Salvia divinorum

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Collections

Details Top

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

Description Top

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Synonyms Top

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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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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 Southwest

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_041381175.1	UTM_Sdiv_1.0	Chromosome	University of Toronto Mississauga	2024-08-21	40.0x	516.36 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

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

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

A Critical Review of the Neuropharmacological Effects of Kratom: An Insight from the Functional Array of Identified Natural Compounds

Hossain R, Sultana A, Nuinoon M, Noonong K, Tangpong J, Hossain KH, Rahman MA

Molecules

31-Oct-2023

PMCID:	PMC10648626
doi:	10.3390/molecules28217372
PMID:	37959790

Effects of a dissociative drug on fronto-limbic resting-state functional connectivity in individuals with posttraumatic stress disorder: a randomized controlled pilot study

Danböck SK, Duek O, Ben-Zion Z, Korem N, Amen SL, Kelmendi B, Wilhelm FH, Levy I, Harpaz-Rotem I

Psychopharmacology (Berl)

23-Oct-2023

PMCID:	PMC10806226
doi:	10.1007/s00213-023-06479-4
PMID:	37872291

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 CCCCCCCCCCCCCCCCC(=O)C=C1C(C(C(N1CCC2=CC=C(C=C2)O)CCC)C(=O)OC)O	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
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol	145386	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1016/J.BMC.2005.05.054 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 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
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	15559627	Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C	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 CC1CCC2C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O	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 CC1CCC2(C(C1(C)CCC3=COC=C3)C(CC=C2C(=O)O)O)C	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 CC(=O)OCC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C	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 CC12CCC(C(C1C(CC=C2C(=O)OC)O)(C)CCC3=COC=C3)CO	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 CC(=O)OCC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C	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
Hardwickiic acid	15559629	Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)C	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
methyl (1R,3S,4aR,4bS,6R,8aR,10aR)-3-acetyloxy-6-[(2S,3R,4S,5R)-3,4-dihydroxy-2,5-dimethoxyoxolan-3-yl]-4b,10a-dimethyl-4,8-dioxo-1,2,3,4a,5,6,7,8a,9,10-decahydrophenanthrene-1-carboxylate	71454521	Click to see CC(=O)OC1CC(C2(CCC3C(=O)CC(CC3(C2C1=O)C)C4(C(C(OC4OC)OC)O)O)C)C(=O)OC	526.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2535573/
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 CC12CCC(C(C1C(C(C=C2C(=O)OC)O)O)(C)CCC3=COC=C3)CO	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 CC12CCC(C(C1C(CC=C2C(=O)OC)O)(C)CCC3=COC=C3)C=O	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 CC1CCC2(C(C1(C)CCC3=COC=C3)C(CC=C2C(=O)OC)O)C	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 CC(=O)OCC1CCC2(C(C1(C)CCC3=COC=C3)C(CC=C2C(=O)OC)O)C	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 CC12CCC3C(OC(CC3(C1C(C(C=C2C(=O)OC)O)O)C)C4=COC=C4)O	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 CC12CCC(C(C1C(C(C=C2C(=O)OC)O)O)(C)CCC3=COC=C3)CO	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 CC12CCC(C(C1C(CC=C2C(=O)OC)O)(C)CCC3=COC=C3)CO	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 CC(=O)OCC1CCC2(C(C1(C)CCC3=COC=C3)C(CC=C2C(=O)OC)O)C	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 CC12CCC(C(C1C(CC=C2C(=O)OC)O)(C)CCC3=COC=C3)C=O	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 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
> 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 CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C	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 CC(=O)OC1CC(C2(CCC(C(C2C1=O)(C)C=CC3=CC(=O)OC3O)C(=O)O)C)C(=O)OC	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 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/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 CC(=O)OC1CC(C2(CCC(C(C2C1=O)(C)C=CC3=CC(=O)OC3O)C(=O)O)C)C(=O)OC	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 CC(=O)OC1CC(C2(CCC(C(C2C1=O)(C)C=CC3=CC(=O)OC3O)C(=O)O)C)C(=O)OC	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 CC(=O)OC1CC(C2(CCC(C(C2C1=O)(C)C=CC3=CC(=O)OC3O)C(=O)O)C)C(=O)OC	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 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
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 CC(=O)OC1CC(C2(CCC3C(=O)OC(CC3(C2C1=O)C)C4=COC=C4)C)C(=O)OC	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 CC(=O)OC1C2C(CCC3C2(CC(OC3=O)C4=COC=C4)C)(C(=CC1=O)C(=O)OC)C	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 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/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 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/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 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
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 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 (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 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 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 CC(=O)OC1C2C(CCC3C2(CC(OC3=O)C4=COC=C4)C)(C(=CC1=O)C(=O)OC)C	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 CC(=O)OC1C(C=C(C2(C1C3(CC(OC(=O)C3CC2)C4=COC=C4)C)C)C(=O)OC)O	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 CC12CCC3C(=O)OC(CC3(C1C(C(C=C2C(=O)OC)O)O)C)C4=COC=C4	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 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 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 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 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 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 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 CC(=O)OC1C=C(C2(CCC3C(=O)OC(CC3(C2C1O)C)C4=COC=C4)C)C(=O)OC	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 CC(=O)OC1CC(C2(CCC3C(=O)OC(CC3(C2C1=O)C)C4=COC=C4)C)C(=O)OC	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 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/
Salvinorin A	128563	Click to see CC(=O)OC1CC(C2(CCC3C(=O)OC(CC3(C2C1=O)C)C4=COC=C4)C)C(=O)OC	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 CC(=O)OC1CC(C2(CCC3C(=O)OC(CC3(C2C1=O)C)C4=COC=C4)C)C(=O)OC	432.50	unknown	https://doi.org/10.1016/J.TETLET.2010.08.033
Salvinorin B	11440685	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/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 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
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1021/NP030313I
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	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
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
Beta-Sitosterol	222284	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 CC(=CC1CC(C2N1C(=N)N(C2)CC(CCOC3C(C(C(CO3)O)O)O)O)C(=O)O)C	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 C(=O)C(C(C(C(C(=O)O)O)O)O)O	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
Protocatechualdehyde	8768	Click to see C1=CC(=C(C=C1C=O)O)O	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-tetrahydrobenzofuran-2(4H)-one	14334	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	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 C1=CC=C2C(=C1)C=CN2	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 CC1=C2CC3CCCCC3(CC2(OC1=C)OC)C	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 C1=CC(=CN=C1)O	95.10	unknown	https://doi.org/10.1016/J.TETLET.2010.08.033
> Organoheterocyclic compounds / Pyridines and derivatives / Methylpyridines
3-Hydroxy-2-methylpyridine	70719	Click to see CC1=C(C=CC=N1)O	109.13	unknown	https://doi.org/10.1016/J.TETLET.2010.08.033
> Organoheterocyclic compounds / Pyrrolopyrazines
Pyrocoll	10241527	Click to see C1=CN2C(=C1)C(=O)N3C=CC=C3C2=O	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
Caffeic acid methyl ester	689075	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	194.18	unknown	https://doi.org/10.1021/NP078001T https://doi.org/10.1021/NP060456F
Methyl 3,4-dihydroxycinnamate	92202	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	194.18	unknown	https://doi.org/10.1021/NP060456F
Nepetoidin B	5316819	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 https://doi.org/10.1021/NP078001T

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Salvia divinorum

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