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Scutellaria scandens

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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 UUID643fecac91fcc802407680
Scientific name Scutellaria scandens
Authority Buch.-Ham. ex D.Don
First published in Prodr. Fl. Nepal. : 110 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Scutellaria angulosa Benth. Pl. Asiat. Rar. 1: 67 (1830)
Scutellaria celtidifolia A.Ham. Esq. Monogr. Scutellaria : 27 (1832)

Common names Top

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Language Common/alternative name
Chinese 棱茎黄芩

Subspecies (abbr. subsp./ssp.) Top

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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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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-0000308430
Tropicos 17600346
KEW urn:lsid:ipni.org:names:458641-1
The Plant List kew-189685
Open Tree Of Life 6085746
NCBI Taxonomy 2802346
IPNI 458641-1
iNaturalist 950308
GBIF 5608241
EOL 2894283

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
Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo Studies De S, Paul S, Manna A, Majumder C, Pal K, Casarcia N, Mondal A, Banerjee S, Nelson VK, Ghosh S, Hazra J, Bhattacharjee A, Mandal SC, Pal M, Bishayee A Cancers (Basel) 03-Feb-2023
PMCID:PMC9913554
doi:10.3390/cancers15030993
PMID:36765950
Phytochemicals in the Prevention and Treatment of SARS-CoV-2—Clinical Evidence Bijelić K, Hitl M, Kladar N Antibiotics (Basel) 13-Nov-2022
PMCID:PMC9686831
doi:10.3390/antibiotics11111614
PMID:36421257
A Review of Medicinal Plants of the Himalayas with Anti-Proliferative Activity for the Treatment of Various Cancers Regassa H, Sourirajan A, Kumar V, Pandey S, Kumar D, Dev K Cancers (Basel) 12-Aug-2022
PMCID:PMC9406073
doi:10.3390/cancers14163898
PMID:36010892
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. IX. On the flavonoid constituents of the root of scutellaria scandens BUCH.-HAM. ex D. DON. YUKINORI MIYAICHI, YOSHITAKA IMOTO, TSUYOSHI TOMIMORI, TUSNEO NAMBA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.36.2371
Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies Khadem S, Marles RJ Molecules 08-Nov-2010
PMCID:PMC6259451
doi:10.3390/molecules15117985
PMID:21060304

