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Salvia phlomoides

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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 UUID643febdd7b857675703071
Scientific name Salvia phlomoides
Authority Asso
First published in Intr. Oryctogr. Aragon. : 158 (1784)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salvia montana Salisb. Prodr. Stirp. Chap. Allerton : 74 (1796)
Salvia phlomoides var. arachnoidea (Noë ex Walp.) Nyman Consp. Fl. Eur. 569 1881

Common names Top

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Language Common/alternative name
Arabic قصعين أفلومسي

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Salvia phlomoides subsp. africana (Maire) Greuter & Burdet Willdenowia 14: 301 (1984 publ. 1985)
Salvia phlomoides subsp. boissieri (Noë) Rosua & Blanca Collect. Bot. (Barcelona) 17: 230 (1988 publ. 1989)
Salvia phlomoides subsp. phlomoides Unknown

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301908
KEW urn:lsid:ipni.org:names:456939-1
The Plant List kew-183490
Open Tree Of Life 5800975
Observations.org 138496
NCBI Taxonomy 1520037
IPNI 456939-1
iNaturalist 513849
GBIF 7307924
EPPO SALPH
Elurikkus 623525
USDA GRIN 449170
GBIF 7819681

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
Targeting SARS-CoV-2 Non-Structural Proteins Tam D, Lorenzo-Leal AC, Hernández LR, Bach H Int J Mol Sci 20-Aug-2023
PMCID:PMC10455537
doi:10.3390/ijms241613002
PMID:37629182
Abietane diterpenoids from the root of Salvia phlomoides J HUESORODRIGUEZ, M JIMENO, B RODRIGUEZ, G SAVONA, M BRUNO Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80033-8
Salvifarin and salvifaricin, neo-clerodane diterpenoids from salvia farinacea Giuseppe Savona, Demetrio Raffa, Mauricio Bruno, Benjamín Rodríguez Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86989-7

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bS,8aS,9R,10R)-9,10-dihydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione 162953224 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C3(CCCC(C3C(C2O)O)(C)C)C 332.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
1,1,4a-Trimethyl-7-propan-2-yl-2,3,4,5,6,9,10,10a-octahydrophenanthrene 74428055 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
11-Hydroxysugiol 10403490 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
https://doi.org/10.1016/0031-9422(83)80033-8
14-deoxycoleon U 10735190 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(=C3C2(CCCC3(C)C)C)O)O)O 330.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
https://doi.org/10.1016/0031-9422(83)80033-8
4-Hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-3,9-dione 275527 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/10.1016/S0031-9422(00)86989-7
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/10.1016/0031-9422(83)80033-8
https://doi.org/10.1016/S0031-9422(00)86989-7
5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 14136733 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
5,6,10-trihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 85249733 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(=C3C2(CCCC3(C)C)C)O)O)O 330.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
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(00)86989-7
https://doi.org/10.1016/0031-9422(83)80033-8
6,11-Dihydroxyabieta-7,9(11),13-trien-12-one 457961 Click to see CC(C)C1=CC2=CC(C3C(CCCC3(C2=C(C1=O)O)C)(C)C)O 316.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
7-Isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene 86869 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
9,10-Dihydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione 162953223 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C3(CCCC(C3C(C2O)O)(C)C)C 332.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
Abietatriene 6432211 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
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/10.1016/S0031-9422(00)86989-7
https://doi.org/10.1016/0031-9422(83)80033-8
Palustradiene 443473 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
Royleanone 442084 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C)O 316.40 unknown https://doi.org/10.1016/0031-9422(83)80033-8
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(00)86989-7
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/10.1016/0031-9422(83)80033-8
https://doi.org/10.1016/S0031-9422(00)86989-7
Taxodone 275528 Click to see CC(C)C1=CC2=CC(C3C(CCCC3(C2=C(C1=O)O)C)(C)C)O 316.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
https://doi.org/10.1016/0031-9422(83)80033-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4aR,7aS)-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4,4a,5,7a-tetrahydro-3H-cyclopenta[c]pyran-1-one 49788109 Click to see C1COC(=O)C2C1CC=C2COC3C(C(C(C(O3)CO)O)O)O 330.33 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(3-hydroxy-4b,8,8-trimethyl-4-oxo-2-propan-2-yl-5,6,7,8a,9,10-hexahydro-1H-phenanthren-1-yl) acetate 162872612 Click to see CC(C)C1=C(C(=O)C2=C(C1OC(=O)C)CCC3C2(CCCC3(C)C)C)O 360.50 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
[(1R,4bS,8aS)-3-hydroxy-4b,8,8-trimethyl-4-oxo-2-propan-2-yl-5,6,7,8a,9,10-hexahydro-1H-phenanthren-1-yl] acetate 162872613 Click to see CC(C)C1=C(C(=O)C2=C(C1OC(=O)C)CCC3C2(CCCC3(C)C)C)O 360.50 unknown https://doi.org/10.1016/S0031-9422(00)86989-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3aR,4R,5R,9aR,9bS)-5-acetyloxy-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 162926507 Click to see CC1C(O1)(C)C(=O)OC2C3C(C4C(=CC(=O)C4=C(C2OC(=O)C)C)C)OC(=O)C3=C 416.40 unknown https://doi.org/10.1016/S0031-9422(00)86989-7

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