Glycyrrhiza flavonol A

Details

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Internal ID f9dc6c9e-c8b7-4d8b-b700-4dfa3d0d8578
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 3-prenylated flavones
IUPAC Name 3,5,7-trihydroxy-2-(3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)chromen-4-one
SMILES (Canonical) CC1(C(CC2=C(O1)C=CC(=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)C
SMILES (Isomeric) CC1(C(CC2=C(O1)C=CC(=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)C
InChI InChI=1S/C20H18O7/c1-20(2)15(23)6-10-5-9(3-4-13(10)27-20)19-18(25)17(24)16-12(22)7-11(21)8-14(16)26-19/h3-5,7-8,15,21-23,25H,6H2,1-2H3
InChI Key UFWHTSBKDGUFOX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H18O7
Molecular Weight 370.40 g/mol
Exact Mass 370.10525291 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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3,5,7-trihydroxy-2-(3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)chromen-4-one
RefChem:1086104
197304-01-1
Glycyrrhizaflavonol A
Glycyrrhiza-flavonol A
[2,6'-Bi-4H-1-benzopyran]-4-one, 2',3'-dihydro-3,3',5,7-tetrahydroxy-2',2'-dimethyl-
orb1984193
CHEMBL5430013
CHEBI:175752
DTXSID601133444
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Glycyrrhiza flavonol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9807 98.07%
Caco-2 - 0.5791 57.91%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6746 67.46%
OATP2B1 inhibitior + 0.5797 57.97%
OATP1B1 inhibitior + 0.8075 80.75%
OATP1B3 inhibitior + 0.9271 92.71%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6827 68.27%
P-glycoprotein inhibitior - 0.6495 64.95%
P-glycoprotein substrate + 0.5154 51.54%
CYP3A4 substrate + 0.6804 68.04%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.7891 78.91%
CYP3A4 inhibition + 0.5463 54.63%
CYP2C9 inhibition - 0.6977 69.77%
CYP2C19 inhibition - 0.7544 75.44%
CYP2D6 inhibition - 0.8337 83.37%
CYP1A2 inhibition - 0.6841 68.41%
CYP2C8 inhibition + 0.9085 90.85%
CYP inhibitory promiscuity - 0.7775 77.75%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6422 64.22%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.8338 83.38%
Skin irritation - 0.7000 70.00%
Skin corrosion - 0.9075 90.75%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4122 41.22%
Micronuclear + 0.5659 56.59%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8127 81.27%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7299 72.99%
Acute Oral Toxicity (c) III 0.7277 72.77%
Estrogen receptor binding + 0.8702 87.02%
Androgen receptor binding + 0.7873 78.73%
Thyroid receptor binding + 0.6400 64.00%
Glucocorticoid receptor binding + 0.8781 87.81%
Aromatase binding + 0.6982 69.82%
PPAR gamma + 0.8912 89.12%
Honey bee toxicity - 0.8383 83.83%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.8939 89.39%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.59% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.02% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.57% 89.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 96.04% 96.12%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.42% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 93.69% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.35% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.05% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 91.12% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.91% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.72% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.39% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.87% 99.23%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 87.51% 95.64%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.45% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.17% 90.71%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 86.91% 85.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.73% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.15% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 84.98% 94.73%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.01% 95.78%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.56% 95.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.27% 97.09%
CHEMBL3194 P02766 Transthyretin 80.89% 90.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Glycyrrhiza uralensis
Glycyrrhiza uralensis

Cross-Links

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PubChem 5317765
NPASS NPC171821
LOTUS LTS0086210
wikiData Q105272178