutting too deeply increases mortality and weakens those plants which do manage to recover.
The one existing study on the subject was published in Terry & Mauseth 2006. Using a histological evaluation, it was established that only the stem tissue was capable of producing new growth. Root tissue could only grow roots. A visible clear and sharp line of division was noted to exist between the two tissues.

Peyote harvesters often use a shovel with sharpened edge or a machete. Both of those tools can work great for cutting at ground level or they can be mis-employed and produce a deeply angled cut.

 

a cut peyote

Peyote plant after the crown has been removed

 

What do we know about the impact of peyote harvesting on wild populations?

A simple overview:

More complete details concerning the items in this list can be gleaned at the Cactus Conservation Institute website or in Kalam et al. 2013, Klein et al. 2015, Terry et al 2011, 2012, 2013 & 2014.

1) Peyote harvest causes a small increase in mortality.

2) If harvesting is repeated too frequently, this rate of mortality increases.

3) Harvesting also reduces the amount of harvestable biomass of sacrament per plant.

4) The aforementioned observation (3) is initially obscured by the increase in numbers due to the common occurrence of multiple regrowth. However, the sum total biomass of head (crown) tissue per plant, even after 4 years of uninterrupted regrowth, was still significantly smaller than the biomass of the original single head that had been harvested four years before. The study to determine the minimum sustainable recovery period after harvesting is still not complete, but it now clear that the time required for recovery from a single harvesting event is greater than six years.

5) Analysis has also shown that even after four years the regrowth had regained only half the potency of the original crown. It is not yet known how long it takes for the original potency to be re-established in the regrowth buttons.

6) Current and future seed production contributions to the local population are lost along with the harvested plants. The typical fate for peyote seeds following a harvest is into the trash or compost.
During the late 1990s, Leo Mercado was able to successfully recover (and plant) many thousands of seeds from the piles of hairs and tufts that accumulated from the peyote cleaned in preparation for a large ceremony. That event, at an annual NAC meeting at Mirando City, consumed more than a thousand crowns. (Information from a personal communication with Leo in 1998.)

7) The oldest and largest plants have been selected for by their environment as those are the plants which are best suited to survive the peak adverse periods of weather. These are commonly preferentially harvested – precluding any future contribution they might have made to the genetics of the population.
This last point may be subtle but played out over a long time can become significant. Following the removal of these genetically superior products of natural selection, future adverse periods of weather will likely begin to produce an increased adverse impact on the remaining population.

 

multiple regrowth

Peyote plant with multiple regrowth

 

Recovery

Let’s go over through that overview again but this time from a slightly different angle of thought and consider those factors in terms of recovery.
Recovery after harvesting is a core concept for this subject as it interweaves an impact assessment with a determination of sustainability. If the harvesting of a natural renewable resource is not sustainable, both harvesting and availability are temporary and transient phenomena with an inevitable end point involving either the loss or increased scarcity of that resource. /span>
There is nothing mysterious or unclear about what is being witnessed. A dramatic multiplication of undersized individuals is in fact the classical model resulting from harvesting activities involving an overexploited natural resource, be it fish or ginseng roots. (See Terry & Trout 2013. This link is a PDF file.)

Recovery is best understood not by looking at recovery of the individuals which are involved but of the health of local populations which are composed of many individuals.
Recovery of a population will accordingly have several factors based on what we looked at in our overview:

1) Replacement of the plants which die as a result of harvesting. (Replacement in this case is being considered only in terms of the natural recruitment of new seedlings although cultivation and wildcrafting would also enter the picture in this area. Wildcrafting is the conscious planting of seeds or return of plants in such locations where the plant formerly occurred naturally or could have occurred naturally.) This decrease in survival is thankfully a fairly low rate but it is not insignificant if a field is revisited as each subsequent visit may result in the reharvesting of plants which are still drawing their sustenance from the original reserves of the remaining taproot fragment from their mother and have not yet had time to manage to grow a replacement taproot.
The rate of mortality has increased with each time that reharvesting occurred in what limited study of the topic has occurred so mindfulness is needed not just of how deeply a plant is cut but also when it was last cut. Until after the point that a plant can regrow a taproot it is vulnerable to outright death from loss of its photosynthetic tissues as occurs in harvesting. This subtle but simple fact is somehow often either missed or trivialized: when the crown tissue has been removed the peyote plant loses its ability to use the sunlight. This remains true until after a new crown can be made and it reaches the surface of the ground where it can absorb sunlight to once again photosynthesize and feed itself. Repeated cutting too frequently forces the plant to exhaust its limited reserves and interferes with good regrowth and survival.
Plants that have been harvested need adequate time to replace their missing storage tissues (by photosynthesis in the crowns of the regrowth pups) before being reharvested or their death rate increases; eventually requiring their actual replacement.

2) Regrowing new crown tissue to replace the harvested crown with its equivalent prior to reharvesting.
Even though multiple crowns commonly result following harvesting, it takes some point greater than six years for their combined total weight to match that of the original crown. (The study to determine how long it takes for the sum of the regrowth buttons to equal the weight of the original harvested crown is still ongoing.)
Harvesting prior to following that point of recovery will provide smaller and steadily decreasing volumes of harvests. This is a practice which feeds into the spiral towards smaller, weaker plants with higher loss rates.

3) Recovering the original level of alkaloids.
After four years the average alkaloid level of new growth was only half that of the original crown. It is presently unknown how long it takes for the preharvest alkaloid level to be restored. Harvesting prior to following that point of potency recovery will provide an inferior quality of harvests, requiring consumers to ingest more plants, which also feeds into the extinction vortex towards smaller, weaker plants with higher loss rates.

4) The population also has to recover from the impact of however many years it would take seeds from those harvested plants to be replaced by new seed-producing crowns, and this must be taken into account if wanting to accurately assess the impact of harvesting. Every plant which is taken means that many less seeds are available for the local population for at least a handful of years. This is not insignificant as wild peyote in nature primarily reproduces via seeds. Removing a plant means removing all future seed contribution by that plant.
If older plants are preferentially harvested and as numbers dwindle the age of first harvest also decreases, it rapidly produces a situation where the only plants to harvest may have flowered only once or twice or not at all, creating a huge seed production deficit for the local population.
In the event of adverse weather (whether prolonged drought or beyond average freezing) causing an above average loss rate, this adds to the risk that the local population may not recover.

I’ll let you, the reader, do the math for yourself.

 

reharvested L. williamsii

This plant was previously harvested multiple times and the severed crowns sold through the licensed distributors. While the harvesting was conservative enough to not lose the original taproot, this individual strains the concept of “sustainability“. Also notice the steep angle showing careless cutting during two previous harvests.

 

What about the sustainability of harvesting?

Peyote harvesting appears to be a sustainable practice, at least in potential or in theory. In its present-day application however, the slow attrition process leading to the endangered species path has already clearly begun. It is clear that the consumers of peyote still have plenty of peyote to last for some years to come. Maybe even for the rest of our lifetimes, especially if you are middle aged like me.
Sustainability is not something defined by the here-and-now though. A commonly cited definition of sustainability is found in the 1987 Brundtland Report for The United Nations World Commission on Environment and Development, meeting the needs of the present without compromising the ability of future generations to meet their own needs”
As Kimberly Cover pointed out in 2005, that report’s definition is curiously similar to the Iroquois concept of thinking with responsibility for the next seven generations.

Much more study is needed to better define what was seen in the limited harvesting studies that exist but this is how it looks at the moment: The increased rate of mortality that results from a one time harvest is low enough so as not to adversely impact the long term survival of a population. That only appears to be true when adequate time is permitted between harvests. Some period greater than six years is all we can say about that number pending future data emerging. If enough plants of adequate size and potency exist to fill the anticipated needs of the active NAC membership and those plants are being reharvested no more often than they can regrow and return to being what they were prior to the point when they were first cut, harvesting appears to be sustainable.
Anything which creates an average result that achieves less than that, such as is presently the case, is not a sustainable practice.

 

So, let’s come back to our question, “Why ISN’T peyote cultivated?”

Probably the single most important element as to why cultivation is not already a part of the picture is the simple fact that none of the non-NAC people who are legally involved in the supply side have actual legal protection permitting them to cultivate peyote. They are in general law-abiding respected citizens who want to stay out of any trouble. Additionally, the peyote distributors can lose their licenses for violating the law.
As the licensed distributor Mauro Morales told Franks in 2007 . You have to make sure you don’t have a problem with the law, you know?

The portion of South Texas where peyote occurs naturally is commonly referred to as the Peyote Gardens, despite there being a complete lack of historical peyote cultivation. There are presently at least two pertinent stumbling blocks preventing this land from actually being used for creating a real peyote garden (or otherwise addressing the fatal long-term flaws that are inherent within the existing distribution system). Those are located within the Texas DPS (Department of Public Safety) regulations concerning peyote harvesting:

One for the Distributors:
Ҥ13.42. Peyote Distributor Registration. (d) Activity not authorized. A distributor registration does not authorize the distributor to: (1) manufacture or cultivate peyote; (2) ingest or use peyote; (3) deliver to an individual who is an Indian as the term is defined in AIRFA, unless the individual is also an Indian as the term is defined in this subchapter; or (4) import or export peyote except as permitted by federal law.

&
Another for the Ranchers has two pertinent features of interest:

“§13.55 adopted to be effective July 18, 2001, 26 Tex Reg 5266 (only a part is being included below) Nothing in this subchapter affects the ability of a landowner to: […] (2) burn or clear land for purposes unrelated to harvesting, cutting, collecting, or possessing peyote.” and within that same subsection, (b) Prohibited. Unless registered as a distributor or reported to the director as a current employee of a distributor, a landowner may not sell, harvest, cut, collect, transport, or possess peyote. A landowner does not possess peyote in violation of the Act or this subchapter if the peyote is unharvested and growing in its natural state.”

Landowners are permited to charge access fees for peyote harvesting but interestingly there is another clause in this same regulation that adds:
“(d) Harvest fee limitation. Unless the landowner is registered as a distributor, the director will deem the landowner to be selling or distributing peyote if the landowner bases the fee charged or collected under subsection (c)(1) of this section on the amount of peyote harvested, cut, or collected by the Indian using or entering the land”

Notice that this is a dysfunctional “one-price-regardless-of-harvest-size” scenario that actually encourages the maximum possible harvesting to occur per visit. Since the law further sets the retail price as being per piece (i.e. per button) and not by weight there is just as much financial motivation to harvest tiny plants as older ones. Increasing difficulty in gaining access adds additional motivation to maximize the harvests recovered on every visit.

Many ranchers don’t like peyote or peyote harvesting or peyote people and express a familiar bias directed against them. A not untypical attitude is Sahagun’s 1994 quote of ranch owner Robert East. I don’t want them here. That’s all there is to it. I think it’s a dope business, that peyote.” Racism and bigotry often still exist close to the surface in South Texas, in all directions. When talking with ranchers, several times I’ve heard it said that the cause for the disappearance of peyote wasover-grazing by the Indians.”

While that degrading analogy blames the “Indians” there is actually a highly valuable insight if we look at what IS actually real within that notion — namely, as is also true for a rancher’s grazing animals, the NAC is in fact being constrained and provided with its Medicine in a regulated and controlled manner rather than having the freedom to do as they choose. Blaming Native Americans for the, ahem, “over-grazing” problem is about as sound as a rancher blaming their grazing animals for “eating too much” rather than, in this case, correctly recognizing that any “overgrazing” was the direct result of negligent planning, counter-productive activities and incompetent management on the part of the ranch manager.

Similarly the fees charged by ranchers for access are high enough to stimulate maximizing the harvesting per visit as well. Johnson has mentioned ranchers’ greed raising access costs from what once was a pittance to something more significant.

Grant gave a 2000 estimation of it then typically costing $1,500 or $2,000 a month for a peyote lease; which provided a small work crew with access to locate and harvest crowns that were then being sold at the retail level for around $0.15 each.

There is no question that the public perception of the peyote trade being profitable contributed to that increase in peyote lease fees. Not everyone shares completely identical motivations. Sahagun 1994 described rancher Rick Walker as being fed up with trespassers. But he suggested another reason for guarding the peyote gardens on his land. Peyote, he said, may one day become a hot commodity – for ranchers.”

There is at least one rancher in South Texas, the identity of whom is being withheld, who has discovered a unique way to legally make money from his peyote and still protect them from any harm. Instead of leasing his land for the harvest of peyote buttons, he instead “showcases” his peyote plants. He permits organized “eco-tours” to bring visitors onto his property in a bus as part of a fee-based tour. They are allowed to visit his property under tightly controlled circumstances in order to witness and photograph his healthy population of peyote plants. The tour bus also takes the visitors away at the end of the visit so there is no risk of theft.
That population is, just as importantly, also located far enough away from the nearest road to ensure that none of their visitors will be able to return on foot.

While this may sound cynical, one other highly significant factor in the perpetuation of the status quo is that the peyote distributors actually derive a very good living from their trade.

Despite the low cost per button, it is actually a moderately lucrative profession in what is historically an economically depressed region of Texas since the three remaining peyote distributors combined now typically report a total sales of a little under a half million dollars per year ($530,230 in 2013, $434,609 in 2012, $466,590 in 2011, $459,699 in 2010 and $493,834 in 2009 according to DPS records). This reflects their combined totals so in reality it is split into uneven thirds based on how much they actually sell. Each distributor’s total sales pays for their lease fees, their expenses and is also what they pay to the small group of their ’employees’ who help them harvest peyote. In most cases their employees are their relatives.
Unlike the ranches, the distributors are authorized to pay and charge a fee on a per-button basis. Resale prices to their consumers had risen from around $0.09 in 1990 to $0.15 in 2000 and to $0.33 per button in 2011. (A hidden cost factor within that is that the rise in cost had been accompanied by a decrease in size and potency which meant people were required to eat more buttons. See Terry et al. 2012. Link goes to the PDF at CCI’s website.)
A perceived threat to their income and livelihood is no doubt going to be an important motivating factor and can add some illumination to the larger picture and help us to better understand why there is such resistance to change at the distributor level.

