Scientific name	Authority	First published in
Ramona stachyoides	Briq.	Nat. Pflanzenfam. 4(3a): 287 (1896)
Audibertia spinulosa	Nutt. ex Benth.	Prodr. 12: 359 (1848)
Audibertia stachyoides	Benth.	Labiat. Gen. Spec. : 313 (1833)
Audibertiella stachyoides	Briq.	Bull. Herb. Boissier 2: 73 (1894)
Salvia mellifera var. jonesii	Munz	Bull. S. Calif. Acad. Sci. 26: 24, fig. 20, 21. 1927
Salvia mellifera subsp. jonesii	Abrams	Ill. Fl. Pacific States 3: 641 (1951)
Salvia mellifera var. revoluta	Munz	Bull. S. Calif. Acad. Sci. 26: 23 (1927)
Salvia mellifera subsp. revoluta	Abrams	Ill. Fl. Pacific States 3: 641 (1951)

Common names Top

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Filter by language:

Language	Common/alternative name
English	black sage
Czech	šalvěj černá
German	kalifornischer salbei
Chinese	蜜腺鼠尾草

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

Northern America click to expand
- Mexico
  - Mexico Northwest
- Southwestern U.S.A.
  - California

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000301567
UNII	SG3NE0O808
USDA Plants	SAME3
Tropicos	17601712
KEW	urn:lsid:ipni.org:names:289832-2
The Plant List	kew-183169
Open Tree Of Life	1609
NCBI Taxonomy	392671
Nature Serve	2.142490
IPNI	289832-2
iNaturalist	50643
GBIF	2926986
Freebase	/m/03tttz
FEIS	plants/shrub/salmel
EPPO	SALMF
EOL	578475
Calflora (Californian flora)	7311
USDA GRIN	430895
Wikipedia	Salvia_mellifera

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

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023

Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A

EFSA J

15-Dec-2023

PMCID:	PMC10722330
doi:	10.2903/j.efsa.2023.8477
PMID:	38107375

Testing the contribution of dispersal to microbial succession following a wildfire

Barbour KM, Weihe C, Walters KE, Martiny JB

mSystems

25-Sep-2023

PMCID:	PMC10654055
doi:	10.1128/msystems.00579-23
PMID:	37747204

Plant physiological indicators for optimizing conservation outcomes

Schönbeck L, Arteaga M, Mirza H, Coleman M, Mitchell D, Huang X, Ortiz H, Santiago LS

Conserv Physiol

12-Sep-2023

PMCID:	PMC10498484
doi:	10.1093/conphys/coad073
PMID:	37711583

Honeybees (Apis mellifera) decrease the fitness of plants they pollinate

Travis DJ, Kohn JR

Proc Biol Sci

28-Jun-2023

PMCID:	PMC10291720
doi:	10.1098/rspb.2023.0967
PMID:	37357853

Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022

Gibin D, Pasinato L, Delbianco A

EFSA J

13-Jun-2023

PMCID:	PMC10262070
doi:	10.2903/j.efsa.2023.8061
PMID:	37325259

Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach

De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K

In Silico Pharmacol

28-Apr-2023

PMCID:	PMC10141836
doi:	10.1007/s40203-023-00143-7
PMID:	37131867

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2022

Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M

EFSA J

09-Jan-2023

PMCID:	PMC9827234
doi:	10.2903/j.efsa.2023.7726
PMID:	36628332

Chemical Authentication and Speciation of Salvia Botanicals: An Investigation Utilizing GC/Q-ToF and Chemometrics

Lee J, Wang M, Zhao J, Avula B, Chittiboyina AG, Li J, Wu C, Khan IA

Foods

19-Jul-2022

PMCID:	PMC9322183
doi:	10.3390/foods11142132
PMID:	35885375

Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2021

Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M

EFSA J

15-Jun-2022

PMCID:	PMC9198695
doi:	10.2903/j.efsa.2022.7356
PMID:	35734284

Allelopathic Properties of Lamiaceae Species: Prospects and Challenges to Use in Agriculture

Islam AK, Suttiyut T, Anwar MP, Juraimi AS, Kato-Noguchi H

Plants (Basel)

31-May-2022

PMCID:	PMC9182988
doi:	10.3390/plants11111478
PMID:	35684250

Is it best to add native shrubs to a coastal sage scrub restoration project as seeds or as seedlings?

