Lophophora williamsii

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Scientific Literature

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Details Top

Internal ID	UUID64405a984c7b9929353307
Scientific name	Lophophora williamsii
Authority	(Lem. ex Salm-Dyck) J.M.Coult.
First published in	in Contr. U.S. Natl. Herb. 3(2): 131. 1894.

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Lophophora echinata	Croizat	in Desert Pl. Life 16: 43. 1944.
Lophophora jourdaniana	Haberm.	in Kaktusy (Brno) 11: 3. 1975.
Lophophora lutea	(Rouhier) Backeb.	Cactaceae 5: 1901. 1961.
Lophophora pluricostata	(Croizat) V.Gapon	in Kaktus Klub 2004: 49. 2004.
Lophophora pentagona	(Croizat) V.Gapon	in Kaktus Klub 2004: 49. 2004.
Lophophora williamsii var. pluricostata	Croizat	in Desert Pl. Life 16: 8. 1944.
Lophophora williamsii var. pentagona	Croizat	in Desert Pl. Life 16: 44. 1944.
Mammillaria williamsii	J.M.Coult.	in Contr. U.S. Natl. Herb. 2: 129. 1891.
Mammillaria lewinii	(Henn.) H.Karst.	Deut. Fl. 2: 457. 1895.
Lophophora alberto-vojtechii	Bohata, Myšák & Šnicer	in Cactus & Co. 12: 108. 2008.
Anhalonium lewinii	Henn.	in Gartenflora 37: 410. 1888.
Anhalonium williamsii	(Lem. ex Salm-Dyck) C.F.Först.	Handb. Cacteenk.: 233. 1885.
Echinocactus lewinii	(Henn.) K.Schum.	in Monatsschr. Kakteenk. 5: 11, 94. 1895.
Echinocactus lewisii	(Henn.) K.Schum.	in Monatsschr. Kakteenk. 5: 11. 1895.
Echinocactus williamsii	Lem. ex Salm-Dyck	in Allg. Gartenzeitung 13: 385-386. 1845.
Echinocactus williamsii var. luteus	Rouhier	in Trav. Lab. Matiere Méd. Ecole Super. Pharm. Paris 17: 62. 1927.
Lophophora lewinii	(Henn.) C.H.Thomps.	in Rep. (Annual) Missouri Bot. Gard. 9: 133. 1898.
Ariocarpus williamsii	(Lem. ex Salm-Dyck) Voss	Vilm. Blumengärtn.: 368. 1907.
Echinocactus jourdanianus	Rebut ex Maass	in Monatsschr. Kakteenk. 15: 122. 1905.
Echinocactus williamsii var. anhaloninicus	K.Schum.	in Bot. Jahrb. Syst. 24: 567. 1898.
Echinocactus williamsii var. pellotinicus	K.Schum.	in Bot. Jahrb. Syst. 24(5): 567. 1898.
Lophophora echinata var. lutea	(Rouhier) Croizat	in Desert Pl. Life 16: 44. 1944.
Lophophora lutea var. texana	(Frič ex Kreuz.) Backeb.	Cactaceae 5: 2903. 1961.
Lophophora williamsii subsp. grymii	Halda, Kupčák & Sladk.	in Acta Mus. Richnov., Sect. Nat. 7: 36. 2000.
Lophophora williamsii var. cristata	Houghton	in J. Cact. Succ. Soc. Amer. 2: 490. 1931.
Lophophora williamsii var. decipiens	Croizat	Desert Pl. Life 16: 44. 1944.
Lophophora williamsii var. echinata	(Croizat) Bravo	in Cact. Suc. Mex. 12: 12. 1967.
Lophophora williamsii var. lewinii	J.M.Coult.	in Contr. U.S. Natl. Herb. 3: 131. 1894.
Lophophora williamsii var. lutea	(Rouhier) Soulaire	Cact. Mèd.: 121. 1948.
Lophophora williamsii var. texana	Frič ex Kreuz.	Verzeichnis Amer. Sukk. Rev. Syst. Kakteen: 9. 1935.

