GSK-269984A is a Prostaglandin E2 Receptor 1 (EP1) antagonist with a pIC 50 of 7.9. In Vitro Results from [ 3 H]-PGE 2 binding assay in CHO cells overexpressing the human EP 1 receptor demonstrate that GSK-269984A is an antagonist of EP 1 receptor with a pIC 50 of 7.9. GSK-269984A is found to cause a concentration-dependent rightward shift of the PGE 2 dose-response curve and Schild analysis shows that GSK-269984A is a competitive antagonist with pA 2 8.1±0.3 and slope 1.0. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo GSK-269984A demonstrates an ED 50 of 2.6 mg/kg (po), with the 10 mg/kg dose showing equivalent reversal of hypersensitivity to the standard. GSK-269984A displays moderate blood clearance in the rat and dog and high clearance in the monkey which is reflected in the half-life for each species . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:EP1 7.9 (pIC 50 )
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GSK-269984A
CAS number:892664-04-9 molecular formula:C20H14Cl2FNNaO3
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| Chinese alias | - | ||
| English alias | Q27280309 | GSK269984A | GSK-269984A | 2-Pyridinecarboxylic acid, 6-((5-chloro-2-((4-chloro-2-fluorophenyl)methoxy)phenyl)methyl)-, sodium salt (1:1) | Sodium 6-((5-chloro-2-(((4-chloro-2-fluorophenyl)methyl)oxy)phenyl)methyl)-2-pyridinecarboxylate | UNII | ||
| CAS number | 892664-04-9 | molecular formula | C20H14Cl2FNNaO3 |
| molecular weight | 429.22 g/mol | Exact mass | ≥99% |
| PSA | 62.300 Ų | logp | - |
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