McGuire KD, Schmidt KT, Ta P, Long JJ, Yurko M, Kimball S

PLoS One

08-Feb-2022

PMCID:	PMC8824352
doi:	10.1371/journal.pone.0262410
PMID:	35134054

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2021

Delbianco A, Gibin D, Pasinato L, Morelli M

EFSA J

12-Jan-2022

PMCID:	PMC8753584
doi:	10.2903/j.efsa.2022.7039
PMID:	35035582

Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2020

Delbianco A, Gibin D, Pasinato L, Morelli M

EFSA J

23-Jun-2021

PMCID:	PMC8220458
doi:	10.2903/j.efsa.2021.6674
PMID:	34188716

Exchange of medicinal plant information in California missions

McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL

J Ethnobiol Ethnomed

15-Jun-2020

PMCID:	PMC7296748
doi:	10.1186/s13002-020-00388-y
PMID:	32539795

Drought and plant litter chemistry alter microbial gene expression and metabolite production

Malik AA, Swenson T, Weihe C, Morrison EW, Martiny JB, Brodie EL, Northen TR, Allison SD

ISME J

22-May-2020

PMCID:	PMC7608424
doi:	10.1038/s41396-020-0683-6
PMID:	32444813

Phytochemical Profile Top

Add a new one!

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Pisiferal	13785026	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O	300.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8S,10S)-5-[(2S)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-3,4-diol	162931432	Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O)O	332.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(4aR,10aS)-5,6-dihydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carbaldehyde	162943540	Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O)O	332.40	unknown	https://doi.org/10.1016/0031-9422(91)83468-Z
(4aR,10aS)-5,6-dihydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	162950519	Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	348.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(4aR,10aS)-7-[(2S)-1-acetyloxypropan-2-yl]-5,6-dihydroxy-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	162881462	Click to see CC(COC(=O)C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	390.50	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(4bR,8aS)-4b-(hydroxymethyl)-2-[(2S)-1-hydroxypropan-2-yl]-8,8-dimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-diol	162956023	Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O)O	334.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
11,20-Dihydroxyferruginol	15602222	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O)O	318.40	unknown	https://doi.org/10.1016/0031-9422(91)83468-Z
4aH-Dibenzo[a,d]cycloheptene-4a,6,7-triol, 1,2,3,4,5,10,11,11a-octahydro-1,1-dimethyl-8-(1-methylethyl)-, trans-(9CI)	11809306	Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)O	318.40	unknown	https://doi.org/10.1016/0031-9422(91)83468-Z
4b-(Hydroxymethyl)-2-(1-hydroxypropan-2-yl)-8,8-dimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-diol	162956022	Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O)O	334.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
4b-(Hydroxymethyl)-8,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-diol	15602221	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O)O	318.40	unknown	https://doi.org/10.1016/0031-9422(91)83468-Z
5-(1-Hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-3,4-diol	162931431	Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O)O	332.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
5,6-Dihydroxy-7-(1-hydroxypropan-2-yl)-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carbaldehyde	85446789	Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O)O	332.40	unknown	https://doi.org/10.1016/0031-9422(91)83468-Z
5,6-Dihydroxy-7-(1-hydroxypropan-2-yl)-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	14527199	Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	348.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
5,6-Dihydroxy-7-(1-hydroxypropan-2-yl)-1,1-dimethyl-2,3,9,10-tetrahydrophenanthren-4-one	162864792	Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3=C2C(=O)CCC3(C)C)O)O	316.40	unknown	https://doi.org/10.1016/S0040-4020(01)80415-4
5,6-dihydroxy-7-[(2R)-1-hydroxypropan-2-yl]-1,1-dimethyl-2,3,9,10-tetrahydrophenanthren-4-one	162864793	Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3=C2C(=O)CCC3(C)C)O)O	316.40	unknown	https://doi.org/10.1016/S0040-4020(01)80415-4
7-(1-Acetyloxypropan-2-yl)-5,6-dihydroxy-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	74403601	Click to see CC(COC(=O)C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	390.50	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
Carnosic acid	65126	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	332.40	unknown	https://doi.org/10.1016/0031-9422(91)83468-Z https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/0031-9422(90)80149-B https://doi.org/10.1016/0031-9422(92)80282-J
Carnosicacid	5024746	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	332.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
Demethylsalvicanol	11666872	Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)O	318.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/0031-9422(91)83468-Z
From the seeds of Chamaecyparis pisifera	355228	Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O	302.50	unknown	https://doi.org/10.1080/10575639908045430
Isopimara-7,15-diene	13969536	Click to see CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C	272.50	unknown	https://doi.org/10.1016/S0040-4020(01)80415-4
Podocarp-8(14)-ene, 13beta-methyl-13-vinyl-	519326	Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C	272.50	unknown	https://doi.org/10.1016/S0040-4020(01)80415-4
Sageone	6481824	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3=C2C(=O)CCC3(C)C)O)O	300.40	unknown	https://doi.org/10.1016/0031-9422(92)83493-I
Salvicanol	101607178	Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)OC	332.50	unknown	https://doi.org/10.1080/10575639908045430 https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/0031-9422(91)83468-Z https://doi.org/10.1016/0031-9422(90)80149-B
Sandaracopimaradiene	443469	Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C	272.50	unknown	https://doi.org/10.1016/S0040-4020(01)80415-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
1,6,6-Trimethyl-1,2,6,7,8,9-hexahydrophenanthro[1,2-b]furan-10,11-dione	496348	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	296.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/S0040-4020(01)80415-4