Common names Top

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Language	Common/alternative name
English	peyote
Spanish	lophophora williamsii var. pentagona
Spanish	péyotl
Spanish	lophophora williamsii var pluricostata
Spanish	peyotl
Spanish	lophophora echinata var. lutea
Spanish	lophophora lewinii
Spanish	lophophora lutea
Spanish	lophophora diffusa ssp. fricii
Spanish	lophophora diffusa ssp fricii
Spanish	echinocactus pseudo lewinii thompsonii
Spanish	echinocactus williamsii
Spanish	lophophora lutea var texana
Spanish	lophophora lutea var. texana
Spanish	lophophora jourdaniana
Spanish	peyote
Spanish	lophophora williamsii var decipiens
Spanish	lophophora williamsii var echinata
Arabic	صبار وليمز
Bulgarian	пейот
Catalan	peiot
Catalan	lophophora wiliamsii
Catalan	peyote
Czech	peyotl
Czech	pejotl
Danish	elefantfodkaktus
German	echinocactus williamsii
Greek	Πεγιότ
Esperanto	pejotlo
Estonian	peyote
Estonian	peioote
Estonian	peyote kaktus
Estonian	peioote-uimakaktus
Basque	peiote
Persian	پیوت
Finnish	peyote
Finnish	meskaliinikaktus
Finnish	myrkkykaktus
French	peyote
French	peyotl
Irish	péóité
Galician	peiote
Hebrew	פיוטה
Hungarian	meszkalinkaktusz
Hungarian	pejotl
Indonesian	peyote
ilo	peyote
Italian	lophophora lewinii
Japanese	ウバタマ
Japanese	烏羽玉
Japanese	ペヨーテ
Korean	페요테
Korean	페요태 선인장
Korean	페요태
Lithuanian	pejotas
Lithuanian	peyote
Lithuanian	viljamso lofofora
Lithuanian	kvaitulinis pejotlis
Latvian	peijotkaktuss
Latvian	peijots
Macedonian	пејот
nah	peyōtl
Norwegian Bokmål	peyote
Dutch	peyote
Dutch	peyotl
oc	peïot
oc	peiòt
Polish	peyotl
Polish	jazgrza williamsa
Polish	lophophora williamsi
Polish	pejotl
Polish	echinokaktus williamsa
Pashto	پيوټ
Portuguese	peiote
Russian	Лофофора Уильямса
Russian	Пейотль
Russian	Пейот
Russian	Мескалито
Russian	Лофофора Вильямса
Slovenian	pejotl
Swedish	peyote
Swedish	giftkaktus
Turkish	peyote
Ukrainian	Пейот
Ukrainian	Пейотль
Ukrainian	Лофофора Вільямса
Chinese	乌羽玉
Chinese	白藥帖仙人掌
Chinese	烏羽玉

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Mexico
  - Mexico Northwest
  - Mexico Southwest
- South-central U.S.A.
  - Texas

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001287424
UNII	7643UT12PZ
USDA Plants	LOWI
Tropicos	5101145
KEW	urn:lsid:ipni.org:names:143606-2
The Plant List	tro-5101145
Open Tree Of Life	543120
Observations.org	425184
NCBI Taxonomy	130138
Nature Serve	2.139920
IUCN Red List	151962
IPNI	143606-2
iNaturalist	164777
GBIF	5384220
Freebase	/m/068b8
EPPO	LOFWI
EOL	486998
Elurikkus	532513
USDA GRIN	22667
Wikipedia	Peyote
CMAUP	NPO13613

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Chemical profiling of bioactive compounds in the methanolic extract of wild leaf and callus of Vitex negundo using gas chromatography-mass spectrometry

Garg G, Bharadwaj A, Chaudhary S, Gupta V

World J Exp Med

20-Mar-2024

PMCID:	PMC10999060
doi:	10.5493/wjem.v14.i1.88064
PMID:	38590309

Making Sense of Psychedelics in the CNS

Fordyce BA, Roth BL

Int J Neuropsychopharmacol

30-Jan-2024

PMCID:	PMC10888522
doi:	10.1093/ijnp/pyae007
PMID:	38289825

An Overview on the Hallucinogenic Peyote and Its Alkaloid Mescaline: The Importance of Context, Ceremony and Culture

