Details Top

Internal ID UUID643febabe4f50958256570
Scientific name Salvia divinorum
Authority Epling & Játiva
First published in Bot. Mus. Leafl. 20: 75. 1962

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.

Salvia divinorum is most famously used by the Mazatec of Oaxaca, Mexico, who traditionally chew the fresh leaves or brew them into a tea to induce a short‑lived visionary experience. The same practice is recorded among the Mixtec of Oaxaca (Bennett et al., 2021) and the Zapotec of Oaxaca (Bennett et al., 2021), where the leaves are either macerated in water or steeped as a decoction before consumption. In all three cultures the infusion is prepared from the fresh or dried leaves, the part of the plant that contains the psychoactive compounds, and is consumed orally in small doses, typically one or two cups per session.

A simple, safe preparation for a mild tea is as follows: take 5 g of dried Salvia divinorum leaves and place them in a pot with 250 ml of boiling water. Allow the mixture to steep for 5 minutes, then strain the liquid into a cup. Drink one cup at a time, waiting at least 30 minutes between doses. Because the plant’s active constituents are potent, it is advisable to avoid use during pregnancy, in children, or by individuals with a history of psychiatric illness. A single cup per day is generally considered the upper limit for recreational use.

The pharmacological activity of Salvia divinorum is largely attributed to the diterpene salvinorin A, which is present in the leaves at concentrations up to 0.5 % of dry weight. Salvinorin B, a closely related compound, is also found in smaller amounts and may contribute to the overall effect profile. These compounds are unique in that they act as selective kappa‑opioid receptor agonists, a mechanism that underlies the plant’s hallucinogenic properties. Other minor diterpenes have been identified, but salvinorin A remains the primary active constituent responsible for the traditional psychoactive use.

Today, Salvia divinorum continues to be studied for its unusual kappa‑opioid activity, with research exploring potential therapeutic applications and the risks of abuse. The plant is regulated in many countries, and in the United States it is a Schedule I controlled substance, although it remains available in some online markets as dried leaves or tinctures for research purposes. Its continued use by indigenous communities and interest from the scientific community underscore its enduring relevance.

General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English diviner's sage
English yerba de la pastora
English ska maría pastora
English ska maria pastora
English seer's sage
Spanish ojos de la pastora
Spanish ska pastora
Spanish ska maría
Spanish ska maria
Spanish s. divinorum
Spanish s divinorum
Arabic قصعين الكهان
Belarusian Шалвея вяшчуноў
Belarusian Шалфей вешчуноў
Czech šalvěj divotvorná
German aztekensalbei
German göttersalbei
German pipiltzitzintl
German wahrsage-salbei
German wahrsagesalbei
German zaubersalbei
German azteken-salbei
Esperanto dia salvio
Esperanto divenista salvio
Estonian luulusalvei
Persian سالویا دیوینوروم
Persian مایش ازتکی
Persian مایش آزتکی
Finnish mazatecinsalvia
French sauge des devins
Hebrew סאלוויה
Hebrew סלוויה דיווינורום
Hebrew סלוויה דיוינורום
Hebrew סאלביה
Hebrew סלוויה
Hebrew סאלויה דיוינורום
Hebrew סאלוויה דיווינורום
Hebrew סאלביה דיבינורום
Croatian prorokova kadulja
Hungarian látnokzsálya
Japanese 幻覚性サルビア
Lithuanian kvaitulinis šalavijas
Latvian dievišķā salvija
Macedonian пророчка жалфија
Polish szałwia czarownika
Polish szałwia wieszcza
Polish szałwia prorocza
Russian Шалфей предсказателей
Russian Шалфей прорицателей
Russian Шалфей наркотический
Russian Сальвия Дивинорум
Slovak Šalvia divotvorná
Swedish profetsalvia
Swahili msalvia