Sahagun 1994 quoted Johnson as saying,

I love what I do, enjoy the hell out of it. But hey, you don’t get rich picking peyote.

It is not a huge amount of money but in a region where relatively few other alternative options for similarly lucrative employment opportunities exist it is certainly something that the people involved are going to care about. Relatively few of the distributors and harvesters could successfully turn into peyote growers without investing resources and time in buying land and/or learning skill sets they do not presently possess. Even if they decided to take that path, it would put them on equal footing at the starting gate along with their new competition only if they had the same level of interest, education and skills as a professional gardener or nursery operator.

While the state law that was mentioned previously as granting the distributors their licensing specifically prohibits the distributors from cultivating peyote, the federal law also recognizes that the NAC, or anyone else who is producing peyote for the NAC, has a need to “manufacture” their Medicine (21 CFR 1307.31). [The regulation says “Any person who manufactures peyote for or distributes peyote to the Native American Church, however, is required to obtain registration annually and to comply with all other requirements of law.” That potentially open door for cultivation would apply to any person, NAC or otherwise. There is no special restriction to NAC members in this regulation.] Manufacturing a plant obviously requires growing it or else modern technology has become much farther advanced than I am aware.

Congress has further added an affirmative clause that suggests NAC cultivation was at least being envisioned as enough of a possibility that its regulation needed inclusion.

(b) Use, possession, or transportation of peyote
(1) Notwithstanding any other provision of law, the use, possession, or transportation of peyote by an Indian for bona fide traditional ceremonial purposes in connection with the practice of a traditional Indian religion is lawful, and shall not be prohibited by the United States or any State. No Indian shall be penalized or discriminated against on the basis of such use, possession or transportation, including, but not limited to, denial of otherwise applicable benefits under public assistance programs.
(2) This section does not prohibit such reasonable regulation and registration by the Drug Enforcement Administration of those persons who cultivate, harvest, or distribute peyote as may be consistent with the purposes of this section and section 1996 of this title. (In 42 USC § 1996a.) [Again, this applies to all persons, but it certainly includes the NAC.]

Which, at the very least, suggests that the road to the future cultivation of peyote by the NAC appears to be open as an available option that is protected by federal law. As AIRFAA treats cultivation in exactly the same manner as it does distribution, and because regulated distribution requires a long-standing registration process that functions daily before our very eyes, it would seem to be obvious that Congress intended cultivation to be not merely a hypothetical possibility, but a real option that should be realizable by the act of registration (to be defined and regulated, of course, by DEA).

 

peyote-buttons-Safford-1916

Dried peyote buttons from Safford 1916

 

 

Robledo 2006 included a thought-provoking comment that was left unexplained but touches on an often overlooked contribution to peyote harvesting by the NAC:

Out of the approximate 5 million buttons sold legally each year in the U.S. and Canada, deep South Texas provides about 2 million, with Salvador and his team of peyoteros providing at least 1 million themselves.
What is not mentioned by Robledo is what source provides the other 3 million of those buttons. It is noteworthy that the amount being estimated as procured independently of the activities of the licensed distributors exceeds their total output by 50%. It is reasonable to assume that he refers to the peyote that is being provided by the independent NAC members who are harvesting their own peyote. This brings us to another element in the story that we will return to again later – in the second part of this chapter.
Before moving onward this also is a great example of how much of the current “wisdom” about the peyote trade is based on untraceable rumor rather than documented fact. In the case of Robledo’s intriguing assertion of an actual numeric value for the unregulated peyote trade there are two glaring and inescapable facts that might be easily overlooked: 1) The claim lacks mention of its actual source or providing any indication about where or how this information came into Robledo’s awareness, and 2) it is an absolute impossibility for anyone to keep track of, much less tally with accuracy, the actual extent of the peyote trade occurring independently of the licensed distributors.

 

In 1988, after interviewing the active licensed distributors, John Morthland commented:

Dealers worry constantly about running out of stock, so they keep sources secret from outsiders and even from each other. They are also afraid that if Indians ever discovered the choice growing areas, they might try to bypass the dealers.”

An actual attempt by some peyote distributors to control the peyote trade and deliberately try to prevent cultivation by their customers actually goes back a very long time. Some comments from BIA Special Agent “Pussyfoot” Johnson were featured in an intriguing account by his supervisor that appears in a 1909 issue of the Indian School Journal, entitled “History, Use and Effects of Peyote.”

About twenty-three years ago a white man appeared at Laredo from the Territory in quest of peyotes.
He learned from the Indians up north that in a range of hills about forty miles east of Laredo, these peyotes could be found, He employed Mexicans to gather a supply, which he took north with him. He came in contact with a shipper by the name of Villegas, founder of the house known as L. Villegas and Company. Villegas then began buying these peyotes of ignorant Mexicans and shipping them north to the Indians. This house has been doing this for more than twenty years, but the business has been kept as secret as possible. Villegas has always refused to give the Indians any information as to the source of supply and has also refused all these years to supply Indians with the whole plant, fearing that they would transplant them and thus establish their own source of supply. Half a dozen years ago a member of the firm named Wormser withdrew and established the house of Wormser Brothers, of course taking the secret of the peyotes with him.
These two houses very craftily called these peyotes by the name of Japanese buttons, and created the impression locally that they were for some mysterious use by the Japanese.
These two houses, in this way, have built up a commercial monopoly in peyotes for the whole United States, practically.
About forty miles east of Laredo and four miles from the Texas-Mexican Railway, is an ancient Mexican town of about fifteen families, called Los Ojuelos. It has a graveyard larger than the town itself. It is located close to the edge of some rough, rocky graveled hills, on which these peyotes grow wild; none are cultivated anywhere. They grow wild under the shelter of a bush on these rocky ledges.
[…]
The Mexicans who gather the plant do not pull it up by the roots, but merely cut off the tops, leaving the potato itself in the ground. The top part of this potato then rots. The lower roots then grow and three or four peyotes often thereby appear where there originally was but one. It requires from one to two months’ time properly to dry these peyote tops for the market.
In this village, Los Ojuelos, are two small stores run by V. Laurel and Bro., and the other by Gayetasio Ochoa, the latter being postmaster. The villagers gather these peyotes and turn them into these two stores for supplies, getting about $2.50 a thousand for them. An industrious worker can not gather more than two hundred per day.

 

Modern workers appear to be able to harvest faster.

It used to be you’d go out for a couple of hours and you’d find 500 to 1,000 plants,” he said. “Now, you go out for six hours and you don’t come back with much.
Mauro Morales in Roebuck 2004.

In three hours his two brothers gathered about five potato sacks, some 4000 buttons in all.”
De Cordoba 2004 speaking of his time with Salvador Johnson.

 

Some statistics from the Texas Department of Public Safety (DPS)

Year

# of Buttons

Reported Sold

Total Sales

($US)

Price per Thousand

($US)

Notes

1986 1,913,212 $149,307.52 $ 78
1987 1,766,409 $137,046.30 $ 78
1988 1,575,766 $129,051.01 $ 82
1989 1,572,102 $129,619.62 $ 82
1990 1,772,126 $156.607.29 $ 88
1991 1,859,189 $182,544.02 $ 97
1992 1,886,434 $192,695.25 $102
1993 No data. No data. na [data from DPS in 2005]
1993 1,978,646 $210,247.60 $106 [data from DPS in 2011]
1994 No data. No data. na [data from DPS in 2005]
1994 2,184,739 $246,632.94 $113 [data from DPS in 2011]
1995 No data. No data. na [data from DPS in 2005]
1995 2,252,174 $234,750.20 $104 [data from DPS in 2011]
1996 2,258,993 $278,579.50 $123
1997 2,317,380 $274,500.62 $118
1998 2,076,167 $277,119.71 $133
1999 2,093,335 $335,823.02 $160
2000 2,057,020 $310,722.10 $151
2001 1,934,600 $360,676.00 $186
2002 1,820,847 $422,289.50 $232 [data from DPS in 2005]
2002 1,703,914 $404,859.50 $237 [data from DPS in 2011]
2003 1,779,170 $416,727.00 $234 [data from DPS in 2005]
2003 1,781,170 $416,727.00 $234 [data from DPS in 2011]
2004 1,658,195 $393,572.50 $237 [data from DPS in 2005]
2004 1,304,691 $304,002.50 $237 [data from DPS in 2006]
2004 1,669,806 $393,572.50 $236 [data from DPS in 2011]
2005 1,565,534 $407,789.50 $260
2006 1,619,115 $463,714.75 $286
2007 1,605,345 $474,321.80 $296
2008 1,475,469 $463,148.00 $314
2009 1,604,623 $493,834.00 $308
2010 1,483,697 $459,699.00 $310
2011 1,413,846 $466,590.50 $330
2012 1,106,209 $434,609.00 $393
2013 1,363,978 $530,230.00 $389
2014 1,128,787 $426,300.00 $378

The above reflects the reported activities of the licensed distributors (and their employees) based on figures provided by the Texas Department of Public Safety (DPS).

There are presently three peyote distributors and this has been true since 2006. Four licensed peyote dealers were still in operation in 2003-2005. Prior to that there were five and before that there were more. I have heard that a fourth has submitted her paperwork to DPS.

It is an interesting point of clarity that the licensed distributors who sell peyote prefer to be called “peyote dealers” rather than peyoteros.

Math in the fourth column is mine so any mistakes there are mine.

The late 1990s is when the average size plummeted for the buttons showing up in NAC meetings in central Texas. In the late 1990s sacks of Mexican peyote became more common.

 

It is very easy to see that a lot more peyote populations exist in Mexico than are inside of the USA.

The distribution of Lophophora williamsii

map-Anderson-Koehres

The suggested distribution of peyote
Composite map created from Anderson1980 & Koehres

Concerning this map:
It is important to be aware that peyote grows only in soils that are acceptable to it. This is true within any region it occurs, and therefore this map suggests there is a far more substantial distribution and many more populations than really exist (or have ever existed) within the shaded zones.

Anderson created this map by placing the reported herbarium collections, some of which are now known to be erroneous, as dots on a map and then drawing a line encircling them all.
For those reasons reason it is extremely doubtful that any peyote actually lives within large sections of the indicated areas. To put it another way, the presence of a solidly shaded area does not imply a continuous peyote population anywhere within it. It certainly does not indicate a lawn of Lophophora.

Koehres created his map similarly but incorporates his own field information which is superior to that of Anderson.

 

How difficult is peyote to grow?

It is easy to find it said that peyote is difficult or even impossible to grow.

After interviewing peyoteros in 1988 John Morthland wrote,

Indeed, peyote is almost impossible to cultivate. Once a seed germinates, the plant takes five years to grow big enough for picking, and the root of a harvested peyote takes nearly that long to bloom again.

 

Morthland’s “almost impossible” estimates are actually optimistic despite being shorter than reality. A professional cactus cultivator would consider them to be more typical than impossible and would simply take those numbers in stride in his or her production planning.
The reality is that peyote is among the easiest and the most forgiving of the cactus species to grow from seed.

Peyote, like any other cactus species, is fairly slow growing which is why what is developing contains the elements of a crisis-in-the-making. After cultivation begins in a meaningful way, more than a decade can be expected to elapse prior to the first acceptable harvest.

The widely circulated meme that cultivation is somehow either a difficult challenge or an absolute impossibility is probably just simple propaganda that conveniently serves licensed distributors, law enforcement and the powers-that-be alike.
Cactus cultivators have not reported similar results as the image of what is largely Lophophora diffusa in the next photograph should illustrate. These seedlings shown below are growing in Prague.

 

diffusa-in-prague

It is also surprisingly common to find it said that peyote cannot be cultivated anywhere outside of its natural ranges. People like Leo Mercado who, in theory, have proved this to be in error have actually proven just how right Voltaire was when saying:

It is dangerous to be right in matters on which the established authorities are wrong.”

At least, we now understand WHY peyote cultivation is considered to be impossible: not because of any technical issues but rather because the federal, state and/or local police will come and destroy the peyote plants if they learn of their existence.

The Peyote Foundation 1998

The Peyote Foundation 1998

Leo’s “impossible” shade house in 1998.
Taken with Leo’s permission from their newsletter

 

That is only the beginning of this story as it is clear that the cultivation of peyote is easy. Cultivation of someone else’s spiritual sacrament, however, rapidly becomes a quite different subject altogether.
The one very significant hurdle for the cultivation of peyote is a lack of acceptance by more than a relatively few members of the NAC.

This will be explored in more detail when this commentary continues.

 

More is still to come with part 2.

 

Related Reading Off-Site – Cactus Conservation Institute’s website

 

Additional Related Reading Off-Site – Edward Anderson’s thoughts on the Peyote Crisis.

 

Pereskiopsis

Pereskiopsis Britton & Rose

Pereskiopsis-porterii-MG

Pereskiopsis porterii from Mesa Garden

 

 

~10 spp. of trees and shrubs from Mexico and Central America.

They are cacti but have thick leaves which are broad and flat.
And, areoles with glochids.
Yellow to red flowers. Lateral, mostly sessile, rotate. Ovary is
leafy.

Umbilicate fruit has a few bony seeds, covered with matted hairs.
Allied to Opuntias but more similar in habit and foliage to Pereskia.
Hortus Third page. 846

The fruit are Opuntia-like, and those of some Mexican species are said to be eaten by cattle during the dry season. Safford mentions that the hair covered seeds are an easy way to distinguish these from the similar Pereskia. Safford 1908. [Pereskia spp. lack glochids & hair.]

