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Scutellaria schachristanica

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fecacb1859702013935
Scientific name Scutellaria schachristanica
Authority Juz.
First published in Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 14: 419 (1951)

Ethnobotanical Use Top

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General Uses 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-0000308432
Tropicos 17604477
KEW urn:lsid:ipni.org:names:458643-1
The Plant List kew-189687
Open Tree Of Life 6085748
Observations.org 142799
IPNI 458643-1
GBIF 5608235

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)!
Title Authors Publication Released IDs
Chemical components of the aerial part of Scutellaria schachristanica Z. O. Tashmatov, K. A. Eshbakova, Kh. M. Bobakulov Springer Science and Business Media LLC 28-Jul-2011
doi:10.1007/S10600-011-9955-8
Flavonoids from the aerial part of Scutellaria schachristanica Z. O. Tashmatov, K. A. Eshbakova, Kh. M. Babakulov, N. D. Abdullaev Springer Science and Business Media LLC 08-Jan-2010
doi:10.1007/S10600-010-9481-0

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 / O-glycosyl compounds
Hex-2-ulofuranosyl hexopyranoside 1115 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1007/S10600-011-9955-8
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1007/S10600-011-9955-8
> 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/S10600-010-9481-0
Chrysin 5281607 Click to see 254.24 unknown https://doi.org/10.1007/S10600-010-9481-0
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/S10600-010-9481-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown https://doi.org/10.1007/S10600-011-9955-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Chrysin-7-O-glucoronide 14135334 Click to see 430.40 unknown https://doi.org/10.1007/S10600-011-9955-8
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/S10600-011-9955-8
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 444.40 unknown https://doi.org/10.1007/S10600-011-9955-8
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/S10600-011-9955-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5,6-Dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14332446 Click to see 448.40 unknown https://doi.org/10.1007/S10600-010-9481-0
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1007/S10600-010-9481-0
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1007/S10600-010-9481-0
Plantaginin 5320623 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-010-9481-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Galangin 3-methyl ether 5281946 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 284.26 unknown https://doi.org/10.1007/S10600-011-9955-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown https://doi.org/10.1007/S10600-010-9481-0
Oroxylin A 5320315 Click to see 284.26 unknown https://doi.org/10.1007/S10600-011-9955-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see 284.26 unknown https://doi.org/10.1007/S10600-011-9955-8

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