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Cat. No. Product Name Information
PC-26385

JP-2-197

BRD4 degrader

JP-2-197 is a fumarate-based RNF126-dependent BRD4 degrader, induces robust degradation of both long and short BRD4 isoforms in RNF126 wild-type cells but not in RNF126 knockout cells.
PC-26370

HDAC3 degrader GS-1

HDAC3 degrader

GS-1 is a potent, selective HDAC3 degrader with DC50 of 1.24 uM in THP-1 cells, shows minimal degradation of HDAC1 or HDAC2 at 5 uM.
PC-26347

Orevandrodeg

Ligand-directed degrader

Orevandrodeg (BMS-986460, CC-2043137) is a ligand-directed degrader composed of an E3 ubiquitin ligase-binding moiety that is conjugated, via a linker, to a moiety that targets a prostate specific tumor-associated antigen (TAA), with potential antineoplastic activity, androgen receptor degradation inducer.
PC-26284

DZ-865B

BCL6 PROTAC

DZ-865B is a selective BCL6 degrader with DC50 of 2.7 uM and 4.7 uM in DLBCL cell lines OCI-LY-1 and SU-DHL-4 respectively, effectively suppresses DLBCL cell growth.
PC-26247

DFCI-002-06

HCK/BTK PROTAC

DFCI-002-06 is a potent, first-in-class dual HCK/BTK PROTAC degrader with DC50 values of 4.5 nM for BTK and 1.3 nM for HCK, Dmax values of >95% for BTK and 87% for HCK.
PC-26238

USP39_PROTAC_V1

USP39 PROTAC

USP39_PROTAC_V1 is a potent, selective VHL‐based PROTAC degrader of USP39 with KD of 232 nM, DC50 of 1 nM in HeLa cells.
PC-26228

ITRI-148

AR-NTD PROTAC

ITRI-148 is a CRBN-based androgen receptor N-terminal domain (AR-NTD) degrader, degrades AR, AR-V7, and AR mutants with DC50 of 0.05 uM and 0.02 uM for AR and AR-V7in VCaP cells.
PC-26219

XYD270

BRD9 PROTAC

XYD270 is a potent, selective, and orally efficacious BRD9 PROTAC degrader with DC50 of 0.082 nM and 3.9 nM in HS-SY-II cells and MV4;11 cells respectively.
PC-26139

KTX-951

IRAK4 PROTAC

KTX-951 is a potent and orally active degrader of IRAK4 and the Ikaros and Aiolos (IMiD) substrates with DC50 of 13 nM, 14 nM and 13 nM for IRAK4, Ikaros and Aiolos, respectively, induces proteasomal degradation of these key proteins, leading to the dual inhibition of the NF-κB and IRF4 signaling pathways.
PC-26138

KTX-582

IRAK4 PROTAC

KTX-582 is a potent, selective IRAK4 PROTAC degrader with DC50 values of 4 nM and 5 nM for IRAK4 and Ikaros, respectively, induces apoptosis in MYD88MT DLBCL, induces in vivo tumor regressions in lymphoma model.
PC-26133

GDCNF-11

GPX4 degrader

GDCNF-11 is a potent HSP90 interactome-mediated proteolysis targeting chimera (HIM-PROTAC) GPX4 degarder, potently induces ferroptosis via HSP90-mediated ubiquitin-proteasomal degradation of GPX4 in HT-1080 cells with DC50 of 0.08 uM.
PC-26131

GDAz-3

GPX4 degrader

GDAz-3 is a potent GPX4-targeting HSP70-PROTAC, potently and rapidly eliminates GPX4 in HT1080 cells (DC50=0.13 uM), thereby triggering ferroptosis with high selectivity.

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