CAS NO: | 344458-19-1 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | PJ34 is a potent specific inhibitor ofPARPl/2withIC50of 110 nM and 86 nM, respectively. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | PJ34 inhibits the PARP enzyme activity with an IC50of 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 10-7to 10-5M[1]. | ||||||||||||||||
体内研究 (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]. | ||||||||||||||||
分子量 | 295.34 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H17N3O2 | ||||||||||||||||
CAS 号 | 344458-19-1 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 25 mg/mL(84.65 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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