Lophophora williamsii

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.

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Huichol of northwestern Mexico, dried peyote “buttons” are prepared as a mild, bittersweet tea, and the same material is chewed fresh or dry as part of pilgrimage rites and curing ceremonies; the juice may also be pressed from fresh buttons and taken alone (Schaefer and Furst, 1996; Custodio et al., 2012). In the Native American Church of the United States and southern Canada, peyote is placed in a shallow bowl and shared ceremonially; some participants sip the cold aqueous extract from the buttons after the sharing, while others consume the buttons by chewing and swallowing (Slotkin, 1955; Aberle, 1966; Opler, 1938). Among the O’Odham of southern Arizona and northern Sonora, peyote is less frequently encountered, but older accounts describe it being chewed or taken as an infusion for potency and healing (Russell, 1908; Jones, 1908). Across these regions the primary plant part is the crown of the cactus—fresh or dried “buttons” (the uppermost part of the root crown and stem)—and use is tied to ritual fasting, community prayer, divination, and gastrointestinal cleansing.

A concise preparation reflecting reported ceremonial practice is the cold aqueous extract often referred to by NAC members. Place about 6–10 buttons (≈30–45 g) in a bowl and cover with cold water. Let the mixture sit for at least 30 minutes; some ceremonies allow longer steeping. The resulting liquid is sipped as a “dose” while participants rest, and the remaining buttons may be chewed and swallowed. Caution: such use requires culturally supervised setting and group leadership. Individuals with cardiovascular disease, psychiatric conditions, or who are taking certain medications should consult a clinician. Alcohol should not be combined; vomiting may occur as part of the experience, so fluid replacement is important. Do not attempt this preparation in contexts where it is illegal; follow local law and NAC protocol.

Active constituents are well documented and provide a clear chemical rationale for the reported effects. Major alkaloids include mescaline (3,4,5-trimethoxyphenethylamine), together with the imidazole alkaloids hordenine (anhaline), pellotine, and anhalonidine; peyote also contains certain flavonoids and cactaceous-specific lignans. The mescaline-rich fraction is water-soluble and readily extracted by cold infusion, while the other minor alkaloids contribute to the bitter taste and ancillary activity.

Modern relevance is mixed. Although peer‑reviewed pharmacology on mescaline and peyote’s cultural chemistry continues in journals, the cactus itself is protected in Mexico and listed under international narcotics controls, so it is not legally available outside NAC ceremonies in the United States and select jurisdictions; meanwhile, Indigenous communities and scholars continue to document its ceremonial continuity and symbolic life within a legal framework that often restricts broader public access (Aberle, 1966; Custodio et al., 2012).

General Uses Top

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Scientific and model‑organism uses:
Lophophora williamsii is a non‑model cactus used in research on plant systematics, chemotaxonomy, and conservation. Its complete nuclear genome has been sequenced and is publicly accessible, enabling comparative genomics within Cactaceae. Transcriptomic data support phylogenetic analyses and studies of cactus-specific traits. Community databases include herbarium specimens and occurrence records in global biodiversity portals (e.g., GBIF, iNaturalist), as well as ethnobotanical collections and voucher specimens in specialized repositories (e.g., JSTOR Global Plants; herbarium records). These resources underpin taxonomic revision, population genetics, and biosystematic analyses. No established industrial, craft, or culinary uses are reported. The species is protected in Mexico and listed in CITES Appendix II; international commercial trade is restricted.

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.
Peyotl xochimilcensis F.Hern. Hist. Pl. Nov. Hisp. 3: 70. 1790.
Lophophora williamsii var. heptagona Y.Itô Cactaceae: 467. 1981.
Lophophora williamsii var. typica Croizat Desert Pl. Life 16: 8. 1944.

Common names Top

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Language Common/alternative name
English peyote
Spanish echinocactus pseudo lewinii thompsonii
Spanish peyote
Spanish péyotl
Spanish peyotl
Arabic صبار وليمز
Arabic المسكال
Bulgarian пейот
Catalan peyote
Catalan peiot
Czech peyotl
Czech pejotl
Czech lofofora williamsova
Czech ježunka williamsova
Danish elefantfodkaktus
Greek Πεγιότ
Esperanto pejotlo
Estonian peioote
Estonian peyote kaktus
Estonian peioote-uimakaktus
Estonian peyote
Basque peiote
Persian پیوت
Finnish peyote
Finnish meskaliinikaktus
Finnish myrkkykaktus
French peyote
French peyotl
frr peyote kaktus
Irish péóité
Irish an péóité
Galician peiote
Hebrew פיוטה
Hungarian pejotl
Hungarian meszkalinkaktusz
Indonesian peyote
ilo peyote
Japanese ペヨーテ
Japanese 烏羽玉
Japanese ウバタマ
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 peyotl
Dutch peyote
oc peiòt
oc peïot
Polish echinokaktus williamsa
Polish pejotl
Polish peyotl
Polish jazgrza williamsa
Pashto پيوټ
Portuguese peiote
Russian Мескалито
Russian Лофофора Вильямса
Russian Пейот
Russian Пейотль
Russian Лофофора Уильямса
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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northwest
      • Mexico Southwest
    • South-central U.S.A.
      • Texas

