产品
编 号:F085017
分子式:C50H66Cl4N8O10S2
分子量:1145.05
产品类型
结构图
CAS No: 1234423-95-0
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产品详情
生物活性:
Tenapanor (AZD1722) is a potent and orally active sodium/hydrogen exchanger isoform 3 (NHE3) inhibitor. Tenapanor reduces intestinal phosphate absorption predominantly through reduction of passive paracellular phosphate flux. Tenapanor has the potential for the research of hyperphosphatemia.
体内研究:
Tenapanor (0.15、0.5 mg/kg;口服) 减少大鼠的被动细胞旁磷酸盐吸收。Tenapanor (0.15 mg/kg;口服;每天两次,连续 11 天) 增加大鼠尿磷排泄的减少。Animal Model:Rats (intestinal loop model)
Dosage:0.15, 0.5 mg/kg
Administration:P.o.
Result:Reduced passive paracellular phosphate absorption by reduced urinary phosphate and sodium excretion after the high-phosphate meal and increased sodium and phosphate delivery to the cecum.
Animal Model:8 weeks, 250 g male Sprague–Dawley rats
Dosage:0.15 mg/kg in combination with sevelamer (0%, 0.75%, 1.5%, and 3% (wt/wt))
Administration:Oral gavage; twice-daily for 11 consecutive days
Result:Significantly augmented the reduction in urinary phosphorus excretion.