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Salvia staminea

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643febf5927eb997932967
Scientific name Salvia staminea
Authority Montbret & Aucher
First published in Ann. Sci. Nat., Bot. , sér. 2, 6: 41 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salvia armeniaca Grossh. Beih. Bot. Centralbl. 44(2): 237 (1927)
Salvia calvertii Boiss. Fl. Orient. 4: 626 (1879)
Salvia kudjurica Rech.f. Oesterr. Bot. Z. 99: 56 (1952)
Salvia staminea subsp. armeniaca Bordz. Trudy Bot. Sada Imp. Yur'evsk. Univ. 13: 22. 1912 (1912)
Salvia transcaucasica Pobed. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 21: 321 (1961)

Common names Top

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Language Common/alternative name
Persian مریمگلی مازندرانی

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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000302368
Tropicos 100254271
KEW urn:lsid:ipni.org:names:457304-1
The Plant List kew-183920
Open Tree Of Life 912162
NCBI Taxonomy 268934
IPNI 457304-1
iNaturalist 1090725
GBIF 3886824
Freebase /m/05n_smb
EOL 6343208
USDA GRIN 468760
Wikipedia Salvia_staminea

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
Changes in Metabolite Profiling and Expression Levels of Key Genes Involved in the Terpenoid Biosynthesis Pathway in Garden Sage (Salvia officinalis) under the Effect of Hydrazine Hydrate Ali M, Abdelkawy AM, Darwish DB, Alatawi HA, Alshehri D, Al-Amrah H, Soudy FA Metabolites 29-Jun-2023
PMCID:PMC10385164
doi:10.3390/metabo13070807
PMID:37512514
Higher Resistance of Yersinia enterocolitica in Comparison to Yersinia pseudotuberculosis to Antibiotics and Cinnamon, Oregano and Thyme Essential Oils Hulankova R Pathogens 01-Dec-2022
PMCID:PMC9784965
doi:10.3390/pathogens11121456
PMID:36558790
Phytochemical Screening and Acanthamoebic Activity of Shoots from in Vitro Cultures and in Vivo Plants of Eryngium alpinum L.—The Endangered and Protected Species Kikowska M, Kruszka D, Derda M, Hadaś E, Thiem B Molecules 20-Mar-2020
PMCID:PMC7144402
doi:10.3390/molecules25061416
PMID:32244952
Role of Saponins in Plant Defense Against Specialist Herbivores Hussain M, Debnath B, Qasim M, Bamisile BS, Islam W, Hameed MS, Wang L, Qiu D Molecules 30-May-2019
PMCID:PMC6600540
doi:10.3390/molecules24112067
PMID:31151268
Anti-paralytic medicinal plants – Review Mikawlrawng K, Rani R, Kumar S, Bhardwaj AR, Prakash G J Tradit Complement Med 09-Mar-2017
PMCID:PMC5755955
doi:10.1016/j.jtcme.2017.02.001
PMID:29321983
A Review of the Current Research Trends in the Application of Medicinal Plants as a Source for Novel Therapeutic Agents Against Acanthamoeba Infections Niyyati M, Dodangeh S, Lorenzo-Morales J Iran J Pharm Res 01-Sep-2016
PMCID:PMC5316269
PMID:28243287
Lethal Effects of Helianthemum lippii (L.) on Acanthamoeba castellanii Cysts in Vitro Badria FA, Hetta MH, Sarhan RM, Ezz El-Din MH Korean J Parasitol 26-Jun-2014
PMCID:PMC4096634
doi:10.3347/kjp.2014.52.3.243
PMID:25031463
Studies on di- and triterpenoids from Salvia staminea with cytotoxic activity. Topcu G, Altiner EN, Gozcu S, Halfon B, Aydogmus Z, Pezzuto JM, Zhou BN, Kingston DG Planta Med 01-May-2003
doi:10.1055/S-2003-39705
PMID:12802732
Diterpenoids from Salvia miltiorrhiza. Lin HC, Chang WL Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(99)00433-1
PMID:10820810

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 / Naphthalenes
(1S,13S)-13-hydroxy-1,8,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraene-2,10-dione 10495322 Click to see CC1=C2C(=O)CCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)C)(C)O 312.40 unknown https://doi.org/10.1055/S-2003-39705
Microstegiol 403772 Click to see CC1=C2CCCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)O)(C)C 298.40 unknown https://doi.org/10.1055/S-2003-39705
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 5316143 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC 330.50 unknown https://doi.org/10.1055/S-2003-39705
Cryptojaponol 11724205 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC 330.50 unknown https://doi.org/10.1055/S-2003-39705
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1055/S-2003-39705
Taxodione 73588 Click to see CC(C)C1=CC2=CC(=O)C3C(CCCC3(C2=C(C1=O)O)C)(C)C 314.40 unknown https://doi.org/10.1055/S-2003-39705
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1055/S-2003-39705
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1055/S-2003-39705
> 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 CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1055/S-2003-39705
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1055/S-2003-39705
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
1,2,4a,6a,6b,9,9,12a-octamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-3,10,13-triol 75048981 Click to see CC1C(C2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C 458.70 unknown https://doi.org/10.1055/S-2003-39705
Labd-14-ene, 8,13-epoxy-, (13S)- 6432025 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1055/S-2003-39705
Salvinemorol 44575230 Click to see CC1(CC2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C 458.70 unknown https://doi.org/10.1055/S-2003-39705
> 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/10.1055/S-2003-39705
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/10.1055/S-2003-39705
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/10.1055/S-2003-39705
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/10.1055/S-2003-39705
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-2003-39705
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1055/S-2003-39705
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/10.1055/S-2003-39705
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1055/S-2003-39705
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown https://doi.org/10.1016/S0031-9422(99)00433-1

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