7-Hydroxy-3-(5-hydroxy-2,2-dimethylchromen-6-yl)-5-methoxychromen-2-one

Details

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Internal ID 29cf9dac-9020-49c3-8d43-c43f575f767b
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Pyranoisoflavonoids
IUPAC Name 7-hydroxy-3-(5-hydroxy-2,2-dimethylchromen-6-yl)-5-methoxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H18O6/c1-21(2)7-6-13-16(27-21)5-4-12(19(13)23)14-10-15-17(25-3)8-11(22)9-18(15)26-20(14)24/h4-10,22-23H,1-3H3
InChI Key RVMQSBYTVFSIMB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H18O6
Molecular Weight 366.40 g/mol
Exact Mass 366.11033829 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-3-(5-hydroxy-2,2-dimethylchromen-6-yl)-5-methoxychromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9791 97.91%
Caco-2 + 0.5911 59.11%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8404 84.04%
OATP2B1 inhibitior - 0.7068 70.68%
OATP1B1 inhibitior + 0.8567 85.67%
OATP1B3 inhibitior + 0.8841 88.41%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7192 71.92%
P-glycoprotein inhibitior + 0.7833 78.33%
P-glycoprotein substrate + 0.5369 53.69%
CYP3A4 substrate + 0.6534 65.34%
CYP2C9 substrate - 0.6435 64.35%
CYP2D6 substrate - 0.8312 83.12%
CYP3A4 inhibition - 0.6469 64.69%
CYP2C9 inhibition + 0.5550 55.50%
CYP2C19 inhibition + 0.6399 63.99%
CYP2D6 inhibition - 0.8500 85.00%
CYP1A2 inhibition - 0.8478 84.78%
CYP2C8 inhibition + 0.6044 60.44%
CYP inhibitory promiscuity + 0.6165 61.65%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Danger 0.6068 60.68%
Eye corrosion - 0.9896 98.96%
Eye irritation + 0.7376 73.76%
Skin irritation - 0.7856 78.56%
Skin corrosion - 0.9690 96.90%
Ames mutagenesis - 0.5537 55.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6606 66.06%
Micronuclear + 0.6900 69.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.9079 90.79%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.5551 55.51%
Acute Oral Toxicity (c) III 0.5594 55.94%
Estrogen receptor binding + 0.9578 95.78%
Androgen receptor binding + 0.8477 84.77%
Thyroid receptor binding + 0.7266 72.66%
Glucocorticoid receptor binding + 0.9036 90.36%
Aromatase binding + 0.7827 78.27%
PPAR gamma + 0.7897 78.97%
Honey bee toxicity - 0.7985 79.85%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.9850 98.50%

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 99.56% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.87% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.11% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 94.00% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.98% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.13% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.90% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.86% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 89.13% 93.31%
CHEMBL2535 P11166 Glucose transporter 86.79% 98.75%
CHEMBL4208 P20618 Proteasome component C5 86.35% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 86.22% 90.20%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.52% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.62% 99.23%
CHEMBL3194 P02766 Transthyretin 83.17% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.01% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.42% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.41% 99.15%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.07% 96.67%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.82% 94.42%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.76% 90.71%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.74% 89.50%

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.
Glycyrrhiza aspera

Cross-Links

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PubChem 101664571
LOTUS LTS0103802
wikiData Q105246125