Cryptotanshinone	160254	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	296.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/S0040-4020(01)80415-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50051A035
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/NP50051A035
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1021/NP50051A035
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/NP50051A035
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50051A035
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Gamma-cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8R,10S)-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-9,15-dione	162977601	Click to see CC(C)C1=C(C(=C2C(=C1)C3C(=O)C4C2(CCCC4(C)C)C(=O)O3)O)O	344.40	unknown	https://doi.org/10.1016/0031-9422(92)83493-I
(1R,8R,9R,10S)-3,4,9-trihydroxy-5-[(2S)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	163188738	Click to see CC(CO)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O	362.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8R,9S,10S)-3,4,8-trihydroxy-5-[(2S)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	162996145	Click to see CC(CO)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	362.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8S,10S)-3,4,8-trihydroxy-5-[(2R)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	102271305	Click to see CC(CO)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	362.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8S,9S,10S)-3,4,8-trihydroxy-5-[(2S)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	162996142	Click to see CC(CO)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	362.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8S,9S)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	455261	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/0031-9422(92)80282-J https://doi.org/10.1016/0031-9422(91)83468-Z
(1R)-3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	2579	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
16-Hydroxycarnosol	12966869	Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	346.40	unknown	https://doi.org/10.1016/S0040-4020(01)80415-4 https://doi.org/10.1248/CPB.53.1524
16-Hydroxycarnosol	44566424	Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	346.40	unknown	https://doi.org/10.1016/S0040-4020(01)80415-4
2H-10,4a-(Epoxymethano)phenanthren-12-one, 1,3,4,9,10,10a-hexahydro-5,6,9-trihydroxy-1,1-dimethyl-7-(1-methylethyl)-, (4aR,9R,10S,10aS)-	23243694	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-9,15-dione	162977600	Click to see CC(C)C1=C(C(=C2C(=C1)C3C(=O)C4C2(CCCC4(C)C)C(=O)O3)O)O	344.40	unknown	https://doi.org/10.1016/0031-9422(92)83493-I
3,4-Dihydroxy-5-(1-hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	73178218	Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	346.40	unknown	https://doi.org/10.1248/CPB.53.1524 https://doi.org/10.1016/S0040-4020(01)80415-4
3,4,8-Trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	9884612	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
3,4,8-Trihydroxy-5-(1-hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	74026716	Click to see CC(CO)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	362.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
3,4,9-Trihydroxy-11,11-dimethyl-5-(propan-2-yl)-16-oxatetracyclo[6.6.2.0^{1,10}.0^{2,7}]hexadeca-2(7),3,5-trien-15-one	11996616	Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
3,4,9-Trihydroxy-5-(1-hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	162975294	Click to see CC(CO)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O	362.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
7-O-Methylrosmanol	23243692	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O	360.40	unknown	https://doi.org/10.1016/0031-9422(92)80282-J
Carnosol	442009	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/0031-9422(91)83468-Z https://doi.org/10.1016/0031-9422(92)80282-J
Galdosol	13966127	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C3C4C2(CCCC4(C)C)C(=O)O3)O)O	344.40	unknown	https://doi.org/10.1016/0031-9422(91)83468-Z https://doi.org/10.1016/0031-9422(92)80282-J https://doi.org/10.1016/0031-9422(93)85463-2
Isorosmanol	13820511	Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/0031-9422(91)83468-Z https://doi.org/10.1016/0031-9422(92)80282-J
Rosmanol	13966122	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/0031-9422(91)83468-Z https://doi.org/10.1016/0031-9422(92)80282-J
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1080/10575639908048785
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(90)80149-B
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/10.1080/10575639908048785
Oleanolic acid acetate	6708573	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C	498.70	unknown	https://doi.org/10.1016/0031-9422(90)80149-B
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1080/10575639908048785
> 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/10.1080/10575639908048785 https://doi.org/10.1080/10575639908045430
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1080/10575639908048785 https://doi.org/10.1080/10575639908045430
> Organoheterocyclic compounds / Benzofurans
(-)-Rosmadial	72996596	Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	344.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
(1'S,3R)-7-hydroxy-6-[(2S)-1-hydroxypropan-2-yl]-2',2'-dimethyl-2-oxospiro[1-benzofuran-3,6'-cyclohexane]-1',4-dicarbaldehyde	163187068	Click to see CC(CO)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	360.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
7-Hydroxy-6-(1-hydroxypropan-2-yl)-2',2'-dimethyl-2-oxospiro[1-benzofuran-3,6'-cyclohexane]-1',4-dicarbaldehyde	163076522	Click to see CC(CO)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	360.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2
Rosmadial	15801061	Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	344.40	unknown	https://doi.org/10.1016/0031-9422(93)85463-2 https://doi.org/10.1016/0031-9422(91)83468-Z https://doi.org/10.1016/0031-9422(92)80282-J

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Salvia mellifera

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