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Cat. No. Product Name Information
PC-72149

AMXI-5001

PARP inhibitor

AMXI-5001 (AMXI 5001) is a novel, highly potent, orally active dual PARP1/2 (IC50 5/0.05 nM) and microtubule polymerization inhibitor, inhibits intracellular PAR formation with IC50 of 7 nM.
PC-38102

Venadaparib

PARP inhibitor

Venadaparib (IDX-1197) is a potent, selective PARP inhibitor with IC50 of 1.4 nM and 1.0 nM for PARP1 and PARP2, respectively.
PC-38045

DR2313

PARP inhibitor

DR2313 is a PARP inhibitor, inhibits poly(ADP-ribosyl)ation in nuclear extracts of rat brain in vitro (Ki=0.23 uM).
PC-36037

Fluzoparib

PARP inhibitor

Fluzoparib (Fuzuloparib, SHR-3162) is a novel, potent and orally available inhibitor of PARP with IC50 of 1.46 nM (PARP1).
PC-36012

PARP10 inhibitor 22

PARP10 inhibitor

PARP10 inhibitor 22 is a selective, cell-active inhibitor of PARP10 with IC50 of 1.8 uM, exhibits >10-fold selectivity over a large subset of other PARP family members.
PC-36007

MSC2504877

TNKS1/2 inhibitor

MSC2504877 (M2912) is a novel small molecule selective tankyrase inhibitor with IC50 of 0.7/0.8 nM against TNKS1/2, shows 771-fold selectivity for TNKS1 over PARP1 (IC50=0.54 uM).
PC-35720

PARP11 inhibitor ITK7

PARP11 inhibitor

PARP11 inhibitor ITK7 (ITK7) is a potent and selective PARP11 inhibitor with IC50 of 14 nM, displays >200-fold selectivity over other PARPs.
PC-35703

RK-287107

TNKS1/2 inhibitor

RK-287107 (RK287107) is a novel potent, tankyrase-specific inhibitor with IC50 of 14.3 and 10.6 nM for tankyrase-1 (TNKS1) and tankyrase-2 (TNKS2) respectively, shows no activity against PARP-1.
PC-35646

Gemcabene calcium

PARP activator

Gemcabene (PD-72953, PD72953) is a first-in-class lipid-lowering agent and activator of PARP.
PC-35643

Gemcabene

PARP activator

Gemcabene (PD-72953, PD72953) is a first-in-class lipid-lowering agent and activator of PARP.
PC-35508

ME0328

ARTD3/PARP3 inhibitor

ME0328 (ME-0328) is a potent, selective inhibitor of ADP-ribosyltransferase ARTD3/PARP3 with IC50 of 0.89 uM.
PC-35506

ZYTP1

PARP1/2 inhibitor

ZYTP1 is a novel, oral PARP inhibitor that inhibits PARP1, PARP2, Tankyrase-1 and Tankyrase-2 with IC50 of 5.4, 0.7, 133.3 and 289.8 nM, respectively.

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