Sometimes this is spelled Peireskiopsis. Many authors use this spelling in spite of its potential conflict with the Code of Nomenclature. Some have claimed that the Code has been specifically amended to allow this.

See also Backeberg 1958, pages 130-136 and Britton & Rose 1919; 1: 25-30

Most species apparently lack analysis.

Pereskiopsis-Lophophora-graft-01

Many growers use Pereskiopsis as grafting stock to graft young seedlings or small cuttings until they get large enough to be regrafted onto a larger sized stock or their own roots. They are also used to decrease the time required for seed production due to their ability to accelerate the growth rate of their scions.

The tiny glochids do require a little care in handling but they are valuable tools for plant propagation & cactus conservation.

My thanks to Cactus Conservation for letting me use these two images!

 Pereskiopsis-Lophophora-graft-02

Pereskiopsis scandens Britton & Rose

Now considered a synonym of Pereskiopsis kellermanii Rose (1908) Smithsonian Miscellaneous Collections, 50 (4): 332.

Or

Grusonia kellermanii ( Rose ) G.D.Rowley Tephrocactus Study Group, 12(3): 42. 2006.

 

Mescaline is present in trace amounts.

 [An image is presently unavailable to me but LOTS of them exist at Google Images under Pereskiopsis kellermanii.]

Etymology: scandens is in reference to its apparent “climbing” habit due to sprawling across shrubbery (“scandent”).
kellermanii was named for botanist William Ashbrook Kellerman who collected the species.

Distribution & occurrence: Occurs in Yucatan, Izamal and Merida in Mexico. Kellerman collected P. kellermannii in Guatamala.

Original description:
“Stems glabrous, herbaceous, weak and clambering over shrubs,about 2 cm. in diameter ; second year’s branches with cherry-colored bark; old stem spineless (?) ; young branches spineless or with a single short spine ; glochids numerous, brownish ; leaves glabrous, orbicular to ovate, 3 cm. long by 2 to 2.5 cm. broad, acute; flowers not seen ; fruit red, glabrous, leafy, 6 cm. long ; seeds covered with matted hairs.
Collected by W. A. Kellerman at Trapichite, Guatemala, January 1, 1907 (no. 6025).
Type in U. S. National Museum, no. 575,464.”
p. 332 in Britton & Rose 1908.

Backeberg 1977: page 408:
Clambering shrub to 10 meter tall. Stems are grey in color, round in cross section and smooth.
Leaves are smooth, tapering and ovate; up to 2 cm in length.
1 short (5 mm) spine is borne from the woolly white areoles.
They bear brown glochids.
Yellow flowers form slender, more or less tubercled, fruit which mature slowly and contain few seeds.

 

Reported analysis:

Using tlc and GC:
3,4-Dimethoxy-β-phenethylamine observed at 0.0029% in the dry plant.
Mescaline was found as 0.0022% of the dry plant material. (440 mg. per 2 kg. dry wt.; ~20+ lb. fresh?)
Using tlc, Tyramine was found to be also present.
Doetsch et al. 1980

Despite the low value it might be suggested that this and additional species be looked at more closely with an eye to alkaloid concentrations in the plant’s various tissues and possible seasonal fluctuations.

Abbreviations used in Sacred Cacti

A simple listing of the technical abbreviations used in the 4th edition

µm = micrometer = micron

ml = milliliter

Å = angstrom

MLD = minimum lethal dose reported in literature

BCE = before current era

mM = milliMolar

BP = before present

mm = millimeter

bp= boiling point

mmp = mixed melting point

cm = centimeter

mp = melting point

dec. = with decomposition

ms = mass spectroscopy

dm = decimeter (10 cm.)

na = not available/applicable

et al. = et alia (“& others”)

nd = not detected

f = forma

nm = nanometer

ft = foot

nn = nomen nudum (named but lacking any description)

gc = gas chromatography

RT = room temperature

gm = gram

sc = subcutaneous

in = inch

sn = sine numero(lacking a collection number)

im = intramuscular

sp = species (singular)

ip = intraperitoneal

spp = species (plural)

ir = infrared

ssp = subspecies

iv = intravenous

subsp = subspecies

kg = kilogram

TD = toxic dose

kV = kilovolt

TLC = thin-layer chromatography

LD100 = lethal dose 100%

uv = ultraviolet

LD50 = lethal dose 50%

v = volt

mm = millimicron (= nm)

var = variety

m = meter

X = indicates a hybrid

ma = milliamp

MAO = monoamine oxidase

MAOI = mao inhibitor

 

 

Chemical synonyms crosslisting

including compound index, pharmaceutical names, chemical formula, Chemical Abstract Registry numbers, NIOSH numbers & MW.

Names followed by the word “structure” lack an entry but include a structural diagram and/or their chemical formula. Iodides do not occur in cacti. Formation of the iodide is how the quaternary alkaloids are most often isolated from cacti.

Links to the actual compound entries have not yet been completed. All of the entries can be found in the PDF of the book The Cactus Alkaloids.

