Ratni H, Baumann K, Bellotti P, Cook X A, Green L G, Luebbers T, Reutlinger M, Stepan A F, Vifian W
pRED, Pharma Research & Early Development, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd. Grenzacherstrasse 124 4070 Basel Switzerland
RSC Med Chem. 2021 Apr 12;12(5):758-766. doi: 10.1039/d1md00043h. eCollection 2021 May 26.
Phenyl rings are one of the most prevalent structural moieties in active pharmaceutical ingredients, even if they often contribute to poor physico-chemical properties. Herein, we propose the use of a bridged piperidine (BP) moiety as a phenyl bioisostere, which could also be seen as a superior phenyl alternative as it led to strongly improved drug like properties, in terms of solubility and lipophilicity. Additionally, this BP moiety compares favorably to the recently reported saturated phenyl bioisosteres. We applied this concept to our γ-secretase modulator (GSM) project for the potential treatment of Alzheimer's disease delivering clinical candidates.
苯环是活性药物成分中最常见的结构部分之一,即便它们常常导致不良的物理化学性质。在此,我们提出使用桥连哌啶(BP)部分作为苯基生物电子等排体,由于它在溶解度和亲脂性方面带来了显著改善的类药物性质,它也可被视为一种更优的苯基替代物。此外,该BP部分与最近报道的饱和苯基生物电子等排体相比具有优势。我们将这一概念应用于我们的γ-分泌酶调节剂(GSM)项目,用于阿尔茨海默病的潜在治疗并推出临床候选药物。