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首页-抗体药物偶连体和PROTACs-PROTAC

Request The Product List ofPROTAC PROTAC

Cat. No. Product Name Information
PC-23795

XYD049

GSPT1 degrader

XYD049 is a potent, selective CRBN-interacting molecular glue degrader of G1 to S phase transition 1 (GSPT1) with DC50 of 19 nM in 22Rv1 cells.
PC-23771

RET PROTAC RD-23

RET PROTAC

RET PROTAC RD-23 is a potent, selective and orally bioavailable RET PROTAC degrader with DC50 of 5.6 nM, Dmax =92% in BaF3 cells.
PC-23735

TEAD PROTAC H122

TEAD PROTAC

TEAD PROTAC H122 is a potent, selective TEAD PROTAC degrader with DC50 of 3.0 nM in MSTO-211H cells, shows TEAD1 binding affinity with Ki of 0.3 nM, promotes the degradation of TEAD1, TEAD3, and TEAD4 with similar potency.
PC-23715

PT-129

G3BP1/2 PROTAC

PT-129 is the first potent, selective, and efficacious G3BP1/2 PROTAC degrader, induces degradation of G3BP1 and G3BP2 with DC50 of 5 and 10 μM respectively in L929 cells, Dmax=95%.
PC-23675

SMD-3040

SMARCA2 PROTAC

SMD-3040 is a highly potent, exceptionally selective SMARCA2 PROTAC degrader with DC50 of 12 nM and Dmax = 96% in Hela cells, >500-fold selectivity over SMARC4.
PC-23674

SMD-3236

SMARCA2 PROTAC

SMD-3236 is a highly potent, exceptionally selective SMARCA2 PROTAC degrader with DC50 of 0.5 nM and Dmax = 96% in H838 NSCLC cells, >2000-fold selectivity over SMARC4.
PC-23665

dTAGV-1 hydrochloride

FKBP12 degrader

dTAGV-1 hydrochloride is an exclusively selective VHL-recruiting dTAG molecule, to rapidly degrade FKBP12F36V-tagged proteins.
PC-23651

PARP1 PROTAC 180055

PARP1 PROTAC

PARP1 PROTAC 180055 is a potent, PARP1-specific degradation PROTAC compound with DC50 of 180  nM and 240 nM in T47D and MDA-MB-231 cell lines, respectively.
PC-23566

YB-3-17

GSPT1 degrader, mTOR inhibitor

YB-3-17 is a potent dual-target, dual-mechanism molecule, robustly inhibits mTOR (IC50=0.22 nM) and selectively degrades GSPT1 (DC50=5 nM, U87 cells).
PC-23565

LZK PROTAC-21A

LZK PROTAC

LZK PROTAC-21A is a potent, selective LZK (Leucine zipper-bearing kinase, MAP3K13)-targeting PROTAC with binding affinity of 35 nM.
PC-23554

YZ-836P

PRMT5 PROTAC

YZ-836P is a CRBN-recruiting PRMT5 PROTAC degrader, exerts cytotoxic effects in TNBC, promotes the ubiquitination and degradation of PRMT5 in a CRBN-dependent manner, downregulates key downstream target protein KLF5 in TNBC.
PC-23543

dCK1α-2

CK1α degrader

dCK1α-2 is a potent, selective and orally bioavailable CK1α degrader with DC50 of 146 nM, Dmax of 84% in MOLM13 cells.

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