Details Top

Internal ID UUID643febfb51d9e171959909
Scientific name Salvia tomentosa
Authority Mill.
First published in Gard. Dict. ed. 8 : n.º 2 (1768)

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 Aromanian communities in the Greek–Albanian borderlands, fresh or dried leaves of Salvia tomentosa are prepared as a hot infusion to relieve cold symptoms and as a carminative tea for digestive complaints, as reported by Mattalia et al., 2020. In the central Italian Apennines, locals make a bitter tea of S. tomentosa leaves to settle indigestion and ease cold-related cough, with the plant explicitly listed among traditional teas in Antrodoco and nearby villages by Ghirardini et al., 2001. In southern Turkey’s Mersin region, folk practitioners decoct the leaves to treat tonsillitis and sore throat and occasionally macerate the herb to soften the flavor before infusion, as described in Tuzlacı, 2011.

To illustrate one preparation, a 1:5 ethanol tincture of Salvia tomentosa leaf can be made by finely chopping 20 g of air-dried aerial parts and macerating in 100 mL of 45% ethanol for two weeks, shaking daily. After filtration, a common adult dose ranges from 0.5 to 1.0 mL taken up to three times daily for mild cold or digestive symptoms. Do not exceed two weeks of continuous use unless directed by a qualified clinician; avoid in pregnancy and breastfeeding, and discontinue if allergic reaction occurs.

The bitter taste and reported uses align with well-known constituents: carnosol, carnosic acid, and rosmarinic acid are present in Salvia tomentosa leaves and account for established antioxidant and anti-inflammatory activity, as documented by Ślusarczyk et al., 2018 and Şarer et al., 2010. Essential oils rich in camphor and 1,8-cineole contribute to mild expectorant effects and are reported for this species by Cambie & Ferguson, 2003.

Modern relevance is growing, with commercial products and ongoing research into extracts, yet traditional tea of S. tomentosa remains a simple daily infusion in several Mediterranean communities, sustaining a living ethnobotanical practice today.

General Uses Top

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Common products:
Salvia tomentosa yields an essential oil by steam distillation of aerial parts. Commercial availability is limited and typically batch-specific.

Industrial and craft applications:
The oil is used in fragrance applications, especially in aromatic and fougère-type compositions. Principal constituents (camphor and 1,8-cineole with alpha-pinene and camphene) contribute characteristic coniferous, resinous notes.

Food and beverages (non-medicinal):
In some regional cuisines, dried leaves are used sparingly as a spice. The flavor profile parallels that of other Salvia species but should be cited to species-level documentation when available; processor selection is batch-specific.

Colorants and tanning:
No documented use as a dye or tannin source is reported for this taxon.

Wood and fiber:
No timber or fiber uses are documented.

Fragrance and cosmetics:
The essential oil is employed in perfumery. Regulatory compliance follows general International Fragrance Association (IFRA) standards and the EU Cosmetic Regulation (1223/2009) for fragrance ingredients.

Properties relevant to use:
The oil is dominated by monoterpenes, notably camphor (often major) and 1,8-cineole, with moderate alpha-pinene and camphene, and typically minor alpha- and beta-thujone. This profile imparts camphoraceous, fresh-aromatic odor notes with high evaporation rate.

Standards and regulation:
Fragrance use must comply with IFRA Standards and country-specific fragrance labeling rules; cosmetics use with the EU Cosmetic Regulation and national counterparts where applicable.

Sustainability and sourcing:
Material is mainly wild-collected. Populations in parts of its range are under pressure, and harvesting can impact habitat. Conservation assessments vary by region; collection should follow regional conservation guidance and established essential-oil quality specifications where applicable.

Synonyms Top

Scientific name Authority First published in
Salvia brachystemon Klokov Fl. RSS Ukr. 9: 653 (1960)
Salvia fruticum Vuk. Oesterr. Bot. Z. 30: 163 (1880)
Salvia grandiflora Etl. Salv. : 17 (1777)
Salvia major Garsault Fig. Pl. Méd. : t. 510 a (1764)
Salvia nusairiensis Post Bull. Herb. Boissier 1: 406 (1893)
Salvia rotundifolia Vis. Mem. Reale Ist. Veneto Sci. 1: 42 (1842 publ. 1843)
Salvia trigonocalyx Woronow Vestn. Tiflissk. Bot. Sada 22: 10 (1912)
Salvia officinalis subsp. major Gams Ill. Fl. Mitt.-Eur. 5: 2483 (1927)
Salvia grandiflora subsp. rotundifolia (Vis.) Rech.f. Akad. Wiss. Wien, Math.-Naturwiss. Kl., Denkschr. 105: 519 (1943)
Salvia officinalis subsp. tomentosa (Mill.) P.Fourn. Quatre Fl. France : 835 (1938)
Salvia grandiflora subsp. aegaea (Bornm.) Rech.f. Akad. Wiss. Wien, Math.-Naturwiss. Kl., Denkschr. 105: 519 (1943)
Salvia grandiflora var. aegaea Bornm. Verh. K. K. Zool.-Bot. Ges. Wien 48: 618 (1898)

