PJ34 HCl Cas 344458-15-7 PARP Inhibitors
PJ34 HCl PARP Inhibitors Cas 344458-15-7 With Potential Anticancer
| Product name:PJ34 HCl | Purity:98.0% min |
| CAS NO:344458-15-7 | Solubility:H2O : ≥ 6 mg/mL (18.08 mM) |
| Molecular Formula:C17H17ClN2O2 | Package:Package according to customer requirements. |
| Molecular Weight:316.782 | Storage:Store at -20℃ |
PJ-34 is a novel and potent PARP-1 inhibitor with potential anticancer activity. PJ34 has a high affinity for PARP-1 (IC(50) = 20 nM). PJ-34 inhibits PARP-1 expression and ERK phosphorylation in glioma-conditioned brain microvascular endothelial cells. PJ-34 reduces mesenteric vascular injury induced by experimental cardiopulmonary bypass with cardiac arrest. PJ-34 reduce cell inflammation and damage that follow PARP-1 overexpression. PJ-34 negatively modulate proinflammatory commitment of human glioblastoma cells.
PJ34 HCl is an inhibitor of PARP1/2 with IC50 of 110 nM and 86 nM, respectively.
PARP Inhibitors Related Products:
Veliparib hcl; Olaparib; XAV-939; Rucaparib; Talazoparib; A-966492; Niraparib; Pamiparib; WIKI4; G007-LK; AZD2461; Saroglitazar; Veliparib
[1]. Iwashita A, et al. A novel and potent poly(ADP-ribose) polymerase-1 inhibitor, FR247304 (5-chloro-2-[3-(4-phenyl-3,6-dihydro-1(2H)-pyridinyl)propyl]-4(3H)-quinazolinone), attenuates neuronal damage in in vitro and in vivo models of cerebral ischemia. J Ph
[2]. Haddad M, et al. Anti-inflammatory effects of PJ34, a poly(ADP-ribose) polymerase inhibitor, in transient focal cerebral ischemia in mice. Br J Pharmacol. 2006 Sep;149(1):23-30.
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