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Cat. No. Product Name Information
PC-24376

MS115

PRMT5 PROTAC

MS115 is a potent, selective best-in-class PRMT5 PROTAC degrader, induces rapid and robust degradation of PRMT5 (DC50=17.4 nM) and its binding partner MEP50 (DC50=11.3 nM, MDAMB468 cells), in a time-, concentration-, VHL- and UPS-dependent manner.
PC-24355

MS2133

DOT1L PROTAC

MS2133 is a first-in-class, potent and selective DOT1L PROTAC degrader with a DC50 of 56 nM and Dmax of 69 in THP-1 cells and a DC50 of 25 nM and Dmax of 93 in MV4-11 cells.
PC-24279

YX0597

CDK9 PROTAC

YX0597 is a potent, selective CDK9 PROTAC degrader, potently inhibits GEAC cell growth, especially in radiation-resistant tumor cells.
PC-24278

TO-1187

HDAC6 PROTAC

TO-1187 is a potent, selective, cereblon (CRBN)-based HDAC6 PROTAC degrader with DC50 of 5.81 nM in MM.1S cells (6 h), Dmax of 94%.
PC-24265

HDAC6 PROTAC 17c

HDAC6 PROTAC

HDAC6 PROTAC 17c is a potent, selective CRBN- and VHL-recruiting PROTAC degrader of HDAC6 with DC50 of 14 nM in MM.1S cells, Dmax of 91%, high selective over other HDACs.
PC-24242

BT-O2C

p300 PROTAC

BT-O2C is a potent, selective PROTAC degrader of p300, potently degrades p300 while sparing CBP, is cytotoxic in CIC::DUX4 sarcoma (CDS) cell lines (IC50=152-221 nM).
PC-24233

PP-C8

CDK12 PROTAC

PP-C8 is a potent, selective CDK12-cyclin K complex PROTAC degrader with DC50 of DC50 of 416 nM and 412 nM for CDK12 and CycK protein levels respectively, does not affect CDK13.
PC-24107

ANXA3 degrader 18a5

ANXA3 degrader

ANXA3 degrader 18a5 is a highly selective ANXA3 degrader with SPR KD of 0.08 uM, exhibits antiproliferative activity against with IC50 of 0.71 and 1.05 uM, DC50 of 3.12 uM and 1.32 uM in MDA-MB-468 and MDA-MB-231 cells, respectively.
PC-24090

cGAS PROTAC TH35

cGAS degrader

cGAS PROTAC TH35 is an effective, selective CRBN-recruiting cGAS-targeting PROTAC degrader with DC50 of 0.9 uM and 4.6 uM in THP-1 and RAW 264.7 cells respectively, Dmax >90% at 20 uM.
PC-24083

SK2188

Aurora A PROTAC

SK2188 is a potent, highly selective PROTAC degrader of Aurora A with DC50 of 3.9 nM and Dmax of 89% in NGP neuroblastoma cells, induces subsequent reduction of MYCN.
PC-24082

JB170

Aurora A PROTAC

JB170 is a potent, highly selective PROTAC degrader of Aurora A with DC50 of 28 nM and Dmax of 300 nM in MV4-11 cells, linking alisertib to the cereblon-binding molecule Thalidomide.
PC-24081

JB300

Aurora A PROTAC

JB300 is a potent, highly selective PROTAC degrader of Aurora A with DC50 of 30 nM.

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