α-(3,4-dihydroxyphenyl)-β-aminoethane. See as Dopamine
α-(3,4-dihydroxyphenyl)-α-hydroxy-β-dimethylaminoethane. See as
N-Methyladrenaline
α-(3,4-dihydroxyphenyl)-2-dimethylaminoethanol. See as
N-Methyladrenaline
α-(4-hydroxyphenyl)-β-aminoethane. See as Tyramine
α-(Aminomethyl)-3,4,5-trimethoxybenzenemethanol. See as
β-Hydroxymescaline
α-(Aminomethyl)-3,4-dihydroxybenzyl alcohol. See as Norepinephrine
α-(Aminomethyl)-4-hydroxy-3-methoxybenzenemethanol. Normetanephrine
α-(Aminomethyl)-vanillyl alcohol. Normetanephrine
α-Desoxyadrenaline. See as Epinine
α-(Dimethylaminomethyl)-3,4-dihydroxybenzyl alcohol. See as
N-Methyladrenaline
α-(Dimethylaminomethyl)proto-catechuyl alcohol. See as
N-Methyladrenaline
α-(Methylaminomethyl)-vanillyl alcohol. See as Metanephrine
α-[(Dimethylamino)methyl]-3,4-dimethoxybenzenemethanol. See as
Macromerine
α-[(Dimethylamino)methyl]benzenemethanol. See as Ubine
α-[(Dimethylamino)methyl]benzyl alcohol. See as Ubine
α-[(Dimethylamino)methyl]veratryl alcohol. See as Macromerine
α-[(Methylamino)methyl]vanillyl alcohol. See as Metanephrine
β-Aminoethylbenzen(e). See as Phenethylamine
β-Hydroxy-3,4,5-trimethoxyphenethylamine. See as β-Hydroxymescaline
β-Hydroxy-3,4-dihydroxy-N-methylphenethylamine. See as Epinephrine.
β-Hydroxy-3,4-dihydroxyphenethylamine. See as Norepinephrine.
β-Hydroxy-3,4-dimethoxy-N-methylphenethylamine. See as Normacromerine
β-Hydroxy-3-methoxy-N,N-dimethyltyramine. See as
N-Methyl-metanephrine
β-Hydroxy-4-methoxy-N,N-dimethylphenethylamine. See as
N,N-Dimethyl-4-methoxy-β-hydroxyphenethylamine
β-Hydroxy-4-methoxy-N-methylphenethylamine. See as
N-Methyl-4-methoxy-β-hydroxyphenethylamine
β-Hydroxy-4-methoxyphenethylamine. See as
4-Methoxy-β-hydroxyphenethylamine
β-Hydroxy-N,N-dimethyl-DMPEA. See as Macromerine
β-Hydroxy-N,N-dimethylphenethylamine. See as Ubine
β-Hydroxy-N-methyl-3,4-dimethoxyphenethylamine. See as Normacromerine
β-Hydroxy-N-methyl-4-hydroxyphenethylamine. See as
Synephrine  
β-Methoxy-dehydroxycandicine. See as Coryphanthine
β-Methoxy-N,N,N-trimethylphenethylamine. See as Coryphanthine
β-Methylamino-a(4-hydroxyphenyl)ethyl alcohol. See as Synephrine
β-O-Methylmacromerine. See as
β-Methoxy-3,4-dimethoxy-N,N-dimethylphenethylamine
β-O-Methylnormacromerine. See as
β-Methoxy-3,4-dimethoxy-N-methylphenethylamine
β-Phenethylamine. See as Phenethylamine
β-Phenethyldimethylamine. See as N,N-Dimethylphenethylamine
β-Phenethylmethylamine. See as N-Methylphenethylamine
b,4-Dihydroxy-3-methoxy-N-methylphenethylamine. See as Metanephrine
b,4-Dihydroxyphenethylamine. See as Octopamine
?-Hydroxy-?-trimethoxy-2-methyl-isoquinoline. See as  ?
Mono-OH-tri-MeO-2-Methyl-isoquinoline
?-Mono-Methoxy-1-Methyl-THIQ. See as  ?-Methoxy-1-methyl-THIQ
1-(β-3’,4’,5’-Trimethoxyphenethyl)-pyrrole-2-carboxylic acid. See as
Peyonine
1-(3,4-dihydroxyphenyl)-2-aminoethanol. See as Norepinephrine
1-(4-Hydroxy-3-methoxyphenyl)-2-aminoethanol. Normetanephrine
1-(4-Hydroxy-3-methoxyphenyl)-2-methylaminoethanol. See as
Metanephrine
1-(4-Hydroxyphenyl)-2-methylaminoethanol. See as Synephrine
1-(Dimethylamino)-2-(4-hydroxyphenyl)ethane. See as Hordenine
1,2,3,4-Tetradehydropachycereine. See as Isopachycereine
1,2,3,4-tetrahydro-1-isobutyl-6-methoxy-2-methylisoquinolin-7-ol.
See as Lophocerine
1,2,3,4-Tetrahydro-2-methyl-4,8-isoquinolinediol. See as
Longimammamine
1,2,3,4-Tetrahydro-4,8-dihydroxy-2-methylisoquinoline. See as
Longimammamine
1,2,3,4-Tetrahydro-5,6,7,8-tetramethoxy-1,2-dimethylisoquinoline.
See as N-Methylpachycereine
1,2,3,4-Tetrahydro-5,6,7,8-tetramethoxy-1-methylisoquinoline. See as
Pachycereine
1,2,3,4-Tetrahydro-5,6,7,8-Tetramethoxy-2-methylisoquinoline. See as
Weberine
1,2,3,4-Tetrahydro-5,6,7,8-tetramethoxyisoquinoline. See as
Norweberine
1,2,3,4-Tetrahydro-5,6,7-trimethoxy-2-methylisoquinoline. See as
Tehuanine
1,2,3,4-Tetrahydro-5,6,7-trimethoxy-isoquinoline. See as Nortehuanine
1,2,3,4-Tetrahydro-5-hydroxy-6,7-dimethoxy-1,2-dimethylisoquinoline.
See as Gigantine
1,2,3,4-Tetrahydro-5-methoxy-2-methyl-7-isoquinolinol. See as Uberine
1,2,3,4-Tetrahydro-6,7,8-trimethoxy-1-methyl-1-isoquinolinecarboxylic
acid. See as O-Methylpeyoruvic acid. See as O- Methylpeyoxylic acid
1,2,3,4-Tetrahydro-6,7,8-trimethoxy-1-methyl-isoquinoline. See as
O-Methylanhalonidine
1,2,3,4-Tetrahydro-6,7,8-trimethoxy-2-methylisoquinoline. See as
N-Methylanhalinine
1,2,3,4-Tetrahydro-6,7,8-trimethoxy-2-methyl-isoquinoline. See as
O-Methylanhalidine
1,2,3,4-Tetrahydro-6,7,8-trimethoxy-isoquinoline. See as Anhalinine
1,2,3,4-Tetrahydro-6,7,8-trimethoxy-N-methyl-isoquinoline. See as
O-Methylanhalidine
1,2,3,4-Tetrahydro-6,7-dimethoxy-1,2-dimethyl-5-isoquinolinol. See
as Gigantine
1,2,3,4-Tetrahydro-6,7-dimethoxy-1,2-dimethyl-8-isoquinolinol. See
as Pellotine
1,2,3,4-Tetrahydro-6,7-dimethoxy-1,2-dimethylisoquinoline. See as
Carnegine
1,2,3,4-Tetrahydro-6,7-dimethoxy-1-methyl-8-isoquinolinol. See as
Anhalonidine
1,2,3,4-Tetrahydro-6,7-dimethoxy-1-methyl-8-methoxy-isoquinoline.
See as O-Methylanhalonidine
1,2,3,4-Tetrahydro-6,7-dimethoxy-1-methyl-isoquinoline. See as
Salsolidine
1,2,3,4-Tetrahydro-6,7-dimethoxy-2-methyl-8-isoquinolinol. See as
Anhalidine
1,2,3,4-Tetrahydro-6,7-dimethoxy-2-methylisoquinoline. See as
N-Methylheliamine
1,2,3,4-Tetrahydro-6,7-dimethoxy-8-isoquinolinol. See as Anhalamine
1,2,3,4-Tetrahydro-6,7-dimethoxyisoquinoline. See as Heliamine
1,2,3,4-Tetrahydro-6,7-dimethoxy-N-methyl-8-methoxy-isoquinoline.
See as O-Methylanhalidine
1,2,3,4-Tetrahydro-6-hydroxy-2-methylisoquinoline. See as
Longimammosine
1,2,3,4-Tetrahydro-6-hydroxy-7,8-dimethoxy-1,2-dimethylisoquinoline.
See as Isopellotine
1,2,3,4-Tetrahydro-6-hydroxy-7,8-dimethoxy-1-methylisoquinoline. See
as Isoanhalonidine
1,2,3,4-Tetrahydro-6-hydroxy-7,8-dimethoxy-2-methylisoquinoline. See
as Isoanhalidine
1,2,3,4-Tetrahydro-6-hydroxy-7-methoxy-1-methylisoquinoline. See as
Salsoline
1,2,3,4-Tetrahydro-6-methoxy-1,2-dimethyl-7,8-methylenedioxyisoquinoline.
See as Lophophorine
1,2,3,4-Tetrahydro-6-methoxy-1,2-dimethyl-7-isoquinolinol. See as
N-Methylisosalsoline
1,2,3,4-Tetrahydro-6-methoxy-1-methyl-7-isoquinolinol. See as
Isosalsoline
1,2,3,4-Tetrahydro-6-methoxy-2-methyl-1-(2-methyl-propyl)-7-isoquinolinol.
See as Lophocerine
1,2,3,4-Tetrahydro-6-methoxyisoquinoline. See as Longimammatine
1,2,3,4-Tetrahydro-6-methoxy-N-methyl-7-isoquinolinol. See as
Corypalline
1,2,3,4-Tetrahydro-7,8-dimethoxy-1,2-dimethyl-6-isoquinolinol. See
as Isopellotine
1,2,3,4-Tetrahydro-7,8-dimethoxy-1,2-dimethylisoquinoline. See as
Tepenine
1,2,3,4-Tetrahydro-7,8-dimethoxy-1-methyl-6-isoquinolinol. See as
Isoanhalonidine
1,2,3,4-Tetrahydro-7,8-dimethoxy-2-methyl-6-isoquinolinol. See as
Isoanhalidine
1,2,3,4-Tetrahydro-7,8-dimethoxyisoquinoline. See as Lemaireocereine
1,2,3,4-Tetrahydro-7-hydroxy-1-isobutyl-6-methoxy-2-methylisoquinoline.
See as Lophocerine
1,2,3,4-Tetrahydro-7-hydroxy-5-methoxy-2-methylisoquinoline. See as
Uberine
1,2,3,4-Tetrahydro-7-hydroxy-6-methoxy-1,2-dimethylisoquinoline. See
as N-Methylisosalsoline
1,2,3,4-Tetrahydro-7-hydroxy-6-methoxy-1-methylisoquinoline. See as
Isosalsoline
1,2,3,4-Tetrahydro-7-methoxy-1-methyl-6-isoquinolinol. See as
Salsoline
1,2,3,4-Tetrahydro-7-methoxy-1-methyl-8-isoquinolinol. See as
Arizonine
1,2,3,4-Tetrahydro-7-methoxyisoquinoline. See as Weberidine
1,2,3,4-Tetrahydro-8-hydroxy-2-methylisoquinoline. See as
Longimammidine
1,2,3,4-Tetrahydro-8-hydroxy-6,7-dimethoxy-1-methyl-1-isoquinolinecarboxylic
acid. See as Peyoruvic acid. See as Peyoxylic acid
1,2,3,4-Tetrahydro-8-hydroxy-6,7-dimethoxy-1-methylisoquinoline. See
as Anhalonidine
1,2,3,4-Tetrahydro-8-hydroxy-6,7-dimethoxy-2-methylisoquinoline. See
as Anhalidine
1,2,3,4-Tetrahydro-8-hydroxy-7-methoxy-1-methylisoquinoline. See as
Arizonine
1,2,3,4-Tetrahydro-ar-hydroxy-ar-trimethoxy-2-methylisoquinoline.
See as  ? Mono-OH-tri-MeO-2-Methyl-isoquinoline
1,2,3,4-Tetrahydro-ar-methoxy-1-methylisoquinoline. See as
?-Methoxy-1-methyl-THIQ
1,2,3,6a,7,8,9,12α-Octahydro-5,11-dimethoxy-1,7-dimethyl-6a,12α-bis(2-methylpropyl)-6,12-dioxα-1,7-diazadibenzo[def,mno]chrysene.
See as Lophocine
1,2-Didehydropachycereine. See as Dehydropachycereine
1,2-Didehydrosalsolidine. See as Dehydrosalsolidine
1,2-Dimethyl-6,7,8-trimethoxytetrahydroisoquinoline. See as
O-Methylpellotine
1,2-Dimethyl-6,7-dimethoxy-8-hydroxy-1,2,3,4-tetrahydroisoquinoline.
See as Pellotine
1,2-Dimethyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner
salt, 146
1-[2-(3,4,5-Trimethoxyphenyl)ethyl]-1H-pyrrole-2-carboxylic acid.
See as Peyonine
1-[2-(3,4,5-Trimethoxyphenyl)ethyl]-2,5-pyrrolidine-dione. See as
Mescaline succinamide
1-[2-(3,4,5-Trimethoxyphenyl)ethyl]-3,4-didehydro-2,5-pyrrolidine-dione.
See as Mescaline maleimide
1-[2-(3,4,5-Trimethoxyphenyl)ethyl]-3-hydroxy-2,5-pyrrolidine-dione.
See as Mescaline malimide
1-Amino-2-phenylethane. See as Phenethylamine
1-Demethyl-O-methyl-pellotine. See as O-Methylanhalidine
1-Hydroxy-8-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline. See as
Arizonine
1-Hydroxymethyl-2-methyl-5-β-O-glucosyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline.
See as Pterocereine
1-Hydroxymethyl-2-methyl-5-hydroxy-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline.
See as Deglucopterocereine
1-Hydroxymethyl-2-methyl-5-hydroxy-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-N-oxide.
See as Deglucopterocereine-N-oxide
1-Hydroxymethyl-2-methyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-5-β-O-glucopyranoside.
See as Pterocereine
1-i-Butyl-7-hydroxy-6-methoxy-2-methyl-THIQ. See as Lophocerine
1-iso-Butyl-1,2,3,4-tetrahydro-7-hydroxy-6-methoxy-2-methylisoquinoline.
See as Lophocerine
1-isobutyl-2-methyl-6-methoxy-7-hydroxy-1,2,3,4-tetrahydroisoquinoline.
See as Lophocerine
1-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline, 137
1-Methyl-6-methoxy-7,8-methylenedioxy-1,2,3,4-tetrahydroisoquinoline.
See as Anhalonine
1-Methylcorypalline. See as N-Methylisosalsoline
1-OH-8-MeO-2-Me-THIQ. See as Arizonine
2-(3,4,5-Trimethoxy-phenyl)-ethylamin(e). See as Mescaline
2-(3,4-Dihydroxyphenyl)ethylamine. See as Dopamine
2-(4-Methoxyphenyl)ethylamine. See as 4-Methoxyphenethylamine
2-(Methylamino)ethylbenzene. See as N-Methylphenethylamine
2-(p-Hydroxyphenyl)-ethylamine. See as Tyramine
2-Amino-1-(3,4,5-trimethoxyphenyl)ethanol. See as β-Hydroxymescaline
2-Amino-1-(3,4-dihydroxyphenyl)ethanol. See as Norepinephrine
2-Chloro-3,4,5-trimethoxyphenethylamine. See as 2-Chloro-mescaline
2-Dimethylamino-1-phenylethanol. See as Ubine
2-Ethyl-6-methoxy-7,8-methylenedioxy-1-methyl-THIQ. See as
Peyophorine
2-Methyl-5,6,7-trimethoxy-1,2,3,4-tetrahydroisoquinoline. See as
Tehuanine
2-Methyl-6,7,8-trimethoxy-THIQ. See as O-Methylanhalidine
2-Methyl-6,7-dimethoxy-1,2,3,4-tetrahydro-8-isoquinolinol. See as
Anhalidine
2-Phenethylamine. See as Phenethylamine
