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

Add a new one! Suggest a correction!

Filter by language:

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

Suggest a correction or add new data!

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 click to expand
- Caucasus
  - Transcaucasus
- Western Asia
  - East Aegean Islands
  - Lebanon-Syria
  - Turkey

Europe click to expand
- 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

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

Add a new one!

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 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
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 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

Biological Material Top

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Salvia tomentosa

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