3-(5-Methyl-6-oxopyran-2-yl)but-2-enoic acid

Details

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Internal ID 8a1f8f96-83a7-44e5-b2e1-6ab0945437cb
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-(5-methyl-6-oxopyran-2-yl)but-2-enoic acid
SMILES (Canonical) CC1=CC=C(OC1=O)C(=CC(=O)O)C
SMILES (Isomeric) CC1=CC=C(OC1=O)C(=CC(=O)O)C
InChI InChI=1S/C10H10O4/c1-6-3-4-8(14-10(6)13)7(2)5-9(11)12/h3-5H,1-2H3,(H,11,12)
InChI Key MQNNRPUVAMHCCO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O4
Molecular Weight 194.18 g/mol
Exact Mass 194.05790880 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.44
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(5-Methyl-6-oxopyran-2-yl)but-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9746 97.46%
Caco-2 + 0.7430 74.30%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8755 87.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9329 93.29%
OATP1B3 inhibitior + 0.9744 97.44%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9026 90.26%
P-glycoprotein inhibitior - 0.9723 97.23%
P-glycoprotein substrate - 0.9458 94.58%
CYP3A4 substrate - 0.6501 65.01%
CYP2C9 substrate - 0.8005 80.05%
CYP2D6 substrate - 0.9180 91.80%
CYP3A4 inhibition - 0.8354 83.54%
CYP2C9 inhibition - 0.5232 52.32%
CYP2C19 inhibition + 0.5903 59.03%
CYP2D6 inhibition - 0.8740 87.40%
CYP1A2 inhibition - 0.7647 76.47%
CYP2C8 inhibition - 0.8398 83.98%
CYP inhibitory promiscuity - 0.7410 74.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7917 79.17%
Carcinogenicity (trinary) Non-required 0.6172 61.72%
Eye corrosion - 0.9254 92.54%
Eye irritation + 0.9169 91.69%
Skin irritation + 0.6276 62.76%
Skin corrosion - 0.8857 88.57%
Ames mutagenesis - 0.6370 63.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7198 71.98%
Micronuclear + 0.8059 80.59%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.6003 60.03%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7914 79.14%
Acute Oral Toxicity (c) III 0.4930 49.30%
Estrogen receptor binding - 0.8625 86.25%
Androgen receptor binding - 0.6167 61.67%
Thyroid receptor binding - 0.8043 80.43%
Glucocorticoid receptor binding - 0.8353 83.53%
Aromatase binding - 0.5952 59.52%
PPAR gamma - 0.6527 65.27%
Honey bee toxicity - 0.9488 94.88%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9705 97.05%

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 92.49% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.52% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.07% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 86.54% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.13% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.29% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 81.89% 92.51%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.68% 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 73657206
LOTUS LTS0092140
wikiData Q104171969