2-p-Hydroxyphenylethylamine. See as Tyramine
3,4 dm PEA. See as 3,4-Dimethoxyphenethylamine
3,4,5-Trihydroxyphenethylamine, 64
3,4,5-Trimethoxy-β-phenethylamine. See as Mescaline
3,4,5-Trimethoxybenzeneethanamine. See as Mescaline
3,4,5-Trimethoxy-benzolethanamin. See as Mescaline
3,4,5-Trimethoxy-N-methylphenethylamine. See as N-Methylmescaline
3,4,5-Trimethoxyphenethylamine. See as Mescaline
3,4,5-trimethoxyphenethylglycine. See as as
3,4,5-trimethoxyphenylalanine
3,4,5-Trimethoxy-phenethyl-N,N,N-trimethylammonium hydroxide, 101
3,4,5-trimethoxyphenylalanine, 102
3,4-Didehydro-N-(3,4,5-trimethoxyphenyl)-succinamide. See as
Mescaline maleimide
3,4-Dihydro-5,6,7,8-tetramethoxy-1-methylisoquinoline. See as
Dehydropachycereine
3,4-Dihydro-5,6,7,8-tetramethoxydihydroisoquinoline. See as
Dehydronorweberine
3,4-Dihydro-5,6,7,8-tetramethoxyisoquinoline. See as
Dehydronorweberine
3,4-Dihydro-6,7-dimethoxy-1-methyl-8-isoquinolinol. See as
1-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
3,4-Dihydro-6,7-dimethoxy-1-methylisoquinoline. See as
Dehydrosalsolidine
3,4-Dihydro-6,7-dimethoxy-8-isoquinolinol. See as
6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
3,4-Dihydro-6,7-dimethoxyisoquinoline. See as Dehydroheliamine
3,4-Dihydro-7,8-dimethoxyisoquinoline. See as Dehydrolemaireocereine
3,4-Dihydro-8-hydroxy-6,7-dihydroisoquinolinium inner salt. See as
6,7-Dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner salt
3,4-Dihydro-8-hydroxy-6,7-dimethoxy-1,2-dimethylisoquinolinium inner
salt. See as
1,2-Dimethyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner
salt
3,4-Dihydro-8-hydroxy-6,7-dimethoxy-1-methylisoquinoline. See as
1-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
3,4-Dihydro-8-hydroxy-6,7-dimethoxy-1-methylisoquinolinium inner
salt. See as 1-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
3,4-Dihydro-8-hydroxy-6,7-dimethoxy-2-methylisoquinolinium inner
salt. See as 2-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium
inner salt
3,4-Dihydro-8-hydroxy-6,7-dimethoxyisoquinoline. See as
6,7-Dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
3,4-Dihydro-ar-trimethoxy-1-methylisoquinoline. See as  ?
Tri-MeO-1-Methyl-1,2,3,4-tetrahydro-isoquinoline
3,4-Dihydronorephedrine. See as Norepinephrine
3,4-Dihydroxy-α-[(methylamino)methyl]benzyl alcohol. See as
Epinephrine.
3,4-Dihydroxy-β-hydroxy-N-methylphenethylamine. See as Epinephrine.
3,4-Dihydroxy-β-hydroxyphenethylamine. See as Norepinephrine.
3,4-Dihydroxy-N,N,N-trimethylphenethylamine. See as Coryneine
3,4-Dihydroxy-N-methylphenethylamine. See as Epinine
3,4-Dihydroxyphenethylamine. See as Dopamine
3,4-Dihydroxy-phenethyl-trimethyl-ammonium cation. See as Coryneine
3,4-Dimethoxy-α-[(dimethylamino)methyl]benzylalcohol. See as
Macromerine
3,4-Dimethoxy-β-phenethylamine. See as 3,4-Dimethoxyphenethylamine
3,4-Dimethoxy-5-hydroxyphenethylamine. See as
3-Hydroxy-4,5-dimethoxyphenethylamine
3,4-Dimethoxy-N,N,N-trimethylammonium phenethylamine. See as
Coryneine
3,4-Dimethoxy-N,N-dimethyl-β-hydroxyphenethylamine. See as
Macromerine
3,4-Dimethoxy-N-acetylphenylethylamine. See as N-Acetyl-DMPEA
3,4-Dimethyldopamine. See as 3,4-Dimethoxyphenethylamine
3,5-Dimethoxy-4-hydroxyphenethylamine. See as
4-Hydroxy-3,5-dimethoxyphenethylamine
3,5-Dimethoxytyramine. See as 4-Hydroxy-3,5-dimethoxyphenethylamine
3:4:5:Trimetossifenilethamina. See as Mescaline
3-Demethylmescaline. See as 3-Hydroxy-4,5-dimethoxyphenethylamine
3-Demethyltrichocereine. See as
N,N-Dimethyl-3-hydroxy-4,5-dimethoxyphenethylamine
3-Hydroxy-4,5-dimethoxy-N,N-dimethylphenethylamine. See as
N,N-Dimethyl-3-hydroxy-4,5-dimethoxyphenethylamine
3-Hydroxy-4,5-dimethoxy-N-methylphenethylamine. See as
N-Methyl-3-hydroxy-4,5-dimethoxyphenethylamine
3-Hydroxy-N-(3,4,5-Trimethoxyphenyl)succinamide. See as Mescaline
malimide
3-Hydroxytyramine. See as Dopamine
3-Methoxy-β-hydroxytyramine. Normetanephrine
3-Methoxy-4,5-dihydroxyphenethylamine. See as
3,4-Dihydroxy-5-methoxyphenethylamine
3-Methoxy-4-hydroxy-N,N-dimethylphenethylamine. See as
N,N-Dimethyl-3-methoxytyramine
3-Methoxy-4-hydroxy-N-methylphenethylamine. See as
N-Methyl-3-methoxytyramine
3-Methoxy-4-hydroxyphenethylamine. See as 3-Methoxytyramine
3-Methoxy-N,N-dimethyltyramine. See as N,N-Dimethyl-3-methoxytyramine
3-Methoxynoradrenaline. Normetanephrine
3-Methoxynorepinephrine. Normetanephrine
3-O-Methyladrenaline. See as Metanephrine
3-O-Methylarterenol. Normetanephrine. Normetanephrine
3-O-Methylepinephrine. See as Metanephrine
3-O-Methylnoradrenaline. Normetanephrine
3-O-Methylnorepinephrine. Normetanephrine
4-(β-Amino-α-hydroxyethyl)catechol. See as Norepinephrine
4-(β-Methylaminoethyl)catechol. See as Epinine
4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol. See as Norepinephrine
4-(2-Aminoethyl)-1,2-benzenediol. See as Dopamine
4-(2-Aminoethyl)phenol. See as Tyramine
4-(2-Aminoethyl)-pyrocatechol. See as Dopamine
4,β-Dihydroxy-3-methoxyphenethylamine. Normetanephrine
4,8-Dihydroxy-2-methyl-THIQ. See as Longimammamine
4,8-Dihydroxy-N-methyl-THIQ. See as Longimammamine
4-[2-(Dimethylamino)-1-hydroxyethyl]-1,2-benzenediol. See as
N-Methyladrenaline
4-[2-(Dimethylamino)ethyl]phenol. See as Hordenine
4-[2-(Methylamino)ethyl]-1,2-benzenediol. See as Epinine
4-[2-(Methylamino)ethyl]phenol. See as N-Methyltyramine
4-[2-(Methylamino)-ethyl]-pyrocatechol. See as Epinine
4-Demethylmescaline. See as 4-Hydroxy-3,5-dimethoxyphenethylamine
4-Hydroxy-α-[(methylamino)methyl]-benzenemethanol. See as Synephrine
4-Hydroxy-3-methoxy-α-(aminomethyl)benzyl alcohol. Normetanephrine
4-Hydroxy-3-methoxy-α-[(methylamino)methyl]benzenemethanol. See as
Metanephrine
4-Hydroxy-3-methoxy-N,N-dimethylphenethylamine. See as
N,N-Dimethyl-3-methoxytyramine
4-Hydroxy-3-methoxy-N-methylphenethylamine. See as
N-Methyl-3-methoxytyramine
4-Hydroxy-3-methoxyphenethylamine. See as 3-Methoxytyramine
4-Hydroxy-3-nitrophenethylamine. See as 3-Nitrotyramine
4-Hydroxy-6,7-dimethoxy-1,2-dimethyl-THIQ, 138
4-Hydroxy-N,N,N-trimethylphenethylamine. See as Candicine
4-Hydroxy-N,N-dimethylphenethylamine. See as Hordenine
4-Hydroxy-N-methylphenethylamine. See as N-Methyltyramine
4-Hydroxyphenethylamine. See as Tyramine
4-Methoxybenzeneethanamine. See as 4-Methoxyphenethylamine
4-Methoxy-N,N,N-trimethylphenethylamine. See as O-Methylcandicine
4-Methoxy-N,N-dimethylbenzeneethanamine. See as
N,N-Dimethyl-4-methoxyphenethylamine
4-Methoxy-N-methylbenzeneethanamine. See as
N-Methyl-4-methoxyphenethylamine
4-Methoxy-N-methylphenethylamine. See as
N-Methyl-4-methoxyphenethylamine
5-(2-Aminoethyl)-2-methoxyphenol. See as
3-Hydroxy-4-methoxyphenethylamine
5,6,7,8-Tetramethoxy-1,2-dimethyl-THIQ. See as N-Methylpachycereine
5,6,7,8-Tetramethoxy-1-methyl-3,4-dihydroisoquinoline. See as
Dehydropachycereine
5,6,7,8-Tetramethoxy-1-methylisoquinoline. See as Isopachycereine
5,6,7,8-Tetramethoxy-1-methyl-tetrahydroisoquinoline. See as
Pachycereine
5,6,7,8-Tetramethoxy-2-methyl-THIQ. See as Weberine
5,6,7,8-Tetramethoxy-dihydroisoquinoline. See as Dehydronorweberine
5,6,7,8-Tetramethoxyisoquinoline. See as Isonorweberine
5,6,7,8-Tetramethoxy-tetrahydroisoquinoline. See as Norweberine
5,6,7-Trimethoxy-2-methyl-THIQ. See as Tehuanine
5,6,7-Trimethoxy-dihydroisoquinoline. See as Dehydronortehuanine
5,6,7-Trimethoxy-isoquinoline. See as Isonortehuanine
5,6,7-Trimethoxy-THIQ. See as Nortehuanine
5-Hydroxy-3,4-dimethoxyphenethylamine. See as
3-Hydroxy-4,5-dimethoxyphenethylamine
5-Hydroxy-6,7-dimethoxy-1,2-dimethyl-THIQ. See as Gigantine
5-Hydroxycarnegine. See as Gigantine
5-Hydroxymethyl-1-[2-(3,4,5-trimethoxyphenyl)ethyl]-2-pyrrolecarboxaldehyde.
See as Peyoglunal
5-Methoxy-7-hydroxy-2-methyl-1,2,3,4-tetrahydroisoquinoline. See as
Uberine
5-Methylanhalonine. See as Lophophorine
6,7,8,9-Tetrahydro-4-methoxy-8,8,9-trimethyl-1,3-dioxolo[4,5-h]-isoquinolinium.
See as Lophotine
6,7,8,9-Tetrahydro-4-methoxy-8,9-dimethyl-1,3-dioxolo[4,5-h]isoquinoline.
See as Lophophorine
6,7,8,9-Tetrahydro-4-methoxy-9-methyl-1,3-dioxolo[4,5-h]isoquinoline.
See as Anhalonine
6,7,8-Trimethoxy-1,2,3,4-tetrahydroisoquinoline. See as Anhalinine
6,7,8-Trimethoxy-1,2-dimethyl-1,2,3,4-tetrahydroisoquinoline. See as
O-Methylpellotine
6,7,8-Trimethoxy-2-methyl-THIQ. See as O-Methylanhalidine
6,7,8-Trimethoxy-N-methyl-1,2,3,4-tetrahydro-isoquinoline. See as
O-Methylanhalidine
6,7-diMeO-1,2-diMe-THIQ. See as Carnegine
6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline. See as Heliamine
6,7-Dimethoxy-1,2-dimethyl-1,2,3,4-tetrahydroisoquinoline. See as
Carnegine
6,7-Dimethoxy-1,2-dimethyl-1,2,3,4-tetrahydroisoquinoline-8-ol. See
as Pellotine
6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline. See as
Salsolidine
6,7-Dimethoxy-1-methyl-dihydroisoquinoline. See as Dehydrosalsolidine
6,7-Dimethoxy-1-methyl-isoquinoline. See as Isosalsolidine
6,7-Dimethoxy-2-methyl-THIQ. See as N-Methylheliamine
6,7-Dimethoxy-3,4-dihydroisoquinoline. See as Dehydroheliamine
6,7-Dimethoxy-8-hydroxy-1,2,3,4-tetrahydroisoquinoline. See as
Anhalamine
6,7-Dimethoxy-8-hydroxy-1-methyl-1,2,3,4-tetrahydroisoquinoline. See
as Anhalonidine
6,7-Dimethoxy-isoquinoline. See as Backebergine
6,7-Dimethoxy-THIQ. See as Heliamine
6,7-Dimethyl-salsolinol. See as Salsolidine
6-Hydroxy-2-methyl-THIQ; 6-Hydroxy-N-methyl-THIQ. See as
Longimammosine
6-Hydroxy-7,8-dimethoxy-1,2-dimethyl-THIQ. See as Isopellotine
6-Hydroxy-7,8-dimethoxy-2-methyl-THIQ. See as Isoanhalidine
6-Hydroxy-7,8-dimethoxy-THIQ. See as Isoanhalamine
6-Hydroxy-7-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline. See as
Salsoline
6-Hydroxy-N-methyl-THIQ. See as Longimammidine
6-MeO-THIQ. See as Longimammatine
6-Methoxy-1,2,3,4-tetrahydroisoquinoline. See as Longimammatine
6-Methoxy-7,8-methylenedioxy-1,2-dimethyl-1,2,3,4-tetrahydroisoquinoline.
See as Lophophorine
6-Methoxy-7,8-methylenedioxy-1-methyl-2-ethyl-THIQ. See as
Peyophorine
6-Methyl-salsolinol. See as Isosalsoline
6-OH-2-Me-THIQ. See as Longimammosine
6-OH-7,8-diMeO-1-Me-THIQ. See as Isoanhalonidine
7,8-Dimethoxy-1,2-dimethyl-THIQ. See as Tepenine
7,8-Dimethoxy-1-methyl-6-hydroxytetrahydroisoquinolinol. See as
Isoanhalonidine
7,8-dimethoxy-2-methyl-1,2,3,4-tetrahydro-6-isoquinolinol. See as
Isoanhalidine
7,8-Dimethoxy-3,4-dihydroxyisoquinoline, 112
7,8-Dimethoxy-dihydroisoquinoline. See as Dehydrolemaireocereine
7,8-Dimethoxy-isoquinoline. See as Isobackebergine
7,8-Dimethoxy-THIQ. See as Lemaireocereine
7-Hydroxy-6-methoxy-1,2-dimethyl-THIQ. See as N-Methylisosalsoline
7-Hydroxy-6-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline. See as
Isosalsoline
7-Hydroxy-6-methoxy-2-methyl-THIQ. See as Corypalline
7-MeO-THIQ. See as Weberidine
7-Methoxy-1,2,3,4-tetrahydroisoquinoline. See as Weberidine
7-Methyl-salsolinol. See as Salsoline
7-OH-5-MeO-2-Me-THIQ. See as Uberine
7-OH-5-MeO-N-Me-THIQ. See as Uberine
7-OH-6-MeO-1,2-diMe-THIQ. See as N-Methylisosalsoline
