Nádasdi L, Medzihradszky K
Peptides. 1983 Mar-Apr;4(2):137-44. doi: 10.1016/0196-9781(83)90103-1.
A steric parameter (Y gamma) has been derived for alpha-amino acids to characterize the steric hindrances near to the alpha-carbon atom. This easily computable variable is suitable for quantitative structure-activity relationship (QSAR) calculations for peptide hormones. Successful multivariate analyses were performed for oxytocin and angiotensin II analogs with the help of parameters describing the lipophilic and steric properties and the measure of dispersion forces. In the case of position 4 substituted oxytocin analogs, the steric, lipophilic and H-bridge forming properties equally account for the different biological activities of the derivatives. In the case of position 5 substituted angiotensin II analogs, primarily the steric parameters account for the biological activity of the series of derivatives.
已为α-氨基酸推导了一个空间参数(Yγ),以表征α-碳原子附近的空间位阻。这个易于计算的变量适用于肽激素的定量构效关系(QSAR)计算。借助描述亲脂性和空间性质以及色散力度量的参数,对催产素和血管紧张素II类似物进行了成功的多变量分析。对于4位取代的催产素类似物,空间、亲脂性和形成氢键的性质同样决定了衍生物的不同生物活性。对于5位取代的血管紧张素II类似物,主要是空间参数决定了该系列衍生物的生物活性。