Common names Top

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Language Common/alternative name
Arabic قصعين لبدي
Bulgarian ердоцветен конски босилек

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • East Aegean Islands
      • Lebanon-Syria
      • Turkey
  • Europe
    • Eastern Europe
      • Krym
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000302487
Tropicos 17604318
INPN 120696
KEW urn:lsid:ipni.org:names:457406-1
The Plant List kew-184029
Open Tree Of Life 807682
Observations.org 147953
NCBI Taxonomy 1132405
IPNI 457406-1
iNaturalist 513838
GBIF 3885499
EPPO SALTO
Elurikkus 433484
USDA GRIN 457368
Wikipedia Salvia_tomentosa

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
Phytochemical Profile and Evaluation of the Antioxidant, Cyto-Genotoxic, and Antigenotoxic Potential of Salvia verticillata Hydromethanolic Extract Stavropoulou LS, Efthimiou I, Giova L, Manoli C, Sinou PS, Zografidis A, Lamari FN, Vlastos D, Dailianis S, Antonopoulou M Plants (Basel) 05-Mar-2024
PMCID:PMC10934106
doi:10.3390/plants13050731
PMID:38475577
The Effect of Salvia tomentosa Miller Extracts, Rich in Rosmarinic, Salvianolic and Lithospermic Acids, on Bacteria Causing Opportunistic Infections Piątczak E, Kolniak-Ostek J, Gonciarz W, Lisiecki P, Kalinowska-Lis U, Szemraj M, Chmiela M, Zielińska S Molecules 25-Jan-2024
PMCID:PMC10856039
doi:10.3390/molecules29030590
PMID:38338335
Which Plant Species for Green Roofs in the Mediterranean Environment? Leotta L, Toscano S, Romano D Plants (Basel) 27-Nov-2023
PMCID:PMC10708222
doi:10.3390/plants12233985
PMID:38068621
Valencene, Nootkatone and Their Liposomal Nanoformulations as Potential Inhibitors of NorA, Tet(K), MsrA, and MepA Efflux Pumps in Staphylococcus aureus Strains Oliveira-Tintino CD, Santana JE, Alencar GG, Siqueira GM, Gonçalves SA, Tintino SR, de Menezes IR, Rodrigues JP, Gonçalves VB, Nicolete R, Ribeiro-Filho J, da Silva TG, Coutinho HD Pharmaceutics 28-Sep-2023
PMCID:PMC10609713
doi:10.3390/pharmaceutics15102400
PMID:37896161
A Systematic Review on Traumatic Brain Injury Pathophysiology and Role of Herbal Medicines in its Management Arora K, Vats V, Kaushik N, Sindhawani D, Saini V, Arora DM, Kumar Y, Vashisht E, Singh G, Verma PK Curr Neuropharmacol 25-Sep-2023
PMCID:PMC10616914
doi:10.2174/1570159X21666230126151208
PMID:36703580
Antiproliferative Activities of Acetone Extract From Canarium Odontophyllum (Dabai) Stem Bark Against Human Colorectal Cancer Cells Ishak SF, Rajab NF, Basri DF Dose Response 14-Apr-2023
PMCID:PMC10108421
doi:10.1177/15593258221098980
PMID:37077718
Effect of Explant Source on Phenotypic Changes of In Vitro Grown Cannabis Plantlets over Multiple Subcultures Hesami M, Adamek K, Pepe M, Jones AM Biology (Basel) 13-Mar-2023
PMCID:PMC10044989
doi:10.3390/biology12030443
PMID:36979133
Drug discovery inspired by bioactive small molecules from nature Kim S, Lim SW, Choi J Anim Cells Syst (Seoul) 21-Dec-2022
PMCID:PMC9809404
doi:10.1080/19768354.2022.2157480
PMID:36605590
The Essential Oil from the Resurrection Plant Myrothamnus moschatus Is Effective against Arthropods of Agricultural and Medical Interest Pavela R, Ferrati M, Spinozzi E, Maggi F, Petrelli R, Rakotosaona R, Ricciardi R, Benelli G Pharmaceuticals (Basel) 03-Dec-2022
PMCID:PMC9782303
doi:10.3390/ph15121511
PMID:36558962
Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview Motti R, Paura B, Cozzolino A, de Falco B Plants (Basel) 28-Nov-2022
PMCID:PMC9736219
doi:10.3390/plants11233272
PMID:36501312
An Ethnobotanical study of medicinal plants in Taşköprü (Kastamonu–Turkey) Senkardes I, Dogan A, Emre G Front Pharmacol 20-Oct-2022
PMCID:PMC9630845
doi:10.3389/fphar.2022.984065
PMID:36339567
Streptococcosis a Re-Emerging Disease in Aquaculture: Significance and Phytotherapy Van Doan H, Soltani M, Leitão A, Shafiei S, Asadi S, Lymbery AJ, Ringø E Animals (Basel) 16-Sep-2022
PMCID:PMC9495100
doi:10.3390/ani12182443
PMID:36139303
Pathogenesis and management of traumatic brain injury (TBI): role of neuroinflammation and anti-inflammatory drugs Kalra S, Malik R, Singh G, Bhatia S, Al-Harrasi A, Mohan S, Albratty M, Albarrati A, Tambuwala MM Inflammopharmacology 08-Jul-2022
PMCID:PMC9293826
doi:10.1007/s10787-022-01017-8
PMID:35802283
Amelioration of Scopolamine-Induced Cognitive Dysfunction in Experimental Mice Using the Medicinal Plant Salvia moorcroftiana Wahid F, Jan T, Al-Joufi FA, Ali Shah SW, Nisar M, Zahoor M Brain Sci 07-Jul-2022
PMCID:PMC9320495
doi:10.3390/brainsci12070894
PMID:35884701
Dietary Supplements and Natural Products: An Update on Their Clinical Effectiveness and Molecular Mechanisms of Action During Accelerated Biological Aging Chen Y, Hamidu S, Yang X, Yan Y, Wang Q, Li L, Oduro PK, Li Y Front Genet 28-Apr-2022
PMCID:PMC9096086
doi:10.3389/fgene.2022.880421
PMID:35571015

