Porter Roger J, Kupferberg Harvey J, Hessie Bettie Jean
Int J Clin Pharmacol Ther. 2015 Jan;53(1):9-12. doi: 10.5414/CP202212.
To determine the efficacy of the Anticonvulsant Screening Program (ASP) of the National Institute of Neurological Disorders and Stroke (NINDS) in identifying new anti-seizure drugs with new mechanisms of action (MOA). The ASP does not itself identify the nature of the MOA, but on further basic investigation, many of these drugs prove eventually to have a wide variety of new and novel MOA.
Data were tabulated from multiple sources, including the ASP and the literature.
Since it was established in 1975, the ASP has contributed to the identification of at least 9 new anti-seizure drugs. The effectiveness of the program was evaluated by ascertaining the number of MOA of the anti-seizure drugs discovered by the ASP screening techniques. Considering the MOA of drugs marketed after 1975 - and the MOA of investigational compounds not yet marketed - the ASP has contributed to the identification of anti-seizure drugs that possess 16 distinctly different MOA.
The ever-evolving screening approach of the ASP has many characteristics of a final common pathway for anti-seizure drug discovery.
确定美国国立神经疾病与中风研究所(NINDS)的抗惊厥药物筛选计划(ASP)在识别具有新作用机制(MOA)的新型抗癫痫药物方面的功效。ASP本身并不能确定作用机制的本质,但在进一步的基础研究中,这些药物中的许多最终被证明具有各种各样新的和新颖的作用机制。
数据来自多个来源,包括ASP和文献,并制成表格。
自1975年成立以来,ASP已助力识别出至少9种新型抗癫痫药物。通过确定ASP筛选技术发现的抗癫痫药物的作用机制数量来评估该计划的有效性。考虑到1975年后上市药物的作用机制以及尚未上市的研究性化合物的作用机制,ASP已助力识别出具有16种明显不同作用机制的抗癫痫药物。
ASP不断发展的筛选方法具有抗癫痫药物发现最终共同途径的许多特征。