Ukrainian Шавлія віщунів
Chinese 墨西哥鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300879
USDA Plants SADI7
Tropicos 50003023
KEW urn:lsid:ipni.org:names:456121-1
The Plant List kew-182532
Open Tree Of Life 595171
NCBI Taxonomy 28513
IPNI 456121-1
iNaturalist 281359
GBIF 2927020
Freebase /m/012zsr
EPPO SALDI
EOL 483858
US Library of Congress sh97001502
USDA GRIN 400324
Wikipedia Salvia_divinorum

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_055755735.1 HU-SaDiv-2.2 Chromosome Hainan University 2026-03-09 20 532.18 Mb

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
Targeting autophagy with natural products as a potential therapeutic approach for diabetic microangiopathy Liu F, Zhao L, Wu T, Yu W, Li J, Wang W, Huang C, Diao Z, Xu Y Front Pharmacol 10-Apr-2024
PMCID:PMC11039818
doi:10.3389/fphar.2024.1364616
PMID:38659578
An efficient behavioral screening platform classifies natural products and other chemical cues according to their chemosensory valence in C. elegans Fryer E, Guha S, Rogel-Hernandez LE, Logan-Garbisch T, Farah H, Rezaei E, Mollhoff IN, Nekimken AL, Xu A, Selin Seyahi L, Fechner S, Druckmann S, Clandinin TR, Rhee SY, Goodman MB bioRxiv 03-Apr-2024
PMCID:PMC10274637
doi:10.1101/2023.06.02.542933
PMID:37333363
Class II terpene cyclases: structures, mechanisms, and engineering Pan X, Rudolf JD, Dong LB Nat Prod Rep 20-Mar-2024
PMCID:PMC10954422
doi:10.1039/d3np00033h
PMID:38105714
The influence of cultivation conditions on the formation of psychoactive salvinorin A, salvinorin B, rosmarinic acid and caffeic acid in Coleus scutellarioides Jakobina M, Łyczko J, Szumny A, Galek R Sci Rep 20-Mar-2024
PMCID:PMC10954737
doi:10.1038/s41598-024-57399-y
PMID:38509159
Research Progress of Plant-Derived Natural Products against Drug-Resistant Cancer Liu W, Wang Y, Xia L, Li J Nutrients 11-Mar-2024
PMCID:PMC10975298
doi:10.3390/nu16060797
PMID:38542707
Psychedelic substitution: altered substance use patterns following psychedelic use in a global survey Glynos NG, Aday JS, Kruger D, Boehnke KF, Lake S, Lucas P Front Psychiatry 22-Feb-2024
PMCID:PMC10917882
doi:10.3389/fpsyt.2024.1349565
PMID:38455520
Treatment of Dissociative Identity Disorder: leveraging neurobiology to optimize success Purcell JB, Brand B, Browne HA, Chefetz RA, Shanahan M, Bair ZA, Baranowski KA, Davis V, Mangones P, Modell RL, Palermo CA, Robertson EC, Robinson MA, Ward L, Winternitz S, Kaufman M, Lebois LA Expert Rev Neurother 15-Feb-2024
PMCID:PMC10950423
doi:10.1080/14737175.2024.2316153
PMID:38357897
Study of Dandelion (Taraxacum mongolicum Hand.-Mazz.) Salt Response and Caffeic Acid Metabolism under Saline Stress by Transcriptome Analysis Wu Z, Meng R, Feng W, Wongsnansilp T, Li Z, Lu X, Wang X Genes (Basel) 09-Feb-2024
PMCID:PMC10888437
doi:10.3390/genes15020220
PMID:38397210
Xuebijing improves inflammation and pyroptosis of acute lung injury by up-regulating miR-181d-5p-mediated SPP1 inactivation Wu X, Xin R, Zhang Y, Yang C, Sun F, Wang Y, Zheng F Clinics (Sao Paulo) 06-Feb-2024
PMCID:PMC10862507
doi:10.1016/j.clinsp.2024.100336
PMID:38325020
Synthetic surprise as the foundation of the psychedelic experience De Filippo R, Schmitz D Neurosci Biobehav Rev 01-Feb-2024
PMCID:PMC10839673
doi:10.1016/j.neubiorev.2024.105538
PMID:38220035
Third-Generation Antipsychotics and Lurasidone in the Treatment of Substance-Induced Psychoses: A Narrative Review Ricci V, De Berardis D, Maina G Healthcare (Basel) 29-Jan-2024
PMCID:PMC10855531
doi:10.3390/healthcare12030339
PMID:38338224
Study on the effect of compound cultivation on the growth feature and active ingredients content of Salvia miltiorrhiza Zhang L, Tao S, Zhang Y, Yang Y, Peng F, Liao H, Mao C, Wan X, Wu Y, Xu Z, Zhang C Front Plant Sci 18-Jan-2024
PMCID:PMC10854009
doi:10.3389/fpls.2023.1238896
