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Scutellaria immaculata

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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 UUID643fec94330cf062627360
Scientific name Scutellaria immaculata
Authority Nevski ex Juz.
First published in Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 14: 428 (1951)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Uzbek koʻkamaron

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000307923
Tropicos 17604385
KEW urn:lsid:ipni.org:names:458350-1
The Plant List kew-189203
Open Tree Of Life 6085577
Observations.org 128942
NCBI Taxonomy 2721167
IPNI 458350-1
iNaturalist 905623
GBIF 5609203
Elurikkus 556326

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
Untargeted Metabolomics Analysis of the Orchid Species Oncidium sotoanum Reveals the Presence of Rare Bioactive C-Diglycosylated Chrysin Derivatives Zorzi G, Gambini S, Negri S, Guzzo F, Commisso M Plants (Basel) 02-Feb-2023
PMCID:PMC9920315
doi:10.3390/plants12030655
PMID:36771739
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
Different compounds against Angiotensin-Converting Enzyme 2 (ACE2) receptor potentially containing the infectivity of SARS-CoV-2: an in silico study Shahbazi B, Mafakher L, Teimoori-Toolabi L J Mol Model 05-Mar-2022
PMCID:PMC8898033
doi:10.1007/s00894-022-05059-1
PMID:35249180
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
In Vitro Biological Activities of Fruits and Leaves of Elaeagnus multiflora Thunb. and Their Isoprenoids and Polyphenolics Profile Lachowicz S, Kapusta I, Świeca M, Stinco CM, Meléndez-Martínez AJ, Bieniek A Antioxidants (Basel) 17-May-2020
PMCID:PMC7278795
doi:10.3390/antiox9050436
PMID:32429578
Flavonoids from the Aerial Part of Scutellaria intermedia A. M. Karimov, T. N. Slobodyanyuk, E. Kh. Botirov Springer Science and Business Media LLC 19-Jul-2017
doi:10.1007/S10600-017-2107-Z
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
Flavonoids of Scutellaria immaculata Roots M. P. Yuldashev, A. Karimov Springer Science and Business Media LLC 10-Jun-2005
doi:10.1007/S10600-005-0068-0

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
> 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/S10600-005-0068-0
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/S10600-005-0068-0
Isoscutellarein 5281665 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/S10600-005-0068-0
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/S10600-005-0068-0
> 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/S10600-017-2107-Z
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/S10600-017-2107-Z
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/S10600-017-2107-Z
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-8-methoxy-2-phenyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74977902 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1007/S10600-005-0068-0
Apigenin 7-O-glucoside 5385553 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 432.40 unknown https://doi.org/10.1007/S10600-005-0068-0
Apigetrin 5280704 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 432.40 unknown https://doi.org/10.1007/S10600-005-0068-0
https://doi.org/10.1007/S10600-017-2107-Z
Immaculoside 44258561 Click to see COC1=CC(=C(C2=C1C(=O)C=C(O2)C3=CC=CC=C3)OC)OC4C(C(C(C(O4)CO)O)O)O 460.40 unknown https://doi.org/10.1007/S10600-017-2107-Z
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/S10600-017-2107-Z
wogonin 7-O-glucoside 51136398 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1007/S10600-005-0068-0
> 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/S10600-005-0068-0
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/S10600-005-0068-0
> 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/S10600-005-0068-0
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/S10600-005-0068-0
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/S10600-005-0068-0

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