CAS NO: | 892664-04-9 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | GSK-269984A is aProstaglandin E2 Receptor 1 (EP1)antagonist with apIC50of 7.9. | ||||||||||||||||
IC50& Target | pIC50: 7.9 (Prostaglandin E2 Receptor 1 (EP1))[1] | ||||||||||||||||
体外研究 (In Vitro) | Results from [3H]-PGE2binding assay in CHO cells overexpressing the human EP1receptor demonstrate that GSK-269984A is an antagonist of EP1receptor with a pIC50of 7.9. GSK-269984A is found to cause a concentration-dependent rightward shift of the PGE2dose-response curve and Schild analysis shows that GSK-269984A is a competitive antagonist with pA28.1±0.3 and slope 1.0[1]. | ||||||||||||||||
体内研究 (In Vivo) | GSK-269984A demonstrates an ED50of 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[1]. | ||||||||||||||||
分子量 | 429.22 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H14Cl2FNNaO3 | ||||||||||||||||
CAS 号 | 892664-04-9 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 7 mg/mL(16.31 mM;ultrasonic and warming and heat to 60℃) 配制储备液
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