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Internal ID UUID643fecb43ea1c940340571
Scientific name Scutellaria viscidula
Authority Bunge
First published in Enum. Pl. China Bor. : 52 (1833)

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 黄芩
Chinese 黄芩子
Chinese 腺毛黄芩
Chinese 土黄芩
Chinese 粘毛黄芩
Chinese 粘毛黄芩(黄花黄芩)
Chinese 黏毛黄芩
Chinese 下巴子
Chinese 黄花黄芩

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-0000308611
Tropicos 17605816
KEW urn:lsid:ipni.org:names:458765-1
The Plant List kew-189850
Open Tree Of Life 393212
Observations.org 455259
NCBI Taxonomy 512023
IPNI 458765-1
iNaturalist 1030047
GBIF 5607891
EOL 2894305
Elurikkus 555900
USDA GRIN 423539
CMAUP NPO19994

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
Cloning, expression and activity analysises of chalcone synthase genes in Carthamus tinctorius Tang X, Ren C, Hu J, Chen J, Wang J, Wang R, Wu Q, Liao W, Pei J Chin Herb Med 16-Feb-2023
PMCID:PMC10230621
doi:10.1016/j.chmed.2022.12.005
PMID:37265765
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
Analyses on Flavonoids and Transcriptome Reveals Key MYB Gene for Proanthocyanidins Regulation in Onobrychis Viciifolia Jin Z, Jiang W, Luo Y, Huang H, Yi D, Pang Y Front Plant Sci 24-Jun-2022
PMCID:PMC9263696
doi:10.3389/fpls.2022.941918
PMID:35812930
Tissue-specific transcriptome analyses reveal candidate genes for stilbene, flavonoid and anthraquinone biosynthesis in the medicinal plant Polygonum cuspidatum Wang X, Hu H, Wu Z, Fan H, Wang G, Chai T, Wang H BMC Genomics 17-May-2021
PMCID:PMC8127498
doi:10.1186/s12864-021-07658-3
PMID:34000984
Contribution of potassium channels, beta2-adrenergic and histamine H1 receptors in the relaxant effect of baicalein on rat tracheal smooth muscle Saadat S, Boskabadi J, Boskabady MH Iran J Basic Med Sci 01-Nov-2019
PMCID:PMC7038427
doi:10.22038/ijbms.2019.36377.8666
PMID:32128101
Transcriptomic analysis of early fruit development in Chinese white pear (Pyrus bretschneideri Rehd.) and functional identification of PbCCR1 in lignin biosynthesis Su X, Zhao Y, Wang H, Li G, Cheng X, Jin Q, Cai Y BMC Plant Biol 11-Oct-2019
PMCID:PMC6788021
doi:10.1186/s12870-019-2046-x
PMID:31604417
Medicinal wild plants used by the Mongol herdsmen in Bairin Area of Inner Mongolia and its comparative study between TMM and TCM Wurchaih, Huar, Menggenqiqig, Khasbagan J Ethnobiol Ethnomed 03-Jul-2019
PMCID:PMC6609360
doi:10.1186/s13002-019-0300-9
PMID:31269968
A Novel β-Glucuronidase from Talaromyces pinophilus Li-93 Precisely Hydrolyzes Glycyrrhizin into Glycyrrhetinic Acid 3-O-Mono-β-d-Glucuronide Xu Y, Feng X, Jia J, Chen X, Jiang T, Rasool A, Lv B, Qu L, Li C Appl Environ Microbiol 17-Sep-2018
PMCID:PMC6146983
doi:10.1128/AEM.00755-18
PMID:30054355
Identification and Characterization of Flavonoid Biosynthetic Enzyme Genes in Salvia miltiorrhiza (Lamiaceae) Deng Y, Li C, Li H, Lu S Molecules 16-Jun-2018
PMCID:PMC6099592
doi:10.3390/molecules23061467
PMID:29914175
The Chloroplast Genome Sequence of Scutellaria baicalensis Provides Insight into Intraspecific and Interspecific Chloroplast Genome Diversity in Scutellaria Jiang D, Zhao Z, Zhang T, Zhong W, Liu C, Yuan Q, Huang L Genes (Basel) 13-Sep-2017
PMCID:PMC5615360
doi:10.3390/genes8090227
PMID:28902130
A new species of Scutellaria (Scutellarioideae, Lamiaceae) from Sichuan Province in southwest China Zhao F, Liu ED, Peng H, Xiang CL PeerJ 08-Aug-2017
PMCID:PMC5550825
doi:10.7717/peerj.3624
PMID:28804694
A specialized flavone biosynthetic pathway has evolved in the medicinal plant, Scutellaria baicalensis Zhao Q, Zhang Y, Wang G, Hill L, Weng JK, Chen XY, Xue H, Martin C Sci Adv 08-Apr-2016
PMCID:PMC4846459
doi:10.1126/sciadv.1501780
PMID:27152350
Isolation and Functional Characterization of a Phenylalanine Ammonia-Lyase Gene (SsPAL1) from Coleus (Solenostemon scutellarioides (L.) Codd) Zhu Q, Xie X, Lin H, Sui S, Shen R, Yang Z, Lu K, Li M, Liu YG Molecules 16-Sep-2015
PMCID:PMC6332037
doi:10.3390/molecules200916833
PMID:26389875
Commercialized non-Camellia tea: traditional function and molecular identification Long P, Cui Z, Wang Y, Zhang C, Zhang N, Li M, Xiao P Acta Pharm Sin B 24-Mar-2014
PMCID:PMC4629065
doi:10.1016/j.apsb.2014.02.006
PMID:26579387
Molecular cloning and expression profiling of a chalcone synthase gene from hairy root cultures of Scutellaria viscidula Bunge Lei W, Tang SH, Luo KM, Sun M Genet Mol Biol 01-Jun-2010
PMCID:PMC3036846
doi:10.1590/S1415-47572010005000031
PMID:21637484

