GlaxoSmithKline Medicines Research Centre, Gunnels Wood Road, Stevenage, SG1 2NY, UK.
Angew Chem Int Ed Engl. 2012 Jan 27;51(5):1114-22. doi: 10.1002/anie.201105840. Epub 2012 Jan 3.
The pharmaceutical industry remains solely reliant on synthetic chemistry methodology to prepare compounds for small-molecule drug discovery programmes. The importance of the physicochemical properties of these molecules in determining their success in drug development is now well understood but we present here data suggesting that much synthetic methodology is unintentionally predisposed to producing molecules with poorer drug-like properties. This bias may have ramifications to the early hit- and lead-finding phases of the drug discovery process when larger numbers of compounds from array techniques are prepared. To address this issue we describe for the first time the concept of lead-oriented synthesis and the opportunity for its adoption to increase the range and quality of molecules used to develop new medicines.
制药行业仍然仅仅依赖于合成化学方法来为小分子药物发现计划制备化合物。这些分子的物理化学性质对于确定它们在药物开发中的成功至关重要,但我们在这里提供的数据表明,许多合成方法有意无意地倾向于产生具有较差药物性质的分子。当使用阵列技术制备更多数量的化合物时,这种偏见可能会对药物发现过程的早期命中和先导发现阶段产生影响。为了解决这个问题,我们首次描述了导向先导合成的概念及其采用的机会,以增加用于开发新药的分子的范围和质量。