Links to other databases Top

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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

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_964133935.1 Lwill_v1 Contig weizmann institute of science 2024-06-04 11 3.10 Gb

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
New perspective on sustained antidepressant effect: focus on neurexins regulating synaptic plasticity Ruan Y, Yuan R, He J, Jiang Y, Chu S, Chen N Cell Death Discov 01-May-2024
PMCID:PMC11063156
doi:10.1038/s41420-024-01974-9
PMID:38693106
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
Psychedelic Drugs or Hallucinogens: Exploring Their Medicinal Potential Raj P, Rauniyar S, Sapkale B Cureus 13-Nov-2023
PMCID:PMC10716812
doi:10.7759/cureus.48719
PMID:38094517
Imaging plant metabolism in situ Horn PJ, Chapman KD J Exp Bot 27-Oct-2023
PMCID:PMC10938046
doi:10.1093/jxb/erad423
PMID:37889862
In Vitro and In Vivo Evaluation of Pellotine: A Hypnotic Lophophora Alkaloid Poulie CB, Chan CB, Parka A, Lettorp M, Vos J, Raaschou A, Pottie E, Bundgaard MS, Sørensen LM, Cecchi CR, Märcher-Rørsted E, Bach A, Herth MM, Decker A, Jensen AA, Elfving B, Kretschmann AC, Stove CP, Kohlmeier KA, Cornett C, Janfelt C, Kornum BR, Kristensen JL ACS Pharmacol Transl Sci 18-Sep-2023
PMCID:PMC10580395
doi:10.1021/acsptsci.3c00142
PMID:37854625
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

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 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 138.19 unknown via CMAUP database
Hordenine 68313 Click to see 165.23 unknown https://doi.org/10.2307/4117899
Mescaline 4076 Click to see 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 225.28 unknown https://doi.org/10.1016/0021-9673(92)80380-D
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
5-(2-Aminoethyl)-1,2-benzene-3,4,6-d3-diol 11993858 Click to see 156.20 unknown via CMAUP database
> Benzenoids / Phenols / Cresols / Meta cresols
M-Cresol 342 Click to see 108.14 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
[D] Tyrosol 10773058 Click to see 140.18 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Triacontene 87639 Click to see 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 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 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 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 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
(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 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
[(5R,6S,8S,9Z)-8-methoxy-3,6,10-trimethyl-4-oxo-6,7,8,11-tetrahydro-5H-cyclodeca[b]furan-5-yl] acetate 101149318 Click to see 320.40 unknown via CMAUP database
Furanodienone 6506548 Click to see 230.30 unknown via CMAUP database
Isofuranodiene 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 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 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
rel-1S,2S-epoxy-4R-furanogermacr-10(15)-en-6-one 10444597 Click to see 246.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
3,4-Dihydro-8-hydroxy-6-methoxy-3-methyl-1H-2-benzopyran-1-one 93040 Click to see 208.21 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydroisoquinolines
6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinolin-8-ol 136652044 Click to see 221.25 unknown https://doi.org/10.1248/YAKUSHI1947.92.4_482
6,7-Dimethoxy-3,4-dihydroisoquinolin-8-ol 135817517 Click to see 207.23 unknown https://doi.org/10.1248/YAKUSHI1947.92.4_482
> Organoheterocyclic compounds / Naphthofurans
(9aS)-9a-hydroxy-3,5,8-trimethyl-4,9-dihydrobenzo[f][1]benzofuran-2-one 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 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 237.29 unknown https://doi.org/10.1002/PAUZ.19850140502
https://doi.org/10.1016/0021-9673(92)80380-D
(1S)-6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-8-ol 87201 Click to see 223.27 unknown https://doi.org/10.1016/0021-9673(92)80380-D
https://doi.org/10.1248/YAKUSHI1947.92.4_482
6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-8-ol 199214 Click to see 223.27 unknown https://doi.org/10.1248/YAKUSHI1947.92.4_482
6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinolin-8-ol 65742 Click to see 237.29 unknown https://doi.org/10.1248/YAKUSHI1947.92.4_482
Ambalonine 16637831 Click to see CC1C2=C3C(=C(C=C2CCN1)OC)OCO3 221.25 unknown https://doi.org/10.1016/0021-9673(92)80380-D
https://doi.org/10.1002/PAUZ.19850140502
Anhalamine 69510 Click to see 209.24 unknown https://doi.org/10.1002/ARDP.18992370306
https://doi.org/10.1016/0021-9673(92)80380-D
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
Lophophorine 442315 Click to see CC1C2=C3C(=C(C=C2CCN1C)OC)OCO3 235.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see 132.16 unknown via CMAUP database

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