5-Hydroxy-7-methyl-2-(3-oxobutyl)chromen-4-one

Details

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Internal ID 0494f44b-e186-4587-8a1f-c90f618c5754
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5-hydroxy-7-methyl-2-(3-oxobutyl)chromen-4-one
SMILES (Canonical) CC1=CC(=C2C(=C1)OC(=CC2=O)CCC(=O)C)O
SMILES (Isomeric) CC1=CC(=C2C(=C1)OC(=CC2=O)CCC(=O)C)O
InChI InChI=1S/C14H14O4/c1-8-5-11(16)14-12(17)7-10(4-3-9(2)15)18-13(14)6-8/h5-7,16H,3-4H2,1-2H3
InChI Key RXZXZFWJLWOGFC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O4
Molecular Weight 246.26 g/mol
Exact Mass 246.08920892 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-7-methyl-2-(3-oxobutyl)chromen-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 + 0.9792 97.92%
Caco-2 + 0.9261 92.61%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6377 63.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9292 92.92%
OATP1B3 inhibitior + 0.9749 97.49%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6875 68.75%
P-glycoprotein inhibitior - 0.8632 86.32%
P-glycoprotein substrate - 0.8834 88.34%
CYP3A4 substrate - 0.5483 54.83%
CYP2C9 substrate + 0.6197 61.97%
CYP2D6 substrate - 0.8321 83.21%
CYP3A4 inhibition + 0.5339 53.39%
CYP2C9 inhibition - 0.8687 86.87%
CYP2C19 inhibition - 0.8786 87.86%
CYP2D6 inhibition - 0.8997 89.97%
CYP1A2 inhibition + 0.7347 73.47%
CYP2C8 inhibition - 0.8639 86.39%
CYP inhibitory promiscuity - 0.8884 88.84%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6805 68.05%
Eye corrosion - 0.9771 97.71%
Eye irritation + 0.6457 64.57%
Skin irritation - 0.7046 70.46%
Skin corrosion - 0.8909 89.09%
Ames mutagenesis + 0.5499 54.99%
Human Ether-a-go-go-Related Gene inhibition - 0.5683 56.83%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8996 89.96%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7906 79.06%
Acute Oral Toxicity (c) III 0.8113 81.13%
Estrogen receptor binding - 0.5205 52.05%
Androgen receptor binding + 0.6437 64.37%
Thyroid receptor binding - 0.7539 75.39%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.5341 53.41%
PPAR gamma + 0.7214 72.14%
Honey bee toxicity - 0.9244 92.44%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9125 91.25%

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 98.42% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.73% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.46% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.20% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.81% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.06% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.13% 96.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.48% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.08% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.79% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.18% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.60% 94.80%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.04% 93.65%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101637248
LOTUS LTS0230324
wikiData Q105247396