Salvia glutinosa, also known as glutinous sage, sticky sage, Jupiter's sage, or Jupiter's distaff, is a perennial herb belonging to the Lamiaceae family. It grows up to 40-60 centimetres tall and has bright green hairy leaves that are deciduous and toothed. The plant is covered in sticky glandular hairs, giving it its name "glutinosa". It is the main host plant for the plant bug Macrotylus quadrilineatus and has pale yellow flowers with maroon speckles. Salvia glutinosa is native to Central and East Europe and West Asia and is commonly found in forested areas with calcareous soils. It is often grown in gardens and has a flowering period from June to September. This species also contains salvinorin A, a psychoactive compound, and is found at altitudes of 100-1,600 metres above sea level.

Synonyms Top

Scientific name	Authority	First published in
Sclarea glutinosa	Mill.	Gard. Dict. ed. 8 : n.º 11 (1768)
Drymosphace glutinosa	Opiz	Seznam : 38 (1852)
Glutinaria acuminata	Raf.	Autik. Bot. : 122 (1840)
Glutinaria glutinosa	Raf.	Fl. Tellur. 3: 93 (1837)

Common names Top

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Filter by language:

Language	Common/alternative name
English	jupiter's sage
English	sticky clary
English	sticky sage
English	jupiter's distaff
English	hardy sage
English	glutinous sage
Arabic	مريمية دبقية
Arabic	سلفيا غلوتينية
Arabic	قصعين
Azerbaijani	vəzili adaçayı
Bulgarian	жълт конски босилек
Czech	šalvěj lepkavá
Welsh	clari gludiog
Danish	klæbrig salvie
German	kleb-salbei
German	klebriger salbei
Estonian	kollane salvei
Persian	مریمگلی جنگلی
Finnish	keltasalvia
French	sauge glutineuse
Croatian	ljepljiva kadulja
Upper Sorbian	lěpjaca želbija
Georgian	შალამანდილი
Dutch	kleverige salie
Polish	szałwia lepka
Russian	Шалфей клейкий
Russian	Шалфей железистый
Russian	или Шалфей клейкий
Slovak	šalvia lepkavá
Slovenian	lepljiva kadulja
Swedish	klibbsalvia
Turkish	yapışkan adaçayı
Turkish	okluşalba
Turkish	oklu şalba
Chinese	银紫丹参
Chinese	膠質鼠尾
Chinese	胶质鼠尾
Chinese	胶质鼠尾草

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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No subvariety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Western Asia
  - Iran
  - Turkey

Europe click to expand
- Eastern Europe
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Germany
  - Hungary
  - Poland
  - Switzerland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Spain

Northern America click to expand
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000301096
USDA Plants	SAGL12
Tropicos	17600295
INPN	120643
Flora of Italy	4672
KEW	urn:lsid:ipni.org:names:456289-1
The Plant List	kew-182731
Open Tree Of Life	1025161
Observations.org	126683
NCBI Taxonomy	49211
NBN Atlas	NBNSYS0000014568
Nature Serve	2.141360
IPNI	456289-1
iNaturalist	143418
GBIF	2927026
Freebase	/m/05lfk2
EPPO	SALGL
EOL	485078
Elurikkus	215081
USDA GRIN	32931
Wikipedia	Salvia_glutinosa

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

Novel Insights on Ferroptosis Modulation as Potential Strategy for Cancer Treatment: When Nature Kills

Consoli V, Fallica AN, Sorrenti V, Pittalà V, Vanella L

Antioxid Redox Signal

17-Jan-2024

PMCID:	PMC10824235
doi:	10.1089/ars.2022.0179
PMID:	37132605

Cytotoxic diterpenoids from Salvia glutinosa and comparison with the tanshinone profile of danshen (Salvia miltiorrhiza)

Ayvazyan A, Deutsch L, Zidorn C, Kircher B, Çiçek SS

Front Plant Sci

04-Dec-2023

PMCID:	PMC10729661
doi:	10.3389/fpls.2023.1269710
PMID:	38116152

In Vitro Antibacterial, Antioxidant, Anticholinesterase, and Antidiabetic Activities and Chemical Composition of Salvia balansae

Mokhtar A, Souhila T, Nacéra B, Amina B, Alghonaim MI, Öztürk M, Alsalamah SA, Miara MD, Boufahja F, Bendif H

Molecules

27-Nov-2023

PMCID:	PMC10708212
doi:	10.3390/molecules28237801
PMID:	38067531

Chemical Composition and Future Perspectives of Essential Oil Obtained from a Wild Population of Stachys germanica L. Distributed in the Balkan Mountains in Bulgaria

Ivanova S, Pashova S, Dyankov S, Georgieva Y, Ivanov K, Benbassat N, Koleva N, Bozhkova M, Karcheva-Bahchevanska D

Int J Anal Chem

31-Oct-2023

PMCID:	PMC10630024
doi:	10.1155/2023/4275213
PMID:	37942231

Ursolic acid: biological functions and application in animal husbandry

Liu G, Qin P, Cheng X, Wu L, Wang R, Gao W

Front Vet Sci

25-Oct-2023

PMCID:	PMC10642196
doi:	10.3389/fvets.2023.1251248
PMID:	37964910

In vitro Antimicrobial Activity of Some Extracts of Salvia spp Harvested from the Oltenia Flora Using Different Solvents

