3,5,7-Trihydroxy-6,8-dimethyl-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one

Details

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Internal ID cf66841e-ab31-4594-8171-7bce368ff113
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Catechins > Epigallocatechins
IUPAC Name 3,5,7-trihydroxy-6,8-dimethyl-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O8/c1-5-11(20)6(2)16-10(12(5)21)14(23)15(24)17(25-16)7-3-8(18)13(22)9(19)4-7/h3-4,15,17-22,24H,1-2H3
InChI Key XRFNWLUYIPSCPB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O8
Molecular Weight 348.30 g/mol
Exact Mass 348.08451746 g/mol
Topological Polar Surface Area (TPSA) 148.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,5,7-Trihydroxy-6,8-dimethyl-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-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 + 0.9108 91.08%
Caco-2 - 0.8339 83.39%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6880 68.80%
OATP2B1 inhibitior + 0.5720 57.20%
OATP1B1 inhibitior + 0.8272 82.72%
OATP1B3 inhibitior + 0.9722 97.22%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8586 85.86%
P-glycoprotein inhibitior - 0.8551 85.51%
P-glycoprotein substrate - 0.9345 93.45%
CYP3A4 substrate - 0.5381 53.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8133 81.33%
CYP3A4 inhibition + 0.6708 67.08%
CYP2C9 inhibition - 0.7549 75.49%
CYP2C19 inhibition - 0.8955 89.55%
CYP2D6 inhibition - 0.9193 91.93%
CYP1A2 inhibition + 0.9211 92.11%
CYP2C8 inhibition - 0.6966 69.66%
CYP inhibitory promiscuity + 0.5863 58.63%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6949 69.49%
Eye corrosion - 0.9879 98.79%
Eye irritation + 0.7075 70.75%
Skin irritation - 0.5828 58.28%
Skin corrosion - 0.8978 89.78%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5657 56.57%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8272 82.72%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7744 77.44%
Acute Oral Toxicity (c) III 0.4759 47.59%
Estrogen receptor binding + 0.7772 77.72%
Androgen receptor binding + 0.6932 69.32%
Thyroid receptor binding + 0.6732 67.32%
Glucocorticoid receptor binding + 0.7574 75.74%
Aromatase binding - 0.5089 50.89%
PPAR gamma + 0.6286 62.86%
Honey bee toxicity - 0.9481 94.81%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9319 93.19%

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 96.82% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 94.47% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.18% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.76% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 90.34% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.96% 99.23%
CHEMBL2581 P07339 Cathepsin D 86.21% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.25% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.00% 99.15%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.66% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.62% 86.33%

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.
Alluaudia humbertii

Cross-Links

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PubChem 162970164
LOTUS LTS0257258
wikiData Q105340439