Details Top

Internal ID UUID643febb6309ed742930576
Scientific name Salvia glutinosa
Authority L.
First published in Sp. Pl. : 26 (1753)

Ethnobotanical Use Top

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

Among the Greek folk healers of the Peloponnese, the dried leaves of Salvia glutinosa are prepared as a mild tea to alleviate cough and to reduce fever; Pieroni et al., 2005 recorded this use in a 2005 ethnobotanical survey. In northern Albania, a decoction of the aerial parts is taken for stomach pain and dyspepsia; Gashi et al., 2020 reported the practice in a 2020 field study of the Shkodër region. Serbian herbalists in the Vojvodina plain use an infusion of the same plant as a gargle for sore throat, a practice noted by Stojanović & Milanović, 2017. Austrian rural physicians of the nineteenth century noted a decoction of the dried herb taken for fevers (Keller, 1863), and in the Italian Apennines fresh leaves are sometimes pounded into a poultice for minor skin irritations, as described by Ballini & Marsili, 2014.

A simple mild tea is prepared by placing one to two teaspoons (≈1–2 g) of dried Salvia glutinosa leaves in a cup, pouring 250 ml of freshly boiled water over them, covering the cup, and allowing the mixture to steep for eight to ten minutes. The infusion is then strained and may be taken two to three times daily while symptoms persist. The same preparation can be cooled and used as a gargle. Safety notes: the tea should not be consumed by pregnant or breastfeeding women, and the daily intake should not exceed three cups, because high doses can cause mild gastrointestinal upset in sensitive individuals.

Chemical analyses confirm that Salvia glutinosa contains rosmarinic acid, a phenolic acid with recognized anti‑inflammatory and antispasmodic activity (Sava et al., 2020). The herb also supplies flavonoids such as luteolin and apigenin (Gökmen et al., 2014), which contribute antioxidant protection. Its essential oil, rich in camphor (≈13 %) and 1,8‑cineole (≈22 %), provides the characteristic aromatic scent and has been shown in vitro to exert mild antimicrobial effects (Erdemoglu et al., 2005). These compounds plausibly explain the traditional cough‑relieving and digestive actions reported across the various regions.

Modern research continues to explore the anti‑inflammatory potential of rosmarinic acid and the antimicrobial activity of the essential oil, while commercial herbal suppliers now sell dried Salvia glutinosa as “sticky sage tea” and the plant remains a staple in many rural health practices of southern Europe.

General Uses Top

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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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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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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
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Turkey
  • Europe
    • 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

Links to other databases Top

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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 278.30 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
Dihydroisotanshinone Ii 44425164 Click to see 278.30 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
Isotanshinone Ii 44425166 Click to see 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 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 296.40 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
15-Epi-Danshenol-A 102004790 Click to see 336.40 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
2-Isopropyl-8-methylphenanthrene-3,4-dione 135872 Click to see 264.30 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
8,9-Dihydro-4,8-dimethylphenanthro(3,2-b)furan-7,11-dione 89406 Click to see 278.30 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
Cryptotanshinone 160254 Click to see 296.40 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
Danshenol A 3083514 Click to see 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 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 278.30 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
Isotanshinone I 623940 Click to see 276.30 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
Isotanshinone IIA 626354 Click to see 294.30 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
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
(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 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 456.70 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-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
alpha-Amyrin acetate 92842 Click to see 468.80 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 (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 89432794 Click to see 470.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Methyl 3-hydroxyolean-12-en-28-oate 122541 Click to see 470.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Methyl Oleanolate 92900 Click to see 470.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Methyl Ursolate 636516 Click to see 470.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Npc25529 293754 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Ursolic acid methyl ester 621719 Click to see 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
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
(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 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 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
7alpha-Hydroxysitosterol 161816 Click to see 430.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00042-3
Stigmasterol 5280794 Click to see 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 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 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 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 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 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 344.30 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
Jaranol 5318869 Click to see 314.29 unknown https://doi.org/10.1016/S0031-9422(01)00415-0

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