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
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1248/CPB.46.988
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Multijugenol 70566040 Click to see CC1=CCC2C(CC2(C)C)C(=C)CCC1O 220.35 unknown https://doi.org/10.1248/CPB.46.988
Clovanediol 15599878 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)O)C 238.37 unknown https://doi.org/10.1248/CPB.46.988
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epioleanolic acid 11869658 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/10.1248/CPB.46.988
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Citrusin C 9945189 Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown https://doi.org/10.1248/CPB.46.988
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1S,4R,10R)-4,12,12-trimethyl-5-oxatricyclo[8.2.0.04,6]dodecan-9-one 129317138 Click to see CC1(CC2C1CCC3(C(O3)CCC2=O)C)C 222.32 unknown https://doi.org/10.1248/CPB.46.988
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Osmanthuside B 10438425 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC=C(C=C3)O)CO)OCCC4=CC=C(C=C4)O)O)O)O)O 592.60 unknown https://doi.org/10.1248/CPB.46.988
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Dihydrobaicalein 9816931 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC=CC=C3 272.25 unknown https://doi.org/10.1248/CPB.36.2371
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Baicalein 5281605 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O 270.24 unknown https://doi.org/10.1248/CPB.36.2371
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1248/CPB.36.2371
Norwogonin 5281674 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O 270.24 unknown https://doi.org/10.1248/CPB.36.2371
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Baicalin 64982 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.36.2371
Chrysin-7-O-glucuronide 14135335 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O 430.40 unknown https://doi.org/10.1248/CPB.36.2371
Dihydrobaicalin 14135325 Click to see C1C(OC2=CC(=C(C(=C2C1=O)O)O)OC3C(C(C(C(O3)C(=O)O)O)O)O)C4=CC=CC=C4 448.40 unknown https://doi.org/10.1248/CPB.36.2371
Oroxindin 3084961 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 460.40 unknown https://doi.org/10.1248/CPB.36.2371
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
(2S)-5,7-dihydroxy-2-[5-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6-methoxy-2,3-dihydrochromen-4-one 14135327 Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 480.40 unknown https://doi.org/10.1248/CPB.36.2371
(2s)-5,7,2',5'-Tetrahydroxy-6-methoxyflavanone 14135322 Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=CC(=C3)O)O)O 318.28 unknown https://doi.org/10.1248/CPB.36.2371
[(2S,3R,4S,5S,6R)-2-[2-[(2S)-5,7-dihydroxy-6-methoxy-4-oxo-2,3-dihydrochromen-2-yl]-4-hydroxyphenoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 14135329 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3=C(C=C(C=C3)O)C4CC(=O)C5=C(O4)C=C(C(=C5O)OC)O)CO)O)O)O 656.60 unknown https://doi.org/10.1248/CPB.36.2371
[(2S,3R,4S,5S,6R)-2-[2-[(2S)-5,7-dihydroxy-6-methoxy-4-oxo-2,3-dihydrochromen-2-yl]-4-hydroxyphenoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 14135331 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OC3=C(C=C(C=C3)O)C4CC(=O)C5=C(O4)C=C(C(=C5O)OC)O)CO)O)O 686.60 unknown https://doi.org/10.1248/CPB.36.2371
[2-[2-(5,7-Dihydroxy-6-methoxy-4-oxo-2,3-dihydrochromen-2-yl)-4-hydroxyphenoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162914501 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3=C(C=C(C=C3)O)C4CC(=O)C5=C(O4)C=C(C(=C5O)OC)O)CO)O)O)O 656.60 unknown https://doi.org/10.1248/CPB.36.2371
[2-[2-(5,7-Dihydroxy-6-methoxy-4-oxo-2,3-dihydrochromen-2-yl)-4-hydroxyphenoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 162858873 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OC3=C(C=C(C=C3)O)C4CC(=O)C5=C(O4)C=C(C(=C5O)OC)O)CO)O)O 686.60 unknown https://doi.org/10.1248/CPB.36.2371
5,7-Dihydroxy-2-[5-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6-methoxy-2,3-dihydrochromen-4-one 14135326 Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 480.40 unknown https://doi.org/10.1248/CPB.36.2371
5,7,2',5'-Tetrahydroxy-6-methoxyflavanone 14135321 Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=CC(=C3)O)O)O 318.28 unknown https://doi.org/10.1248/CPB.36.2371
Dihydrooroxylin A 5316733 Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 286.28 unknown https://doi.org/10.1248/CPB.36.2371
Oroxylin A 5320315 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O 284.26 unknown https://doi.org/10.1248/CPB.36.2371
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown https://doi.org/10.1248/CPB.36.2371
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2S,3R,4S,5S,6R)-2-[2-[(2S)-5,7-dihydroxy-6-methoxy-4-oxo-2,3-dihydrochromen-2-yl]-4-hydroxyphenoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 4-hydroxy-3-methoxybenzoate 14135333 Click to see COC1=C(C=CC(=C1)C(=O)OC2C(C(C(OC2OC3=C(C=C(C=C3)O)C4CC(=O)C5=C(O4)C=C(C(=C5O)OC)O)CO)O)O)O 630.50 unknown https://doi.org/10.1248/CPB.36.2371
[2-[2-(5,7-Dihydroxy-6-methoxy-4-oxo-2,3-dihydrochromen-2-yl)-4-hydroxyphenoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 4-hydroxy-3-methoxybenzoate 14135332 Click to see COC1=C(C=CC(=C1)C(=O)OC2C(C(C(OC2OC3=C(C=C(C=C3)O)C4CC(=O)C5=C(O4)C=C(C(=C5O)OC)O)CO)O)O)O 630.50 unknown https://doi.org/10.1248/CPB.36.2371

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