Geysen H M, Wagner C D, Bodnar W M, Markworth C J, Parke G J, Schoenen F J, Wagner D S, Kinder D S
Glaxo Wellcome, Inc., Research Triangle Park, NC 27709, USA.
Chem Biol. 1996 Aug;3(8):679-88. doi: 10.1016/s1074-5521(96)90136-2.
Combinatorial chemistry using solid-phase synthesis is a rapidly developing technology that can result in a significant reduction in the time required to find and optimize lead compounds. The application of this approach to traditional medicinal chemistry has led to the construction of libraries of small organic molecules on resin beads. A major difficulty in developing large combinatorial libraries is the lack of a facile encoding and decoding methodology to identify active compounds.
Several encoding schemes are described which use the ability of mass spectrometry to ascertain isotopic distributions. Molecular tags are attached to resin beads in parallel or on the linker used for chemical library synthesis. The tags are encoded via a controlled ratio of a number of stable isotopes on the tagging molecules, and range from a single to a complex isotopic distribution.
A novel coding scheme is described that is useful for the generation of large encoded combinatorial libraries. The code can be cleaved after assay and analyzed by mass spectrometry in an automated fashion. An important element of the combinatorial discovery process is the ability to extract the structure-activity relationship (SAR) information made available by library screening. The speed and sensitivity of the mass-encoding scheme has the potential to determine the full SAR for a given library.
采用固相合成的组合化学是一项快速发展的技术,它能够显著减少寻找和优化先导化合物所需的时间。将这种方法应用于传统药物化学已促使在树脂珠上构建小分子有机化合物库。开发大型组合库的一个主要困难在于缺乏一种简便的编码和解码方法来识别活性化合物。
描述了几种利用质谱确定同位素分布能力的编码方案。分子标签并行地或附着于用于化学库合成的连接子上,连接到树脂珠上。标签通过标记分子上多种稳定同位素的可控比例进行编码,范围从单一同位素分布到复杂同位素分布。
描述了一种对生成大型编码组合库有用的新型编码方案。该编码在分析后可被裂解,并以自动化方式通过质谱进行分析。组合发现过程的一个重要要素是能够提取通过库筛选获得的构效关系(SAR)信息。质量编码方案的速度和灵敏度有可能确定给定库的完整SAR。