2-(4-Hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-enyl)chromen-4-one

Details

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Internal ID 336ccb87-c01a-4513-8c2f-5c63f0886c99
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 6-prenylated flavones
IUPAC Name 2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=CC2=C(C=C1OC)OC(=CC2=O)C3=CC=C(C=C3)O)C
SMILES (Isomeric) CC(=CCC1=CC2=C(C=C1OC)OC(=CC2=O)C3=CC=C(C=C3)O)C
InChI InChI=1S/C21H20O4/c1-13(2)4-5-15-10-17-18(23)11-20(14-6-8-16(22)9-7-14)25-21(17)12-19(15)24-3/h4,6-12,22H,5H2,1-3H3
InChI Key BVTZAHKRSBADDO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O4
Molecular Weight 336.40 g/mol
Exact Mass 336.13615911 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.68
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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BDBM50084041

2D Structure

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2D Structure of 2-(4-Hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-enyl)chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.6780 67.80%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7935 79.35%
OATP2B1 inhibitior - 0.5769 57.69%
OATP1B1 inhibitior + 0.8763 87.63%
OATP1B3 inhibitior + 0.9123 91.23%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8786 87.86%
P-glycoprotein inhibitior + 0.8305 83.05%
P-glycoprotein substrate - 0.5364 53.64%
CYP3A4 substrate + 0.5627 56.27%
CYP2C9 substrate - 0.8217 82.17%
CYP2D6 substrate - 0.7552 75.52%
CYP3A4 inhibition - 0.7230 72.30%
CYP2C9 inhibition + 0.8275 82.75%
CYP2C19 inhibition + 0.9435 94.35%
CYP2D6 inhibition - 0.7767 77.67%
CYP1A2 inhibition + 0.8005 80.05%
CYP2C8 inhibition + 0.7678 76.78%
CYP inhibitory promiscuity + 0.9227 92.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.6596 65.96%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.7217 72.17%
Skin irritation - 0.7755 77.55%
Skin corrosion - 0.9713 97.13%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3700 37.00%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.6167 61.67%
skin sensitisation - 0.8324 83.24%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6573 65.73%
Acute Oral Toxicity (c) III 0.7369 73.69%
Estrogen receptor binding + 0.9407 94.07%
Androgen receptor binding + 0.8823 88.23%
Thyroid receptor binding + 0.5791 57.91%
Glucocorticoid receptor binding + 0.9291 92.91%
Aromatase binding + 0.7843 78.43%
PPAR gamma + 0.9407 94.07%
Honey bee toxicity - 0.8017 80.17%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9915 99.15%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 175.5 nM
488.8 nM
Ki
IC50
via Super-PRED
PMID: 25978962

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.98% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.63% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.48% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.38% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.37% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.12% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.99% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.32% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.00% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.98% 99.17%
CHEMBL3922 P50579 Methionine aminopeptidase 2 87.34% 97.28%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.17% 90.71%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.10% 91.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.38% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.86% 99.15%
CHEMBL2535 P11166 Glucose transporter 80.72% 98.75%

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

Cross-Links

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PubChem 44584224
NPASS NPC110969
ChEMBL CHEMBL458053
LOTUS LTS0242940
wikiData Q104946851