Bioactivity | JNJ-40255293 is a high-affinity human A 2A receptor antagonist with a KiKi of 7.5 nM. JNJ-40255293 can be used in the research of neurodegenerative diseases such as Parkinson's disease[1]. |
In Vivo | JNJ-40255293 (0.1-10 mg/kg, p.o.) 可以逆转氟哌啶醇 (HY-14538) 诱导的雄性 Balb/c 小鼠僵直症。在雄性 Wistar 大鼠中,JNJ-40255293 也可以剂量依赖性地逆转氟哌啶醇(0.63 mg/kg,皮下注射)诱导的强直性昏厥,增强主动觉醒,显着逆转利血平(HY-N0480)引起的运动活性缺陷[1]。 |
Name | JNJ-40255293 |
CAS | 1147271-25-7 |
Formula | C23H22N4O3 |
Molar Mass | 402.45 |
Transport | Room temperature in continental US; may vary elsewhere. |
Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Reference | [1]. John R Atack, et al. JNJ-40255293, a novel adenosine A2A/A1 antagonist with efficacy in preclinical models of Parkinson's disease. ACS Chem Neurosci. 2014 Oct 15;5(10):1005-19. |