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
Antimycin A19 56600064 Click to see CCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)C(C)C 548.60 unknown via CMAUP database
Antimycin A20 54764156 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C 506.50 unknown via CMAUP database
Antimycin A2a 447434 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)C 534.60 unknown via CMAUP database
Antimycin A3 245869 Click to see CCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C 520.60 unknown via CMAUP database
Antimycin A3a 2'R-epimer 86278330 Click to see CCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)CC 520.60 unknown via CMAUP database
Benzoic acid, 3-(formylamino)-2-hydroxy- 15409159 Click to see C1=CC(=C(C(=C1)NC=O)O)C(=O)O 181.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Methyl-3-hydroxyanthranilic acid 95222 Click to see CC1=C(C(=C(C=C1)C(=O)O)N)O 167.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Virginiae butanolide A 10036830 Click to see CC(C)CCCC(C1C(COC1=O)CO)O 230.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(10R,13S)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-[1-[5-methyl-6-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]ethyl]-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 11968816 Click to see CC1CCC(OC1OC2C(C(C(C(O2)C)O)O)O)C(C)C3CCC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C 887.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids and derivatives
antimycin A1 14957 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C 548.60 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Ketomycin 19489 Click to see C1CC(CC=C1)C(=O)C(=O)O 154.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
Oleandomycin 72493 Click to see CC1CC(C(C(O1)OC2C(CC3(CO3)C(=O)C(C(C(C(OC(=O)C(C(C2C)OC4CC(C(C(O4)C)O)OC)C)C)C)O)C)C)O)N(C)C 687.90 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
9-[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]-3H-purin-6-one 21785357 Click to see C1C(C(C(C(O1)N2C=NC3=C2NC=NC3=O)O)O)O 268.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
(alphaR,2R)-alpha,5alpha-Dimethyl-6alpha-[(1E,3E,5E,7E,9S)-1,9-diethyl-14-oxo-14-(1H-pyrrole-2-yl)-1,3,5,7-tetradecatetraenyl]tetrahydro-2H-pyran-2beta-acetic acid 101789368 Click to see CCC(CCCCC(=O)C1=CC=CN1)C=CC=CC=CC=C(CC)C2C(CCC(O2)C(C)C(=O)O)C 495.70 unknown via CMAUP database
Indanomycin 10345604 Click to see CCC1CCC2C1C=CC(C2C(=O)C3=CC=CN3)C=CC=C(CC)C4C(CCC(O4)C(C)C(=O)O)C 493.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(2R)-6',10-Dihydroxy-7',9'-dimethoxy-4',5',9-trioxo-4,4',5',9-tetrahydrospiro[benzo[1,2-b:5,4-c']dipyran-2(3H),2'(3'H)-naphtho[1,2-b]furan]-7-carboxylic acid methyl ester 97042233 Click to see COC1=CC(=C(C2=C1C3=C(CC4(O3)CCC5=C(O4)C(=C6C(=C5)C=C(OC6=O)C(=O)OC)O)C(=O)C2=O)O)OC 536.40 unknown via CMAUP database
gamma-Rubromycin 5464075 Click to see COC1=CC(=O)C2=C(C1=O)C(=C3C(=C2O)CC4(O3)CCC5=C(O4)C(=C6C(=C5)C=C(OC6=O)C(=O)OC)O)O 522.40 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinoxalines / Phenazines and derivatives
6-Acetylphenazine-1-carboxylic acid 443635 Click to see CC(=O)C1=C2C(=CC=C1)N=C3C(=N2)C=CC=C3C(=O)O 266.25 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazodiazepines
Pentostatin 439693 Click to see C1C(C(OC1N2C=NC3=C2NC=NCC3O)CO)O 268.27 unknown via CMAUP database
Vira A deaminase inhibitor 44283251 Click to see C1C(C(OC1N2C=NC3=C2NC=NCC3O)CO)O 268.27 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4R,5S)-3-hexyl-4-hydroxy-5-methyloxolan-2-one 11030843 Click to see CCCCCCC1C(C(OC1=O)C)O 200.27 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
beta-Skytanthine 442552 Click to see CC1CCC2C1CN(CC2C)C 167.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Anthracyclines
Cinerubin B 73593 Click to see CCC1(CC(C2=C(C3=C(C=C2C1C(=O)OC)C(=O)C4=C(C=CC(=C4C3=O)O)O)O)OC5CC(C(C(O5)C)OC6CC7C(C(O6)C)OC8C(O7)CC(=O)C(O8)C)N(C)C)O 825.80 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(3S,4S,6S)-6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 44258403 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 via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S,3S,4S,5R)-2,3,4,5-Tetrahydroxy-5-(5-hydroxy-8-methoxy-4-oxo-2-phenyl-4H-chromen-7-yl)-6-oxohexanoic acid 29927693 Click to see COC1=C2C(=C(C=C1C(C=O)(C(C(C(C(=O)O)O)O)O)O)O)C(=O)C=C(O2)C3=CC=CC=C3 460.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-6,8-dimethoxyflavone 5321859 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)O 346.30 unknown via CMAUP database
Ganhuangenin 5271991 Click to see COC1=C(C=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
Skullcapflavone II 124211 Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 374.30 unknown via CMAUP database
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Woodorien 192694 Click to see COC(=O)C1=CC(=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown via CMAUP database

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