PROTAC PRMT1 degrader-1 (compound 4) is a PRMT1 PROTAC degrader, with an IC50 of 185.7 nM against human PRMT1. PROTAC PRMT1 degrader-1 recruits the CRBN E3 ubiquitin ligase to induce proteasome-dependent degradation of PRMT1, it also forms a ternary complex with PRMT1 and CRBN, promoting ubiquitination and subsequent proteasomal degradation of PRMT1. PROTAC PRMT1 degrader-1 reduces the level of asymmetric dimethylarginine in cancer cells, as well as the level of asymmetric dimethylation of arginine 3 on histone H4, while inhibiting the growth of various cancer cells. PROTAC PRMT1 degrader-1 can be used in the research of breast cancer and melanoma[1].
Molecular Weight:
752.94
Formula:
C43H56N6O6
Target:
Histone Methyltransferase,PROTACs
Application Notes:
MCE Product type: Reference compound
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