2'-Methoxy-3',4',7-trihydroxyisoflavone

Details

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Internal ID f87595b1-89d3-4ce2-93ca-406b53ad4af3
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 3-(3,4-dihydroxy-2-methoxyphenyl)-7-hydroxychromen-4-one
SMILES (Canonical) COC1=C(C=CC(=C1O)O)C2=COC3=C(C2=O)C=CC(=C3)O
SMILES (Isomeric) COC1=C(C=CC(=C1O)O)C2=COC3=C(C2=O)C=CC(=C3)O
InChI InChI=1S/C16H12O6/c1-21-16-9(4-5-12(18)15(16)20)11-7-22-13-6-8(17)2-3-10(13)14(11)19/h2-7,17-18,20H,1H3
InChI Key XFAMBGFUJZVEQW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O6
Molecular Weight 300.26 g/mol
Exact Mass 300.06338810 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2'-Methoxy-3',4',7-trihydroxyisoflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9577 95.77%
Caco-2 + 0.6789 67.89%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7944 79.44%
OATP2B1 inhibitior + 0.5549 55.49%
OATP1B1 inhibitior + 0.9178 91.78%
OATP1B3 inhibitior + 0.9965 99.65%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7626 76.26%
P-glycoprotein inhibitior - 0.8012 80.12%
P-glycoprotein substrate - 0.7845 78.45%
CYP3A4 substrate + 0.5654 56.54%
CYP2C9 substrate - 0.8397 83.97%
CYP2D6 substrate - 0.7876 78.76%
CYP3A4 inhibition - 0.7179 71.79%
CYP2C9 inhibition + 0.5494 54.94%
CYP2C19 inhibition + 0.6827 68.27%
CYP2D6 inhibition - 0.9018 90.18%
CYP1A2 inhibition + 0.9263 92.63%
CYP2C8 inhibition + 0.5325 53.25%
CYP inhibitory promiscuity + 0.6056 60.56%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5596 55.96%
Eye corrosion - 0.9766 97.66%
Eye irritation + 0.7429 74.29%
Skin irritation - 0.5899 58.99%
Skin corrosion - 0.9443 94.43%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7012 70.12%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9318 93.18%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6538 65.38%
Acute Oral Toxicity (c) III 0.6733 67.33%
Estrogen receptor binding + 0.9141 91.41%
Androgen receptor binding + 0.8640 86.40%
Thyroid receptor binding + 0.7071 70.71%
Glucocorticoid receptor binding + 0.9126 91.26%
Aromatase binding + 0.8641 86.41%
PPAR gamma + 0.6358 63.58%
Honey bee toxicity - 0.9072 90.72%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8838 88.38%

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 99.68% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.64% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.59% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.08% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.37% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.02% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.89% 86.33%
CHEMBL242 Q92731 Estrogen receptor beta 89.71% 98.35%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 88.92% 80.78%
CHEMBL1951 P21397 Monoamine oxidase A 87.63% 91.49%
CHEMBL2535 P11166 Glucose transporter 86.74% 98.75%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 84.05% 98.21%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.64% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.72% 99.17%
CHEMBL3194 P02766 Transthyretin 80.84% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 80.50% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.35% 93.65%

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.
Clinopodium vulgare
Commiphora sphaerocarpa
Erythrina speciosa
Helichrysum drakensbergense
Piper divaricatum
Prosopis africana
Prunus prostrata
Richteria pyrethroides
Santolina pectinata

Cross-Links

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PubChem 101785462
NPASS NPC250800