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首页-小分子抑制剂&激动剂-Cell Cycle/DNA Damage-PARP

Request The Product List ofPARP PARP

Cat. No. Product Name Information
PC-42837

INO-1001

PARP inhibitor

INO-1001 is a potent, selective poly(ADP-ribose) polymerase (PARP).
PC-42830

BSI-201

PARP1 inhibitor

BSI-201 (Iniparib, NSC 746045, IND-71677, SAR240550) is a potent, small molecule PARP1 inhibitor with strong anti-neoplastic effect, demonstrates the potential treatment of breast cancer.
PC-62699

AZ9482

PARP inhibitor

AZ9482 is a potent PARP inhibitor with IC50 of 1/1/46/9/160/640 nM for PAPR1/PARP2/PARP3/TNKS1/TNKS2/PAPR6 respectively.
PC-62698

AZ0108

PARP inhibitor

AZ0108 is an orally bioavailable phthalazinone PARP inhibitor with enzyme IC50 of <30/<30/83 nM for PARP1/2/6 respectively.
PC-62410

Gallotannin

PARG inhibitor

Gallotannin (Tannic acid, Gallotannic acid) is a potent PARG (poly(ADP-ribose) glycohydrolase) inhibitor that produces significant reductions in H2O2-induced cell death in cultured murine astrocytes.
PC-61950

Simmiparib

PARP1/2 inhibitor

Simmiparib is a novel potent, orally active PARP1/2 inhibitor with IC50 of 1.75/0.22 nM, inhibits PARP1 >90-fold more potently than the other PARPs (PARP3, TNKS1, TNKS2).
PC-61949

Mefuparib hydrochloride

PARP1/2 inhibitor

Mefuparib hydrochloride is a potent, highly selective, competitive PARP1/2 inhibitor with IC50 of 3.2/1.9 nM, respectively.
PC-61158

PARP14 inhibitor H10

PARP14 inhibitor

PARP14 inhibitor H10 (H10) is a potent, selective, cell-active PARP14 inhibitor with IC50 of 490 nM, with good selectivity over other PARPs (24-fold and 18-fold over PARP1 and TNKS1, respectively).
PC-60483

Pamiparib

PARP1/2 inhibitor

Pamiparib (BGB-290, BGB290) is a highly potent, selective and brain penetrant PARP1/2 inhibitor with IC50 of 0.9 nM and 0.5 nM for PARP1 and PARP2, respectively.
PC-60367

TNKS-IN-41

Tankyrase inhibitor

TNKS-IN-41 is a highly potent and selective tankyrase inhibitor with pIC50 of 8.5 and 8.1 for TNKS1 and TNKS2, respectively.
PC-60021

GeA-69

PARP14 inhibitor

GeA-69 (GeA69) is a potent, selective, allosteric, cell-active PARP14 macrodomain 2 (MD2) inhibitor with Kd of 0.86 uM in ITC assays.
PC-42680

Rucaparib

PARP inhibitor

Rucaparib (AG014699, PF-01367338) is a potent inhibitor of PARP with Ki of 1.4 nM for PARP1 in a cell-free assay, also showing binding affinity to eight other PARP domains.

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