3-(3,4-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-5,7-dihydroxychromen-4-one

Details

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Internal ID eecd000f-31c2-4426-a1cb-af495d72b2ba
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Pyranoisoflavonoids
IUPAC Name 3-(3,4-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-5,7-dihydroxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H18O7/c1-20(2)19(25)18(24)11-5-9(3-4-14(11)27-20)12-8-26-15-7-10(21)6-13(22)16(15)17(12)23/h3-8,18-19,21-22,24-25H,1-2H3
InChI Key DRLOYLLHCWGYLF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O7
Molecular Weight 370.40 g/mol
Exact Mass 370.10525291 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(3,4-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-5,7-dihydroxychromen-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 + 0.9236 92.36%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7695 76.95%
OATP2B1 inhibitior + 0.5710 57.10%
OATP1B1 inhibitior + 0.9034 90.34%
OATP1B3 inhibitior + 0.9718 97.18%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4838 48.38%
P-glycoprotein inhibitior - 0.6247 62.47%
P-glycoprotein substrate - 0.6956 69.56%
CYP3A4 substrate + 0.6639 66.39%
CYP2C9 substrate - 0.6412 64.12%
CYP2D6 substrate - 0.8243 82.43%
CYP3A4 inhibition + 0.6068 60.68%
CYP2C9 inhibition - 0.6188 61.88%
CYP2C19 inhibition - 0.7226 72.26%
CYP2D6 inhibition - 0.9076 90.76%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition + 0.8152 81.52%
CYP inhibitory promiscuity - 0.6023 60.23%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6670 66.70%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.8199 81.99%
Skin irritation - 0.6913 69.13%
Skin corrosion - 0.8944 89.44%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6108 61.08%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8211 82.11%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.6970 69.70%
Acute Oral Toxicity (c) III 0.6604 66.04%
Estrogen receptor binding + 0.7660 76.60%
Androgen receptor binding + 0.7205 72.05%
Thyroid receptor binding + 0.6683 66.83%
Glucocorticoid receptor binding + 0.7607 76.07%
Aromatase binding + 0.6296 62.96%
PPAR gamma + 0.7525 75.25%
Honey bee toxicity - 0.8069 80.69%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9391 93.91%

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
CHEMBL2581 P07339 Cathepsin D 98.72% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.65% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.15% 89.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 96.85% 96.12%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.65% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 88.11% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.03% 95.56%
CHEMBL3922 P50579 Methionine aminopeptidase 2 87.01% 97.28%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.79% 96.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 86.66% 95.78%
CHEMBL3038469 P24941 CDK2/Cyclin A 86.27% 91.38%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.03% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.35% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.46% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.34% 94.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.88% 95.53%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.83% 93.10%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.26% 96.38%
CHEMBL3194 P02766 Transthyretin 80.25% 90.71%

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.
Genista corsica

Cross-Links

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PubChem 163002758
LOTUS LTS0229897
wikiData Q104987478