3,5,7-Trihydroxy-2-(4-hydroxy-2-methoxyphenyl)chromen-4-one

Details

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Internal ID 8d42db1c-3066-4089-bf0c-58344e122921
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > Flavonols
IUPAC Name 3,5,7-trihydroxy-2-(4-hydroxy-2-methoxyphenyl)chromen-4-one
SMILES (Canonical) COC1=C(C=CC(=C1)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
InChI InChI=1S/C16H12O7/c1-22-11-5-7(17)2-3-9(11)16-15(21)14(20)13-10(19)4-8(18)6-12(13)23-16/h2-6,17-19,21H,1H3
InChI Key KOGSTTPXQAYLHK-UHFFFAOYSA-N
Popularity 0 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 1.90
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 3,5,7-Trihydroxy-2-(4-hydroxy-2-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 + 0.9524 95.24%
Caco-2 - 0.7892 78.92%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6494 64.94%
OATP2B1 inhibitior - 0.5107 51.07%
OATP1B1 inhibitior - 0.4544 45.44%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.7195 71.95%
P-glycoprotein substrate - 0.5370 53.70%
CYP3A4 substrate + 0.5932 59.32%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.7348 73.48%
CYP2C9 inhibition + 0.7560 75.60%
CYP2C19 inhibition + 0.8648 86.48%
CYP2D6 inhibition - 0.6993 69.93%
CYP1A2 inhibition + 0.9218 92.18%
CYP2C8 inhibition + 0.8788 87.88%
CYP inhibitory promiscuity + 0.8546 85.46%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6176 61.76%
Eye corrosion - 0.9767 97.67%
Eye irritation + 0.8666 86.66%
Skin irritation - 0.5841 58.41%
Skin corrosion - 0.9319 93.19%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7972 79.72%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.9240 92.40%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7233 72.33%
Acute Oral Toxicity (c) III 0.7362 73.62%
Estrogen receptor binding + 0.9144 91.44%
Androgen receptor binding + 0.8311 83.11%
Thyroid receptor binding + 0.5856 58.56%
Glucocorticoid receptor binding + 0.8711 87.11%
Aromatase binding + 0.8588 85.88%
PPAR gamma + 0.8403 84.03%
Honey bee toxicity - 0.8962 89.62%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.8321 83.21%

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 98.59% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.86% 91.49%
CHEMBL2581 P07339 Cathepsin D 95.80% 98.95%
CHEMBL3194 P02766 Transthyretin 94.89% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.25% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.65% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.63% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.36% 86.33%
CHEMBL4208 P20618 Proteasome component C5 88.10% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.57% 99.17%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 86.51% 98.21%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.91% 94.42%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.84% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 82.76% 94.73%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 81.85% 95.64%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.59% 96.09%
CHEMBL2535 P11166 Glucose transporter 81.08% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.87% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.59% 99.15%
CHEMBL242 Q92731 Estrogen receptor beta 80.56% 98.35%

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.
Anaxagorea luzonensis

Cross-Links

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PubChem 10018620
LOTUS LTS0011859
wikiData Q105143816