Home   >  
Cell Cycle/DNA Damage
  • Epigenetics
∨
  >  
PARP

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

PARP

Chemical Structure Cat. No. Product Name CAS No.
MSC2504877 Chemical Structure
 BCP48087 MSC2504877 1460286-21-8
MSC2504877 is a novel tankyrase inhibitor, enhancing the effects of clinical cdk4/6 inhibitors.
RBN3143 Chemical Structure
 BCP47990 RBN3143 RBN3143
RBN-3143 is a PARP-14 inhibitor. PARP14 is over-expressed in tissues with inflammatory diseases.
E7016 Chemical Structure
 BCP46932 E7016 902128-92-1
E7016 is an inhibitor of the nuclear enzyme poly(ADP-ribose) polymerase (PARP) with potential chemo- and/or radiosensitizing activity. PARP inhibitor E7016 selectively binds to PARP and prevents PARP mediated DNA repair of single strand DNA breaks via the base-excision repair pathway.
EB 47 Chemical Structure
 BCP46739 EB 47 366454-36-6
EB 47 is a potent inhibitor of poly(ADP-ribose) polymerase-1 (PARP-1).
KSQ-4279 Chemical Structure
 BCP46572 KSQ-4279 2446480-97-1
KSQ-4279 is a USP1 and PARP inhibitor.
Senaparib Chemical Structure
 BCP44003 Senaparib 1401682-78-7
Senaparib is an orally bioavailable inhibitor of the nuclear enzymes poly (ADP-ribose) polymerase (PARP) 1 and 2, with potential antineoplastic activity.
NVP-TNKS656 Chemical Structure
 BCP28685 NVP-TNKS656 1419949-20-4
NVP-TNKS656 is a highly potent, selective, and orally active TNKS2 inhibitor with IC50 of 6 nM, and is > 300 fold selectivity against PARP1 and PARP2.
Venadaparib Chemical Structure
 BCP42946 Venadaparib 1681017-83-3
Venadaparib is an antineoplastic.Venadaparib is a potent, selective and orally active PARP inhibitor with IC50s of 1.4 nM and 1.0 nM for PARP1 and PARP2, respectively.
RBN012759 Chemical Structure
 BCP42877 RBN012759 2360851-29-0
RBN012759 is a potent and selective inhibitor of PARP14 with IC50 of <3 nM and 5 nM for human catalytic domain and mouse catalytic domain, respectively. RBN012759 contributes to anti-tumor immune response.
AZD-5305 Chemical Structure
 BCP41765 AZD-5305 2589531-76-8
AZD5305 is a potent and oral active, second-generation PARP (highly selective PARP1) inhibitor.
123下一页末页共 58 条记录 1 / 6 页 
0086-13720134139