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KB-5492 free base

    级别和纯度:
  • ≥99%
  • CAS编号: 113594-64-2
  • 分子式: C23H30N2O6
  • 分子量: 430.49
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货号 (SKU) 包装规格 是否现货 价格 数量
K648251-5mg
5mg 期货 Stock Image
K648251-10mg
10mg 期货 Stock Image
K648251-25mg
25mg 期货 Stock Image
K648251-50mg
50mg 期货 Stock Image
K648251-100mg
100mg 期货 Stock Image

基本描述

别名 KB-5492 游离碱
规格或纯度 ≥99%
英文名称 KB-5492 free base
生化机理 KB-5492 游离碱是一种强效的σ受体选择性抑制剂,可抑制[3 H]1,3-二(2-甲苯基)胍(DTG)与σ受体的特异性结合,IC 50 为 3.15 μM。KB-5492 游离碱是一种抗溃疡剂。
储存温度 -20°C储存
运输条件 超低温冰袋运输
作用类型 抑制剂
产品介绍


KB-5492 free base is a potent and selective inhibitor of sigma receptor , inhibits specific [ 3 H]1,3-di(2-tolyl)guanidine (DTG) binding to the sigma receptor with an IC 50 of 3.15 μM. KB-5492 free base is an anti-ulcer agent

In Vitro

KB-5492 (0.001-100 μM) free base inhibits specific [ 3 H]DTG binding in a concentration-dependent manner. KB-5492 (0.1-1 mM) free base significantly and concentration-dependently prevents the ethanol- and acidified aspirin-induced increases in 51 Cr release from gastric epithelial cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

KB-5492 (200 mg/kg; p.o.) free base prevents macroscopic lesions in the gastric mucosa. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male Sprague-Dawley rats weighing 210-240 g are induced gastric mucosal damageDosage: 200 mg/kg Administration: Oral gavage Result: Reduced the lesion length as compared with the control. Prevented the deep mucosal lesions and exfoliation of surface epithelial cells.

Form:Solid

IC50& Target:IC50: 3.15 μM (sigma receptor)

纯度 ≥99%

名称和识别符

分子量 430.49

化学和物理性质

溶解性 DMSO : 100 mg/mL (232.29 mM; Need ultrasonic)

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:

溶液计算器