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Cat. No. Product Name Information
PC-20167

TMX-4153

PIP4K2C PROTAC

TMX-4153 (TMX4153) is a bivalent PIP4K2C degrader (MOLT4 cells, DC50=24 nM, Dmax=921% at 1 uM) based on TMX-4084, rapidly and selectively degrades endogenous PIP4K2C.
PC-20153

TMX-4100

PDE6D PROTAC

TMX-4100 (TMX4100) is a highly potent PDE6D degrader with DC50 of <200 nM in MOLT4 cells, does not degrade CK1α and IKZF1/IKZF3.
PC-20152

TMX-4113

PDE6D PROTAC

TMX-4113 (TMX4113) is a highly potent PDE6D degrader with DC50 of 40 nM in MM.1S cells, does not degrade CK1α, IKZF1/IKZF3.
PC-20151

TMX-4116

CK1α PROTAC

TMX-4116 (TMX4116) is a highly potent casein kinase 1α (CK1α) degrader with DC50 of <200 nM (CK1α) in MOLT4 cells, does not degrade PDE6D and IKZF1/IKZF3.
PC-20149

FPFT-2216

KZF1 and CK-1α degrader

FPFT-2216 (FPFT2216) is a thalidomide derivative cereblon modulator that shows an inhibitory effect toward IKZF1 protein level, upregulates the production of IL-2 and degrades IKZF1 as well as CK-1α among ubiquitin–proteasomal degradative substrates of IMiDs.
PC-20148

UNC7700

PRC2 PROTAC

UNC7700 (UNC-7700) is a potent EED-targeted PRC2 degrader, contains a unique cis-cyclobutane linker and potently degrades all PRC2 components EED (DC50=111 nM; Dmax=84%), EZH2WT/EZH2Y641N (DC50=275 nM; Dmax=86%) and SUZ12 (Dmax=44%) in DLBCL cells.
PC-20147

UNC6852

PRC2 PROTAC

UNC6852 (UNC-6852) is a chemical degrader of PRC2, contains an EED226-derived ligand and a ligand for VHL, induces proteasomal degradation of PRC2 components, EED (DC50=0.61 uM), EZH2WT/EZH2Y641N (DC50=0.67 uM) and SUZ12.
PC-20145

NVP-DKY709

IKZF2 degrader

NVP-DKY709 (DKY709) is a first-in-class, selective CRBN glue degrader of IKZF2 with DC50 of 4 nM in cellular assays, completely spares degradation of IKZF1/3.
PC-20007

GMB-475

BCR-ABL1 PROTAC

GMB-475 (GMB475) is an allosteric BCR-ABL1 PROTAC with DC50 of 340 nM, degrades the BCR-ABL1 through the ubiquitin-proteasome pathway.
PC-49672

MS3227

MDM2 PROTAC

MS3227 is a proteolysis-targeting chimera (PROTAC) that targets MDM2 by recruiting the E3 ligase VHL, resulting in proteasome-dependent degradation of MDM2.
PC-49629

AK-2292

STAT5 PROTAC

AK-2292 (AK2292) is a first, potent and selective small-molecule degrader of both STAT5A and STAT5B isoforms.
PC-49622

MS147

PRC1 degrader

MS147 (MS 147) is the first degrader of PRC1 core components, BMI1 and RING1B, comprises an EED small-molecule binder (EED226, Cat. PC-42321) linked to a ligand of the E3 ligase von Hippel-Lindau (VHL), degrades BMI1/RING1B in an EED-, VHL-, ubiquitination-, and time-dependent manner.

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