7-Hydroxy-6,8-dimethoxy-4-(4-methoxyphenyl)chromen-2-one

Details

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Internal ID 42ee2d2b-9cff-423d-bd92-5c9a071f5a1e
Taxonomy Phenylpropanoids and polyketides > Neoflavonoids > Neoflavones
IUPAC Name 7-hydroxy-6,8-dimethoxy-4-(4-methoxyphenyl)chromen-2-one
SMILES (Canonical) COC1=CC=C(C=C1)C2=CC(=O)OC3=C(C(=C(C=C23)OC)O)OC
SMILES (Isomeric) COC1=CC=C(C=C1)C2=CC(=O)OC3=C(C(=C(C=C23)OC)O)OC
InChI InChI=1S/C18H16O6/c1-21-11-6-4-10(5-7-11)12-9-15(19)24-17-13(12)8-14(22-2)16(20)18(17)23-3/h4-9,20H,1-3H3
InChI Key SABAAVUCEBCQPO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O6
Molecular Weight 328.30 g/mol
Exact Mass 328.09468823 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-6,8-dimethoxy-4-(4-methoxyphenyl)chromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9702 97.02%
Caco-2 + 0.7780 77.80%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7377 73.77%
OATP2B1 inhibitior - 0.7262 72.62%
OATP1B1 inhibitior + 0.9051 90.51%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6677 66.77%
P-glycoprotein inhibitior + 0.6401 64.01%
P-glycoprotein substrate - 0.8878 88.78%
CYP3A4 substrate + 0.5512 55.12%
CYP2C9 substrate - 0.8431 84.31%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.8205 82.05%
CYP2C9 inhibition - 0.9311 93.11%
CYP2C19 inhibition - 0.8473 84.73%
CYP2D6 inhibition - 0.9525 95.25%
CYP1A2 inhibition + 0.5484 54.84%
CYP2C8 inhibition + 0.7261 72.61%
CYP inhibitory promiscuity - 0.5745 57.45%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5155 51.55%
Eye corrosion - 0.9803 98.03%
Eye irritation + 0.6714 67.14%
Skin irritation - 0.7287 72.87%
Skin corrosion - 0.9851 98.51%
Ames mutagenesis - 0.6070 60.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6000 60.00%
Micronuclear + 0.8459 84.59%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.9612 96.12%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8649 86.49%
Acute Oral Toxicity (c) II 0.6012 60.12%
Estrogen receptor binding + 0.9254 92.54%
Androgen receptor binding + 0.9135 91.35%
Thyroid receptor binding + 0.7301 73.01%
Glucocorticoid receptor binding + 0.9181 91.81%
Aromatase binding + 0.8283 82.83%
PPAR gamma + 0.7061 70.61%
Honey bee toxicity - 0.9090 90.90%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5249 52.49%
Fish aquatic toxicity + 0.9374 93.74%

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 98.41% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.80% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 95.84% 93.31%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.38% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.22% 99.15%
CHEMBL2581 P07339 Cathepsin D 92.57% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.23% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.17% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.76% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.37% 92.62%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 86.05% 96.47%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.96% 86.92%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 84.93% 95.53%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.58% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.56% 85.14%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.50% 91.71%
CHEMBL5747 Q92793 CREB-binding protein 84.27% 95.12%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.99% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.93% 96.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.33% 92.94%
CHEMBL2535 P11166 Glucose transporter 80.69% 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.
Calophyllum polyanthum

Cross-Links

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PubChem 46856033
LOTUS LTS0141812
wikiData Q105248729