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Facing Chirality in the 21st Century: Approaching the Challenges in the Pharmaceutical Industry

机译:面向21世纪的手性:应对制药行业的挑战

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How is process R & D organized and operated in today's phermaceutical industry at the dawn of the 21st century? A way to respond to the challenges with regard to reduced time to market is to build on early involvement and a front-loading approach. This means that activities are initiated during the lead optimization phase starting up to 2 years ahead of candidate drug nomination and a model built on this concept covering the stages through to commercial launch is advocated as the appropriate way forward. However, given the high attrition rate in a pharma R & D pipeline focused risk management needs to be applied and options judiciously evaluated. From a molecular perspective, the chemical targets in many instances present a formidable complexity both with regard to the overall structure but increasingly also when it comes to their stereochemical features. Thus, a novel triazolo pyrimidine compound with six stereogenic centers requiring 28 transformations for its assembly is examined to underscore this, but also the difficulties in designing a feasible route for the relatively simple (S)-azetidinecarboxylic acid are highlighted. Furthermore, the successful development of a unique and highly efficient catalytic asymmetric sulfide oxidation to the corresponding (S)-sulfoxide esomeprazole is discussed, together with the remarkable effect that normal sea sand has on the stereoselectivity of a steroid trans-acetalization.
机译:在21世纪初,当今的机电行业如何进行过程研发的组织和运作?应对缩短上市时间的挑战的一种方法是在早期参与和前瞻性方法的基础上发展。这意味着,活动应在潜在客户最优化阶段开始,直到候选药物提名之前的2年,并且倡导以此概念为基础的模型,涵盖从开发到商业发布的各个阶段,是前进的适当方法。但是,鉴于制药研发管线中的高流失率,需要采用针对性的风险管理,并明智地评估选择方案。从分子的角度看,化学靶在许多情况下不仅在整体结构方面而且在立体化学特征方面也表现出极大的复杂性。因此,研究了具有六个立体异构中心的新颖的三唑并嘧啶化合物,其组装需要28个转化,以强调这一点,但是也突出了在设计相对简单的(S)-氮杂环丁烷羧酸的可行路线方面的困难。此外,还讨论了独特高效的催化不对称硫化物向相应的(S)-亚砜esomeprazole氧化的成功开发,以及普通海砂对类固醇反缩醛化的立体选择性的显着影响。

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