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Pharmacological Studies of FUT-175, Nafamstat Mesilate

机译:甲磺酸萘非司他FUT-175的药理研究

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References(41) Cited-By(125) FUT-175, 6-amidino-2-naphthyl p-guanidinobenzoate dimethanesulfonate (nafamstat mesilate), a novel synthetic protease-inhibiting agent, was studied to determine its in vitro effects against various proteases and other enzymes, as well as to determine its in vivo protease inhibitory effects. FUT-175 was found to inhibit, in an intense, specific and reversible way, the enzyme activities of trypsin, C1r, C1s, thrombin, kallikrein and plasmin with IC50 values of the order of 10-6-10-8 M. FUT-175 also inhibited complement-mediated hemolysis, including both classical and alternative pathways, sites of inhibition being on C1r and C1s as evidenced by the intermediate-cell technique. In animal model reactions in which the complement system is known to be involved as pathogenetic factors, e.g., Forssman shock, Forssman cutaneous vasculitis, zymosan-induced paw edema, endotoxin shock and local Shwartzman reaction, FUT-175 was highly effective in that, for example, intravenous dosing at 3 mg/kg could completely protect guinea pigs from the lethal Forssman shock. FUT-175 was also found to be effective in trypsin-induced shock in mice, in lethality due to thrombin-thrombosis in mice and in kinin formation in the inflammatory process in rats.
机译:参考文献(41)被引用的By(125)FUT-175、6--基-2-萘基对胍基苯甲酸酯二甲磺酸盐(萘甲磺胺甲磺酸盐)是一种新型的合成蛋白酶抑制剂,旨在确定其对多种蛋白酶和化合物的体外作用。其他酶,以及确定其体内蛋白酶抑制作用。发现FUT-175以强烈,特异性和可逆的方式抑制胰蛋白酶,C1r,C1s,凝血酶,激肽释放酶和纤溶酶的酶活性,IC50值为10-6-10-8M。 175还抑制补体介导的溶血,包括经典途径和替代途径,其中抑制位点在C1r和C1s上,如中间细胞技术所证明。在动物模型反应中,补体系统被认为是致病因素,例如,福斯曼休克,福斯曼皮肤血管炎,酵母聚糖诱导的爪水肿,内毒素休克和局部Shwartzman反应,FUT-175在其中非常有效例如,静脉注射3 mg / kg剂量可以完全保护豚鼠免受致命的Forssman休克。还发现FUT-175可有效治疗胰蛋白酶引起的小鼠休克,小鼠因凝血酶血栓形成的致死性以及大鼠炎症过程中激肽的形成。

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