8-Ethyl-6,7,8,9-tetrahydro-4-methoxy-9-methyl-1,3-dioxo[4,5-h]-isoquinoline.
See as Peyophorine
8-Hydroxy-2-methyl-THIQ. See as Longimammidine
8-Hydroxy-6,7-dimethoxy-1,2-dimethyl-1,2,3,4-tetrahydroisoquinoline.
See as Pellotine
8-Hydroxy-6,7-dimethoxy-2-methyl-THIQ. See as Anhalidine
Acordin. See as Synephrine
Adnephrin(e). See as Epinephrine
Adrenal. See as Epinephrine
Adrenalin. See as Epinephrine
Adrenalin(e). See as Epinephrine
Adrenaline. See as Epinephrine
adrenaline, Nor-. See as Norepinephrine
Adrenamine. See as Epinephrine
Adrenan. See as Epinephrine
Adrenapax. See as Epinephrine
Adrenasol. See as Epinephrine
Adrenatrate. See as Epinephrine
Adrenine. See as Epinephrine
Adrenodis. See as Epinephrine
Adrenohorma. See as Epinephrine
Adrenor. See as Norepinephrine
Adrenosan. See as Epinephrine
Adrenutol. See as Epinephrine
Adrin(e). See as Epinephrine
Aethahen. See as Synephrine
Aktamin. See as Norepinephrine
Analeptin. See as Synephrine
Andirine. See as N-Methyltyramine
Angeline. See as N-Methyltyramine
Anhalidine methiodide. See as Anhalotine (iodide)
Anhaline. See as Hordenine
Antiasthmatique. See as Epinephrine
Arterenol. See as Norepinephrine
Asmatane Mist. See as Epinephrine
Asthma Meter Mist. See as Epinephrine
Asthmα-Nefrin. See as Epinephrine
Astmahalin. See as Epinephrine
Astminhal. See as Epinephrine
Balmadren. See as Epinephrine
Benzeneethanamine. See as Phenethylamine
Bernarenin. See as Epinephrine
Binodrenal. See as Norepinephrine
Biorenine. See as Epinephrine
Bisnormacromerine. See as 3,4-Dimethoxy-β-hydroxyphenethylamine
Bosmin. See as Epinephrine
Brevirenin. See as Epinephrine
C10H12NO2. See as Longimammamine
C10H13NO. See as Longimammidine. See as Longimammosine. See as
Weberidine. See as Longimammatine
C10H15NO. See as N-Methyl-4-methoxyphenethylamine. See as Hordenine.
See as Hordenine. See as Ubine
C10H15NO2. See as 3,4-Dimethoxyphenethylamine. See as
N-Methyl-3-methoxytyramine
C10H15NO3. See as 3-Hydroxy-4,5-dimethoxyphenethylamine. See as
Metanephrine. See as N-Methyladrenaline
C11H11NO2. See as Isobackebergine. See as Backebergine
C11H13NO2. See as Dehydrolemaireocereine. See as Dehydroheliamine
C11H13NO3. See as 6,7-Dimethoxy-8-hydroxy-3,4- dihydroisoquinolinium
inner salt
C11H15NO. See as ?-Methoxy-1-methyl-THIQ
C11H15NO2. See as Corypalline. See as Uberine. See as Isosalsoline.
See as Salsoline. See as Lemaireocereine. See as Heliamine. See as
Arizonine
C11H15NO3. See as Isoanhalamine. See as Anhalamine. See as NAMT
C11H17NO. See as N,N-Dimethyl-4-methoxyphenethylamine
C11H17NO2. See as N,N-Dimethyl-3-methoxytyramine
C11H17NO3. See as Mescaline. See as
N-Methyl-3-hydroxy-4,5-dimethoxyphenethylamine. N-Methylmetanephrine.
See as Coryneine
C11H17NO4. See as β-Hydroxymescaline
C11H19NO2. See as Candicine
C12H15NO. See as N-Methylheliamine
C12H15NO2. See as Dehydrosalsolidine
C12H15NO3. See as Anhalonine. See as
2-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner salt.
See as 1-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
C12H15NO4. See as N-Formylanhalamine
C12H15NO5. See as Peyoxylic acid
C12H17NO2. See as N-Methylisosalsoline. See as Salsolidine. See as
N-Methylisosalsoline
C12H17NO3. See as Anhalidine. See as Isoanhalidine. See as
Anhalonidine. See as Isoanhalonidine. See as Nortehuanine. See as
Anhalinine. See as N-Acetyl DMPEA
C12H17NO4. See as N-Formylmescaline. See as
N-Acetyl-3-hydroxy-4,5-dimethoxyphenethylamine
C12H19NO3. See as N-Methylmescaline. See as
N,N-Dimethyl-3-hydroxy-4,5-dimethoxyphenethylamine. See as Macromerine
C12H20ClNO. See as O-Methylcandicine
C12H20NO+. See as O-Methylcandicine
C13H15NO3. See as ? Tri-MeO-1-Methyl-1,2-dihydro-isoquinoline
C13H15NO4. See as N-Formylanhalonine
C13H17NO3. See as O-Methylpeyoxylic acid. See as
1,2-Dimethyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner
salt. See as Lophophorine. See as ?
Tri-MeO-1-Methyl-1,2,3,4-tetrahydro-isoquinoline. See as
N,N-Dimethylmescaline
C13H17NO4. See as Dehydronorweberine. See as N-Formylanhalonidine.
See as N-Formylanhalinine. See as N-Acetylanhalamine
C13H17NO5. See as Peyoruvic acid
C13H17NO7. See as β-O-Methylsynephrine
C13H19NO2. See as Tepenine. See as Carnegine
C13H19NO3. See as Pellotine. See as Isopellotine. See as Gigantine.
See as Tehuanine. See as O-Methyl-anhalidine. See as
O-Methylanhalonidine. See as N-Methylanhalinine
C13H19NO4. See as Norweberine. See as Deglucopterocereine. See as
Tehuanine-N-oxide. See as N-Acetylmescaline
C13H19NO5. See as Deglucopterocereine-N-oxide. See as Mescaloxylic
acid
C13H20NO3I. See as Anhalotine. See as Anhalotine
C14H17NO4. See as Isopachycereine. See as N-Acetylanhalonine. See as
Peyoglutam. See as N-Acetyl-Anhalonine. See as Peyoglutam
C14H19NO3. See as Peyophorine
C14H19NO4. See as Dehydropachycereine. See as
N-Formyl-O-methylanhalonidine
C14H19NO5. See as O-Methylpeyoruvic acid
C14H20NO3+. See as Lophotine
C14H20NO3I. See as Lophotine
C14H21NO3. See as O-Methylpellotine
C14H21NO4. See as Weberine
C14H21NO5. See as Mescaloruvic acid
C14H22NO3I. See as Peyotine
C15H19NO4. See as Mescalotam. See as Mescalotam
C15H19NO5. See as Mescaline maleimide . See as Mescaline malimide .
See as Mescaline succinamide
C15H23NO2. See as Lophocerine
C15H23NO4. See as N-Methylpachycereine
C16H19NO5. See as Peyonine
C17H19NO7. See as Mescaline isocitrimide lactone
C17H21NO5. See as Peyoglunal
C17H21NO8. See as Mescaline citrimide
C19H25NO2. Normetanephrine
C19H29NO9. See as Pterocereine
C30H40N2O4. See as Lophocine
C45H65N3O6. See as Piloceredine. See as Pilocereine
C8H11N. See as N-Methylphenethylamine. See as Phenethylamine
C8H11NO. See as Tyramine
C8H11NO2. See as Dopamine. See as Octopamine
C8H11NO3. See as Norepinephrine
C9H13NO. See as 4-Methoxyphenethylamine. See as N-Methyltyramine
C9H13NO2. See as 3-Methoxytyramine. See as Epinine. See as Synephrine
C9H13NO3. See as 3,4-Dihydroxy-5-methoxyphenethylamine. See as
Epinephrine
CA Reg No.: 97-31-4. Normetanephrine
CA Reg. No.: 104-14-3. See as Octopamine
CA Reg. No.: 120-20-7. See as 3,4-Dimethoxyphenethylamine
CA Reg. No.: 138-65-8. Norepinephrine
CA Reg. No.: 14097-39-3. See as Longimammosine
CA Reg. No.: 14788-32-0. See as Longimammidine
CA Reg. No.: 149-95-1. Norepinephrine
CA Reg. No.: 16620-96-5. See as N-Methylheliamine
CA Reg. No.: 1745-06-8. See as Nortehuanine
CA Reg. No.: 1745-07-9. See as Heliamine
CA Reg. No.: 17627-77-9. See as Anhalonidine
CA Reg. No.: 19267-93-7. See as Anhalotine
CA Reg. No.: 19267-94-8. See as  Lophotine
CA Reg. No.: 19445-62-6. See as Anhalotine iodide
CA Reg. No.: 19485-63-3. See as Lophocerine
CA Reg. No.: 19717-25-0. See as Peyonine
CA Reg. No.: 2202-68-8. See as Ubine (racemic)
CA Reg. No.: 2245-94-5. See as Anhalidine
CA Reg. No.: 2552-47-8. See as Pilocereine
CA Reg. No.: 25526-36-7. See as Peyotine
CA Reg. No.: 29193-99-5. See as Peyoxylic acid
CA Reg. No.: 29194-00-1. See as Peyoruvic acid
CA Reg. No.: 30147-93-4. See as Tehuanine
CA Reg. No.: 31241-40-4. See as
1-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
CA Reg. No.: 3213-30-7. See as 3-Hydroxy-4-methoxyphenethylamine
CA Reg. No.: 32829-58-6. See as Gigantine
CA Reg. No.: 3382-18-1. See as Dehydroheliamine
CA Reg. No.: 34222-77-0. See as Longimammidine
CA Reg. No.: 34319-92-1. See as Tepenine
CA Reg. No.: 35048-35-2. See as N-Methylisosalsoline.
CA Reg. No.: 35646-08-3. See as O-Methylanhalonidine
CA Reg. No.: 35803-88-4. See as N-Methyl-4-methoxyphenethylamine
CA Reg. No.: 370-98-9. See as N-Methyltyramine
CA Reg. No.: 37484-64-3. See as Isoanhalidine
CA Reg. No.: 37484-65-4. See as Isoanhalonidine
CA Reg. No.: 37484-66-5. See as Isopellotine
CA Reg. No.: 38221-25-9. See as (S)-Carnegine
CA Reg. No.: 3851-33-0. See as Anhalonidine (±)-form
CA Reg. No.: 38520-68-2. See as Salsolidine
CA Reg. No.: 4091-50-3. See as N-Methyl-4-methoxyphenethylamine
CA Reg. No.: 411136-36-1. See as Normacromerine
CA Reg. No.: 41303-72-4. See as O-Methylpeyoruvic acid
CA Reg. No.: 41303-73-5. See as O- Methylpeyoxylic acid
CA Reg. No.: 42923-77-3. See as Longimammatine
CA Reg. No.: 43207-78-9. See as Weberidine
CA Reg. No.: 4593-89-9. See as N-Acetylmescaline
CA Reg. No.: 4593-97-9. See as Isosalsoline
CA Reg. No.: 4838-96-4. See as N-Methylmescaline
CA Reg. No.: 490-53-9. See as Carnegine
CA Reg. No.: 493-48-1. See as S-(-)-Salsolidine
CA Reg. No.: 4973-61-9. See as O-Methylpellotine
CA Reg. No.: 5001-33-2. See as Metanephrine
CA Reg. No.: 501-15-5. See as Epinine
CA Reg. No.: 51-41-2. Norepinephrine
CA Reg. No.: 51424-33-0. See as R-(+)-Salsoline
CA Reg. No.: 51-43-4. See as Epinephrine
CA Reg. No.: 51-61-6. See as Dopamine
CA Reg. No.: 51-67-2. See as Tyramine
CA Reg. No.: 51745-28-9. See as (R)- Carnegine
CA Reg. No.: 52759-08-7. See as Lemaireocereine
CA Reg. No.: 529-58-8. See as Anhalonidine R-(-)-form
CA Reg. No.: 529-91-9. See as N,N-Dimethylmescaline
CA Reg. No.: 5308-58-7. See as Isoanhalamine
CA Reg. No.: 54-04-6. See as Mescaline
CA Reg. No.: 54193-08-7. See as R-(+)-Salsolidine
CA Reg. No.: 55-81-2. See as 4-Methoxyphenethylamine
CA Reg. No.: 57196-60-8. See as Longimammosine
CA Reg. No.: 57196-62-0. See as Longimammatine
CA Reg. No.: 57236-57-4. See as Longimammamine
CA Reg. No.: 57286-92-7. See as Longimammidine
CA Reg. No.: 57286-93-8. See as
N-Methyl-4-methoxy-β-hydroxyphenethylamine
CA Reg. No.: 582-84-3. See as Longimammidine
CA Reg. No.: 60508-83-0. See as Arizonine
CA Reg. No.: 63596-58-7. See as Uberine
CA Reg. No.: 64-04-0. See as Phenethylamine
CA Reg. No.: 642-30-8. See as Anhalinine
CA Reg. No.: 643-60-7. See as Anhalamine
CA Reg. No.: 6853-14-1. See as Ubine
CA Reg. No.: 74046-24-5. See as Weberine
CA Reg. No.: 74046-25-6. See as N-Methylpachycereine
CA Reg. No.: 74991-76-7. See as Lophocine
CA Reg. No.: 775-33-7. See as N,N-Dimethyl-4-methoxyphenethylamine
CA Reg. No.: 82261-02-7. See as Dehydropachycereine
CA Reg. No.: 82261-04-9. See as Pachycereine
CA Reg. No.: 833-14-7. See as Pellotine
CA Reg. No.: 85769-25-1. See as Tehuanine-N-oxide
CA Reg. No.: 89-31-6. See as S-(-)-Salsoline
CA Reg. No.: 93474-27-2. See as Isopachycereine
CA Reg. No.: 939-45-7. See as Ubine hydrochloride (S-form)
CA Reg. No.:13079-18-0. See as β-Hydroxymescaline
CA Reg. No.:7738-40-1. See as Mescaloxylic acid
CA Reg. No.:7738-43-4. See as Mescaloruvic acid
CA Reg. No: 17627-78-0. See as Lophophorine
Calipamine. See as β-Methoxy-3,4-dimethoxy-N-methylphenethylamine
Cardiodynamin. See as Synephrine
Chelafrin. See as Epinephrine
Corazol. See as Synephrine
Corisol. See as Epinephrine
Corvasymtom. See as Synephrine
DA. See as Dopamine
Demethyltehuanine. See as Nortehuanine
Deoxyepinephrine. See as Epinine
Desoxyepinephrine. See as Epinine
Dihydroxyphenethylmethylamine. See as Epinine
Dimethoxyphenylethanolamine. See as
3,4-Dimethoxy-β-hydroxyphenethylamine
Dimethylaminomethyl-(3,4-dihydroxyphenyl) carbinol. See as
