[(2R,3S,4S)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate

Details

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Internal ID 65ca95b7-038e-41e7-83bd-b3e3b9d40690
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Biflavonoids and polyflavonoids
IUPAC Name [(2R,3S,4S)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H30O16/c38-16-10-22(42)30-28(11-16)51-34(14-6-23(43)31(48)24(44)7-14)36(53-37(50)15-8-25(45)32(49)26(46)9-15)29(30)17-2-4-19(39)18-12-27(47)33(52-35(17)18)13-1-3-20(40)21(41)5-13/h1-11,27,29,33-34,36,38-49H,12H2/t27-,29-,33+,34+,36-/m0/s1
InChI Key DIJCYCDPYBWOEN-NDOOJUEJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H30O16
Molecular Weight 730.60 g/mol
Exact Mass 730.15338487 g/mol
Topological Polar Surface Area (TPSA) 288.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 16
H-Bond Donor 12
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,3S,4S)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8367 83.67%
Caco-2 - 0.9169 91.69%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.5726 57.26%
OATP2B1 inhibitior - 0.7025 70.25%
OATP1B1 inhibitior + 0.8389 83.89%
OATP1B3 inhibitior - 0.5698 56.98%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8673 86.73%
P-glycoprotein inhibitior + 0.7359 73.59%
P-glycoprotein substrate - 0.6028 60.28%
CYP3A4 substrate + 0.6795 67.95%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.7126 71.26%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.9429 94.29%
CYP2C19 inhibition - 0.9118 91.18%
CYP2D6 inhibition - 0.9417 94.17%
CYP1A2 inhibition - 0.9403 94.03%
CYP2C8 inhibition + 0.8479 84.79%
CYP inhibitory promiscuity - 0.9256 92.56%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6306 63.06%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.8745 87.45%
Skin irritation - 0.6568 65.68%
Skin corrosion - 0.9547 95.47%
Ames mutagenesis + 0.6146 61.46%
Human Ether-a-go-go-Related Gene inhibition + 0.8315 83.15%
Micronuclear + 0.8759 87.59%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8377 83.77%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7058 70.58%
Acute Oral Toxicity (c) IV 0.4212 42.12%
Estrogen receptor binding + 0.8003 80.03%
Androgen receptor binding + 0.8077 80.77%
Thyroid receptor binding + 0.5836 58.36%
Glucocorticoid receptor binding + 0.5929 59.29%
Aromatase binding - 0.6003 60.03%
PPAR gamma + 0.7167 71.67%
Honey bee toxicity - 0.7595 75.95%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.8606 86.06%

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 99.64% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.18% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.25% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.22% 97.09%
CHEMBL3194 P02766 Transthyretin 93.46% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.29% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.26% 89.00%
CHEMBL236 P41143 Delta opioid receptor 91.97% 99.35%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 91.97% 83.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.51% 99.15%
CHEMBL2581 P07339 Cathepsin D 89.47% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.26% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.84% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.91% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.58% 95.56%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 85.44% 95.78%
CHEMBL3401 O75469 Pregnane X receptor 85.14% 94.73%
CHEMBL2535 P11166 Glucose transporter 84.80% 98.75%
CHEMBL4208 P20618 Proteasome component C5 81.98% 90.00%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 80.59% 96.37%

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.
Quercus dentata

Cross-Links

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PubChem 162994515
LOTUS LTS0080499
wikiData Q104981406