PMID:38343765
Progress of nanopreparation technology applied to volatile oil drug delivery systems Ye ZW, Yang QY, Lin QH, Liu XX, Li FQ, Xuan HD, Bai YY, Huang YP, Wang L, Wang F Heliyon 08-Jan-2024
PMCID:PMC10825498
doi:10.1016/j.heliyon.2024.e24302
PMID:38293491
Double-Blind Comparison of the Two Hallucinogens Dextromethorphan and Psilocybin: Experience-Dependent and Enduring Psychological Effects in Healthy Volunteers Mathai DS, Hilbert S, Sepeda ND, Strickland JC, Griffiths RR, Garcia-Romeu A Psychedelic Med (New Rochelle) 13-Dec-2023
PMCID:PMC10750378
doi:10.1089/psymed.2023.0035
PMID:38152462
Development of the Protective Strategies for Psychedelics Scale: A novel inventory to assess safety strategies in the context of psychedelics Mian MN, Altman BR, Low F, Earleywine M J Psychopharmacol 04-Dec-2023
PMCID:PMC10851634
doi:10.1177/02698811231214060
PMID:38050326

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 / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown https://doi.org/10.1021/NP060456F
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Plakoridine A 10257462 Click to see 571.80 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
https://doi.org/10.1021/NP900181Q
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(2R,4E,8E)-2-[(5E)-6,10-dimethylundeca-1,5,9-trien-2-yl]-5,9,13-trimethyltetradeca-4,8,12-trien-1-ol 10550383 Click to see CC(=CCCC(=CCCC(=CCC(CO)C(=C)CCC=C(C)CCC=C(C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP030313I
2-(6,10-Dimethylundeca-1,5,9-trien-2-yl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-ol 53632003 Click to see 426.70 unknown https://doi.org/10.1021/NP030313I
3,7,11,15-Tetramethylhexadec-2-en-1-ol 145386 Click to see 296.50 unknown https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP030313I
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(-)-Hardwickiic acid 15559629 Click to see 316.40 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP900181Q
(+)-Hardwickiic Acid 15559627 Click to see 316.40 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
(4aR,5S,6R,8aR)-6-(acetyloxymethyl)-5-[2-(furan-3-yl)ethyl]-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 162874777 Click to see CC(=O)OCC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C 374.50 unknown https://doi.org/10.1021/NP030313I
(7S,8R)-7-(2-(3-Furyl)ethyl)-7,8-dimethylbicyclo[4.4.0]dec-2-ene-2-carboxylic acid 479908 Click to see 302.40 unknown https://doi.org/10.1021/NP900181Q
5-[2-(Furan-3-yl)ethyl]-4-hydroxy-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 85300785 Click to see 332.40 unknown https://doi.org/10.1021/NP030313I
6-(Acetyloxymethyl)-5-[2-(furan-3-yl)ethyl]-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 73099829 Click to see 374.50 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
Divinatorin A 10882157 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)C(CC=C2C(=O)O)O)C 332.40 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP030313I
https://doi.org/10.1021/NP900181Q
Divinatorin B 11057551 Click to see 362.50 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP030313I
https://doi.org/10.1021/NP900181Q
Divinatorin C 11783681 Click to see 374.50 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP900181Q
methyl (2S,4R,4aR,6aR,9S,10R,10aR,10bR)-2-(furan-3-yl)-4,9,10-trihydroxy-6a,10b-dimethyl-2,4,4a,5,6,9,10,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 16099524 Click to see CC12CCC3C(OC(CC3(C1C(C(C=C2C(=O)OC)O)O)C)C4=COC=C4)O 392.40 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
methyl (2S,4R,4aR,6aR,9S,10R,10aR,10bR)-9-acetyloxy-2-(furan-3-yl)-4,10-dihydroxy-6a,10b-dimethyl-2,4,4a,5,6,9,10,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 44234703 Click to see CC(=O)OC1C=C(C2(CCC3C(OC(CC3(C2C1O)C)C4=COC=C4)O)C)C(=O)OC 434.50 unknown https://doi.org/10.1021/NP900181Q
