The 2012 Garrod Lecture: Discovery of antibacterial drugs in the 21st century

被引:63
作者
Chopra, Ian [1 ,2 ]
机构
[1] Univ Leeds, Sch Mol & Cellular Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, Antimicrobial Res Ctr, Leeds LS2 9JT, W Yorkshire, England
基金
英国医学研究理事会;
关键词
Antibiotics; screening; structure-based design; targets; BACTERIAL RNA-POLYMERASE; STRUCTURE-BASED DESIGN; ANTIBIOTIC-RESISTANCE; CELL-WALL; NATURAL-PRODUCTS; GLOBAL NEED; INHIBITORS; CHALLENGES; TARGET; AGENTS;
D O I
10.1093/jac/dks436
中图分类号
R51 [传染病];
学科分类号
100201 [内科学];
摘要
The discovery and development of antibacterial drugs in the twentieth century were major scientific and medical achievements that have had profound benefits for human society. However, in the twenty-first century the widespread global occurrence of bacteria resistant to the antibiotics and synthetic drugs discovered in the previous century threatens to reverse our ability to treat infectious diseases. Although some new drugs are in development they do not adequately cover growing medical needs. Furthermore, these drugs are mostly derivatives of older classes already in use and therefore prone to existing bacterial resistance mechanisms. Thus, new drug classes are urgently needed. Despite investment in antibacterial drug discovery, no new drug class has been discovered in the past 20 years. In this review, based upon my career as a research scientist in the field of antibacterial drug discovery, I consider some of the technical reasons for the recent failure and look to the future developments that may help to reverse the poor current success rate. Diversification of screening libraries to include new natural products will be important as well as ensuring that the promising drug hits arising from structure-based drug design can achieve effective concentrations at their target sites within the bacterial cell.
引用
收藏
页码:496 / 505
页数:10
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