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FR167344 free base is an orally active, nonpeptide antagonist of the bradykinin receptor B2, exhibiting high-affinity binding (IC50: 65 nM) and showing no binding affinity for the B1 receptor.
FR167344 free base is an orally active, nonpeptide antagonist of the bradykinin receptor B2, exhibiting high-affinity binding (IC50: 65 nM) and showing no binding affinity for the B1 receptor.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
100 mg | 询价 | 期货 | |
500 mg | 询价 | 期货 |
产品描述 | FR167344 free base is an orally active, nonpeptide antagonist of the bradykinin receptor B2, exhibiting high-affinity binding (IC50: 65 nM) and showing no binding affinity for the B1 receptor. |
靶点活性 | Bradykinin receptor B2:65 nM |
体外活性 | FR167344 shows no stimulatory effects on PI hydrolysis. FR167344 inhibits the B2 receptor-mediated phosphatidylinositol (PI) hydrolysis and produces a concentration-dependent rightward shift in the dose-response curve to bradykinin, in competitive experiments using membranes prepared from Chinese hamster ovary cells expressing the bradykinin receptor subtypes. This shift is accompanied by a progressive reduction of maximal response. Estimated pA2 values for the antagonism of bradykinin-induced PI hydrolysis by FR167344 is 8.0 [1]. |
体内活性 | FR167344 (p.o.; 2h; carrageenin injection) inhibits carrageenin-induced paw oedema in rats (ID50: 2.7 mg/kg). FR167344 (p.o.) inhibits kaolin-induced writhing in mice (ID50: 2.8 mg/kg in 10 min writhing and 4.2 mg/kg in 15 min writhing). FR167344(p.o.) inhibits caerulein-induced pancreatic oedema (ID50: 13.8 mg/kg) and it also increases in amylase and lipase of blood samples (ID50: 10.3 and 7.4 mg/kg, respectively, in rats) [2]. |
分子量 | 673.38 |
分子式 | C30H28BrCl2N5O4 |
CAS No. | 215258-13-2 |
密度 | 1.43 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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