N-Methyladrenaline
Dimethylaminomethyl-3,4-dimethoxyphenyl-carbinol. See as Macromerine
DIMPEA. See as 3,4-Dimethoxyphenethylamine
DME. See as 3,4-Dimethoxy-β-hydroxyphenethylamine
DMP. See as 3,4-Dimethoxyphenethylamine
DMPA. See as 3,4-Dimethoxyphenethylamine
DMPE. See as 3,4-Dimethoxyphenethylamine
DMPEA. See as 3,4-Dimethoxyphenethylamine
Dopamine-3-methyl ether. See as 3-Methoxytyramine
Drenamist. See as Epinephrine
Dylephrin. See as Epinephrine
Dynatra. See as Dopamine
Dyspne-Inhal. See as Epinephrine
EΑ-1302. See as 3-Methoxyphenethylamine
EΑ-1306. See as Mescaline
Ephinine. See as Epinine
Epifrin. See as Epinephrine
Epine. See as Epinine
Epinefrina. See as Epinephrine
Epinephran. See as Epinephrine
Epinephrin. See as Epinephrine
Epinin. See as Epinine
Epinine dimethyl ether. See as 3,4-Dimethoxy-N-methylphenethylamine
Epirenamine. See as Epinephrine
Epirenan. See as Epinephrine
Epirenin. See as Epinephrine
Episcorb. See as Epinephrine
Epitrate. See as Epinephrine
Eppy. See as Epinephrine
Eremursine. See as Hordenine
Euvasol. See as Synephrine
Exadrin. See as Epinephrine
Glaucosan. See as Epinephrine
Glycirenan. See as Epinephrine
Goeffroyine. See as N-Methyltyramine
Gordenine. See as Hordenine
Haemostasin. See as Epinephrine
Haemostatin. See as Epinephrine
HAYWARD: 6{R(OM)}3RR(CCZ)R. See as Mescaline
Hayward: 6{R(OM)}3RYLLNHLMY. See as O-Methylanhalonidine
Hayward: 6{R(OM)}3RYLLNHLY. See as Anhalinine
Hayward: 6LMN(CM)LLYRR(OM)Y5OLOYY. See as Peyophorine
Hayward: 6LMNHLLYRR(OM)R(OM)RQY. See as Anhalonidine
Hayward: 6LMNMLLYRR(OM)R(OM)RQY. See as Pellotine
Hayward: 6LMNMLLYRR(OM)Y5OLOYY. See as Lophophorine
Hayward: 6R(CC@5NL(CVQ)=LL=L)R{R(OM)}3R. See as Peyonine
Hayward: 6R(CCNHCVM)RR(OM)RQRR. See as NAMT
Hayward: 6R(CCNHCVM)RRQRQRR. See as N-Acetyl DMPEA
Hayward: 6R(CCNHM)RRQRQRR. See as Epinine
Hayward: 6R(CCNHM)RRRQRR. See as N-Methyltyramine
Hayward: 6R(CCZ)R5. See as Phenethylamine
Hayward: 6R(CCZ)RRQRQRR. See as Dopamine
Hayward: 6R(CQCNHM)RRQRQRR. See as Epinephrine
Hayward: 6R(CQCNM2)RR(OM)R(OM)RR. See as Macromerine
Hayward: 6R(CQCNM2)RRQRQRR. See as N-Methyladrenaline
Hayward: 6R(CQCZ)RRQRQRR. Norepinephrine
Hayward: 6R(CQCZ)RRRQRR. See as Octopamine
Hayward: 6R(CVCNHM)RRRQRR. See as Synephrine
Hayward: 6R(OM)R(OM)RR(CCZ)RR. See as 3,4-Dimethoxyphenethylamine
Hayward: 6R(OM)RR(CQCZ)RRRQ. Normetanephrine
Hayward: 6R(OM)RRR(CCZ)RR. See as 4-Methoxyphenethylamine
Hayward: 6R)CCZM)RRR(CF3)RR. See as Tyramine
Hayward: 6RR(OM)R(OM)RQYLNHLLY. See as Anhalamine
Hayward: 6RR(OM)R(OM)RQYLNMLLY. See as Anhalidine
Hayward: LMNHLLYRR(OM)Y5OLOYY. See as Anhalonine
Hektalin. See as Epinephrine
Hemisine. See as Epinephrine
Hemostasin. See as Epinephrine
Hemostatin(e). See as Epinephrine
Homoanisylamine. See as 4-Methoxyphenethylamine
Homovanilylamine. See as 3-Methoxytyramine
Homoveratrylamine. See as 3,4-Dimethoxyphenethylamine
Hydroxytyramine. See as Dopamine
Hypernephrin. See as Epinephrine
Hyporenin. See as Epinephrine
Intranefrin. See as Epinephrine
Intropin. See as Dopamine hydrochloride.
Isoquinolines: See by name or consult Isoquinoline structural table
Jaxartinine. See as N-Methyltyramine
Kidoline. See as Epinephrine
Levarterenol. See as Norepinephrine
Levonorepinephrine. See as Norepinephrine
Levophed. See as Norepinephrine
Levorenin(e). See as Epinephrine
Longimammine. See as N-Methyl-4-methoxy-β-hydroxyphenethylamine
Lophocereine. See as Lophocerine
Lyophrin. See as Epinephrine
M. See as Mescaline
Medihaler-EPI. See as Epinephrine
Mescalin. See as Mescaline
Mescalina. See as Mescaline
Meskalin. See as Mescaline
Metanephrin. See as Epinephrine
Methadren(e). See as N-Methyladrenaline
Methylaminomethyl 4-hydroxyphenyl carbinol. See as Synephrine
Methylarterenol. See as Epinephrine
Mezcalin(e). See as Mescaline
Mezcalina. See as Mescaline
Mezkalin. See as Mescaline
MPEA. See as 4-Methoxyphenethylamine
Mucidrina. See as Epinephrine
MW 121.18. See as Phenethylamine
MW 121.2. See as Phenethylamine
MW 137.18. See as Tyramine
MW 137.2. See as Tyramine
MW 151.208. See as 4-Methoxyphenethylamine. See as N-Methyltyramine
MW 153.180. See as Dopamine
MW 163.219. See as Longimammidine. See as Longimammosine. See as
Weberidine. See as Longimammatine
MW 165.23. See as Hordenine
MW 165.235. See as N-Methyl-4-methoxyphenethylamine. See as Ubine
MW 165.24. See as Hordenine
MW 167.20. See as Synephrine
MW 167.207. See as Epinine
MW 167.21. See as Epinine
MW 169.18. Norepinephrine
MW 175.253. See as Uberine
MW 177 (MIKES). See as ?-Methoxy-1-methyl-THIQ
MW 177.246. See as ?-Methoxy-1-methyl-THIQ
MW 179.218. See as Longimammamine
MW 179.261. See as N,N-Dimethyl-4-methoxyphenethylamine
MW 180.20. See as Epinephrine
MW 183.20. Normetanephrine
MW 189 (MIKES). See as Isobackebergine. See as Backebergine
MW 189.213. See as Isobackebergine. See as Backebergine
MW 191 (MIKES). See as Dehydrolemaireocereine. See as
Dehydroheliamine
MW 191.229. See as Dehydrolemaireocereine. See as Dehydroheliamine
MW 193 (MIKES). See as Lemaireocereine. See as Heliamine
MW 193.24. See as Salsoline
MW 193.245. See as Isosalsoline. See as Salsoline. See as
Lemaireocereine. See as Heliamine. See as Arizonine
MW 194.296 (ion). See as O-Methylcandicine
MW 197.23. See as Metanephrine. See as N-Methyladrenaline
MW 197.233. See as Metanephrine
MW 203 (MIKES). See as Isosalsolidine
MW 203.24. See as Isosalsolidine
MW 205 (MIKES). See as Dehydrosalsolidine
MW 205.256. See as Dehydrosalsolidine
MW 207 (MIKES). See as N-Methylheliamine
MW 207.0892. See as 6,7-Dimethoxy-8-hydroxy-3,4-
dihydroisoquinolinium inner salt
MW 207.229. See as 6,7-Dimethoxy-8-hydroxy-3,4-
dihydroisoquinolinium inner salt
MW 207.272. See as N-Methylheliamine. See as Salsolidine. See as
N-Methylisosalsoline
MW 209.1048. See as Isoanhalamine. See as Anhalamine
MW 209.24. See as Anhalamine
MW 209.25. See as Anhalamine
MW 211.25. See as Mescaline
MW 211.26. See as Mescaline
MW 211.260. See as Mescaline. N-Methylmetanephrine
MW 211.29. See as Mescaline
MW 214.4. See as 3,4-Dimethoxyphenethylamine
MW 219 (MIKES). See as Isonortehuanine
MW 221 (MIKES). See as Dehydronortehuanine. See as Carnegine
MW 221.1048. See as Anhalonine. See as
2-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner salt.
See as 1-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
MW 221.16. See as Anhalonine
MW 221.25. See as Anhalonine
MW 221.255. See as
2-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner salt.
See as 1-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinoline
MW 221.27. See as Dehydronortehuanine
MW 221.29. See as Carnegine
MW 221.299. See as Tepenine. See as Carnegine
MW 223 (MIKES). See as Anhalidine. See as Anhalonidine. See as
Nortehuanine
MW 223.1204. See as Anhalidine. See as Isoanhalidine. See as
Anhalonidine. See as Isoanhalonidine. See as Anhalinine
MW 223.24. See as Anhalonidine
MW 223.271. See as Anhalidine. See as Isoanhalidine. See as
Anhalonidine. See as Isoanhalonidine. See as Nortehuanine. See as
Anhalinine
MW 223.28. See as Anhalonidine
MW 225.28. See as Macromerine
MW 225.287. See as N-Methylmescaline
MW 227.25. See as β-Hydroxymescaline
MW 227.260. See as β-Hydroxymescaline
MW 233 (MIKES). See as ? Tri-MeO-1-Methyl-1,2-dihydro-isoquinoline
MW 233.266. See as ? Tri-MeO-1-Methyl-1,2-dihydro-isoquinoline
MW 235 (MIKES). See as ?
Tri-MeO-1-Methyl-1,2,3,4-tetrahydro-isoquinoline
MW 235.1204. See as
1,2-Dimethyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner
salt. See as Lophophorine
MW 235.27. See as Lophophorine
MW 235.282. See as
1,2-Dimethyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium inner
salt. See as Lophophorine. See as ?
Tri-MeO-1-Methyl-1,2,3,4-tetrahydro-isoquinoline. See as
N,N-Dimethylmescaline
MW 237 (MIKES). See as Tehuanine
MW 237.0097. See as N-Formyl-anhalamine
MW 237.1360. See as Pellotine. See as Isopellotine. See as
O-Methyl-anhalidine. See as OMethyl-anhalonidine
MW 237.255. See as N-Formylanhalamine
MW 237.29. See as Pellotine
MW 237.298. See as Pellotine. See as Isopellotine. See as Gigantine.
See as Tehuanine. See as O-Methyl-anhalidine. See as
O-Methylanhalonidine. See as N-Methylanhalinine
MW 237.30. See as Pellotine. See as Gigantine
MW 238.306. See as Anhalotine
MW 239.271. See as N-Formylmescaline
MW 249 (MIKES). See as Isonorweberine
MW 249.0997. See as N-Formylanhalonine
MW 249.1360. See as Peyophorine
MW 249.266. See as N-Formylanhalonine
MW 249.309. See as Peyophorine
MW 249.352. See as Lophocerine
MW 250.3117. See as Lophotine (ion)
MW 251 (MIKES). See as Dehydronorweberine. See as O-Methylpellotine
MW 251.1153. See as N-Formylanhalinine. See as N-Acetylanhalamine
MW 251.1516. See as O-Methylpellotine
MW 251.282. See as Isonorweberine. See as Dehydronorweberine. See as
N-Formylanhalinine. See as N-Acetylanhalamine
MW 252.1153. See as N-Formylanhalonidine
MW 252.282. See as N-Formylanhalonidine
MW 253 (MIKES). See as Norweberine. See as ?
Mono-OH-tri-MeO-2-Methyl-isoquinoline
MW 253.0946. See as Peyoxylic acid
MW 253.297. See as Norweberine. See as ?
Mono-OH-tri-MeO-2-Methyl-isoquinoline. See as Tehuanine-N-oxide. See as
N-Acetylmescaline
MW 257.22. See as Anhalonine hydrochloride
MW 257.6. See as Carnegine hydrochloride
MW 263. See as Isopachycereine
MW 263.1153. See as N-Acetyl-anhalonine. See as Peyoglutam
MW 263.293. See as Isopachycereine. See as N-Acetylanhalonine. See
as Peyoglutam. See as Peyoglutam
MW 265 (MIKES). See as Dehydropachycereine
MW 265.1309. See as N-Formyl-O-methylanhalonidine
MW 265.308. See as Dehydropachycereine. See as
N-Formyl-O-methylanhalonidine
MW 267. See as Pachycereine
MW 267 (MIKES). See as Weberine
MW 267.1102. See as O-Methylpeyoxylic acid. See as Peyoruvic acid
MW 267.281. See as Peyoruvic acid
MW 267.324. See as Pachycereine
MW 267.324. See as Weberine
MW 269.297. See as Mescaloxylic acid
MW 277. 193. See as Mescalotam
MW 277.1309. See as Mescalotam
MW 277.319. See as Mescalotam
MW 281 (MIKES). See as N-Methylpachycereine
MW 281.1258. See as O-Methylpeyoruvic acid
MW 281.308. See as O-Methylpeyoruvic acid
MW 281.351. See as N-Methylpachycereine
MW 283.324. See as Mescaloruvic acid
MW 291.303. See as Mescaline maleimide
MW 293.319. See as Mescaline succinamide
MW 309.318. See as Mescaline malimide
MW 309.37. See as Mescaline sulfate
MW 319.357. See as Peyoglunal
MW 321.201. See as O-Methylcandicine iodide
MW 349.340. See as Mescaline isocitrimide lactone
MW 365.0483. See as Anhalotine
MW 365.210. See as Anhalotine iodide
MW 367.355. See as Mescaline citrimide
MW 377.0483. See as Lophotine (Iodide)
MW 379.0639. See as Peyotine
MW 492.657. See as Lophocine
MW 744.025. See as Piloceredine. See as Pilocereine
MW C13H15NO4. See as Isonorweberine
MW C14H19NO4. See as Pachycereine
Mydrial. See as Tyramine
Myosthenine. See as Epinephrine
Mytrate. See as Epinephrine
