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Internal ID UUID643febcd726f8730585428
Scientific name Salvia microstegia
Authority Boiss. & Balansa
First published in Diagn. Pl. Orient. , ser. 2, 4: 17 (1859)

Description Top

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It grows to a height of up to 40 cm and has a woody stem. The leaves are opposite, ovate-lanceolate, and have a serrated margin. The plant is used medicinally for treating respiratory and digestive disorders, as well as for its anti-inflammatory and antiseptic properties. It is also used as an ornamental plant in gardens.

Salvia microstegia is a herbaceous perennial plant native to Israel, growing on Mount Hermon. It has white or pale violet flowers, blooming from June to September and grows to a height of up to 40 cm. The leaves are opposite, ovate-lanceolate, and have a serrated margin. The plant is used medicinally for treating respiratory and digestive disorders, as well as for its anti-inflammatory and antiseptic properties. It is also used as an ornamental plant in gardens.

Synonyms Top

Scientific name Authority First published in
Salvia chnoodes Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 50: 98 (1885)

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Language Common/alternative name
Arabic قصعين صغير الغطاء
Hebrew מרווה בוצינית

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Germination/Propagation Top

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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-0000301607
USDA Plants SAMI24
Tropicos 17600596
KEW urn:lsid:ipni.org:names:456706-1
The Plant List kew-183205
Open Tree Of Life 3882802
NCBI Taxonomy 1520034
IPNI 456706-1
iNaturalist 550465
GBIF 3895821
Freebase /m/0n4c8_d
EOL 6342613
USDA GRIN 407906
Wikipedia Salvia_microstegia

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)!
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Title Authors Publication Released IDs
Therapeutic benefits of Salvia species: A focus on cancer and viral infection Ezema CA, Ezeorba TP, Aguchem RN, Okagu IU Heliyon 13-Jan-2022
PMCID:PMC8819530
doi:10.1016/j.heliyon.2022.e08763
PMID:35146151
Diterpenoids from Roots of Salvia lachnocalyx; In-silico and In-vitro Toxicity against Human Cancer Cell Lines Hadavand Mirzaei H, Firuzi O, Jassbi AR Iran J Pharm Res 01-Sep-2020
PMCID:PMC8019878
doi:10.22037/ijpr.2019.15429.13095
PMID:33841524
A review of medicinal plant of Middle East and North Africa (MENA) region as source in tuberculosis drug discovery Dehyab AS, Bakar MF, AlOmar MK, Sabran SF Saudi J Biol Sci 10-Jul-2020
PMCID:PMC7451596
doi:10.1016/j.sjbs.2020.07.007
PMID:32884430
Antifungal, Antibacterial, and Antioxidant Activities of Acacia Saligna (Labill.) H. L. Wendl. Flower Extract: HPLC Analysis of Phenolic and Flavonoid Compounds Al-Huqail AA, Behiry SI, Salem MZ, Ali HM, Siddiqui MH, Salem AZ Molecules 15-Feb-2019
PMCID:PMC6412425
doi:10.3390/molecules24040700
PMID:30781352
RP-HPLC/MS/MS Analysis of the Phenolic Compounds, Antioxidant and Antimicrobial Activities of Salvia L. Species Tohma H, Köksal E, Kılıç Ö, Alan Y, Yılmaz MA, Gülçin İ, Bursal E, Alwasel SH Antioxidants (Basel) 21-Oct-2016
PMCID:PMC5187536
doi:10.3390/antiox5040038
PMID:27775656
Microstegiol, a rearranged diterpene from Salvia microstegia Ayhan Ulubelen, Gulacti Topcu, Nur Tan, Lee-Juian Lin, Geoffrey A. Cordell Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83290-F
Abietane diterpenoids from Salvia microstegia A. Ulubelen, G. Topcu Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85075-B

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
> Benzenoids / Naphthalenes
1-Hydroxy-8,13,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one 50907654 Click to see CC1=C2CCCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)O)(C)C 298.40 unknown https://doi.org/10.1016/0031-9422(92)83290-F
Microstegiol 403772 Click to see CC1=C2CCCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)O)(C)C 298.40 unknown https://doi.org/10.1016/0031-9422(92)83290-F
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Pisiferal 13785026 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O 300.40 unknown https://doi.org/10.1016/0031-9422(91)85075-B
(4bR,8aR)-4b,8,8-trimethyl-2-propan-2-yl-6,7,9,10-tetrahydro-5H-phenanthrene-3,4,8a-triol 15690628 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3(C2(CCCC3(C)C)C)O)O)O 318.40 unknown https://doi.org/10.1016/0031-9422(91)85075-B
1-(6-Hydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-4a-yl)ethanone 162853857 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)C)O 314.50 unknown https://doi.org/10.1016/0031-9422(91)85075-B
1-[(4aR,10aR)-6-hydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-4a-yl]ethanone 162853858 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)C)O 314.50 unknown https://doi.org/10.1016/0031-9422(91)85075-B
4b,8,8-trimethyl-2-propan-2-yl-6,7,9,10-tetrahydro-5H-phenanthrene-3,4,8a-triol 85446139 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3(C2(CCCC3(C)C)C)O)O)O 318.40 unknown https://doi.org/10.1016/0031-9422(91)85075-B
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/0031-9422(91)85075-B

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