Krchnák V, Weichsel A S, Cabel D, Lebl M
Selectide Corporation, Tucson, AZ, USA.
Pept Res. 1995 Jul-Aug;8(4):198-205.
A synthetic library that presents potential pharmacophores in a linear fashion with variable spacing was designed (alpha, beta, gamma-library). To prove the concept, we synthesized a number of individual compounds as well as a model library. Diamino acids connected by amide bonds via their alpha- or side-chain amino groups were used to form the backbone (scaffold) of this library. The remaining amino group of the diamino acids were acylated by a variety of carboxylic acids, generating an appreciable diversity of compounds in this library. The compositions of compounds in the library were identified by reading a peptide tag synthesized concurrently with the library structures. This code contained the information regarding the carboxylic acid coupled, and the diamino acid and amino group to which the acid was coupled.
设计了一个以线性方式呈现具有可变间距的潜在药效团的合成文库(α、β、γ文库)。为了验证这一概念,我们合成了许多单个化合物以及一个模型文库。通过酰胺键经由其α-或侧链氨基连接的二氨基酸用于形成该文库的主链(支架)。二氨基酸的剩余氨基被多种羧酸酰化,从而在该文库中产生了相当多的化合物多样性。通过读取与文库结构同时合成的肽标签来鉴定文库中化合物的组成。该编码包含有关偶联的羧酸以及该酸所偶联的二氨基酸和氨基的信息。