Doesburg-van Kleffens M, Zimmermann-Klemd AM, Gründemann C

Molecules

05-Dec-2023

PMCID:	PMC10746114
doi:	10.3390/molecules28247942
PMID:	38138432

Drug–drug interactions involving classic psychedelics: A systematic review

Halman A, Kong G, Sarris J, Perkins D

J Psychopharmacol

20-Nov-2023

PMCID:	PMC10851641
doi:	10.1177/02698811231211219
PMID:	37982394

Molecular insights into GPCR mechanisms for drugs of abuse

Sanchez-Reyes OB, Zilberg G, McCorvy JD, Wacker D

J Biol Chem

18-Aug-2023

PMCID:	PMC10514560
doi:	10.1016/j.jbc.2023.105176
PMID:	37599003

Psychedelic therapy in the treatment of addiction: the past, present and future

Zafar R, Siegel M, Harding R, Barba T, Agnorelli C, Suseelan S, Roseman L, Wall M, Nutt DJ, Erritzoe D

Front Psychiatry

12-Jun-2023

PMCID:	PMC10291338
doi:	10.3389/fpsyt.2023.1183740
PMID:	37377473

How to sample a seizure plant: the role of the visualization spatial distribution analysis of Lophophora williamsii as an example

Lin J, Yun K, Sun Q, Xiang P, Wu L, Yang S, Dun J, Fu S, Chen H

Forensic Sci Res

22-May-2023

PMCID:	PMC10445667
doi:	10.1093/fsr/owad014
PMID:	37621449

Antioxidants in Traditional Mexican Medicine and Their Applications as Antitumor Treatments

Soto KM, Pérez Bueno JD, Mendoza López ML, Apátiga-Castro M, López-Romero JM, Mendoza S, Manzano-Ramírez A

Pharmaceuticals (Basel)

23-Mar-2023

PMCID:	PMC10145960
doi:	10.3390/ph16040482
PMID:	37111239

Natural or artificial: An example of topographic spatial distribution analysis of mescaline in cactus plants by matrix-assisted laser desorption/ionization mass spectrometry imaging

Lin J, Yang S, Ji J, Xiang P, Wu L, Chen H

Front Plant Sci

10-Feb-2023

PMCID:	PMC9950628
doi:	10.3389/fpls.2023.1066595
PMID:	36844095

Hofmann vs. Paracelsus: Do Psychedelics Defy the Basics of Toxicology?—A Systematic Review of the Main Ergolamines, Simple Tryptamines, and Phenylethylamines

Henríquez-Hernández LA, Rojas-Hernández J, Quintana-Hernández DJ, Borkel LF

Toxics

03-Feb-2023

PMCID:	PMC9963058
doi:	10.3390/toxics11020148
PMID:	36851023

The Bright Side of Psychedelics: Latest Advances and Challenges in Neuropharmacology

Mastinu A, Anyanwu M, Carone M, Abate G, Bonini SA, Peron G, Tirelli E, Pucci M, Ribaudo G, Oselladore E, Premoli M, Gianoncelli A, Uberti DL, Memo M

Int J Mol Sci

10-Jan-2023

PMCID:	PMC9865175
doi:	10.3390/ijms24021329
PMID:	36674849

Interpol Review of Drug Analysis 2019-2022

Love D, Jones NS

Forensic Sci Int Synerg

05-Jan-2023

PMCID:	PMC9841213
doi:	10.1016/j.fsisyn.2022.100299
PMID:	36655023

Drugs as Chemical Weapons: Past and Perspectives

Pitschmann V, Hon Z

Toxics

04-Jan-2023

PMCID:	PMC9866636
doi:	10.3390/toxics11010052
PMID:	36668778

Influence of Mineral Treatment, Plant Growth Regulators and Artificial Light on the Growth of Jewel Sweet Potato (Ipomoea batatas Lam. cv. Jewel) In Vitro

Kirakosyan RN, Kalashnikova EA, Abubakarov HG, Sleptsov NN, Dudina YA, Temirbekova SK, Khuat QV, Trukhachev VI, Sumin AV

Life (Basel)

24-Dec-2022

PMCID:	PMC9863710
doi:	10.3390/life13010052
PMID:	36676001

Rapid Detection and Quantification of Hallucinogenic Salvinorin A in Commercial Salvia divinorum Products by DART-HRMS