BĂLĂȘOIU RM, BIȚĂ A, STĂNCIULESCU EC, BĂLĂȘOIU M, BEJENARU C, BEJENARU LE, PISOSCHI CG

Curr Health Sci J

30-Sep-2023

PMCID:	PMC10832872
doi:	10.12865/CHSJ.49.03.12
PMID:	38314220

The recent progress in the research of extraction and functional applications of basil seed gum

Guan L, Ma Y, Yu F, Jiang X, Jiang P, Zhang Y, Yuan C, Huang M, Chen Z, Liu L

Heliyon

23-Aug-2023

PMCID:	PMC10472252
doi:	10.1016/j.heliyon.2023.e19302
PMID:	37662748

Phylogenetic relationships and biogeography of Asia Callicarpa (Lamiaceae), with consideration of a long-distance dispersal across the Pacific Ocean —insights into divergence modes of pantropical flora

Cai H, Liu X, Wang W, Ma Z, Li B, Bramley GL, Zhang D

Front Plant Sci

15-May-2023

PMCID:	PMC10225572
doi:	10.3389/fpls.2023.1133157
PMID:	37255555

Potential therapeutic applications of infusions and hydroalcoholic extracts of Romanian glutinous sage (Salvia glutinosa L.)

Nicolescu A, Babotă M, Ilea M, Dias MI, Calhelha RC, Gavrilaș L, Rocchetti G, Crișan G, Mocan A, Barros L, Pârvu AE

Front Pharmacol

19-Aug-2022

PMCID:	PMC9437640
doi:	10.3389/fphar.2022.975800
PMID:	36059937

Synopsis of Leptosphaeriaceae and Introduction of Three New Taxa and One New Record from China

Xu R, Su W, Tian S, Bhunjun CS, Tibpromma S, Hyde KD, Li Y, Phukhamsakda C

J Fungi (Basel)

19-Apr-2022

PMCID:	PMC9146790
doi:	10.3390/jof8050416
PMID:	35628672

Diverse in Local, Overlapping in Official Medical Botany: Critical Analysis of Medicinal Plant Records from the Historic Regions of Livonia and Courland in Northeast Europe, 1829–1895

Prakofjewa J, Anegg M, Kalle R, Simanova A, Prūse B, Pieroni A, Sõukand R

Plants (Basel)

13-Apr-2022

PMCID:	PMC9032843
doi:	10.3390/plants11081065
PMID:	35448792

Differentiation of natural scrub communities of the Cotoneastro-Amelanchieretum group in Central Europe

Świerkosz K, Reczyńska K

PLoS One

12-Apr-2022

PMCID:	PMC9004749
doi:	10.1371/journal.pone.0266868
PMID:	35413069

Plant Terpenoids as the Promising Source of Cholinesterase Inhibitors for Anti-AD Therapy

Lai Shi Min S, Liew SY, Chear NJ, Goh BH, Tan WN, Khaw KY

Biology (Basel)

14-Feb-2022

PMCID:	PMC8869317
doi:	10.3390/biology11020307
PMID:	35205173

Non-Alkaloid Cholinesterase Inhibitory Compounds from Natural Sources

Tamfu AN, Kucukaydin S, Yeskaliyeva B, Ozturk M, Dinica RM

Molecules

14-Sep-2021

PMCID:	PMC8472022
doi:	10.3390/molecules26185582
PMID:	34577053

Modulation of Quorum Sensing and Biofilms in Less Investigated Gram-Negative ESKAPE Pathogens

