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Salvia tomentosa

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

Description Top

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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)

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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No subvariety added yet.

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

Suggest others/fix!
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

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
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
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
An ethnobotanical study of medicinal plants in Güce district, north-eastern Turkey Karaköse M Plant Divers 26-Apr-2022
PMCID:PMC9751085
doi:10.1016/j.pld.2022.03.005
PMID:36540712
Phytochemical Investigation and Reproductive Capacity of the Bulgarian Endemic Plant Species Marrubium friwaldskyanum Boiss. (Lamiaceae) Zheljazkov VD, Semerdjieva IB, Stevens JF, Wu W, Cantrell CL, Yankova-Tsvetkova E, Koleva-Valkova LH, Stoyanova A, Astatkie T Plants (Basel) 30-Dec-2021
PMCID:PMC8747201
doi:10.3390/plants11010114
PMID:35009117
Phytochemical profile, antioxidant, antiproliferative, and enzyme inhibition-docking analyses of Salvia ekimiana Celep & Doğan Karatoprak GŞ, Göger F, Çelik İ, Budak Ü, Akkol EK, Aschner M S Afr J Bot 09-Oct-2021
PMCID:PMC8863303
doi:10.1016/j.sajb.2021.09.033
PMID:35210693

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldecane 23415 Click to see CCCCCCCCC(C)C 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 CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 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 CC(C)C1=C(C=C2C3CC(CC(C3CCC2=C1)(C)C)O)O 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 CC(C)C1=C(C=C2C3CC(CC(C3CCC2=C1)(C)C)O)O 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
12-Methoxycarnosic acid 133554352 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)OC 346.50 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 CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 300.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Carnosic acid 65126 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O 332.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Carnosicacid 5024746 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O 332.40 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 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
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 CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 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 CC1=CCC(C=C1)C(C)C 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 CC1C(C(C(C(O1)OC(=O)C23CCC(CC2C4=CCC5C(C4(CC3)CO)(CCC6C5(CC(C(C6(C)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)(C)C)OC8C(C(C(C(O8)C)OC9C(C(C(CO9)O)OC1C(C(CO1)(CO)O)O)O)O)O)O)O 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 CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
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 9884612 Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
Rosmanol 13966122 Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1016/S0031-9422(98)00471-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1021/NP50017A014
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/10.1080/10575639208048902
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 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
https://doi.org/10.1021/NP50013A022
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/10.1080/10575639208048902
https://doi.org/10.1021/NP50013A022
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/10.1021/NP50013A022
https://doi.org/10.1080/10575639208048902
Uvaol 92802 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1021/NP50017A014
Virgatic acid 14489125 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 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 CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C 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
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/10.1080/10575639208048902
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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 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
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
> 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 CCN1CCCC2C1CC(CC2CC3CCC4(C5CC6C(CC(CC6N(C5)C)C)CC4N3)O)C 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
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1021/NP50003A002
Eupatilin 5273755 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1021/NP50017A014
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
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1021/NP50017A014

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