Weight | 138.126 g/mol |
---|---|
Formula | C6H6N2O2 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
methyl pyrimidine-4-carboxylate (2450-08-0)
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- QSAR study of ethyl 2-[(3-methyl-2,5-dioxo(3-pyrrolinyl))amino]-4-(trifluoromethyl) pyrimidine-5-carboxylate: an inhibitor of AP-1 and NF-kappa B mediated gene expression based on support vector machines. (Journal of Chemical Information and Computer Sciences, 2003)
- StructureActivity Relationship Studies of Ethyl 2[(3Methyl2,5dioxo(3pyrrolinyl))amino] 4(trifluoromethyl)pyrimidine5carboxylate: An Inhibitor of AP1 and NFB Mediated Gene Expression. (Bioorganic & Medicinal Chemistry Letters, 2002)
- Novel inhibitors of AP-1 and NF-B mediated gene expression: structureactivity relationship studies of ethyl 4-[(3-Methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)pyrimidine-5-carboxylate (Bioorganic & Medicinal Chemistry Letters, 2000)
- Synthesis and properties of new derivatives of ethyl 7-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrido [2,3-d]pyrimidine-5-carboxylate. (Farmaco, 1990)
- Synthesis of thiazolo[3,2- a ]pyrimidines based on 4-aryl-substituted 3,4-dihydro-pyrimidine(1H)-2-thiones and the crystal structure of ethyl 5-(2,4-dimethoxyphenyl)-7-methyl-3-oxo-3,5-dihydro-2H-thiazolo-[3,2- a ]pyrimidine-6-carboxylate (Chemistry of Heterocyclic Compounds, 2009)
- Antiinflammatory, analgesic, and antipyretic activities of methyl 7-butyl-4,5,6,7-tetrahydro-3-methylamino-4,6-dioxo-5-propyl-2H-pyrazolo[3,4-d]pyrimidine-2-carboxylate (AA-2379), a novel non-acidic agent (Inflammation Research, 1988)
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SMILESCOC(=O)C1=NC=NC=C1
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