methyl (3S,4R,4aR,5S,6R,8aR)-5-[2-(furan-3-yl)ethyl]-3,4-dihydroxy-6-(hydroxymethyl)-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 16099527 Click to see 378.50 unknown https://doi.org/10.1021/NP060456F
methyl (4S,4aR,5R,6R,8aR)-6-formyl-5-[2-(furan-3-yl)ethyl]-4-hydroxy-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 162893425 Click to see 360.40 unknown https://doi.org/10.1016/J.BMC.2005.05.054
methyl (4S,4aR,5S,6R,8aR)-5-[2-(furan-3-yl)ethyl]-4-hydroxy-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 163030040 Click to see 346.50 unknown https://doi.org/10.1021/NP060456F
methyl (4S,4aR,5S,6R,8aR)-6-(acetyloxymethyl)-5-[2-(furan-3-yl)ethyl]-4-hydroxy-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 162915318 Click to see 404.50 unknown https://doi.org/10.1016/J.BMC.2005.05.054
methyl 2-(furan-3-yl)-4,9,10-trihydroxy-6a,10b-dimethyl-2,4,4a,5,6,9,10,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 162988248 Click to see 392.40 unknown https://doi.org/10.1021/NP060456F
Methyl 5-[2-(furan-3-yl)ethyl]-3,4-dihydroxy-6-(hydroxymethyl)-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 162982187 Click to see 378.50 unknown https://doi.org/10.1021/NP060456F
Methyl 5-[2-(furan-3-yl)ethyl]-4-hydroxy-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 163030039 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)C(CC=C2C(=O)OC)O)C 346.50 unknown https://doi.org/10.1021/NP060456F
Methyl 5-[2-(furan-3-yl)ethyl]-4-hydroxy-6-(hydroxymethyl)-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 85383113 Click to see 362.50 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP030313I
Methyl 6-(acetyloxymethyl)-5-[2-(furan-3-yl)ethyl]-4-hydroxy-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 162915317 Click to see 404.50 unknown https://doi.org/10.1016/J.BMC.2005.05.054
Methyl 6-formyl-5-[2-(furan-3-yl)ethyl]-4-hydroxy-5,8a-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylate 162893424 Click to see 360.40 unknown https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP900181Q
methyl 9-acetyloxy-2-(furan-3-yl)-4,10-dihydroxy-6a,10b-dimethyl-2,4,4a,5,6,9,10,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 74959826 Click to see 434.50 unknown https://doi.org/10.1021/NP900181Q
Salvinicin B 71454521 Click to see 526.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2535573/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-Hydroxy-3,5,5-trimethyl-4-(3-oxo-1-butenyl)-2-cyclohexen-1-one 440265 Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C 222.28 unknown https://doi.org/10.1021/NP060456F
Dehydrovomifoliol 688492 Click to see 222.28 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,2R,4aR,5R,7S,8aS)-7-acetyloxy-1-[(E)-2-(2-hydroxy-5-oxo-2H-furan-3-yl)ethenyl]-5-methoxycarbonyl-1,4a-dimethyl-8-oxo-3,4,5,6,7,8a-hexahydro-2H-naphthalene-2-carboxylic acid 16099523 Click to see 464.50 unknown https://doi.org/10.1021/NP078001T
(1R,2R,4aR,5R,7S,8aS)-7-acetyloxy-1-[(E)-2-(2-hydroxy-5-oxo-2H-furan-4-yl)ethenyl]-5-methoxycarbonyl-1,4a-dimethyl-8-oxo-3,4,5,6,7,8a-hexahydro-2H-naphthalene-2-carboxylic acid 16099526 Click to see 464.50 unknown https://doi.org/10.1021/NP078001T
(1R,2R,4aR,5R,7S,8aS)-7-acetyloxy-1-[(E)-2-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]ethenyl]-5-methoxycarbonyl-1,4a-dimethyl-8-oxo-3,4,5,6,7,8a-hexahydro-2H-naphthalene-2-carboxylic acid 163087304 Click to see 464.50 unknown https://doi.org/10.1021/NP060456F
(1R,2R,4aR,5R,7S,8aS)-7-acetyloxy-1-[(E)-2-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]ethenyl]-5-methoxycarbonyl-1,4a-dimethyl-8-oxo-3,4,5,6,7,8a-hexahydro-2H-naphthalene-2-carboxylic acid 162931469 Click to see CC(=O)OC1CC(C2(CCC(C(C2C1=O)(C)C=CC3=CC(OC3=O)O)C(=O)O)C)C(=O)OC 464.50 unknown https://doi.org/10.1021/NP060456F
