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产品名称 | glutaminase ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Telaglenastat |
+++
Glutaminase, IC50: 24 nM |
99%+ | |||||||||||||||||
BPTES |
++
Glutaminase GLS1 (KGA), IC50: 0.16 μM |
98%+ | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | ZED-1227 is a targeted and orally bioavailable inhibitor of transglutaminase 2 (TG2) with an IC50 of 45 nM. It is effective in blocking inflammation-driven TG2 expression and activity, making it a candidate for celiac disease (CeD) research[1].[2]. |
体内研究 | ZED-1227 reduces the activity of intestinal TG2, induced by Polyinosinic:Polycytidylic acid (40 mg/kg), back to normal levels and alleviates intestinal inflammation in mice[1]. At a dose of 5 mg/kg, administered via the oral route, ZED-1227 effectively inhibits TG2 activity in the small intestinal mucosa[2]. |
体外研究 | ZED-1227, at concentrations ranging from 0.1 μM to 1 μM over 24 hours, does not affect the metabolic activity or proliferation of Huh7 and CaCo2 cells, indicating it lacks cytotoxic effects[2]. in vitro, ZED-1227 at dosages between 0.002 and 0.2 mg/mL for 30 minutes, inhibits TG2 activity in the small intestinal mucosa[2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.89mL 0.38mL 0.19mL |
9.46mL 1.89mL 0.95mL |
18.92mL 3.78mL 1.89mL |
CAS号 | 1542132-88-6 |
分子式 | C26H36N6O6 |
分子量 | 528.601 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,Store in freezer, under -20°C |
溶解度 |
DMSO: 120 mg/mL(227.01 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |