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Medchemexpress LLC BSJ-02-162 | 2139329-47-6 | 98.1% | C43H49N11O7 | 100 MG
SDP

Catalog No. 5000354504
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BSJ-02-162 is a potent PROTAC degrader targeting Cyclin-Dependent Kinases 4 and 6. It consists of a thalidomide-based E3 ligase ligand, a Palbociclib-derived target protein ligand, and a PROTAC linker. This compound works by harnessing the cell's ubiquitin-proteasome system to induce the degradation of CDK4/6 proteins, offering an advantage over traditional small-molecule inhibitors. Intended for research use only.

  • Potent PROTAC CDK4/6 degrader with a novel mechanism.
  • Multi-component structure for targeted degradation.
  • High purity of 98.07% for reliable results.
  • Ideal for research in cell cycle, DNA damage, and cancer.
  • Available in various solid and solution quantities.
  • Includes comprehensive documentation for thorough understanding.

Catalog No. 50-003-54504 Supplier Medchemexpress LLC Supplier No. HY144995100MG
May include imposed supplier surcharges.
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BSJ-02-162 is a potent PROTAC degrader targeting Cyclin-Dependent Kinases 4 and 6. It consists of a thalidomide-based E3 ligase ligand, a Palbociclib-derived target protein ligand, and a PROTAC linker. This compound works by harnessing the cell's ubiquitin-proteasome system to induce the degradation of CDK4/6 proteins, offering an advantage over traditional small-molecule inhibitors. Intended for research use only.

  • Potent PROTAC CDK4/6 degrader with a novel mechanism.
  • Multi-component structure for targeted degradation.
  • High purity of 98.07% for reliable results.
  • Ideal for research in cell cycle, DNA damage, and cancer.
  • Available in various solid and solution quantities.
  • Includes comprehensive documentation for thorough understanding.

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