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Salvia flava

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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 UUID643febb25b132345311216
Scientific name Salvia flava
Authority Forrest ex Diels
First published in Notes Roy. Bot. Gard. Edinburgh 5: 235 (1912)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salvia chingii C.Y.Wu ex Sun J. Nanjing Coll. Pharm. 5: 64 1960

Common names Top

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Language Common/alternative name
Persian مریمگلی زرد
Chinese 银紫丹参
Chinese 黄花丹参
Chinese 黄花鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Salvia flava var. flava Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301003
Tropicos 17606665
KEW urn:lsid:ipni.org:names:456217-1
The Plant List kew-182646
Open Tree Of Life 547896
NCBI Taxonomy 342063
IPNI 456217-1
iNaturalist 878611
GBIF 3902420
Freebase /m/05c3nr8
EOL 2894175
Wikipedia Salvia_flava

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
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Unusual patterns of hybridization involving two alpine Salvia species: Absence of both F1 and backcrossed hybrids Chang Y, Zhao S, Xiao H, Liu D, Huang Y, Wei Y, Ma Y Front Plant Sci 18-Oct-2022
PMCID:PMC9623266
doi:10.3389/fpls.2022.1010577
PMID:36330249
Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L J Ethnobiol Ethnomed 23-May-2022
PMCID:PMC9125852
doi:10.1186/s13002-022-00532-w
PMID:35606860
A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M Molecules 20-May-2022
PMCID:PMC9143754
doi:10.3390/molecules27103292
PMID:35630768
Comparative plastomic analysis and insights into the phylogeny of Salvia (Lamiaceae) Wu H, Ma PF, Li HT, Hu GX, Li DZ Plant Divers 25-Jul-2020
PMCID:PMC7987561
doi:10.1016/j.pld.2020.07.004
PMID:33778221
Salvianolic Acid B (Sal B) Protects Retinal Pigment Epithelial Cells from Oxidative Stress-Induced Cell Death by Activating Glutaredoxin 1 (Grx1). Liu X, Xavier C, Jann J, Wu H Int J Mol Sci 03-Nov-2016
PMCID:PMC5133836
doi:10.3390/IJMS17111835
PMID:27827892
Salvianolic acid B stimulates osteogenesis in dexamethasone-treated zebrafish larvae. Luo SY, Chen JF, Zhong ZG, Lv XH, Yang YJ, Zhang JJ, Cui L Acta Pharmacol Sin 01-Sep-2016
PMCID:PMC5057235
doi:10.1038/APS.2016.62
PMID:27569393
Salvianolic Acid B Attenuates Experimental Pulmonary Fibrosis through Inhibition of the TGF-β Signaling Pathway. Liu Q, Chu H, Ma Y, Wu T, Qian F, Ren X, Tu W, Zhou X, Jin L, Wu W, Wang J Sci Rep 09-Jun-2016
PMCID:PMC4899783
doi:10.1038/SREP27610
PMID:27278104
Salvianolic acid J, a depside from Salvia flava Chun-Bo Ai, Qiao-Hong Deng, Wan-Zhi Song, Lian-Niang Li Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90382-0
Polyphenolics of Salvia--a review. Lu Y, Foo LY Phytochemistry 01-Jan-2002
doi:10.1016/S0031-9422(01)00415-0
PMID:11809447

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Salviaflaside 6438919 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 522.50 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(2R,3R)-6-[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-1,4-benzodioxine-3-carboxylic acid 163194055 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3=C(C=C2)OC(C(O3)C(=O)O)C4=CC(=C(C=C4)O)O)O)O 538.50 unknown https://doi.org/10.1016/S0031-9422(00)90382-0
6-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-1,4-benzodioxine-3-carboxylic acid 73005432 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3=C(C=C2)OC(C(O3)C(=O)O)C4=CC(=C(C=C4)O)O)O)O 538.50 unknown https://doi.org/10.1016/S0031-9422(00)90382-0
clinopodic acid E 44537885 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3=C(C=C2)OC(C(O3)C(=O)O)C4=CC(=C(C=C4)O)O)O)O 538.50 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
Salvianolic acid J 24177556 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3=C(C=C2)OC(C(O3)C(=O)O)C4=CC(=C(C=C4)O)O)O)O 538.50 unknown https://doi.org/10.1016/S0031-9422(00)90382-0
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2-({(2E)-3-[(2R,3R)-3-{[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl}-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl}oxy)-3-(3,4-dihydroxyphenyl)propanoic acid 6441188 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown https://doi.org/10.1016/S0031-9422(00)90382-0
(2R)-2-[3-[(2R,3R)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid 92132738 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown https://doi.org/10.1016/S0031-9422(00)90382-0
Salvianic acid B 119177 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899783/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057235/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133836/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)90382-0
> Phenylpropanoids and polyketides / Stilbenes
Salvianolic acid A 5281793 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C(C(=C(C=C2)O)O)C=CC3=CC(=C(C=C3)O)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(00)90382-0

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