3-Methyl-6-(4-oxopent-2-en-2-yl)pyran-2-one

Details

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Internal ID 38c3a063-0e28-4cf4-9d40-cc7d485026b9
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-methyl-6-(4-oxopent-2-en-2-yl)pyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O3/c1-7-4-5-10(14-11(7)13)8(2)6-9(3)12/h4-6H,1-3H3
InChI Key VUBOIQFUPSWOPP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O3
Molecular Weight 192.21 g/mol
Exact Mass 192.078644241 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Methyl-6-(4-oxopent-2-en-2-yl)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 + 0.9912 99.12%
Caco-2 + 0.7053 70.53%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8314 83.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9412 94.12%
OATP1B3 inhibitior + 0.9761 97.61%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8244 82.44%
P-glycoprotein inhibitior - 0.9370 93.70%
P-glycoprotein substrate - 0.9395 93.95%
CYP3A4 substrate - 0.6346 63.46%
CYP2C9 substrate - 0.6101 61.01%
CYP2D6 substrate - 0.8987 89.87%
CYP3A4 inhibition - 0.8519 85.19%
CYP2C9 inhibition - 0.7488 74.88%
CYP2C19 inhibition + 0.5212 52.12%
CYP2D6 inhibition - 0.8993 89.93%
CYP1A2 inhibition + 0.5873 58.73%
CYP2C8 inhibition - 0.8750 87.50%
CYP inhibitory promiscuity - 0.5407 54.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8231 82.31%
Carcinogenicity (trinary) Non-required 0.5876 58.76%
Eye corrosion - 0.8944 89.44%
Eye irritation + 0.7009 70.09%
Skin irritation + 0.6201 62.01%
Skin corrosion - 0.8988 89.88%
Ames mutagenesis - 0.6670 66.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6035 60.35%
Micronuclear + 0.6759 67.59%
Hepatotoxicity + 0.6939 69.39%
skin sensitisation + 0.4768 47.68%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7170 71.70%
Acute Oral Toxicity (c) III 0.5403 54.03%
Estrogen receptor binding - 0.8071 80.71%
Androgen receptor binding - 0.5892 58.92%
Thyroid receptor binding - 0.7657 76.57%
Glucocorticoid receptor binding - 0.7654 76.54%
Aromatase binding + 0.6450 64.50%
PPAR gamma - 0.7532 75.32%
Honey bee toxicity - 0.9390 93.90%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9627 96.27%

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
CHEMBL2581 P07339 Cathepsin D 93.11% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.46% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 90.56% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 88.80% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.82% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.85% 91.11%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 82.96% 90.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.41% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.85% 89.00%

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 162814567
LOTUS LTS0027607
wikiData Q104199788