1. Apoptosis
  2. MDM-2/p53 Apoptosis
  3. DS-5272

DS-5272 是口服有效的 p53-MDM2 抑制剂,IC50 为 20 nM。DS-5272 可抑制 SJSA-1 (p53 野生型,IC50=0.17 μM) 和 DLD-1(p53 突变型) 的增殖。DS-5272 可阻滞细胞周期,并诱导 SJSA-1 细胞凋亡 (apoptosis)。DS-5272 在小鼠中表现出抗肿瘤活性。

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DS-5272 Chemical Structure

DS-5272 Chemical Structure

CAS No. : 1235575-97-9

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  • 生物活性

  • 纯度 & 产品资料

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生物活性

DS-5272 is an orally acitve inhibitor for p53-MDM2 with an IC50 of 20 nM. DS-5272 inhibits the proliferation of SJSA-1 (wildtype p53, IC50=0.17 μM) and DLD-1 (mutant p53). DS-5272 arrest the cell cycle, and induces apoptosis in SJSA-1. DS-5272 exhibits antitumor efficacy in mice[1].

IC50 & Target

IC50: 20 nM (p53-MDM2 interaction)

分子量

703.67

Formula

C34H38Cl2F2N6O2S

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
DS-5272
目录号:
HY-120667
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