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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-72798

AU-15330

SWI/SNF ATPase PROTAC

AU-15330 (AU15330) is a highly specific and VHL-dependent PROTAC degrader of SWI/SNF ATPase components (SMARCA2, SMARCA4 and PBRM1), shows preferential cytotoxicity in enhancer-binding transcription factor-addicted cancers at low nanomolar concentrations.
PC-72782

GSK215

FAK PROTAC

GSK215 is a potent, selective, FAK-degrading Proteolysis Targeting Chimera (PROTAC) based on a binder for the VHL E3 ligase and the known FAK inhibitor VS-4718.
PC-72644

CFT-2718

BRD4 PROTAC

CFT-2718 (CFT2718) is a benzotriazoloazepine-based BRD4 degrader, rapidly and selectively degrade BRD4 in vitro in a CRBN-dependent manner (DC90=10 nM, 293T cells).
PC-72621

ARV-471

ER degrader

ARV-471 (Vepdegestrant) is an investigational orally bioavailable PROTAC protein degrader designed to specifically target and degrade the estrogen receptor (ER) with DC50 of 1.8 nM.
PC-72572

SR-1114

ENL degarder

SR-1114 (SR1114) is a first-in-class ENL PROTAC degarder based on SR-0813 that binds to the E3 substrate adapter cereblon (CRBN), elicits rapid CRBN-dependent degradation of ENL with DC50 of 150 nM in MV4;11 cells.
PC-72497

INY-03-041

AKT PROTAC

INY-03-041 a pan-AKT degrader (PROTAC) consisting of AKT inhibitor GDC-0068 conjugated to lenalidomide, a recruiter of the E3 ubiquitin ligase substrate adaptor Cereblon (CRBN).
PC-72479

IRAK3 PROTAC 23

IRAK3 PROTAC

IRAK3 PROTAC 23 a potent and selective degrader of IRAK3 with DC50 of 2 nM, with a maximum degradation measured of 98%.
PC-72325

MS910

MEK1/2 degrader

MS910 (MS-910) is the first CRBN-recruiting MEK1/2 degrader (PROTC) with HT29 DC50 of 118/55 nM for MEK1/2 degradation, respectively.
PC-72324

MS934

MEK1/2 degrader

MS934 (MS-934) is a VHL-recruiting MEK1/2 degrader (PROTAC) with HT29 DC50 of 18/9 nM for MEK1/2 degradation, respectively.
PC-72322

dBRD9-A

BRD9 PROTAC

dBRD9-A is a chemical degrader (PROTAC) of BRD9, a highly specific binder of the BRD9 bromodomain and elicits near complete BRD9 degradation at low nanomolar concentrations.
PC-72309

DGY-09-192

FGFR degrader

DGY-09-192 is a bivalent degrader (PROTAC) that couples the pan-FGFR inhibitor BGJ398 to a CRL2VHL E3 ligase recruiting ligand,preferentially induces FGFR1/2 degradation while largely sparing FGFR3/4.
PC-72308

HPK1 PROTAC SS47

HPK1 degrader

HPK1 PROTAC SS47 is a heterobifunctional small molecule based on ZYF0033 that simultaneously binds HPK1 and E3 ligase Cereblon (CRBN), induces degradation of HPK1.

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