货号 | 3255/50 |
别名 | N-(5,6-Dihydro-6-oxo-2-phenanthridi |
供应商 | Tocris |
生物活性 | Potent inhibitor of poly(ADP-ribose) polymerase (PARP) (EC50 = 20 nM). ~1000-fold more potent than 3-Aminobenzamide (Cat. No. 0788). Protects primary neuronal cells from oxygen-glucose deprivation in vitro and reduces infarct size following focal cerebral ischemia in vivo. Displays protective effects against cisplatin-induced kidney injury. Also displays activity at Pim-1 and Pim-2 kinases at higher concentrations (IC50 values are 3.7 and 16 μM respectively). |
运输条件 | Blue Ice |
存放说明 | Ambient |
纯度 | >98 % |
计算分子量 | 331.8 |
分子式 | C17H17N3O2.HCl |
可溶性/溶解性 | Soluble to 100 mM in water and to 100 mM in DMSO |
CAS号 | 344458-15-7 |
参考文献 | Antolinet al (2012) Identification of Pim kinases as novel targets for PJ34 with confounding effects in PARP biology. ACS Chem.Biol. 7 1962. PMID: 23025350. Kimet al (2012) Poly(ADP-ribose) polymerase 1 activation is required for cisplatin nephrotoxicity. Kidney Int. 82 193. PMID: 22437413. Gambiet al (2008) Poly(ADPR)polymerase inhibition and apoptosis induction in cDDP-treated human carcinoma cell lines. Biochem.Pharmacol. 75 2356. PMID: 18468580. Abdelkarimet al (2001) Protective effects of PJ34, a novel, potent inhibitor of poly(ADP-ribose) polymerase (PARP) in in vitroandin vivo models of stroke. Int.J.Mol.Med. 7 255. PMID: 11179503. |