3,7-Dimethoxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

Details

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Internal ID 1b4d1242-8444-47b6-a981-c8f2a629be43
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 3,7-dimethoxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O7/c1-22-9-3-4-10-13(7-9)24-16(17(23-2)14(10)20)8-5-11(18)15(21)12(19)6-8/h3-7,18-19,21H,1-2H3
InChI Key NCTYYIJBUOKZRV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O7
Molecular Weight 330.29 g/mol
Exact Mass 330.07395278 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7-Dimethoxy-2-(3,4,5-trihydroxyphenyl)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 + 0.8965 89.65%
Caco-2 - 0.5303 53.03%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6457 64.57%
OATP2B1 inhibitior + 0.5700 57.00%
OATP1B1 inhibitior + 0.9486 94.86%
OATP1B3 inhibitior + 0.9828 98.28%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5973 59.73%
P-glycoprotein inhibitior - 0.4713 47.13%
P-glycoprotein substrate - 0.8039 80.39%
CYP3A4 substrate + 0.5268 52.68%
CYP2C9 substrate - 0.8397 83.97%
CYP2D6 substrate - 0.7876 78.76%
CYP3A4 inhibition + 0.6914 69.14%
CYP2C9 inhibition - 0.8489 84.89%
CYP2C19 inhibition - 0.6694 66.94%
CYP2D6 inhibition - 0.8174 81.74%
CYP1A2 inhibition + 0.8416 84.16%
CYP2C8 inhibition + 0.6565 65.65%
CYP inhibitory promiscuity + 0.6916 69.16%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6616 66.16%
Eye corrosion - 0.9801 98.01%
Eye irritation + 0.6472 64.72%
Skin irritation - 0.6619 66.19%
Skin corrosion - 0.9271 92.71%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6569 65.69%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9068 90.68%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8454 84.54%
Acute Oral Toxicity (c) III 0.5234 52.34%
Estrogen receptor binding + 0.8576 85.76%
Androgen receptor binding + 0.8958 89.58%
Thyroid receptor binding + 0.5299 52.99%
Glucocorticoid receptor binding + 0.7785 77.85%
Aromatase binding + 0.7510 75.10%
PPAR gamma + 0.8261 82.61%
Honey bee toxicity - 0.9396 93.96%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8835 88.35%

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 99.81% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.16% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.00% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.82% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 92.75% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.36% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.66% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.41% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.99% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.38% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.84% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.20% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 83.05% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.63% 99.23%
CHEMBL4208 P20618 Proteasome component C5 82.26% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.69% 94.42%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.40% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.20% 96.00%

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.
Populus nigra

Cross-Links

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PubChem 162882693
LOTUS LTS0234487
wikiData Q105177373