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Internal ID UUID643fecaa71f55505290730
Scientific name Scutellaria repens
Authority Buch.-Ham. ex D.Don
First published in Prodr. Fl. Nepal. : 110 (1825)

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Synonyms Top

Scientific name Authority First published in
Scutellaria cana Wall. Pl. Asiat. Rar. 1: 67 (1830)
Scutellaria wallichiana A.Ham. Esq. Monogr. Scutellaria : 28 (1832)
Scutellaria cana var. diffusa Benth. Pl. Asiat. Rar. 1: 67 (1830)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000308375
Tropicos 17600345
KEW urn:lsid:ipni.org:names:458612-1
The Plant List kew-189631
Open Tree Of Life 6085733
NCBI Taxonomy 2721171
IPNI 458612-1
iNaturalist 820744
GBIF 5608396

Genomes (via NCBI) Top

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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
Medicinal plants used by the Tamang community in the Makawanpur district of central Nepal Luitel DR, Rokaya MB, Timsina B, Münzbergová Z J Ethnobiol Ethnomed 10-Jan-2014
PMCID:PMC3904474
doi:10.1186/1746-4269-10-5
PMID:24410808
Studies on Nepalese Crude Drugs. XXIV. Diterpenoid Constituents of the Leaves of Scutellaria repens BUCH.-HAM. ex D. DON. Haruhisa KIZU, Naohiro SUGITA, Tsuyoshi TOMIMORI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.46.988
[Studies on the Nepalese crude drugs. XIX. On the flavonoid and phenylethanoid constituents of the root of Scutellaria repens Buch.-Ham. ex D. Don]. Matsuura Y, Miyaichi Y, Tomimori T Yakugaku Zasshi 01-Oct-1994
doi:10.1248/YAKUSHI1947.114.10_775
PMID:7528799

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 / Colensane and clerodane diterpenoids
[(1R,2R,3S,4S,4aR,6S,8R,8aS)-4-[(3aR,5S,6aS)-3a-hydroxy-3,4,5,6a-tetrahydro-2H-furo[2,3-b]furan-5-yl]-1,6,8-trihydroxy-8-(hydroxymethyl)-3,4,8a-trimethyl-5-oxo-1,2,3,4a,6,7-hexahydronaphthalen-2-yl] (E)-3-phenylprop-2-enoate 102120214 Click to see 546.60 unknown https://doi.org/10.1248/CPB.46.988
[(1R,2R,3S,4S,4aR,6S,8R,8aS)-4-[(3aS,5S,6aS)-3a-hydroxy-3,4,5,6a-tetrahydro-2H-furo[2,3-b]furan-5-yl]-1,6,8-trihydroxy-8-(hydroxymethyl)-3,4,8a-trimethyl-5-oxo-1,2,3,4a,6,7-hexahydronaphthalen-2-yl] (E)-3-phenylprop-2-enoate 10530620 Click to see CC1C(C(C2(C(C1(C)C3CC4(CCOC4O3)O)C(=O)C(CC2(CO)O)O)C)O)OC(=O)C=CC5=CC=CC=C5 546.60 unknown https://doi.org/10.1248/CPB.46.988
[(1R,2R,3S,4S,4aS,5R,8R,8aR)-4-[(3aR,5S,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-5-acetyloxy-8-formyl-1-hydroxy-3,4,8a-trimethyl-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-yl] (E)-3-phenylprop-2-enoate 10578377 Click to see CC1C(C(C2(C(CCC(C2C1(C)C3CC4CCOC4O3)OC(=O)C)C=O)C)O)OC(=O)C=CC5=CC=CC=C5 540.60 unknown https://doi.org/10.1248/CPB.46.988
[4-(2,3,3a,4,5,6a-Hexahydrofuro[2,3-b]furan-5-yl)-5-acetyloxy-8-formyl-1-hydroxy-3,4,8a-trimethyl-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-yl] 3-phenylprop-2-enoate 85192528 Click to see 540.60 unknown https://doi.org/10.1248/CPB.46.988
[4-(3a-hydroxy-3,4,5,6a-tetrahydro-2H-furo[2,3-b]furan-5-yl)-1,6,8-trihydroxy-8-(hydroxymethyl)-3,4,8a-trimethyl-5-oxo-1,2,3,4a,6,7-hexahydronaphthalen-2-yl] 3-phenylprop-2-enoate 85173965 Click to see 546.60 unknown https://doi.org/10.1248/CPB.46.988
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4S,5S)-5-[(4aS,8aR)-5,5,8a-trimethyl-3-oxo-4a,6,7,8-tetrahydro-4H-naphthalen-2-yl]-4-hydroxy-4-propan-2-yloxolan-2-one 10830575 Click to see 334.40 unknown https://doi.org/10.1248/CPB.46.988
5-(5,5,8a-trimethyl-3-oxo-4a,6,7,8-tetrahydro-4H-naphthalen-2-yl)-4-hydroxy-4-propan-2-yloxolan-2-one 85282297 Click to see CC(C)C1(CC(=O)OC1C2=CC3(CCCC(C3CC2=O)(C)C)C)O 334.40 unknown https://doi.org/10.1248/CPB.46.988
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside 132274946 Click to see 624.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 6-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)- 124222280 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)O 652.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775
Martynoside 5319292 Click to see 652.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
4'-Hydroxywogonin 5322078 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O 300.26 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775
5,7-Dihydroxy-6,8-dimethoxyflavone 11609345 Click to see 314.29 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775
5,7,2'-Trihydroxy-6,8-dimethoxyflavone 9818878 Click to see 330.29 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775
Demethoxysudachitin 3083845 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)O 330.29 unknown https://doi.org/10.1248/YAKUSHI1947.114.10_775

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