1. Apoptosis
  2. MDM-2/p53
  3. RG7112D

RG7112D 是一种有效的 MDM2 抑制剂,通过 HTRF 结合测定抑制 MDM2-p53 和 VHL-HIF1α 的 IC50 分别为 11 nM 和 >10000 nM。RG7112D 通过酰胺键与 VHL-Amine 偶联,形成双功能分子 YX-02-030。YX-02-03 是一种 MDM2-PROTAC,可有效抑制 MDM2-p53 结合 (HTRF IC50 = 63nM)。RG7112D 可以稳定 MDM2 蛋白并提高 p53 蛋白水平。

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RG7112D Chemical Structure

RG7112D Chemical Structure

CAS No. : 2360561-90-4

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生物活性

RG7112D is a potent MDM2 inhibitor with IC50s of 11 nM and >10000 nM and for MDM2-p53 and VHL-HIF1α by binding HTRF assay, respectively. RG7112D is coupled by an amide bond to VHL-Amine, resulting in a bi-functional molecule, YX-02-030. YX-02-03, a MDM2-PROTAC, potently inhibits MDM2-p53 binding (HTRF IC50=63nM). RG7112D can stabilize MDM2 protein and increase p53 protein levels[1].

分子量

665.65

Formula

C36H42Cl2N4O4

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.

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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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RG7112D
目录号:
HY-158685
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