(1S,2R,4aR,5R,7S,8aS)-7-acetyloxy-1-[(E)-2-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]ethenyl]-5-methoxycarbonyl-1,4a-dimethyl-8-oxo-3,4,5,6,7,8a-hexahydro-2H-naphthalene-2-carboxylic acid 163087305 Click to see 464.50 unknown https://doi.org/10.1021/NP060456F
7-acetyloxy-1-[2-(2-hydroxy-5-oxo-2H-furan-3-yl)ethenyl]-5-methoxycarbonyl-1,4a-dimethyl-8-oxo-3,4,5,6,7,8a-hexahydro-2H-naphthalene-2-carboxylic acid 163087303 Click to see 464.50 unknown https://doi.org/10.1021/NP060456F
7-acetyloxy-1-[2-(2-hydroxy-5-oxo-2H-furan-4-yl)ethenyl]-5-methoxycarbonyl-1,4a-dimethyl-8-oxo-3,4,5,6,7,8a-hexahydro-2H-naphthalene-2-carboxylic acid 162931467 Click to see 464.50 unknown https://doi.org/10.1021/NP060456F
CID 72830360 72830360 Click to see CC12CCC3C(=O)OC(CC3(C1C(=O)C(CC2C(=O)OC)O)C)C4=COC=C4 390.40 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
methyl (2S,4aR,10aS)-9-acetyloxy-2-(furan-3-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 11969624 Click to see 432.50 unknown https://doi.org/10.1016/S0379-0738(00)00180-8
https://doi.org/10.1021/JO00198A026
https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<22::AID-PCA428>3.0.CO;2-0
https://doi.org/10.1016/0378-8741(94)90116-3
https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP900181Q
https://doi.org/10.1007/BF02858975
https://doi.org/10.1080/02791072.1994.10472441
https://doi.org/10.1021/NP0205699
methyl (2S,4aR,6aR,10R,10aR,10bR)-10-acetyloxy-2-(furan-3-yl)-6a,10b-dimethyl-4,9-dioxo-2,4a,5,6,10,10a-hexahydro-1H-benzo[f]isochromene-7-carboxylate 24828201 Click to see 430.40 unknown https://doi.org/10.1016/J.BMC.2005.05.054
methyl (2S,4aR,6aR,7R,9S,10aS,10bR)-9-acetyloxy-2-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 162960098 Click to see 464.50 unknown https://doi.org/10.1021/NP060456F
methyl (2S,4aR,6aR,7R,9S,10aS,10bR)-9-acetyloxy-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-dimethoxyoxolan-3-yl]-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 11214688 Click to see CC(=O)OC1CC(C2(CCC3C(=O)OC(CC3(C2C1=O)C)C4(C(C(OC4OC)OC)O)O)C)C(=O)OC 528.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2535573/
methyl (2S,4aR,6aR,7R,9S,10aS,10bR)-9-acetyloxy-2-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 162960097 Click to see 464.50 unknown https://doi.org/10.1021/NP060456F
methyl (2S,4aR,6aR,7R,9S,10aS,10bR)-9-acetyloxy-2-[(2S)-2-hydroxy-5-oxo-2H-furan-4-yl]-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 162940409 Click to see CC(=O)OC1CC(C2(CCC3C(=O)OC(CC3(C2C1=O)C)C4=CC(OC4=O)O)C)C(=O)OC 464.50 unknown https://doi.org/10.1021/NP060456F
methyl (2S,4aR,9S,10R,10aR,10bR)-9,10-diacetyloxy-2-(furan-3-yl)-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 163184949 Click to see 474.50 unknown https://doi.org/10.1021/NP060456F
methyl (2S,4aS,6aR,10aR,10bR)-2-(furan-3-yl)-6a,10b-dimethyl-4,9-dioxo-2,4a,5,6,10,10a-hexahydro-1H-benzo[f]isochromene-7-carboxylate 49804393 Click to see 372.40 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
methyl (2S,4aS,6aR,7R,10aS,10bR)-2-(furan-3-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 11552519 Click to see 374.40 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
methyl 10-acetyloxy-2-(furan-3-yl)-6a,10b-dimethyl-4,9-dioxo-2,4a,5,6,10,10a-hexahydro-1H-benzo[f]isochromene-7-carboxylate 74327193 Click to see 430.40 unknown https://doi.org/10.1016/J.BMC.2005.05.054
Methyl 10-acetyloxy-2-(furan-3-yl)-9-hydroxy-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 72971749 Click to see 432.50 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
https://doi.org/10.1021/NP900181Q
methyl 2-(furan-3-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 73004512 Click to see CC12CCC3C(=O)OC(CC3(C1C(=O)CCC2C(=O)OC)C)C4=COC=C4 374.40 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
