Artificial Macrocycles

被引:24
作者
Abdelraheem, Eman M. M. [1 ,2 ]
Shaabani, Shabnam [1 ]
Domling, Alexander [1 ]
机构
[1] Univ Groningen, Dept Drug Design, A Deusinglaan 1, NL-9713 AV Groningen, Netherlands
[2] Sohag Univ, Dept Chem, Fac Sci, Sohag 82524, Egypt
关键词
macrocycle; multicomponent reaction; bioavailability; convergence; bioactivity; druglike properties; synthetic pathway; property space; BETA-TURN MIMICS; UGI REACTION; MULTICOMPONENT REACTIONS; CONFORMATIONAL MIMICRY; CELL-PERMEABILITY; DRUG DISCOVERY; ONE-POT; PEPTIDE; P53-MDM2; RING;
D O I
10.1055/s-0036-1591975
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Artificial macrocycles recently became popular as a novel research field in drug discovery. As opposed to their natural twins, artificial macrocycles promise to have better control on synthesizability and control over their physicochemical properties resulting in drug like properties. Very few synthetic methods allow for the convergent, fast but diverse access to large macrocycles chemical space. One synthetic technology to access artificial macrocycles with potential biological activity, multicomponent reactions, is reviewed here, with a focus on our own work. We believe that synthetic chemists have to acquaint themselves more with structure and activity to leverage the design aspect of their daily work. 1 Introduction 2 Macrocycle Properties and Receptor Binding 3 Synthetic Approaches towards Artificial Macrocycles Using MCR 4 Design Rules for Membrane Crossing Macrocycles 5 Design Rules for Libraries of Macrocycles 6 Computational Macrocyclic Methods 7 Future View
引用
收藏
页码:1136 / 1151
页数:16
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