PROTAC RIPK degraders -2 is a non-peptide PROTAC based on von Hippel-Lindau and targets serine-threonine kinase RIPK2, which is highly selective to the degradation of RIPK2. PROTAC RIPK degrader-2 acts as an activator to increase cell death and activate ion channels in cancer cells. PROTAC RIPK degrader-2 also can inhibit protein interactions, such as receptors and ligands, involved in a variety of diseases, such as cancer and diabetes[1][2].
Molecular Weight:
1060.31
Purity:
99.89
CAS Number:
[1801547-16-9]
Formula:
C52H65N7O11S3
Target:
PROTACs,RIP kinase
Application Notes:
Reference compound
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