S-Gboxin iodide-抑制剂-深圳欣博盛生物科技有限公司

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S-Gboxin iodide

品牌：Adipogen

官网链接

说明书

折扣/货期

货号：AG-CR1-3533-M001	规格：1 mg	目录价：￥1200
货号：AG-CR1-3533-M005	规格：5 mg	目录价：￥4800

产品详情

* 以下信息仅供参考，详情请以原厂网站为准

产品名称:

S-Gboxin iodide

别名:

1-(2-(((1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-3-methyl-2-(3-(trifluoromethyl)phenyl)-1H-benzo[d]imidazol-3-ium iodide

产品描述:

Potent mitochondrial ATP synthase (ATPases (F0F1)) inhibitor, consequently leading to inhibition of oxidative phosphorylation (OXPHOS). Useful agent for immunometabolism research. Inhibits ATP synthase by blocking its proton channel (F0 subunit), which is necessary for oxidative phosphorylation of ADP to ATP (energy production), significantly reducing electron flow through the electron transport chain. Potent antitumor agent that inhibits oxidative phosphorylation and consequently growth and proliferation of mouse and human glioblastoma (GBM) with an IC50 of 470nM. Shown to rapidly and irreversibly compromise oxygen consumption in glioblastoma cells. This functional Gboxin analog has excellent metabolic stability, enhanced plasma stability and pharmacokinetic properties, and is suitable for in vivo studies. Gboxin-resistant cells require a functional mitochondrial permeability transition pore that regulates pH and thus impedes the accumulation of Gboxin in the mitochondrial matrix. Administration of a metabolically stable Gboxin analog inhibits glioblastoma allografts and patient-derived xenografts. Gboxin toxicity extends to established human cancer cell lines of diverse organ origin and shows that the increased proton gradient and pH in cancer cell mitochondria is a mode of action that can be targeted in the development of antitumor reagents.

保存温度:

+4°C

运输温度:

Ambient

预期分子量:

473.6 . 126.9

产品形式:

solid

产地:

瑞士

纯度:

>98% (1H-NMR)