Gancaonin A

Details

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Internal ID 27e66c7b-921c-47eb-a8fe-4e43bc0c532a
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 6-prenylated isoflavanones
IUPAC Name 5,7-dihydroxy-3-(4-methoxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC)O)C
SMILES (Isomeric) CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC)O)C
InChI InChI=1S/C21H20O5/c1-12(2)4-9-15-17(22)10-18-19(20(15)23)21(24)16(11-26-18)13-5-7-14(25-3)8-6-13/h4-8,10-11,22-23H,9H2,1-3H3
InChI Key JQNSUDIGIIGIOL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O5
Molecular Weight 352.40 g/mol
Exact Mass 352.13107373 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEMBL4453259
5,7-Dihydroxy-4'-methoxy-6-prenylisoflavone
5,7-dihydroxy-3-(4-methoxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one
27762-99-8
SCHEMBL572123
CHEBI:175515
DTXSID001318197
BDBM50535080
LMPK12050225

2D Structure

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2D Structure of Gancaonin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.7363 73.63%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7048 70.48%
OATP2B1 inhibitior - 0.5692 56.92%
OATP1B1 inhibitior + 0.9500 95.00%
OATP1B3 inhibitior + 0.8466 84.66%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7059 70.59%
P-glycoprotein inhibitior + 0.6648 66.48%
P-glycoprotein substrate - 0.8758 87.58%
CYP3A4 substrate + 0.5854 58.54%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.6395 63.95%
CYP2C9 inhibition + 0.8833 88.33%
CYP2C19 inhibition + 0.9477 94.77%
CYP2D6 inhibition - 0.5417 54.17%
CYP1A2 inhibition + 0.8808 88.08%
CYP2C8 inhibition + 0.5646 56.46%
CYP inhibitory promiscuity + 0.9500 95.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6792 67.92%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.4774 47.74%
Skin irritation - 0.7722 77.22%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4883 48.83%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.8343 83.43%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7003 70.03%
Acute Oral Toxicity (c) III 0.6798 67.98%
Estrogen receptor binding + 0.9653 96.53%
Androgen receptor binding + 0.8979 89.79%
Thyroid receptor binding + 0.6561 65.61%
Glucocorticoid receptor binding + 0.8235 82.35%
Aromatase binding + 0.7710 77.10%
PPAR gamma + 0.8991 89.91%
Honey bee toxicity - 0.8389 83.89%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9903 99.03%

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 99.50% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.47% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 94.46% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.36% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.28% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.80% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.61% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.46% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.04% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.12% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.30% 89.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 87.29% 91.71%
CHEMBL1929 P47989 Xanthine dehydrogenase 86.63% 96.12%
CHEMBL4208 P20618 Proteasome component C5 85.82% 90.00%
CHEMBL1907 P15144 Aminopeptidase N 84.83% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 84.81% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.91% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.56% 93.99%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.61% 97.28%

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.
Cullen corylifolium
Garcinia hanburyi
Glycyrrhiza
Glycyrrhiza aspera
Glycyrrhiza uralensis
Glycyrrhiza uralensis
Lotus creticus
Mitracarpus hirtus

Cross-Links

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PubChem 5317478
NPASS NPC40942
LOTUS LTS0216479
wikiData Q105133556