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Cat. No. Product Name Information
PC-42678

A-966492

PARP inhibitor

A-966492 (A966492) is a highly potent and efficacious PARP inhibitor with Ki/EC50 of 1 nM/1 nM for PARP-1.
PC-24241

TDI-012804

TNKS2 inhibitor

TDI-012804 is a potent and selective Tankyrase 2 (TNKS2) inhibitor with IC50 of 3.46 nM in in vitro PARylation assays, has 25-fold selectivity over TNKS1, suppresses WNT signaling in TNKS depleted cells.
PC-24140

Itareparib

PARP1 inhibitor

Itareparib is a potent, selective PARP-1 inhibitor with potential for treatment of cancer, cardiovascular disease, central nervous system injury, and inflammation.
PC-23684

PARP1 inhibitor X

PARP1 inhibitor

PARP1 inhibitor X is a potent, selective poly(ADP-ribose)polymerase-1 (PARP-1) inhibitor with nano-molar activity.
PC-23463

UPF-1069

PARP-2 inhibitor

UPF-1069 is a potent, selective PARP-2 inhibitor with IC50 of 0.3 uM, >25-fold selective over PARP-1 (IC50= 8 uM).
PC-23199

K-756

TNKS1/2 inhibitor

K-756 is a small molecule inhibitor of the Wnt/β-catenin pathway with IC50 of 110 nM in Wnt/β-catenin reporter assay, and selective tankyrase (TNKS) inhibitor with IC50 of 31 and 36 nM for TNKS1 and TNKS2, stabilizes Axin1/2 by inhibiting TNKS1/2.
PC-23088

Lerzeparib

PARP inhibitor

Lerzeparib (TQB3823) is a novel, potent and selective PARP inhibitor with IC50 of  2.8/0.9/629.3 nM for PARP1/PARP2/Tankyrase 1, respectively.
PC-22676

HTMC0435

PARP inhibitor

HTMC0435 is a highly selective small molecule, orally bioavailable PARP inhibitor.
PC-22466

XLY-1

PARP7 inhibitor

XYL-1 is a highly potent, selective PARP7 inhibitor with IC50 of 0.6 nM, weak inhibitory effect on PARP1 (IC50 >1 uM).
PC-22045

K-476

TNKS1/2 inhibitor

K-476 is a highly potent and selective tankyrase (TNKS1/2) inhibitor, potently inhibits Wnt/β-catenin pathway with IC50 of 110 nM in cell-based luciferase assays.
PC-21163

PARP-1 inhibitor Pip5

PARP1 inhibitor

PARP-1 inhibitor Pip5 is an analog of PARP-1 type I inhibitor AZ0108, inhibits PARP-1 auto-PARylation with IC50 of 4-17 nM, shows similar type I inhibition of PARP-1 but is more cytotoxic than AZ0108.
PC-21009

kt-3283

PARP-HDAC inhibitor

kt-3283 is a novel bi-functional PARP-HDAC inhibitor with IC50 of 0.338 nM, 2.19 nM and 1.89 uM for PARP1, PARP2 and HDACs, respectively.

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