CL-F-B1 is a PD-L1 PROTAC degrader, with a DC50 of 2.32 µM. CL-F-B1 promotes the ubiquitination and degradation of PD-L1. CL-F-B1 can be used in the research of colon cancer[1].
Molecular Weight:
947.04
Formula:
C54H54N6O10
Target:
PD-1/PD-L1,PROTACs
Application Notes:
MCE Product type: Reference compound1
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