AGI-5198
面议
药物分子

AGI-5198

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  • 阿拉丁
  • 上海
  • 生产商
  • 现货
  • 3
  • 1
上海阿拉丁生化科技股份有限公司
高级会员 高级会员
产品特点
规格信息
货号 CAS号
A126546-100mg 1355326-35-0
A126546-25mg 1355326-35-0
A126546-5mg 1355326-35-0
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产品描述
  • 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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