5-Hydroxy-3-(3-hydroxy-2-methoxyphenyl)-6,7-dimethoxychromen-4-one

Details

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Internal ID 1f9b2bf7-538b-4aee-95b5-55e1c2abf3fb
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 7-O-methylated isoflavonoids > 7-O-methylisoflavones
IUPAC Name 5-hydroxy-3-(3-hydroxy-2-methoxyphenyl)-6,7-dimethoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O7/c1-22-13-7-12-14(16(21)18(13)24-3)15(20)10(8-25-12)9-5-4-6-11(19)17(9)23-2/h4-8,19,21H,1-3H3
InChI Key IKZJQDUCKJEQJB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O7
Molecular Weight 344.30 g/mol
Exact Mass 344.08960285 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-3-(3-hydroxy-2-methoxyphenyl)-6,7-dimethoxychromen-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 + 0.9711 97.11%
Caco-2 + 0.8035 80.35%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7936 79.36%
OATP2B1 inhibitior - 0.7123 71.23%
OATP1B1 inhibitior + 0.9511 95.11%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7525 75.25%
P-glycoprotein inhibitior + 0.7767 77.67%
P-glycoprotein substrate - 0.7615 76.15%
CYP3A4 substrate + 0.5654 56.54%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7237 72.37%
CYP2C9 inhibition - 0.6863 68.63%
CYP2C19 inhibition + 0.6566 65.66%
CYP2D6 inhibition - 0.8329 83.29%
CYP1A2 inhibition + 0.8642 86.42%
CYP2C8 inhibition + 0.5859 58.59%
CYP inhibitory promiscuity + 0.7231 72.31%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5851 58.51%
Eye corrosion - 0.9825 98.25%
Eye irritation + 0.7849 78.49%
Skin irritation - 0.7275 72.75%
Skin corrosion - 0.9759 97.59%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7610 76.10%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9511 95.11%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6177 61.77%
Acute Oral Toxicity (c) III 0.4741 47.41%
Estrogen receptor binding + 0.8962 89.62%
Androgen receptor binding + 0.6689 66.89%
Thyroid receptor binding + 0.7167 71.67%
Glucocorticoid receptor binding + 0.8432 84.32%
Aromatase binding + 0.7839 78.39%
PPAR gamma + 0.7135 71.35%
Honey bee toxicity - 0.8807 88.07%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8969 89.69%

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 98.00% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.23% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.73% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.67% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.96% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.01% 89.00%
CHEMBL2535 P11166 Glucose transporter 90.63% 98.75%
CHEMBL4302 P08183 P-glycoprotein 1 87.02% 92.98%
CHEMBL1937 Q92769 Histone deacetylase 2 86.93% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.84% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.96% 85.14%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 85.80% 94.03%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.69% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.30% 99.23%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.23% 80.78%
CHEMBL1255126 O15151 Protein Mdm4 83.05% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.35% 96.09%
CHEMBL3194 P02766 Transthyretin 80.02% 90.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 14825813
LOTUS LTS0047224
wikiData Q105115035