2196246-28-1

USP7-IN-20 Chemical Structure
2196246-28-1

Chemical Structure

USP7-IN-20

  • CAS No.: 2196246-28-1
  • Formula:C22H24BrN3O3S
  • Molecular Weight:490.41

InChIKey: NRRXSEFLOFZNSO-OAHLLOKOSA-N

SMILES: O=C1C2=C(C(Br)=CS2)N=CN1CC3(CCN(CC3)C(C[C@H](C4=CC=CC=C4)C)=O)O

Biological Activity: USP7-IN-20 is a highly selective USP7 inhibitor that binds allosterically to the allosteric pocket of USP7 in a non-competitive and reversible manner. USP7-IN-20 downregulates MDM2 protein levels and stabilizes p53, thereby inducing p21 expression and enhancing the ubiquitin-dependent degradation of MDM2. USP7-IN-20 effectively binds endogenous USP7 to inhibit cancer cell proliferation, and also induces apoptosis by promoting the cleavage of PARP and caspase 3. USP7-IN-20 can be widely used in cancer-related basic and translational research.[1]

Cat. No. Product Name Purity Description Pricing
HY-183942
USP7-IN-20 USP7-IN-20 is a highly selective USP7 inhibitor that binds allosterically to the allosteric pocket of USP7 in a non-competitive and reversible manner. USP7-IN-20 downregulates MDM2 protein levels and stabilizes p53, thereby inducing p21 expression and enhancing the ubiquitin-dependent degradation of MDM2. USP7-IN-20 effectively binds endogenous USP7 to inhibit cancer cell proliferation, and also induces apoptosis by promoting the cleavage of PARP and caspase 3. USP7-IN-20 can be widely used in cancer-related basic and translational research.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References