methyl 2-(furan-3-yl)-6a,10b-dimethyl-4,9-dioxo-2,4a,5,6,10,10a-hexahydro-1H-benzo[f]isochromene-7-carboxylate 73813161 Click to see CC12CCC3C(=O)OC(CC3(C1CC(=O)C=C2C(=O)OC)C)C4=COC=C4 372.40 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
Methyl 2-(furan-3-yl)-9,10-dihydroxy-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 73062953 Click to see 390.40 unknown https://doi.org/10.1021/NP060456F
methyl 9-acetyloxy-2-(2-hydroxy-5-oxo-2H-furan-3-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 162960096 Click to see 464.50 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
methyl 9-acetyloxy-2-(2-hydroxy-5-oxo-2H-furan-4-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 162940407 Click to see 464.50 unknown https://doi.org/10.1021/NP060456F
methyl 9-acetyloxy-2-(3,4-dihydroxy-2,5-dimethoxyoxolan-3-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 56670934 Click to see 528.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2535573/
Methyl 9-acetyloxy-2-(furan-3-yl)-10-hydroxy-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 72772891 Click to see 432.50 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
methyl 9-acetyloxy-2-(furan-3-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate 3969708 Click to see 432.50 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMCL.2006.03.062
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/JO00198A026
https://doi.org/10.1039/P19820002505
https://doi.org/10.1021/NP900181Q
https://doi.org/10.1021/NP060456F
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2544632/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025038/
https://doi.org/10.1021/NP0205699
Methyl 9,10-diacetyloxy-2-(furan-3-yl)-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 72793961 Click to see CC(=O)OC1C=C(C2(CCC3C(=O)OC(CC3(C2C1OC(=O)C)C)C4=COC=C4)C)C(=O)OC 474.50 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
https://doi.org/10.1021/OL016820D
salvidivin A 16099522 Click to see CC(=O)OC1CC(C2(CCC3C(=O)OC(CC3(C2C1=O)C)C4=CC(=O)OC4O)C)C(=O)OC 464.50 unknown https://doi.org/10.1021/NP078001T
Salvinicin A 11466688 Click to see 528.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2535573/
Salvinorin A 128563 Click to see 432.50 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMCL.2006.03.062
https://doi.org/10.1007/BF02858975
https://doi.org/10.1016/0378-8741(94)90116-3
https://doi.org/10.1021/NP0205699
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2544632/
https://doi.org/10.1016/J.BMC.2005.05.054
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025038/
https://doi.org/10.1016/S0379-0738(00)00180-8
https://doi.org/10.1016/J.TETLET.2010.08.033
https://doi.org/10.1021/NP078001T
https://doi.org/10.1080/02791072.1994.10472441
https://doi.org/10.1021/NP900181Q
https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<22::AID-PCA428>3.0.CO;2-0
https://doi.org/10.1021/JO00198A026
https://doi.org/10.1039/P19820002505
https://doi.org/10.1021/NP060456F
Salvinorin A (Ester) 21589297 Click to see 432.50 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
Salvinorin B 11440685 Click to see 390.40 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/JO00198A026
https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP900181Q
https://doi.org/10.1007/BF02858975
https://doi.org/10.1021/NP060456F
https://doi.org/10.1080/02791072.1994.10472441
https://doi.org/10.1021/NP0205699
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
[3-(Chloromethyl)-3-hydroxy-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-8-yl] acetate 163001290 Click to see CC(=O)OC1CC2C(C1=C)C3C(CCC2=C)C(C(=O)O3)(CCl)O 340.80 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
https://doi.org/10.1021/NP900181Q
