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组合文库方法在癌症研究与药物发现中的应用。

Application of combinatorial library methods in cancer research and drug discovery.

作者信息

Lam K S

机构信息

Arizona Cancer Center, University of Arizona College of Medicine, Tucson 85724, USA.

出版信息

Anticancer Drug Des. 1997 Apr;12(3):145-67.

PMID:9154108
Abstract

Combinatorial chemistry is now considered as one of the most important recent advances in medicinal chemistry. There are five general approaches in combinatorial peptide library methods: biological libraries; spatially addressable parallel solid phase or solution phase libraries; synthetic library methods requiring deconvolution; the 'one-bead one-compound' library method; and synthetic library methods using affinity chromatography selection. Except for the biological library approach, which is limited to peptide libraries with eukaryotic amino acids, all the other four synthetic approaches are applicable to peptide, non-peptide oligomer or small molecule libraries. Although non-peptide or small molecule libraries are generally prepared by a synthetic approach, recent advances in biosynthetic methods using enzymes may enable one to prepare chemical libraries that are otherwise difficult to synthesize chemically. In the 'one-bead one-compound' library method every member of the library is screened in parallel, but the chemical structure of the positive compound-bead has to be determined either directly or via an encoding strategy. A reliable high-throughput biological assay is needed for a successful combinatorial library screen. Solid-phase binding or functional assays as well as solution phase assays have been used successfully in various library methods. There has been enormous progress in the technological advances of molecular biology and the fundamental understanding of the molecular basis of cancer in recent years. By applying combinatorial chemistry and computational chemistry to the many cancer targets that have recently been identified, it is hopeful that more potent, more specific and less toxic anti-cancer agents will be developed in the foreseeable future. In addition to being a great tool for drug discovery, combinatorial chemistry has also proven to be invaluable in basic research. A few specific examples of the applications of combinatorial chemistry in basic cancer research and drug discovery are described in this mini-review.

摘要

组合化学如今被视为药物化学领域近年来最重要的进展之一。组合肽库方法有五种通用途径:生物文库;空间可寻址平行固相或溶液相文库;需要解卷积的合成文库方法;“一珠一化合物”文库方法;以及使用亲和色谱筛选的合成文库方法。除了生物文库方法(该方法仅限于含真核氨基酸的肽库)外,其他四种合成方法均适用于肽、非肽寡聚物或小分子文库。虽然非肽或小分子文库通常通过合成方法制备,但利用酶的生物合成方法的最新进展可能使人们能够制备出其他难以通过化学方法合成的化学文库。在“一珠一化合物”文库方法中,文库的每个成员都并行进行筛选,但阳性化合物珠子的化学结构必须直接确定或通过编码策略来确定。成功进行组合文库筛选需要可靠的高通量生物学检测。固相结合或功能检测以及溶液相检测已在各种文库方法中成功应用。近年来,分子生物学的技术进步以及对癌症分子基础的基本认识取得了巨大进展。通过将组合化学和计算化学应用于最近发现的许多癌症靶点,有望在可预见的未来开发出更有效、更具特异性且毒性更小的抗癌药物。除了作为药物发现的强大工具外,组合化学在基础研究中也已证明具有不可估量的价值。本综述短文介绍了组合化学在基础癌症研究和药物发现中的一些具体应用实例。

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