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Scutellaria ramosissima

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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 UUID643fecaa0bfc6626551012
Scientific name Scutellaria ramosissima
Authority Popov
First published in Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 5: 155 (1924)

Description Top

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Synonyms Top

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Common names Top

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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-0000308367
Tropicos 17604472
KEW urn:lsid:ipni.org:names:458608-1
The Plant List kew-189624
Open Tree Of Life 6085731
Observations.org 140832
NCBI Taxonomy 2858899
IPNI 458608-1
GBIF 5608400
Elurikkus 556035
USDA GRIN 476376

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
A Background Search on the Potential Role of Scutellaria and Its Essential Oils Zehravi M, Karthika C, Azad AK, Ahmad Z, Khan FS, Rahman MS, Akter R, Rahman MH Biomed Res Int 27-Jul-2022
PMCID:PMC9365597
doi:10.1155/2022/7265445
PMID:35968239
Emerging cellular and molecular mechanisms underlying anticancer indications of chrysin Talebi M, Talebi M, Farkhondeh T, Simal-Gandara J, Kopustinskiene DM, Bernatoniene J, Samarghandian S Cancer Cell Int 15-Apr-2021
PMCID:PMC8050922
doi:10.1186/s12935-021-01906-y
PMID:33858433
Structure-Based Virtual Screening and De Novo Design of PIM1 Inhibitors with Anticancer Activity from Natural Products Park H, Jeon J, Kim K, Choi S, Hong S Pharmaceuticals (Basel) 18-Mar-2021
PMCID:PMC8003278
doi:10.3390/ph14030275
PMID:33803840
Aromatic Medicinal Plants of the Lamiaceae Family from Uzbekistan: Ethnopharmacology, Essential Oils Composition, and Biological Activities Mamadalieva NZ, Akramov DK, Ovidi E, Tiezzi A, Nahar L, Azimova SS, Sarker SD Medicines (Basel) 10-Feb-2017
PMCID:PMC5597069
doi:10.3390/medicines4010008
PMID:28930224
Identification of PPARgamma Partial Agonists of Natural Origin (II): In Silico Prediction in Natural Extracts with Known Antidiabetic Activity Guasch L, Sala E, Mulero M, Valls C, Salvadó MJ, Pujadas G, Garcia-Vallvé S PLoS One 06-Feb-2013
PMCID:PMC3566095
doi:10.1371/journal.pone.0055889
PMID:23405231
Elsholtzia: phytochemistry and biological activities Guo Z, Liu Z, Wang X, Liu W, Jiang R, Cheng R, She G Chem Cent J 05-Dec-2012
PMCID:PMC3536681
doi:10.1186/1752-153X-6-147
PMID:23216850
New flavone glycoside fromScutellaria ramosissima M. P. Yulgashev, �. Kh. Batirov, V. M. Malikov Springer Science and Business Media LLC 15-Feb-2005
doi:10.1007/BF01170224
Flavonoids of the epigeal part of Scutellaria ramosissima M. P. Yuldashev, �. Kh. Batirov, V. M. Malikov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630163
Structures of two new flavonoids fromScutellaria ramosissima M. P. Yuldashev, É. Kh. Batirov, A. Nigmatullaev, V. M. Malikov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00629967

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1007/BF00629967
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1007/BF00629967
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/10.1007/BF00629967
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Chrysin-7-O-beta-D-glucoronide 14135334 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/10.1007/BF00630163
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/10.1007/BF00630163
ethyl (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2S)-5-hydroxy-2-(2-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxane-2-carboxylate 21633173 Click to see CCOC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=O)CC(OC3=C2)C4=CC=CC=C4O)O)O)O)O 476.40 unknown https://doi.org/10.1007/BF00630163
Ethyl 3,4,5-trihydroxy-6-[[5-hydroxy-2-(2-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxane-2-carboxylate 73816174 Click to see CCOC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=O)CC(OC3=C2)C4=CC=CC=C4O)O)O)O)O 476.40 unknown https://doi.org/10.1007/BF00630163
methyl (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2S)-5-hydroxy-2-(2-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxane-2-carboxylate 21770582 Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=O)CC(OC3=C2)C4=CC=CC=C4O)O)O)O)O 462.40 unknown https://doi.org/10.1007/BF00630163
Methyl 3,4,5-trihydroxy-6-[[5-hydroxy-2-(2-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxane-2-carboxylate 73661278 Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=O)CC(OC3=C2)C4=CC=CC=C4O)O)O)O)O 462.40 unknown https://doi.org/10.1007/BF00630163
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(2-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 21769501 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=CC=C4O 434.40 unknown https://doi.org/10.1007/BF00629967
5,7,2'-Trihydroxyflavanone 7-glucoside 42607843 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=CC=C4O 434.40 unknown https://doi.org/10.1007/BF00629967
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
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/10.1007/BF00629967
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(2,6-Dihydroxyphenyl)-5-hydroxy-6,7,8-trimethoxychromen-4-one 1801510 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=C(C=CC=C3O)O)OC)OC 360.30 unknown https://doi.org/10.1007/BF00629967
5,6-Dihydroxy-7,8-dimethoxyflavone 821356 Click to see COC1=C(C(=C2C(=O)C=C(OC2=C1OC)C3=CC=CC=C3)O)O 314.29 unknown https://doi.org/10.1007/BF00629967
Pebrellin 632255 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC 374.30 unknown https://doi.org/10.1007/BF00629967
Rivularin (flavone) 13889022 Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC)O 344.30 unknown https://doi.org/10.1007/BF01170224
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/10.1007/BF00629967

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