Salvia amplexicaulis is a perennial plant found in southeastern Europe. It is closely related to Salvia nemorosa and has stem-clasping leaves without stalks. The plant can grow up to 90 cm tall and produces violet-blue flowers in whorls, creating a continuous spike.

Synonyms Top

Scientific name	Authority	First published in
Salvia exigua	Adamov.	Allg. Bot. Z. Syst. 1905: 3 (1905)
Salvia sylvestris subsp. villicaulis	(Borbás) O.Bolòs & Vigo	Fl. Països Catalans 3: 347 (1995)
Salvia villicaulis	Borbás	Oesterr. Bot. Z. 39: 234 (1889)
Sclarea amplexicaulis	(Lam.) Soják	Cas. Nár. Mus., Odd. Prír. 152: 21 (1983)
Salvia amplexicaulis var. minutiflora	Adamovic	Beitr. Fl. Macedon. 18. 1903
Salvia sylvestris subsp. amplexicaulis	(Lam.) Nyman	Consp. Fl. Eur. 570. 1881 (1881)

Common names Top

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Language	Common/alternative name
Bulgarian	стъблообхващащ конски босилек

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Western Asia
  - Turkey

Europe click to expand
- 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-0000300254
INPN	120622
Flora of Italy	8604
KEW	urn:lsid:ipni.org:names:455630-1
The Plant List	kew-181958
Open Tree Of Life	61887
Observations.org	121714
NCBI Taxonomy	268888
NBN Atlas	NHMSYS0020704620
IPNI	455630-1
iNaturalist	513863
GBIF	3885624
Freebase	/m/0bx_l5g
EPPO	SALAM
EOL	6341566
Elurikkus	591996
USDA GRIN	410525
Wikipedia	Salvia_amplexicaulis

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

Chemometric Analysis Evidencing the Variability in the Composition of Essential Oils in 10 Salvia Species from Different Taxonomic Sections or Phylogenetic Clades

Tomou EM, Fraskou P, Dimakopoulou K, Dariotis E, Krigas N, Skaltsa H

Molecules

29-Mar-2024

PMCID:	PMC11013157
doi:	10.3390/molecules29071547
PMID:	38611827

The Feasibility of Utilizing Cultured Cordyceps militaris Residues in Cosmetics: Biological Activity Assessment of Their Crude Extracts

Pintathong P, Chomnunti P, Sangthong S, Jirarat A, Chaiwut P

J Fungi (Basel)

16-Nov-2021

PMCID:	PMC8621739
doi:	10.3390/jof7110973
PMID:	34829260

Metabolomics and DNA-Based Authentication of Two Traditional Asian Medicinal and Aromatic Species of Salvia subg. Perovskia

Bielecka M, Pencakowski B, Stafiniak M, Jakubowski K, Rahimmalek M, Gharibi S, Matkowski A, Ślusarczyk S

Cells

09-Jan-2021

PMCID:	PMC7826587
doi:	10.3390/cells10010112
PMID:	33435339

Phytochemical Composition and Bioactive Effects of Salvia africana, Salvia officinalis ‘Icterina’ and Salvia mexicana Aqueous Extracts

Afonso AF, Pereira OR, Fernandes Â, Calhelha RC, Silva AM, Ferreira IC, Cardoso SM

Molecules

27-Nov-2019

PMCID:	PMC6930492
doi:	10.3390/molecules24234327
PMID:	31783509

Salvia elegans, Salvia greggii and Salvia officinalis Decoctions: Antioxidant Activities and Inhibition of Carbohydrate and Lipid Metabolic Enzymes

Pereira OR, Catarino MD, Afonso AF, Silva AM, Cardoso SM

Molecules

01-Dec-2018

PMCID:	PMC6321363
doi:	10.3390/molecules23123169
PMID:	30513773

Characterization of Two Triterpenes and a Steroid from the Cultured Roots of<i>Salvia Amplexicaulis</i>

Ş. Arı, U.S. Kolak, S. Hasançebi, H. Birman

Informa UK Limited

27-Jun-2014

doi:	10.1080/13102818.2001.10819125

Cardioactive and antibacterial terpenoids from some Salvia species.

Ulubelen A

Phytochemistry

01-Sep-2003

doi:	10.1016/S0031-9422(03)00225-5
PMID:	12943755

Cardioactive diterpenoids from the roots of Salvia amplexicaulis.

