4-Methoxy-5-methyl-6-(3-methylhexa-1,3-dienyl)pyran-2-one

Details

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Internal ID 4ec7fe7a-9951-44c8-8a6d-1e67a3f16e9e
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 4-methoxy-5-methyl-6-(3-methylhexa-1,3-dienyl)pyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O3/c1-5-6-10(2)7-8-12-11(3)13(16-4)9-14(15)17-12/h6-9H,5H2,1-4H3
InChI Key HKAIFSLAZQJCJF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O3
Molecular Weight 234.29 g/mol
Exact Mass 234.125594432 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.33
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

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-methylhexa-1,3-dienyl)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 + 0.9961 99.61%
Caco-2 + 0.8905 89.05%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7721 77.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9037 90.37%
OATP1B3 inhibitior + 0.9699 96.99%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5982 59.82%
P-glycoprotein inhibitior - 0.7106 71.06%
P-glycoprotein substrate - 0.8296 82.96%
CYP3A4 substrate - 0.5235 52.35%
CYP2C9 substrate - 0.5914 59.14%
CYP2D6 substrate - 0.8530 85.30%
CYP3A4 inhibition - 0.9210 92.10%
CYP2C9 inhibition - 0.8540 85.40%
CYP2C19 inhibition + 0.8026 80.26%
CYP2D6 inhibition - 0.9298 92.98%
CYP1A2 inhibition + 0.6870 68.70%
CYP2C8 inhibition - 0.6517 65.17%
CYP inhibitory promiscuity + 0.8361 83.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8431 84.31%
Carcinogenicity (trinary) Non-required 0.6705 67.05%
Eye corrosion - 0.9232 92.32%
Eye irritation - 0.5368 53.68%
Skin irritation - 0.6090 60.90%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis - 0.6970 69.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6447 64.47%
Micronuclear - 0.6441 64.41%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7194 71.94%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6362 63.62%
Acute Oral Toxicity (c) III 0.7261 72.61%
Estrogen receptor binding + 0.7687 76.87%
Androgen receptor binding - 0.5401 54.01%
Thyroid receptor binding - 0.5532 55.32%
Glucocorticoid receptor binding + 0.6320 63.20%
Aromatase binding + 0.8638 86.38%
PPAR gamma + 0.7338 73.38%
Honey bee toxicity - 0.9133 91.33%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9716 97.16%

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 92.82% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.41% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.47% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.17% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.97% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.67% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.43% 97.21%
CHEMBL2581 P07339 Cathepsin D 87.38% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.22% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 85.89% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.74% 99.17%
CHEMBL1937 Q92769 Histone deacetylase 2 84.13% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.99% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.90% 96.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.46% 93.99%
CHEMBL4208 P20618 Proteasome component C5 80.68% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.64% 85.14%

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 162924446
LOTUS LTS0004954
wikiData Q105029565