3-(2,4-Dimethoxyphenyl)-5,7-dimethoxy-6-(3-methylbut-2-enyl)chromen-2-one

Details

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Internal ID 85d8dedb-85c9-4396-ae1c-79e5a3fb87a5
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-3-enes > Isoflav-3-enones
IUPAC Name 3-(2,4-dimethoxyphenyl)-5,7-dimethoxy-6-(3-methylbut-2-enyl)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26O6/c1-14(2)7-9-17-21(28-5)13-22-19(23(17)29-6)12-18(24(25)30-22)16-10-8-15(26-3)11-20(16)27-4/h7-8,10-13H,9H2,1-6H3
InChI Key CVRRHSSOXTVUSP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O6
Molecular Weight 410.50 g/mol
Exact Mass 410.17293854 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.00
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(2,4-Dimethoxyphenyl)-5,7-dimethoxy-6-(3-methylbut-2-enyl)chromen-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 + 0.9947 99.47%
Caco-2 + 0.8577 85.77%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7300 73.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9113 91.13%
OATP1B3 inhibitior + 0.8892 88.92%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9558 95.58%
P-glycoprotein inhibitior + 0.9559 95.59%
P-glycoprotein substrate - 0.6245 62.45%
CYP3A4 substrate + 0.5791 57.91%
CYP2C9 substrate - 0.6607 66.07%
CYP2D6 substrate - 0.8073 80.73%
CYP3A4 inhibition - 0.7331 73.31%
CYP2C9 inhibition + 0.7432 74.32%
CYP2C19 inhibition + 0.9072 90.72%
CYP2D6 inhibition - 0.8643 86.43%
CYP1A2 inhibition + 0.7787 77.87%
CYP2C8 inhibition - 0.5592 55.92%
CYP inhibitory promiscuity + 0.9381 93.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9713 97.13%
Carcinogenicity (trinary) Non-required 0.6091 60.91%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.7023 70.23%
Skin irritation - 0.7951 79.51%
Skin corrosion - 0.9768 97.68%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7594 75.94%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.5315 53.15%
skin sensitisation - 0.8369 83.69%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8025 80.25%
Acute Oral Toxicity (c) III 0.7248 72.48%
Estrogen receptor binding + 0.9378 93.78%
Androgen receptor binding + 0.8011 80.11%
Thyroid receptor binding + 0.6538 65.38%
Glucocorticoid receptor binding + 0.8260 82.60%
Aromatase binding + 0.6058 60.58%
PPAR gamma + 0.7770 77.70%
Honey bee toxicity - 0.8285 82.85%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9966 99.66%

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 98.97% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.50% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.01% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.45% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.28% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.15% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.40% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 91.16% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 89.34% 94.73%
CHEMBL4208 P20618 Proteasome component C5 87.69% 90.00%
CHEMBL2535 P11166 Glucose transporter 87.63% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 86.42% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.98% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.71% 96.67%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.40% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.33% 92.62%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.77% 89.34%

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 uralensis

Cross-Links

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PubChem 14191849
LOTUS LTS0162180
wikiData Q104970962