Yu Zhen, Cowan James A
Department of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, OH, 43210, USA.
Chemistry. 2017 Oct 12;23(57):14113-14127. doi: 10.1002/chem.201701714. Epub 2017 Aug 21.
Metal complexes that catalyze inactivation and degradation of biomolecular targets can be developed into novel therapeutics (catalytic metallodrugs) against a variety of diseases. Despite recent advances in the field, a lack of substrate selectivity is a major hindrance to the development of catalytic metallodrugs for application in clinical practice. Improved targeting can minimize nonselective activity and the potential for side effects. Herein, we focus on recent developments toward novel metal catalysts that exhibit substrate selectivity against a variety of therapeutically relevant biomolecules. Design strategies for developing selective catalytic metallodrugs are also highlighted.
能够催化生物分子靶点失活和降解的金属配合物可被开发成针对多种疾病的新型治疗药物(催化金属药物)。尽管该领域最近取得了进展,但缺乏底物选择性仍是催化金属药物应用于临床实践发展的主要障碍。改进靶向性可将非选择性活性和副作用的可能性降至最低。在此,我们重点关注针对多种治疗相关生物分子表现出底物选择性的新型金属催化剂的最新进展。还强调了开发选择性催化金属药物的设计策略。