4-Methoxy-5-methyl-6-(3-oxobut-1-enyl)pyran-2-one

Details

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Internal ID 9173b0e9-8de7-4a6a-95bf-3681b402d4fe
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 4-methoxy-5-methyl-6-(3-oxobut-1-enyl)pyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O4/c1-7(12)4-5-9-8(2)10(14-3)6-11(13)15-9/h4-6H,1-3H3
InChI Key BMPQVHKZLQTDRP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O4
Molecular Weight 208.21 g/mol
Exact Mass 208.07355886 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Methoxy-5-methyl-6-(3-oxobut-1-enyl)pyran-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 + 0.9728 97.28%
Caco-2 + 0.7009 70.09%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7655 76.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9317 93.17%
OATP1B3 inhibitior + 0.9834 98.34%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7934 79.34%
P-glycoprotein inhibitior - 0.8866 88.66%
P-glycoprotein substrate - 0.9267 92.67%
CYP3A4 substrate - 0.5592 55.92%
CYP2C9 substrate - 0.7943 79.43%
CYP2D6 substrate - 0.8820 88.20%
CYP3A4 inhibition - 0.8158 81.58%
CYP2C9 inhibition - 0.9622 96.22%
CYP2C19 inhibition - 0.8033 80.33%
CYP2D6 inhibition - 0.9570 95.70%
CYP1A2 inhibition + 0.5263 52.63%
CYP2C8 inhibition - 0.7593 75.93%
CYP inhibitory promiscuity - 0.6153 61.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8441 84.41%
Carcinogenicity (trinary) Non-required 0.5873 58.73%
Eye corrosion - 0.8330 83.30%
Eye irritation + 0.7878 78.78%
Skin irritation - 0.7302 73.02%
Skin corrosion - 0.9673 96.73%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5297 52.97%
Micronuclear + 0.6459 64.59%
Hepatotoxicity + 0.5274 52.74%
skin sensitisation - 0.9186 91.86%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.5519 55.19%
Acute Oral Toxicity (c) II 0.6022 60.22%
Estrogen receptor binding + 0.6109 61.09%
Androgen receptor binding - 0.5465 54.65%
Thyroid receptor binding - 0.8155 81.55%
Glucocorticoid receptor binding - 0.6101 61.01%
Aromatase binding + 0.6741 67.41%
PPAR gamma - 0.5978 59.78%
Honey bee toxicity - 0.9178 91.78%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9417 94.17%

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 94.36% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.25% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.51% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.61% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.33% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.33% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.17% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.89% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.89% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.74% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.15% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.11% 99.23%
CHEMBL2581 P07339 Cathepsin D 80.01% 98.95%

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 85167048
LOTUS LTS0094775
wikiData Q104938488