Brown M L, Brown G B, Brouillette W J
Department of Chemistry, University of Alabama at Birmingham 35294, USA.
J Med Chem. 1997 Feb 14;40(4):602-7. doi: 10.1021/jm960692v.
Binding to the neuronal voltage-dependent sodium channel (NVSC) was evaluated for 12 5-phenylhydantoins which systematically varied either log P and/or 5-phenyl ring orientation. The linear correlation of log P with in vitro sodium channel binding activity (log IC50) for hydantoins 1-12 and diphenylhydantoin (DPH) (r2 = 0.638) suggested that simple partitioning into the lipid phase is important but not sufficient to account for the effects of hydantoins on the NVSC. Comparisons among different hydantoins with the same log P but different low-energy phenyl ring orientations revealed that, in addition to log P, the correct 5-phenyl orientation is important for efficient binding.
对12种5-苯基乙内酰脲进行了与神经元电压依赖性钠通道(NVSC)结合的评估,这些5-苯基乙内酰脲的log P和/或5-苯基环取向有系统地变化。对于乙内酰脲1-12和二苯乙内酰脲(DPH),log P与体外钠通道结合活性(log IC50)的线性相关性(r2 = 0.638)表明,简单地分配到脂质相中很重要,但不足以解释乙内酰脲对NVSC的影响。对具有相同log P但不同低能苯基环取向的不同乙内酰脲进行比较发现,除log P外,正确的5-苯基取向对于有效结合也很重要。