4.5 Article

On drug discovery against infectious diseases and academic medicinal chemistry contributions

期刊

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 18, 期 -, 页码 1355-1378

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.18.141

关键词

antibacterials; frequent hitters; hit to lead chemical library; medicinal chemistry; virtual docking

资金

  1. Region Ile de France [I 06-222/R, I 09-1739/R]

向作者/读者索取更多资源

This perspective paper discusses the challenges medicinal chemists face in drug discovery and emphasizes the importance of academic researchers in addressing these challenges. The paper presents successful examples of drug candidate discoveries and provides suggestions for contributions from academic medicinal chemists. It highlights the need for increased funding support for academic research in drug development.
This perspective is an attempt to document the problems that medicinal chemists are facing in drug discovery. It is also trying to identify relevant/possible, research areas in which academics can have an impact and should thus be the subject of grant calls. Ac-cordingly, it describes how hit discovery happens, how compounds to be screened are selected from available chemicals and the possible reasons for the recurrent paucity of useful/exploitable results reported. This is followed by the successful hit to lead stories leading to recent and original antibacterials which are, or about to be, used in human medicine. Then, illustrated considerations and suggestions are made on the possible inputs of academic medicinal chemists. This starts with the observation that discovering a good hit in the course of a screening campaign still rely on a lot of luck - which is within the reach of academics -, that the hit to lead process requires a lot of chemistry and that if public-private partnerships can be important throughout these stages, they are absolute requirements for clinical trials. Concerning suggestions to improve the current hit success rate, one academic input in organic chemistry would be to identify new and pertinent chemical space, design synthetic accesses to reach these and prepare the corresponding chemical libraries. Concerning hit to lead programs on a given target, if no new hits are available, previously re-ported leads along with new structural data can be pertinent starting points to design, prepare and assay original analogues. In conclusion, this text is an actual plea illustrating that, in many countries, academic research in medicinal chemistry should be more funded, especially in the therapeutic area neglected by the industry. At the least, such funds would provide the intensive to secure series of hopefully relevant chemical entities which appears to often lack when considering the results of academic as well as indus-trial screening campaigns.

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