tcsc1462 PJ34 (hydrochloride)

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Product Description

PJ34 hydrochloride is a potent specific inhibitor of PARPl/2 with IC50 of 110 nM and 86 nM, respectively.

IC50 & Target: IC50: 110 nM (PARP1), 86 nM (PARP2)[1]

In Vitro: PJ34 inhibits the PARP enzyme activity with an IC50 of 110±1.9 nM. To compare the neuroprotective properties of other PARP inhibitors in PC12 cells, PJ34 is evaluated using by LDH assay. PJ34 treatment also significantly and concentration dependently attenuates cell death at a concentration ranging from 10-7 to 10-5 M[1].

In Vivo: To compare the potency and efficacy with other PARP inhibitors, PJ34 is evaluated at the doses of 3.2 and 10 mg/kg, respectively. PJ34 at the dose of 3.2 mg/kg significantly reduces cortical damage by 33%; however, 10 mg/kg dosing shows reversed effect (17% reduction)[1]. PJ34 (25 mg/kg) reduces the levels of TNF-α mRNA in ischemic animals by 70% and these values in treated mice do not differ from that of sham or naive animals. Treatment of ischemic mice with PJ34 reduces the level of E-selectin mRNA by 81% and that of ICAM-1 mRNA by 54%, compared to vehicle-treated ischemic mice[2].

Information

CAS No344458-15-7
FormulaC17H18ClN3O2
Clinical Informationclinicalinformation
PathwayEpigenetics
Cell Cycle/DNA Damage
TargetPARP
PARP

Specifications

Purity / Grade>98%
SolubilityH2O : ≥ 6 mg/mL (18.08 mM)
Smilessmiles

Misc Information

Observed Molecular Weight331.8
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