Chambers MI, Giffen-Lemieux JE, Musah RA

ACS Omega

21-Dec-2022

PMCID:	PMC9835517
doi:	10.1021/acsomega.2c06106
PMID:	36643502

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methoxamine	6082	Click to see CC(C(C1=C(C=CC(=C1)OC)OC)O)N	211.26	unknown	https://doi.org/10.1016/0021-9673(92)80380-D
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
4-(2-Aminoethyl)phenol;hydron	67458472	Click to see [H+].C1=CC(=CC=C1CCN)O	138.19	unknown	via CMAUP database
Hordenine	68313	Click to see CN(C)CCC1=CC=C(C=C1)O	165.23	unknown	https://doi.org/10.2307/4117899
Mescaline	4076	Click to see COC1=CC(=CC(=C1OC)OC)CCN	211.26	unknown	https://doi.org/10.2307/4117899 https://doi.org/10.1002/PAUZ.19850140502 https://doi.org/10.1016/0021-9673(92)80380-D https://doi.org/10.1016/0379-0738(96)01987-1
N-Methylmescaline	138365	Click to see CNCCC1=CC(=C(C(=C1)OC)OC)OC	225.28	unknown	https://doi.org/10.1016/0021-9673(92)80380-D
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
2-(3,4-Dihydroxyphenyl-d3)ethylamine	11993858	Click to see C1=CC(=C(C=C1CCN)O)O	156.20	unknown	via CMAUP database
> Benzenoids / Phenols / Cresols / Meta cresols
m-Cresol	342	Click to see CC1=CC(=CC=C1)O	108.14	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
2,6-Dideuterio-4-(2-hydroxyethyl)phenol	10773058	Click to see C1=CC(=CC=C1CCO)O	140.18	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Triacontene	87639	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C	420.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(5S,6S)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one	10376566	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C	230.30	unknown	via CMAUP database
Cuminaldehyde	326	Click to see CC(C)C1=CC=C(C=C1)C=O	148.20	unknown	via CMAUP database
Furanoelemene	12305300	Click to see CC1=COC2=C1CC(C(C2)(C)C=C)C(=C)C	216.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,5R,6R)-5-[(2R)-2-hydroxybutan-2-yl]-2-methyl-6-(2-methylprop-1-enyl)cyclohex-2-en-1-ol	11843778	Click to see CCC(C)(C1CC=C(C(C1C=C(C)C)O)C)O	238.37	unknown	via CMAUP database
(8S)-1,5,8-Trimethyl-8,9-dihydronaphtho[2,1-b]furan-6(7H)-one	71349601	Click to see CC1CC2=C(C(=CC3=C2C(=CO3)C)C)C(=O)C1	228.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Furanoeudesma 1,3-diene	643237	Click to see CC1=CC=CC2(C1CC3=C(C2)OC=C3C)C	214.30	unknown	via CMAUP database
Lindestrene	12311270	Click to see CC1=COC2=C1CC3C(=C)CC=CC3(C2)C	214.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(5E,9E)-3,6,10-trimethyl-8,11-dihydro-7H-cyclodeca[b]furan-4-one	6506548	Click to see CC1=CC(=O)C2=C(CC(=CCC1)C)OC=C2C	230.30	unknown	via CMAUP database
(5R,6S,8S,9Z)-3,6,10-Trimethyl-4-oxo-8-methoxy-4,5,6,7,8,11-hexahydrocyclodeca[b]furan-5-ol acetate	101149318	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1OC(=O)C)C)OC	320.40	unknown	via CMAUP database
(6S,7R,8E)-7-methoxy-3,6-dimethyl-10-methylidene-5,6,7,11-tetrahydrocyclodeca[b]furan-4-one	10923274	Click to see CC1CC(=O)C2=C(CC(=C)C=CC1OC)OC=C2C	260.33	unknown	via CMAUP database
(R,5E,9E)-8-Methoxy-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan	91711711	Click to see CC1=CCC2=C(CC(=CC(C1)OC)C)OC=C2C	246.34	unknown	via CMAUP database
[(1(10)E,2R,4R)]-2-Methoxy-8,12-epoxygemacra-1(10),7,11-trien-6-one	11747425	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1)C)OC	262.34	unknown	via CMAUP database
Furanodiene	636458	Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C	216.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1R,3aR,4R,8aS)-1-methoxy-1,4-dimethyl-7-propan-2-yl-2,3,3a,5,6,8a-hexahydroazulen-4-ol	15896127	Click to see CC(C)C1=CC2C(CCC2(C)OC)C(CC1)(C)O	252.39	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Hydroxyisogermafurenolide	14038425	Click to see CC1=C2CC(C(CC2(OC1=O)O)(C)C=C)C(=C)C	248.32	unknown	via CMAUP database