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(1R,2R,3R)-2-(4,8-dimethylnona-3,7-dienyl)-2-methyl-3-(2,6,10-trimethylundeca-1,5,9-trienyl)cyclopropyl]methanol 193145 Click to see CC(=CCCC(=CCCC(=CC1C(C1(C)CCC=C(C)CCC=C(C)C)CO)C)C)C 426.70 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
[2-(4,8-Dimethylnona-3,7-dienyl)-2-methyl-3-(2,6,10-trimethylundeca-1,5,9-trienyl)cyclopropyl]methanol 53463597 Click to see 426.70 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1021/NP030313I
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1021/NP030313I
Presqualene alcohol 5471965 Click to see CC(=CCCC(=CCCC(=CC1C(C1(C)CCC=C(C)CCC=C(C)C)CO)C)C)C 426.70 unknown https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(5S,7R,7aR)-2-[2-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-3-imino-5-(2-methylprop-1-enyl)-5,6,7,7a-tetrahydro-1H-pyrrolo[1,2-c]imidazole-7-carboxylic acid 71746449 Click to see 443.50 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
L-Guluronic acid 6857369 Click to see 194.14 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP900181Q
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown https://doi.org/10.1021/NP060456F
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Pseudolarolide F 6711553 Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC5(C=C6C(CCCC4(C3)C)C(OC(=O)C=C6O5)(C)C)O)C 514.60 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
https://doi.org/10.1021/NP900181Q
https://doi.org/10.1021/OL016820D
> Organoheterocyclic compounds / Benzofurans
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one 14334 Click to see 196.24 unknown https://doi.org/10.1021/NP060456F
Isololiolide 11019783 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP50043A031
https://doi.org/10.1021/NP060456F
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole 798 Click to see 117.15 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles / 3-methylindoles
3-Methylindole 6736 Click to see CC1=CNC2=CC=CC=C12 131.17 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
> Organoheterocyclic compounds / Naphthofurans
(4aR,8aR,9aS)-9a-methoxy-3,8a-dimethyl-2-methylidene-4a,5,6,7,8,9-hexahydro-4H-benzo[f][1]benzofuran 163027643 Click to see 248.36 unknown https://doi.org/10.1021/NP900181Q
> Organoheterocyclic compounds / Naphthopyrans
11-Hydroxy-12-methoxy-7,7,10a-trimethyl-1,2,5,6,6a,8,9,10-octahydronaphtho[1,2-h]isochromen-4-one 72988695 Click to see CC1(CCCC2(C1CCC3=C4C(=C(C(=C32)O)OC)CCOC4=O)C)C 344.40 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP030313I
https://doi.org/10.1016/J.BMC.2005.05.054
https://doi.org/10.1021/NP0205699
https://doi.org/10.1021/NP900181Q
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
2-Hydroxypyridine 8871 Click to see C1=CC(=O)NC=C1 95.10 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
> Organoheterocyclic compounds / Pyridines and derivatives / Hydroxypyridines
3-Hydroxypyridine 7971 Click to see 95.10 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
> Organoheterocyclic compounds / Pyridines and derivatives / Methylpyridines
2-Methylpyridin-3-ol 70719 Click to see 109.13 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
> Organoheterocyclic compounds / Pyrrolopyrazines
Pyrocoll 10241527 Click to see 186.17 unknown https://doi.org/10.1016/J.TETLET.2010.08.033
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethenyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 78384837 Click to see C1=CC(=C(C=C1C=CC(=O)OC=CC2=CC(=C(C=C2)O)O)O)O 314.29 unknown https://doi.org/10.1021/NP060456F
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown https://doi.org/10.1021/NP060456F
Methyl Caffeate 689075 Click to see 194.18 unknown https://doi.org/10.1021/NP078001T
https://doi.org/10.1021/NP060456F
Nepetoidin B 5316819 Click to see 314.29 unknown https://doi.org/10.1021/NP060456F
https://doi.org/10.1021/NP078001T

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