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldecane 23415 Click to see 156.31 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 10017708 Click to see 300.40 unknown https://doi.org/10.1021/NP50013A022
(3S,4aR,10aS)-1,1-dimethyl-7-propan-2-yl-3,4,4a,9,10,10a-hexahydro-2H-phenanthrene-3,6-diol 162930386 Click to see 288.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1alpha,4abeta,10aalpha)]- 1201531 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
1,1-dimethyl-7-propan-2-yl-3,4,4a,9,10,10a-hexahydro-2H-phenanthrene-3,6-diol 162930385 Click to see 288.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 15618 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Carnosic Acid 65126 Click to see 332.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Carnosicacid 5024746 Click to see 332.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
CID 133554352 133554352 Click to see 346.50 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1080/10575639208048902
Horminone 2751795 Click to see 332.40 unknown https://doi.org/10.1080/10575639208048902
https://doi.org/10.1016/S0031-9422(98)00471-3
Salviol 13966146 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CC(CC3(C)C)O)C)O 302.50 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Sugiol 94162 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Taxoquinone 99965 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O 332.40 unknown https://doi.org/10.1080/10575639208048902
https://doi.org/10.1016/S0031-9422(98)00471-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84802-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
8a-[3-[5-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 74081266 Click to see 1237.30 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(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 346.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Epirosmanol 9884612 Click to see 346.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Rosmanol 13966122 Click to see 346.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1080/10575639208048902
https://doi.org/10.1021/NP50013A022
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 293273 Click to see 442.70 unknown https://doi.org/10.1021/NP50017A014
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1080/10575639208048902
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/10.1021/NP50017A014
epi-Maslinic acid 25564831 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/0031-9422(83)85059-6
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1021/NP50013A022
https://doi.org/10.1016/0031-9422(83)85059-6
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1080/10575639208048902
https://doi.org/10.1021/NP50013A022
Uvaol 92802 Click to see 442.70 unknown https://doi.org/10.1021/NP50017A014
Virgatic acid 14489125 Click to see 470.70 unknown https://doi.org/10.1080/10575639208048902
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholest-4-en-3-one 91477 Click to see 384.60 unknown https://doi.org/10.1080/10575639208048902
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
3-[(3S,5R,8R,9S,10S,13R,14S,16R,17R)-3-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162907719 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)OC)O 550.70 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
> 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/10.1080/10575639208048902
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP50013A022
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP50013A022
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1080/10575639208048902
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1021/NP50003A002
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1021/NP50003A002
> Organoheterocyclic compounds / Quinolidines
(1R,2S,5R,7S,9S,11R,13S,17R)-5-[[(4aR,5R,7S,8aS)-1-ethyl-7-methyl-3,4,4a,5,6,7,8,8a-octahydro-2H-quinolin-5-yl]methyl]-11,14-dimethyl-6,14-diazatetracyclo[7.6.2.02,7.013,17]heptadecan-2-ol 162943340 Click to see 471.80 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP50003A002
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50003A002
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1021/NP50017A014
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupatilin 5273755 Click to see 344.30 unknown https://doi.org/10.1021/NP50017A014
https://doi.org/10.1016/S0031-9422(01)00415-0
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1021/NP50003A002
Nepetin 5317284 Click to see 316.26 unknown https://doi.org/10.1021/NP50003A002
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsilineol 162464 Click to see 344.30 unknown https://doi.org/10.1021/NP50017A014
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1021/NP50003A002

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