Nisato D, Wagnon J, Callet G, Mettefeu D, Assens J L, Plouzane C, Tonnerre B, Pliska V, Fauchère J L
SANOFI Recherche, Montpellier, France.
J Med Chem. 1987 Dec;30(12):2287-91. doi: 10.1021/jm00395a018.
Free-Wilson and correlation analysis were combined to study a series of 34 pepstatin analogues in which mainly position 2 was varied. A statistically highly significant correlation was found between the inhibitory activity of the analogues on an enriched plasma renin preparation and structural parameters of the amino acid side chain in position 2. The crucial parameters were found to be the NMR chemical shift of the alpha-carbon, the localized electrical (inductive) effect, and the van der Waals radius related steric parameter, which demonstrated the dominating influence of electronic inductive effects compared to steric bulk. The model gives insight into the structural requirements for effective inhibition and suggests the histidine-2 derivative, a positive outlier in this series, as a lead compound for further structure-activity studies.
将Free-Wilson法与相关性分析相结合,对一系列34种胃蛋白酶抑制剂类似物进行研究,其中主要是2位的结构有所变化。在这些类似物对富血浆肾素制剂的抑制活性与2位氨基酸侧链的结构参数之间,发现了具有高度统计学意义的相关性。关键参数为α-碳原子的核磁共振化学位移、局部电学(诱导)效应以及与范德华半径相关的空间参数,这些参数表明与空间位阻相比,电子诱导效应具有主导影响。该模型揭示了有效抑制的结构要求,并提出组氨酸-2衍生物作为该系列中的一个正向离群值,作为进一步构效关系研究的先导化合物。