N-(1-Carboxyethyl)mescaline. See as Mescaloruvic acid
N-(3,4,5-Trimethoxyphenethyl)-alanine. See as Mescaloruvic acid
N-(3,4,5-Trimethoxyphenethyl)malimide. See as Mescaline malimide
N-(3,4,5-Trimethoxyphenyl)-3,4-didehydrosuccinamide. See as
Mescaline maleimide
N-(3,4,5-Trimethoxyphenyl)succinamide. See as Mescaline succinamide
N,N,N-Trimethyl-4-hydroxyphenethylamine. See as Candicine
N,N,N-Trimethyl-4-methoxyphenethylamine. See as O-Methylcandicine
N,N,N-Trimethyldopamine. See as Coryneine
N,N,N-Trimethyltyramine. See as Candicine
N,N-diMe-β-OH-PEA. See as Ubine
N,N-Dimethyl-b,3,4-trimethoxyphenethylamine. See as
β-Methoxy-3,4-dimethoxy-N,N-dimethylphenethylamine
N,N-Dimethyl-β-hydroxyphenethylamine. See as Ubine
N,N-Dimethyl-1-phenylethanolamine. See as Ubine
N,N-Dimethyl-3,4-dimethoxy-β-hydroxyphenethylamine. See as
Macromerine
N,N-Dimethyl-3,4-dimethoxy-β-methoxyphenethylamine. See as
β-Methoxy-3,4-dimethoxy-N,N-dimethylphenethylamine
N,N-Dimethyl-3,4-dimethoxyphenethylamine. See as
3,4-Dimethoxy-N,N-dimethylphenethylamine
N,N-Dimethyl-3-methoxy-β-hydroxytyramine. N-Methylmetanephrine
N,N-Dimethyl-4-hydroxy-3-methoxyphenethylamine. See as
N,N-Dimethyl-3-methoxytyramine
N,N-Dimethyl-4-hydroxyphenethylamine. See as Hordenine
N,N-Dimethyl-DMPEA. See as 3,4-Dimethoxy-N,N-dimethylphenethylamine
N,N-Dimethyl-DMPEA methiodide. See as Coryneine iodide
N,N-Dimethyltyramine. See as Hordenine
N,O-Dimethyltyramine. See as N-Methyl-4-methoxyphenethylamine
N-[2-(3,4,5-Trimethoxyphenethyl)ethyl]acetamide. See as
N-Acetylmescaline
N-[2-(3,4,5-Trimethoxyphenyl)ethyl]alanine. See as Mescaloruvic acid
N-[2-(3,4,5-Trimethoxyphenyl)ethyl]glycine. See as Mescaloxylic acid
N-Acetyl-3,4-dimethoxyphenylethylamine. See as N-Acetyl-DMPEA
N-Acetyl-3-demethylmescaline. See as
N-Acetyl-3-hydroxy-4,5-dimethoxyphenethylamine
NADMPEA. See as N-Acetyl-DMPEA
N-Carboxymethylmescaline. See as Mescaloxylic acid
ND50. See as Octopamine
N-Demethyl-metanephrine. Normetanephrine
Nephedrine. See as Epinephrine
N-Ethylanhalonine. See as Peyophorine
Neupentedrin. See as β-O-Methylsynephrine (as tartrate)
N-Formyl-3-demethylmescaline. See as
N-Formyl-3-hydroxy-4,5-dimethoxyphenethylamine
Nieraline. See as Epinephrine
NIOSH # DN 5950000. Norepinephrine
NIOSH # DN 6125000. Norepinephrine
NIOSH # DN 6300000. Norepinephrine
NIOSH # JI 4800000. See as Lophophorine
NIOSH # NX 5018500. See as S-(-)-Salsolidine
NIOSH # NX 6000000. See as R-(+)-Salsoline
NIOSH # RY 0350000. See as Anhalonidine
NIOSH # SH 7875000. See as 4-Methoxyphenethylamine
NIOSH # SH 8110000. See as N-Methyl-4-methoxyphenethylamine
NIOSH # SI 2625000. See as Mescaline
NIOSH # SJ 5950000. See as Tyramine
NIOSH # SL 8300000. See as N-Methyltyramine
NIOSH # UX 1088000. See as Dopamine
NIOSH # UX 1925000. See as Epinine
N-Methyl-b,3,4-trimethoxyphenethylamine. See as
β-Methoxy-3,4-dimethoxy-N-methylphenethylamine
N-Methyl-β-hydroxy-3,4-dihydroxyphenethylamine. See as Epinephrine.
N-Methyl-2-(3,4-dihydroxyphenyl)ethylamine. See as Epinine
N-Methyl-3,4,5-trimethoxyphenethylamine. See as N-Methylmescaline
N-Methyl-3,4-dihydro-8-hydroxy-6,7-dimethoxyisoquinolinium inner
salt. See as 2-Methyl-6,7-dimethoxy-8-hydroxy-3,4-dihydroisoquinolinium
inner salt
N-Methyl-3,4-dihydroxyphenethylamine. See as Epinine
N-Methyl-3,4-dimethoxy-β-hydroxyphenethylamine. See as Normacromerine
N-Methyl-3,4-dimethoxy-β-methoxyphenethylamine. See as
β-Methoxy-3,4-dimethoxy-N-methylphenethylamine.
N-Methyl-3,4-dimethoxyphenethylamine. See as
3,4-Dimethoxy-N-methylphenethylamine
N-Methyl-3-methoxy-β-hydroxytyramine. See as Metanephrine
N-Methyl-4,β-dihydroxyphenethylamine. See as Synephrine
N-Methyl-4-hydroxy-β-hydroxyphenethylamine. See as Synephrine
N-Methyl-4-hydroxy-3-methoxyphenethylamine. See as
N-Methyl-3-methoxytyramine
N-Methyl-4-hydroxyphenethylamine. See as N-Methyltyramine
N-Methyl-6,7,8-trimethoxy-1,2,3,4-tetrahydroisoquinoline. See as
N-Methylanhalinine
N-Methyl-6,7-dimethoxy-8-hydroxy-1,2,3,4-tetrahydroisoquinoline. See
as Anhalidine
N-Methylanhalamine. See as Anhalidine
N-Methylanhalonidine. See as Pellotine
N-Methylanhalonidine hydriodide. See as Pellotine hydriodide
N-Methylanhalonidine methiodide. See as Pellotine methiodide
N-Methylanhalonine. See as Lophophorine
N-Methyl-DMPEA. See as 3,4-Dimethoxy-N-methylphenethylamine
N-Methyldopamine. See as Epinine
N-Methylepinephrin(e). See as N-Methyladrenaline
N-Methyl-l-anhalonine. See as Lophophorine
N-Methyl-metanephrine
N-Methyl-tyramine O-methyl ether. See as
N-Methyl-4-methoxyphenethylamine
NMN. Normetanephrine
NMPEA. See as N-Methylphenethylamine
NMT. See as N-Methyltyramine
Noradrec. See as Norepinephrine
Noradrenalin(e). See as Norepinephrine
Noradrine. See as Norepinephrine
Norcarnegine. See as Salsolidine
Norefol. See as Norepinephrine
Norepinephrin. See as Norepinephrine
Norepirenamine. See as Norepinephrine
Nor-Epirenan. See as Norepinephrine
Norexadrin. See as Norepinephrine
Norfelol. See as Norepinephrine
Norlevorine. See as Norepinephrine
Normetadrenaline. Normetanephrine
Normethanephrine. Normetanephrine
O3-Demethylmescaline. See as 3-Hydroxy-4,5-dimethoxyphenethylamine
O3-Methyladrenaline. See as Metanephrine
O3-Methyldopamine. See as 3-Methoxytyramine
O-3-Methyldopamine. See as 3-Methoxytyramine
O4-Demethylmescaline. See as 4-Hydroxy-3,5-dimethoxyphenethylamine
O4-Methyldopamine. See as 3-Hydroxy-4-methoxyphenethylamine
O-4-Methyldopamine. See as 3-Hydroxy-4-methoxyphenethylamine
Oksedrin. See as Synephrine
O-Methylanhalamine. See as Anhalinine
O-Methylanhalidine. See as N-Methylanhalinine
O-Methylcorypalline. See as N-Methylheliamine
O-Methylhordenine. See as N,N-Dimethyl-4-methoxyphenethylamine
O-Methyloctopamine. See as 4-Methoxy-β-hydroxyphenethylamine
O-Methylsalsoline. See as Salsolidine
O-Methyltyramine. See as 4-Methoxyphenethylamine
Oxedrin(e). See as Synephrine
Oxedrinum. See as Synephrine
Oxycandicine. See as its synonym: Coryneine
Oxydrine. See as Synephrine
Oxymethylcorypalline. See as N-Methylheliamine
Oxyphenylmethylaminoethanol. See as Synephrine
p-β-aminoethylphenol. See as Tyramine
p-(β-Aminoethyl)-phenol. See as Tyramine
p-(2-Aminoethyl)-phenol. See as Tyramine
Paranephrin(e). See as Epinephrine
Parasympatol. See as Synephrine
PEA. See as Phenethylamine
Pectinin. See as Carnegine
Pectinine. See as Carnegine
Pellotine methiodide, 147. See as Peyotine (as iodide)
Pentedrin. See as β-O-Methylsynephrine (as tartrate). See as
Synephrine
Peyocactin. See as Hordenine
Peyocactine. See as Hordenine
Peyoglutam methyl ether. See as Mescalotam
Peyoruvic acid methyl ether. See as O-Methylpeyoruvic acid. See as
O- Methylpeyoxylic acid
Peyotl. See as Mescaline
Peyotline. See as Pellotine
Phenethylamines:  See by name or consult the Phenethylamine
structural table or look under  -phenethylamine at the start of
the Index.
Phenylephrine. See as Epinephrine
p-Hydroxy-α-[(methylamino)methyl]benzyl alcohol. See as Synephrine
p-Hydroxy-N,N-dimethylphenethylamine. See as Hordenine
p-Hydroxyphenethyl methylamine. See as N-Methyltyramine
p-Hydroxyphenethylamine. See as Tyramine
PM. See as 4-Methoxyphenethylamine
p-Methoxy-β-hydroxy-β-phenethylamine. See as
4-Methoxy-β-hydroxyphenethylamine
p-Methoxyphenethylamine. See as 4-Methoxyphenethylamine
p-Methylaminoethanolphenol. See as Synephrine
p-Oxedrine. See as Synephrine
p-Sympatol. See as Synephrine
p-Synephrine. See as Synephrine
Renagladin(e). See as Epinephrine
Renaglandulin. See as Epinephrine
Renaleptine. See as Epinephrine
Renalina. See as Epinephrine
Renoform. See as Epinephrine
Renostypricin. See as Epinephrine
Renostypticin. See as Epinephrine
Rhatanine. See as N-Methyltyramine
Ro 1-2057. See as O-Methylanhalidine
Salsolinol-O6-methyl ether. See as Isosalsoline
Salsolinol-O7-methyl ether. See as Salsoline
Scurenaline. See as Epinephrine
Simpalon. See as Synephrine
Simpatol. See as Synephrine
Sindrenina. See as Epinephrine
Soladren(e). See as Epinephrine
Sphygmogenin. See as Epinephrine
Stryptirenal. See as Epinephrine
Supranefran. See as Epinephrine
Supranephrane. See as Epinephrine
Supranephrin. See as Epinephrine
Supranol. See as Epinephrine
Suprarenalin(e). See as Epinephrine
Suprarenenin(e). See as Epinephrine
Suprel. See as Epinephrine
Surenine. See as Epinephrine
Surinamine. See as N-Methyltyramine
Surrenine. See as Epinephrine
Susphrine. See as Epinephrine
Symcoral. See as Synephrine
Symcorthal. See as Synephrine
Symcortol. See as Synephrine
Sympadrin. See as Synephrine
Sympaethamin. See as Synephrine
Sympaethaminum. See as Synephrine
Sympalept. See as Synephrine
Sympathin. See as Epinephrine. See as Norepinephrine
Sympathin E. See as Norepinephrine
Sympathol. See as Synephrine
Sympathomin. See as Synephrine
Sympatol. See as Synephrine
Symphetamin. See as Synephrine
Syncalton. See as Synephrine
Synedren. See as Synephrine
Synergol. See as Synephrine
Synthenate. See as Synephrine
Systogen. See as Tyramine
Systogene. See as Tyramine
T.M.P.E.. See as Mescaline
Takamina. See as Epinephrine
Takamine. See as Epinephrine
Tenosin-Wirkstoff. See as Tyramine
TMPEA. See as Mescaline
Tocosin. See as Tyramine
Tocosine. See as Tyramine
Tokamina. See as Epinephrine
Tokosin. See as Tyramine
Tonogen. See as Epinephrine
Trichocereine. See as N,N-Dimethylmescaline
Tyrosam. See as Tyramine
Tyrosamin. See as Tyramine
Tyrosamine. See as Tyramine
Urosympathin. See as Norepinephrine
Uteramin. See as Tyramine
Uteramine. See as Tyramine
Vaponefrin. See as Epinephrine
Vascardyne. See as Synephrine
Vasoconstrictine. See as Epinephrine
Vasoconstrictor. See as Epinephrine
Vasocordin. See as Synephrine
Vasodrine. See as Epinephrine
Vasoton. See as Epinephrine. See as Synephrine
Vasotonin. See as Epinephrine
WLN: 1OR BO1 DYQ1N1&1.  See as Macromerine
WLN: 1VM2R CO1 DO1.  See as N-Acetyl DMPEA
WLN: 1VM2R DQ CO1.  See as NAMT
WLN: QR BQ D2M1.  See as Epinine
WLN: QR BQ DYQ1M1.  See as Epinephrine
WLN: QR BQ DYQ1N1&1.  See as N-Methyladrenaline
WLN: QR D2M1.  See as N-Methyltyramine
WLN: QR DYQ1M1.  See as Synephrine
WLN: T B566 CO EO LM DH&&TJ GO1 M.  See as Anhalonine
WLN: T B566 CO EO LN DH&&TJ GO1 L M.  See as
Lophophorine
WLN: T B566 CO EO LN DH&&TJ GO1 L2 M.  See as
Peyophorine
WLN: T5NJ A2R CO1 DO1 EO1& BVQ.  See as Peyonine
WLN: T66 CMT&J B HO1 IO1 JO1.  See as O-Methylanhalonidine
WLN: T66 CMT&J B HO1 IO1 JQ.  See as Anhalonidine
WLN: T66 CMT&J HO1 IO1 JO1.  See as Anhalinine
WLN: T66 CMT&J HO1 IO1 JQ.  See as Anhalamine
WLN: T66 CNT&J B C HO1 IO1 JQ.  See as Pellotine
WLN: T66 CNT&J HO1 IO1 JQ.  See as Anhalidine
WLN: Z1YQR CQ DQ.  See as Norepinephrine
WLN: Z1YQR DQ CO1.  See as Normetanephrine
WLN: Z2R.  See as Phenethylamine
WLN: Z2R CO1 DO1.  See as 3,4-Dimethoxyphenethylamine
WLN: Z2R CO1 DO1 EO1.  See as Mescaline
WLN: Z2R CQ DQ. See as Dopamine
WLN: Z2R DO1.  See as 4-Methoxyphenethylamine
WLN: Z2R DQ.  See as Tyramine