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Salvia amplexicaulis

Salvia amplexicaulis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643feb9165dd9453983007
Scientific name Salvia amplexicaulis
Authority Lam.
First published in Tabl. Encycl. 1: 68 (1791)

Description Top

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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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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
  • Europe
    • 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
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
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
Urs-12-en-3beta-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-2001-18359
https://doi.org/10.1055/S-0028-1097496
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-2001-18359
https://doi.org/10.1080/13102818.2001.10819125
https://doi.org/10.1055/S-0028-1097496
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/10.1016/S0031-9422(03)00225-5
https://doi.org/10.1055/S-2001-18359
Sitostenone 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
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
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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