Kolak U, Ari S, Birman H, Hasançebi S, Ulubelen A

Planta Med

01-Nov-2001

doi:	10.1055/S-2001-18359
PMID:	11731924

Chemical study of the herba of Salvia amplexicaulis.

Ulubelen A, Brieskorn CH

Planta Med

01-Feb-1977

doi:	10.1055/S-0028-1097496
PMID:	840934

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 CCCCCCCCC(C)C	156.31	unknown	https://doi.org/10.1055/S-2001-18359
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aR,10aR)-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	162952621	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C	284.40	unknown	https://doi.org/10.1055/S-2001-18359
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/10.1055/S-2001-18359
7-Acetylhorminone	2751796	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2OC(=O)C)(C)C)C)O	374.50	unknown	https://doi.org/10.1055/S-2001-18359
Abieta-8,11,13-trien-7-one	11335109	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C	284.40	unknown	https://doi.org/10.1055/S-2001-18359
Abieta-9(11),8(14),12-trien-12-ol	521330	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-2001-18359
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-2001-18359
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/10.1055/S-2001-18359
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(03)00225-5 https://doi.org/10.1055/S-2001-18359
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/10.1055/S-2001-18359
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(1R,4R,4aR,8aS)-4-hydroxy-4,7-dimethyl-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162956442	Click to see CC1=CC2C(CC1)C(CCC2C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)(C)O	400.50	unknown	https://doi.org/10.1055/S-2001-18359 https://doi.org/10.1016/S0031-9422(03)00225-5
> 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/10.1055/S-2001-18359
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aS,6aS,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol	163069311	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/10.1055/S-0028-1097496
(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol	163023159	Click to see CC1CCC2(CCC3(C(C2C1C)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(03)00225-5
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	619165	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C	498.70	unknown	https://doi.org/10.1055/S-2001-18359
3-Hydroxyolean-12-en-28-oic acid	619166	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/10.1055/S-2001-18359 https://doi.org/10.1055/S-0028-1097496
3-O-Acetyloleanolic acid	151202	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C	498.70	unknown	https://doi.org/10.1016/S0031-9422(03)00225-5 https://doi.org/10.1055/S-2001-18359
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1055/S-0028-1097496 https://doi.org/10.1055/S-2001-18359
Acetyloleanolic acid	45050658	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C	498.70	unknown	https://doi.org/10.1055/S-2001-18359
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/10.1055/S-2001-18359 https://doi.org/10.1055/S-0028-1097496
beta-Ursolic acid	220774	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/10.1055/S-2001-18359
Olean-12-en-3beta-ol	225689	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/10.1055/S-0028-1097496
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/10.1055/S-0028-1097496 https://doi.org/10.1080/13102818.2001.10819125 https://doi.org/10.1055/S-2001-18359
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/10.1080/13102818.2001.10819125 https://doi.org/10.1016/S0031-9422(03)00225-5 https://doi.org/10.1055/S-2001-18359
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5R)-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	122411793	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-0028-1097496
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1055/S-2001-18359
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-0028-1097496 https://doi.org/10.1055/S-2001-18359 https://doi.org/10.1080/13102818.2001.10819125
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/10.1080/13102818.2001.10819125 https://doi.org/10.1055/S-2001-18359
Beta-Sitosterol	222284	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-2001-18359 https://doi.org/10.1016/S0031-9422(03)00225-5
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/10.1016/S0031-9422(03)00225-5 https://doi.org/10.1055/S-2001-18359
Stigmast-4-en-3-one, (24S)-	579897	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.1055/S-2001-18359
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1055/S-2001-18359
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
5-[[4-Amino-5-[[1-[[1-carboxy-4-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]butyl]amino]-5-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]-1-oxopentan-2-yl]amino]-5-oxopentyl]-hydroxyamino]-3-methyl-5-oxopent-3-enoic acid	163059045	Click to see CC(=CC(=O)N(CCCC(C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)O)N)O)CC(=O)O	786.80	unknown	https://doi.org/10.1055/S-2001-18359
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin	161271	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O	328.30	unknown	https://doi.org/10.1055/S-2001-18359

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Salvia amplexicaulis

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top