Methyl coumalate

Details

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Internal ID 59849ec5-87e6-4e44-a43a-04712cf8d847
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name methyl 6-oxopyran-3-carboxylate
SMILES (Canonical) COC(=O)C1=COC(=O)C=C1
SMILES (Isomeric) COC(=O)C1=COC(=O)C=C1
InChI InChI=1S/C7H6O4/c1-10-7(9)5-2-3-6(8)11-4-5/h2-4H,1H3
InChI Key HHWWWZQYHPFCBY-UHFFFAOYSA-N
Popularity 34 references in papers

Physical and Chemical Properties

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Molecular Formula C7H6O4
Molecular Weight 154.12 g/mol
Exact Mass 154.02660867 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.43
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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6018-41-3
Methyl 2-oxo-2H-pyran-5-carboxylate
5-(Carbomethoxy)-2-pyrone
2H-Pyran-5-carboxylic acid, 2-oxo-, methyl ester
methyl 6-oxopyran-3-carboxylate
Coumalic acid methyl ester
Coumalic acid, methyl ester
Methyl 2-pyrone-5-carboxylate
Methyl 2-Oxopyran-5-carboxylate
UNII-1S7TMF0R8T
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methyl coumalate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9686 96.86%
Caco-2 + 0.8330 83.30%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.7458 74.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9068 90.68%
OATP1B3 inhibitior + 0.9878 98.78%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9718 97.18%
P-glycoprotein inhibitior - 0.9808 98.08%
P-glycoprotein substrate - 0.9761 97.61%
CYP3A4 substrate - 0.6463 64.63%
CYP2C9 substrate - 0.8140 81.40%
CYP2D6 substrate - 0.8699 86.99%
CYP3A4 inhibition - 0.9285 92.85%
CYP2C9 inhibition - 0.8877 88.77%
CYP2C19 inhibition - 0.7650 76.50%
CYP2D6 inhibition - 0.9507 95.07%
CYP1A2 inhibition + 0.6092 60.92%
CYP2C8 inhibition - 0.7362 73.62%
CYP inhibitory promiscuity - 0.9222 92.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7972 79.72%
Carcinogenicity (trinary) Non-required 0.6270 62.70%
Eye corrosion + 0.7438 74.38%
Eye irritation + 0.9958 99.58%
Skin irritation + 0.5647 56.47%
Skin corrosion - 0.7659 76.59%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7462 74.62%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6408 64.08%
skin sensitisation - 0.9385 93.85%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6065 60.65%
Acute Oral Toxicity (c) III 0.8464 84.64%
Estrogen receptor binding - 0.9421 94.21%
Androgen receptor binding - 0.8930 89.30%
Thyroid receptor binding - 0.9231 92.31%
Glucocorticoid receptor binding - 0.9263 92.63%
Aromatase binding - 0.6570 65.70%
PPAR gamma - 0.9031 90.31%
Honey bee toxicity - 0.9617 96.17%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 0.7649 76.49%

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
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.91% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 88.65% 87.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.60% 86.33%
CHEMBL4208 P20618 Proteasome component C5 87.36% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.33% 91.11%
CHEMBL2581 P07339 Cathepsin D 82.67% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.47% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.37% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 81.48% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Tetradium ruticarpum

Cross-Links

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PubChem 80113
NPASS NPC281278