5,6,7-Trihydroxy-3-(3-hydroxy-4-methoxyphenyl)chromen-4-one

Details

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Internal ID 7f813a61-1a73-4e04-b844-80ec14360a13
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids > 3-hydroxy,4-methoxyisoflavonoids
IUPAC Name 5,6,7-trihydroxy-3-(3-hydroxy-4-methoxyphenyl)chromen-4-one
SMILES (Canonical) COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)O)O)O
SMILES (Isomeric) COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)O)O)O
InChI InChI=1S/C16H12O7/c1-22-11-3-2-7(4-9(11)17)8-6-23-12-5-10(18)15(20)16(21)13(12)14(8)19/h2-6,17-18,20-21H,1H3
InChI Key UTMSPYXAMXSXRW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O7
Molecular Weight 316.26 g/mol
Exact Mass 316.05830272 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.29
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,6,7-Trihydroxy-3-(3-hydroxy-4-methoxyphenyl)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 + 0.9095 90.95%
Caco-2 + 0.6458 64.58%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.6297 62.97%
OATP2B1 inhibitior + 0.5771 57.71%
OATP1B1 inhibitior + 0.9618 96.18%
OATP1B3 inhibitior + 0.9904 99.04%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8727 87.27%
P-glycoprotein inhibitior - 0.8889 88.89%
P-glycoprotein substrate - 0.8780 87.80%
CYP3A4 substrate + 0.5541 55.41%
CYP2C9 substrate - 0.6887 68.87%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition + 0.6330 63.30%
CYP2C9 inhibition - 0.7982 79.82%
CYP2C19 inhibition - 0.6361 63.61%
CYP2D6 inhibition - 0.8687 86.87%
CYP1A2 inhibition + 0.9091 90.91%
CYP2C8 inhibition + 0.7875 78.75%
CYP inhibitory promiscuity + 0.7089 70.89%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6208 62.08%
Eye corrosion - 0.9790 97.90%
Eye irritation + 0.6669 66.69%
Skin irritation - 0.6006 60.06%
Skin corrosion - 0.9153 91.53%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7932 79.32%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9054 90.54%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6668 66.68%
Acute Oral Toxicity (c) III 0.6309 63.09%
Estrogen receptor binding + 0.9319 93.19%
Androgen receptor binding + 0.8283 82.83%
Thyroid receptor binding + 0.6800 68.00%
Glucocorticoid receptor binding + 0.8975 89.75%
Aromatase binding + 0.8337 83.37%
PPAR gamma + 0.7037 70.37%
Honey bee toxicity - 0.8441 84.41%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5551 55.51%
Fish aquatic toxicity + 0.8562 85.62%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.46% 94.00%
CHEMBL2581 P07339 Cathepsin D 97.14% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.21% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.35% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.36% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.11% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.77% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.21% 99.15%
CHEMBL3194 P02766 Transthyretin 87.40% 90.71%
CHEMBL1255126 O15151 Protein Mdm4 86.57% 90.20%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.40% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.86% 99.17%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 85.65% 95.78%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.38% 96.09%
CHEMBL4302 P08183 P-glycoprotein 1 85.15% 92.98%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 84.00% 95.53%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.53% 94.42%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.51% 80.78%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.01% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.89% 95.89%

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.
Iris domestica

Cross-Links

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PubChem 10543410
LOTUS LTS0216255
wikiData Q105278891