BAY 73-1449 是一种选择性前列环素受体 (prostacyclin receptor, IP) 的拮抗剂，在人 HEL 细胞和大鼠 DRG 的 cAMP 分析中具有很高的效价 (IC50 值小于 0.1 nM)。BAY 73-1449 可用于降血压的研究。 BAY 73-1449 is a selective antagonist of prostacyclin receptor (IP) , with high potency ( IC 50 of less than 0.1 nM) in cAMP assays in Human HEL cells and rat DRG. BAY 73-1449 can be used in the research of lowering blood pressure In Vivo BAY 73-1449 (0.1-1 mg/kg; i.v.) does not significantly reduce mesenteric inflow, but significantly reduces splenic shunt vessel outflow in rats . BAY 73-1449 (1-5 mg/kg, s.c. once daily for 7 d) has no effects on the degree of porto-systemic shunting in rats . BAY 73-1449 (1 mg/kg, s.c. once daily for 7 d), has no effects on portal pressures in rats . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male Wistar rats (250-350 g) are ligated portal vein Dosage: 0.1, 1 mg/kg Administration: A single i.v. Result: Significantly reduced shunt flow without affecting mesenteric flow. IC50& Target:IP Receptor
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BAY 73-1449
CAS number：693790-96-4(DMSO) molecular formula：C26H23N3O3
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| Chinese alias | - | ||
| English alias | - | ||
| CAS number | 693790-96-4(DMSO) | molecular formula | C26H23N3O3 |
| molecular weight | 425.48 g/mol | Exact mass | - |
| PSA | - | logp | - |
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