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药物分子

AGI-5198

品牌 厂商性质 产地 货期
阿拉丁 生产商 上海 现货

询价
产品参数
货号 CAS号 操作
A126546-100mg 1355326-35-0 询价
A126546-25mg 1355326-35-0 询价
A126546-5mg 1355326-35-0 询价
产品介绍

  • 分子式 C27H31FN4O2
  • 分子量462.56
  • Beilstein号
  • EC号
  • MDL号
  • PubChem编号

属性

溶解性
  • DMSO 24 mg/mL
  • Water <1 mg/mL
  • Ethanol 14 mg/mL
  • 存贮条件 储存温度-20°C

    描述

    应用 AGI-5198(IDH C35)是剂量依赖的R132H-IDH1抑制剂
    产品介绍 AGI-5198 is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0.07 μM/0.16 μM.
    备注 AGI-5198 is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0.07 μM/0.16 μM.
    生化机理

    Description:
    IC50 Value: N/A
    AGI-5198, a novel R132H-IDH1 inhibitor, identified through a high-throughput screen blocked, in a dose-dependent manner, the ability of the mutant enzyme (mIDH1) to produce R-2-hydroxyglutarate (R-2HG). The recent discovery of mutations in metabolic enzymes has rekindled interest in harnessing the altered metabolism of cancer cells for cancer therapy. Isocitrate dehydrogenase 1 (IDH1) is one potential drug target, which is mutated in multiple human cancers [1].
    in vitro: N/A
    in vivo: N/A
    Clinical trial: N/A
     

    别名 ;IDH-C35;AGI5198;AGI 5198;IDH C35;N-Cycohexyl-2-(N-(3-fluorophenyl)-2-(2-methyl-1H-imidazol-1-yl)acetamido)-2-(o-tolyl)acetamide; N-[2-(Cyclohexylamino)-1-(2-methylphenyl)-2-oxoethyl]-N-(3-fluorophenyl)-2-methyl-1H-imidazole-1-acetamide

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    注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途