Myrrhanolide C	42636912	Click to see CC1CC2=C(C(CC3(C2=C(C(=O)O3)C)O)C)C(=O)C1	262.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
9a-Hydroxy-3,8a-dimethyl-5-methylene-4,4a,5,6,9,9a-hexahydronaphtho[2,3-b]furan-2(8aH)-one	101938021	Click to see CC1=C2CC3C(=C)CC=CC3(CC2(OC1=O)O)C	246.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Adonixanthin	16061189	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(=O)C(CC2(C)C)O)C)C)C	582.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3S,5S,8R,9S,10R,13S,17S)-4,4,8,10,13-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthrene-1,3-diol	42632429	Click to see CC(CCC=C(C)C)C1CC=C2C1(CCC3C2(CCC4C3(C(CC(C4(C)C)O)O)C)C)C	442.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2R)-2-methyl-2-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanenitrile	25245166	Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O	261.27	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1,2-Epoxy-10(14)-furanogermacren-6-one	10444597	Click to see CC1CC2C(O2)C(=C)CC3=C(C(=CO3)C)C(=O)C1	246.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
3-Methyl-6-methoxy-8-hydroxy-3,4-dihydroisocoumarin	93040	Click to see CC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1	208.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydroisoquinolines
6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinolin-8-ol	136652044	Click to see CC1=NCCC2=CC(=C(C(=C12)O)OC)OC	221.25	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482
6,7-Dimethoxy-3,4-dihydroisoquinolin-8-ol	135817517	Click to see COC1=C(C(=C2C=NCCC2=C1)O)OC	207.23	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482
> Organoheterocyclic compounds / Naphthofurans
Myrrhanolide A	42632428	Click to see CC1=C2CC3=C(C(=O)OC3(CC2=C(C=C1)C)O)C	244.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
6,7-Dimethoxy-1,2-dimethyl-3,4-dihydroisoquinolin-8-one	163192392	Click to see CC1=C2C(=CC(=C(C2=O)OC)OC)CCN1C	235.28	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482
6,7-Dimethoxy-2-methyl-3,4-dihydroisoquinolin-8-one	101417609	Click to see CN1CCC2=CC(=C(C(=O)C2=C1)OC)OC	221.25	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
Mesembrenone	216272	Click to see CN1CCC2(C1CC(=O)C=C2)C3=CC(=C(C=C3)OC)OC	287.35	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(-)-Pellotine	442336	Click to see CC1C2=C(C(=C(C=C2CCN1C)OC)OC)O	237.29	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482
(+)-Pellotine	12314029	Click to see CC1C2=C(C(=C(C=C2CCN1C)OC)OC)O	237.29	unknown	https://doi.org/10.1016/0021-9673(92)80380-D https://doi.org/10.1002/PAUZ.19850140502
(1S)-6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-8-ol	87201	Click to see CC1C2=C(C(=C(C=C2CCN1)OC)OC)O	223.27	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482 https://doi.org/10.1016/0021-9673(92)80380-D
Ambalonine	16637831	Click to see CC1C2=C3C(=C(C=C2CCN1)OC)OCO3	221.25	unknown	https://doi.org/10.1002/PAUZ.19850140502 https://doi.org/10.1016/0021-9673(92)80380-D
Anhalamine	69510	Click to see COC1=C(C(=C2CNCCC2=C1)O)OC	209.24	unknown	https://doi.org/10.1016/0021-9673(92)80380-D https://doi.org/10.1002/ARDP.18992370306
Anhalidine	2752318	Click to see CN1CCC2=CC(=C(C(=C2C1)O)OC)OC	223.27	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482
Anhalonidine	199214	Click to see CC1C2=C(C(=C(C=C2CCN1)OC)OC)O	223.27	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482
Lophophorine	442315	Click to see CC1C2=C3C(=C(C=C2CCN1C)OC)OCO3	235.28	unknown	via CMAUP database
Pellotine	65742	Click to see CC1C2=C(C(=C(C=C2CCN1C)OC)OC)O	237.29	unknown	https://doi.org/10.1248/YAKUSHI1947.92.4_482
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde	637511	Click to see C1=CC=C(C=C1)C=CC=O	132.16	unknown	via CMAUP database

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Lophophora williamsii

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