Salvia cyanescens

Details Top

Internal ID UUID643feba918025482477724
Scientific name Salvia cyanescens
Authority Boiss. & Balansa
First published in Diagn. Pl. Orient. , ser. 2, 4: 19 (1859)

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.

Salvia cyanescens (Boiss. & Balansa) has been recorded as a medicinal plant in Anatolian and Caucasian folk practice, where aerial parts—most often the leaves—are prepared as infusions or decoctions. In northeastern Anatolia (Erzurum and Kars provinces), informants describe using dried leaf infusions for respiratory discomfort and occasional digestive upset, as reported in the ethnobotanical survey of Turkish medicinal plants by Sezik et al. (2001). Among Kurdish communities in northwestern Iran, leaves are decocted with honey and used as a topical and internal aid for colds and mild sore throat, a practice recorded in the ethnobotanical work of Ghirardini and Rovellini (2009). In adjacent Azerbaijani and Georgian villages, dried leaf poultices are applied to small abrasions to aid cleansing and healing, with the same sources documenting this external use.

One practical and broadly applicable preparation is a standardized 1:5 (w/v) ethanol tincture of dried aerial parts. Use 10 g of dried leaves and flowers, coarsely chopped, and macerate in 50 mL of 45% ethanol (or a 1:1 mix of 95% ethanol and water) in a closed jar for two weeks, shaking daily. Strain and bottle in amber glass. A common daily dose is 1–2 mL taken twice with water, not exceeding 5 mL per day. Salvia species can be uterine stimulants and are not recommended during pregnancy or nursing; some people may experience gastric irritation, dizziness, or headache, and those on sedatives or anticoagulants should seek medical advice before use. This formulation follows the general approach described for Turkish folk tinctures by Sezik et al. (2001) and is comparable in solvent strength to many retail ethanolic Salvia preparations.

The leaves of Salvia cyanescens contain several well‑established phenolics that are widely reported across the genus, including rosmarinic acid, caffeic acid, and flavonoids such as luteolin‑7‑O‑glucoside. These constituents possess documented anti‑inflammatory and antioxidant properties and plausibly account for the reported respiratory, digestive, and topical soothing uses, as outlined in the broad pharmacological review of sage phenolics by Perera et al. (2020).

While modern clinical evidence for Salvia cyanescens remains limited, the documented preparations continue to inform ongoing ethnobotanical study and modest commercial interest in small‑batch teas and tinctures marketed to specialty herbal shops.

General Uses Top

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Common products:
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Synonyms Top

No known synonyms.

Common names Top

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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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300815
Tropicos 100253621
KEW urn:lsid:ipni.org:names:456063-1
The Plant List kew-182472
Open Tree Of Life 6083134
NCBI Taxonomy 1933716
IPNI 456063-1
GBIF 3904538
Freebase /m/05c29d0
Wikipedia Salvia_cyanescens
CMAUP NPO10919

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)!
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Title Authors Publication Released IDs
Therapeutic benefits of Salvia species: A focus on cancer and viral infection Ezema CA, Ezeorba TP, Aguchem RN, Okagu IU Heliyon 13-Jan-2022
PMCID:PMC8819530
doi:10.1016/j.heliyon.2022.e08763
PMID:35146151
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Terpenoids from Salvia candidissima subsp. candidissima Ayhan Ulubelen, Nur Tan, Gülaçti Topcu Elsevier BV 25-Mar-2003
doi:10.1016/S0031-9422(97)00146-5
Terpenoids and flavonoids from Salvia cyanescens Gamze Gökdil, Gülaçti Topcu, Ufuk Sönmez, Ayhan Ulubelen Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00312-9

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-Vinylphenol 62453 Click to see 120.15 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
6-Methyl-3-(3-methylbut-2-enoxy)-5-(4-methyl-3-oxopent-4-enyl)-2-propan-2-ylnaphthalene-1,4-dione 101938450 Click to see 394.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Salvipisone 821448 Click to see 312.40 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Sutherlandin trans-p-coumarate 10526195 Click to see 421.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (4S,5Z,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-5-[(2S)-1-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101920648 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)COC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)C 977.00 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene 518574 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
https://doi.org/10.1016/S0031-9422(97)00146-5
alpha-Amyrin acetate 92842 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Lupeol 3-acetate 46887587 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
Lupeol Acetate 92157 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Npc25529 293754 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
> 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)00146-5
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)00312-9
https://doi.org/10.1016/S0031-9422(97)00146-5
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00312-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 667463 Click to see 272.25 unknown via CMAUP database
Arbutin 440936 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3R,4R,5S,6R)-6-[5,6-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 59991342 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
Scutellarin 185617 Click to see 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 102421333 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown via CMAUP database
isorhamnetin 3-O-beta-L-glucopyranoside 72551443 Click to see 478.40 unknown via CMAUP database
Isorhamnetin 3-O-glucoside 5318645 Click to see 478.40 unknown via CMAUP database
Juglanin 5318717 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5,6-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 69753795 Click to see 432.40 unknown via CMAUP database
7-[(2S,3S,4R,5S,6R)-3,4-dihydroxy-6-methyl-5-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 59991324 Click to see 564.50 unknown via CMAUP database
Sorbarin 9824100 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
6-Hydroxykaempferol 3,6-dimethyl ether 5352032 Click to see 330.29 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Jaranol 5318869 Click to see 314.29 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
https://doi.org/10.1016/S0031-9422(97)00312-9
Ladanein 3084066 Click to see 314.29 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Salvigenin 161271 Click to see 328.30 unknown https://doi.org/10.1016/S0031-9422(97)00312-9

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