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InChiKey: OBJNFLYHUXWUPF-IZZDOVSWSA-N
Smiles: CC[C@H](C)[C@H]1O[C@@]2(C[C@@H]3C[C@@H](CC=C(C)[C@@H](O[C@H]4C[C@H](OC)[C@@H](O[C@H]5C[C@H](OC)[C@@H](O)[C@H](C)O5)[C@H](C)O4)[C@@H](C)C=CC=C4CO[C@@H]5[C@H](O)C(C)=C[C@@H](C(=O)O3)[C@]45O)O2)C=C[C@@H]1C |c:12
ReACp53 could inhibit p53 amyloid formation and rescue p53 function in cancer cell lines
InChiKey: FNUXMEOWJVTJJE-DTXRQUTOSA-N
InChi: InChI=1S/C20H16N2O4S/c1-26-18-8-4-3-7-17(18)21-20(23)16-6-2-5-9-19(16)27-15-12-10-14(11-13-15)22(24)25/h2-13H
BMS-1166-N-piperidine-CO-N-piperazine 1193 InChiKey: OBJNFLYHUXWUPF-IZZDOVSWSA-NBMS 1166 N piperidine CO N piperazine incorporates a ligand for PD 1 PD L1 immune checkpoint, and a PROTAC linker. BMS 1166 N piperidine CO N piperazine can be used in the synthesis of PROTAC PD 1 PD L1 degrader 1 (HY 131183). PROTAC PD 1 PD L1 degrader 1 inhibits PD 1 PD L1 interaction with an IC50 of 39. 2 nM. Product information CAS Number: 2447066 14 8 Molecular Weight: 707. 26 Formula: C41H43ClN4O5 Chemical Name: 3 [(4 chloro 5 {[3 (2,3 dihydro