Lazar V, Holban AM, Curutiu C, Chifiriuc MC

Front Microbiol

29-Jul-2021

PMCID:	PMC8359898
doi:	10.3389/fmicb.2021.676510
PMID:	34394026

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 / Phenanthrenes and derivatives
Dihydroisotanshine II	75024890	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C4=CC=CC(=C4C=C3)C	278.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Dihydroisotanshinone Ii	44425164	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C4=CC=CC(=C4C=C3)C	278.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Isotanshinone Ii	44425166	Click to see CC1=C2C=CC3=C(C2=CC=C1)C4=C(C(=CO4)C)C(=O)C3=O	276.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
12-Deoxytanshinquinone B	15484930	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C=C(C3=O)C(C)C	264.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(8S)-4,8-dimethyl-8,9-dihydronaphtho[2,1-f][1]benzofuran-7,11-dione	11778300	Click to see CC1COC2=C1C(=O)C3=C(C2=O)C4=CC=CC(=C4C=C3)C	278.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
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/S0031-9422(99)00343-X
15-epi-Danshenol A	102004790	Click to see CC1COC2=C1C(=O)C(C3=C2C=CC4=C(C=CC=C43)C)(CC(=O)C)O	336.40	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
15-Epi-Danshenol-A	73062689	Click to see CC1COC2=C1C(=O)C(C3=C2C=CC4=C(C=CC=C43)C)(CC(=O)C)O	336.40	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
2-Isopropyl-8-methylphenanthrene-3,4-dione	135872	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C(=C3)C(C)C	264.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Cryptotanshinone	160254	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Danshenol A	3083514	Click to see CC1COC2=C1C(=O)C(C3=C2C=CC4=C(C=CC=C43)C)(CC(=O)C)O	336.40	unknown	https://doi.org/10.1016/S0305-1978(98)00043-X https://doi.org/10.1016/S0031-9422(99)00343-X
Danshenxinkun B	5320113	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C(=C3O)C(C)C	280.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Dihydrotanshinone	5316743	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C	278.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Dihydrotanshinone I	11425923	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C	278.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Isotanshinone I	623940	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C4=C(C3=O)C(=CO4)C	276.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Isotanshinone IIA	626354	Click to see CC1=COC2=C1C(=O)C3=C(C2=O)C4=C(C=C3)C(CCC4)(C)C	294.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Phenanthro[3,2-b]furan-7,11-dione, 8,9-dihydro-4,8-dimethyl-	89406	Click to see CC1COC2=C1C(=O)C3=C(C2=O)C4=CC=CC(=C4C=C3)C	278.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Tanshinone I	114917	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C	276.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Tanshinone IIA	164676	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	294.30	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4a-yl)methyl acetate	14777912	Click to see CC(=O)OCC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)(C)C	484.80	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl) acetate	13988561	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2=CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	466.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
[(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4a-yl]methyl acetate	11799091	Click to see CC(=O)OCC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)(C)C	484.80	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
10-Hydroxy-1,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,14b-tetradecahydropicen-13-one	74933427	Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
10-hydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picen-13-one	13996051	Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
11-Oxo-alpha-amyrin	69166285	Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
11-Oxo-beta-amyrin	20055661	Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
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/10.1016/S0031-9422(97)00042-3
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
Acetic acid oleana-9(11),12-diene-3beta-yl ester	13988564	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2=CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	466.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
alpha-Amyrenyl acetate	92842	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
alpha-Amyrin acetate	293754	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
beta-Ursolic acid	220774	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/10.1016/S0031-9422(97)00042-3
Lup-20(29)-en-3-ol, (3beta)-	521518	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/S0031-9422(97)00042-3
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/S0031-9422(97)00042-3
methyl (4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate	122541	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C	470.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
Methyl 3-hydroxyurs-12-en-28-oate	621719	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC	470.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
Methyl oleanolate	92900	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C	470.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
Methyl Ursolate	636516	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC	470.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
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/10.1016/S0031-9422(97)00042-3
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/10.1016/S0031-9422(97)00042-3
Ursolic acid methyl ester	89432794	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC	470.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
[22-(2-Hydroxypropan-2-yl)-1,5,10,10-tetramethyl-11-(3,4,5-trihydroxyoxan-2-yl)oxy-21,25-dioxaheptacyclo[20.2.1.02,19.05,19.06,16.09,14.014,16]pentacosan-3-yl] acetate	85360387	Click to see CC(=O)OC1CC2(C3CCC4C(C(CCC45C3(C5)CCC26C1C7(CCC(O7)(OC6)C(C)(C)O)C)OC8C(C(C(CO8)O)O)O)(C)C)C	662.80	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,7S,8R,9S,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-3,7-dihydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-1-one	163017655	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(C(=O)CC(C4)O)C)O)C)C(C)C	444.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
(3R,7S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-3,7-dihydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-1-one	101712318	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(C(=O)CC(C4)O)C)O)C)C(C)C	444.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
14-(5-Ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-5,9-diol	5318414	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C	430.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
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/S0031-9422(97)00042-3
17-(5-Ethyl-6-methylheptan-2-yl)-3,7-dihydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-1-one	85089123	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(C(=O)CC(C4)O)C)O)C)C(C)C	444.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
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/10.1016/S0031-9422(97)00042-3
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/S0031-9422(97)00042-3
Ikshusterol	161816	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C	430.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(97)00042-3
> Organoheterocyclic compounds / Naphthofurans
(3R,4'R)-4',6-dimethylspiro[benzo[g][2]benzofuran-3,2'-oxolane]-1-one	13965477	Click to see CC1CC2(C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2)OC1	268.31	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
(3S,4'S)-4',6-dimethylspiro[benzo[g][2]benzofuran-3,2'-oxolane]-1-one	13965479	Click to see CC1CC2(C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2)OC1	268.31	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
4',6-Dimethylspiro[benzo[g][2]benzofuran-3,2'-oxolane]-1-one	5316298	Click to see CC1CC2(C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2)OC1	268.31	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Cryptoacetalide	46896125	Click to see CC1CC2(C3=C(C4=C(C=C3)C(CCC4)(C)C)C(=O)O2)OC1	286.40	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
Epidanshenspiroketallactone	102004791	Click to see CC1CC2(C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2)OC1	268.31	unknown	https://doi.org/10.1016/S0031-9422(99)00343-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide	5280862	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	300.26	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin	5280682	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O	344.30	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
Jaranol	5318869	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	314.29	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0

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Salvia glutinosa

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