目錄:MedChemExpress LLC>>生化試劑>> Asapiprant | MCE
CAS | 932372-01-5 | 純度 | 99.58% |
---|---|---|---|
分子量 | 501.55 | 分子式 | C??H??N?O?S |
供貨周期 | 現貨 | 規(guī)格 | 1 mg |
貨號 | HY-16763 | 應用領域 | 醫(yī)療衛(wèi)生,化工,生物產業(yè),制藥 |
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CAS No. : 932372-01-5
產品活性:Asapiprant is a potent and selective DP1 receptor antagonist with a Ki of 0.44 nM.
研究領域:GPCR/G Protein
作用靶點:Prostaglandin Receptor
In Vivo: Oral administration of Asapiprant to sheep at 1 and 3 mg/kg significantly (P<0.01) suppresses the increase in nasal resistance by 82% and 92%, respectively. Oral administration of Asapiprant to sheep at 5 mg/kg suppresses Prostaglandin (PG) D2 (PGD)2-induced nasal resistance by 86%. When orally administered 1 h before the antigen challenge in pigs, Asapiprant (3, 10, and 30 mg/kg) suppresses immediate airway response (IAR) by 52%, 57%, and 96%, and late airway response (LAR) by 67%, 50%, and 79%, respectively. Orally administered with Asapiprant (5 mg/kg) for 4 days, the Asapiprant significantly (P<0.01) suppresses antigen-induced nasal resistance by 73% in sheep. Treatment with 3 and 30 mg/kg of Asapiprant in pigs significantly (P<0.01) suppresses nasal secretion by 53% and 72%, respectively. Treatment with Asapiprant in rats at 10 mg/kg significantly (P<0.05) reduces airway hyper-responsiveness (AHR), infiltration of inflammatory cells, and mucin production in bronchoalveolar lavage fluid (BALF), although treatment with Asapiprant at 0.1 mg/kg does not have a significant effect on any responses.
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