Scutellaria comosa

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Internal ID	UUID643fec8c06fe7926132651
Scientific name	Scutellaria comosa
Authority	Juz.
First published in	Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 14: 381 (1951)

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Synonyms Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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

Asia-temperate click to expand
- Middle Asia
  - Kirgizstan
  - Tadzhikistan
  - Uzbekistan

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Database	ID/link to page
World Flora Online	wfo-0000307730
Tropicos	17604362
KEW	urn:lsid:ipni.org:names:458214-1
The Plant List	kew-189018
Open Tree Of Life	6085514
Observations.org	122072
NCBI Taxonomy	2858894
IPNI	458214-1
iNaturalist	904586
GBIF	5609712
Elurikkus	556534

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

Electrostimulation improves plant growth and modulates the flavonoid profile in aeroponic culture of Scutellaria baicalensis Georgi

Grzelka K, Matkowski A, Ślusarczyk S

Front Plant Sci

01-Mar-2023

PMCID:	PMC10014570
doi:	10.3389/fpls.2023.1142624
PMID:	36938053

Flavonoids of the epigeal part ofScutellaria comosa

M. P. Yuldashev

Springer Science and Business Media LLC

21-Oct-2005

doi:	10.1007/BF02234938

Flavonoids of the roots ofScutellaria comosa

M. P. Yuldashev, �. Kh. Batirov, V. M. Malikov

Springer Science and Business Media LLC

01-Apr-2005

doi:	10.1007/BF01372624

Flavonoids of the roots ofScutellaria comosa

B. Yusupova, R. Atazhanov, I. Toshmatov, Sh. Abdullaev, V. Litvinenko

Springer Science and Business Media LLC

15-Feb-2005

doi:	10.1007/BF01167595

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
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1007/BF01372624 https://doi.org/10.1007/BF01167595
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/10.1007/BF01167595
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/10.1007/BF01372624 https://doi.org/10.1007/BF01167595
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1007/BF02234938
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/BF01167595
Scutellarein	5281697	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O	286.24	unknown	https://doi.org/10.1007/BF02234938
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1007/BF02234938
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
3,4,5-Trihydroxy-6-(5-hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl)oxyoxane-2-carboxylic acid	12004622	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/10.1007/BF01167595 https://doi.org/10.1007/BF01372624
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/10.1007/BF01167595
Breviscapine	6426802	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1007/BF02234938
Chrysin 7-glucuronide	44257628	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/BF01167595
methyl (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(5-hydroxy-4-oxo-2-phenylchromen-7-yl)oxyoxane-2-carboxylate	156020020	Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=CC=C4)O)O)O)O	444.40	unknown	https://doi.org/10.1007/BF01372624
Methyl 3,4,5-trihydroxy-6-(5-hydroxy-4-oxo-2-phenylchromen-7-yl)oxyoxane-2-carboxylate	24769271	Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=CC=C4)O)O)O)O	444.40	unknown	https://doi.org/10.1007/BF01372624
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/10.1007/BF01372624 https://doi.org/10.1007/BF01167595
Oroxylin A glucoronide	14655552	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)OC4C(C(C(C(O4)C(=O)O)O)O)O	460.40	unknown	https://doi.org/10.1007/BF01372624
Oroxylin A-7-o-beta-D-glucuronide	14655551	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)OC4C(C(C(C(O4)C(=O)O)O)O)O	460.40	unknown	https://doi.org/10.1007/BF01372624
Scutellarin	185617	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1007/BF02234938
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Baicalin-7-glucoside	623002	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/BF01167595
Oroxin A	5320313	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/BF01167595
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin	5281628	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O	300.26	unknown	https://doi.org/10.1007/BF02234938
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/BF02234938
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7-dimethoxy-2,3-dihydrochromen-4-one	162908392	Click to see COC1=CC=CC(=C1C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	346.30	unknown	https://doi.org/10.1007/BF01372624
5,2'-Dihydroxy-6,7,6'-trimethoxyflavanone	13889020	Click to see COC1=CC=CC(=C1C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	346.30	unknown	https://doi.org/10.1007/BF01372624
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethoxy-2,3-dihydrochromen-4-one	162945355	Click to see COC1=CC=CC(=C1C2CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O	376.40	unknown	https://doi.org/10.1007/BF01372624
5,2'-Dihydroxy-6,7,8,6'-tetramethoxyflavanone	15838217	Click to see COC1=CC=CC(=C1C2CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O	376.40	unknown	https://doi.org/10.1007/BF01372624
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/BF01167595 https://doi.org/10.1007/BF01372624

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Scutellaria comosa

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top