{"title":"Hit-to-Lead Medicinal Chemistry","authors":"S. Ward, P. Beswick","doi":"10.1002/3527600906.MCB.201600001","DOIUrl":null,"url":null,"abstract":"Hit-to-Lead medicinal chemistry is the process through which “hits” are converted into “leads.” Fundamental to the process is to gain confidence, first that a hit compound can be developed into a robust (lead) series, and second that the leads have the potential to be converted into drug candidates. Such confidence is gained in a stepwise fashion: initially, hit compounds must have their activity confirmed, and second it must be demonstrated that structural modification of the hit can result in changes in biological activity, thus generating a series. Third, members of the series must pass a series of so-called “developability filters,” thus ensuring that there is a high chance of success in the subsequent phase of lead optimization. The hit-to-lead phase is highly important, as chemists are frequently presented with multiple hits from which to identify a small number of series to take forward. Selection at this point will have a direct impact on the success of lead optimization. \n \n \nKeywords: \n \nhit; \nlead; \nlead optimization; \nfragment; \nligand efficiency","PeriodicalId":268680,"journal":{"name":"Reviews in Cell Biology and Molecular Medicine","volume":"81 7 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reviews in Cell Biology and Molecular Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/3527600906.MCB.201600001","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Hit-to-Lead medicinal chemistry is the process through which “hits” are converted into “leads.” Fundamental to the process is to gain confidence, first that a hit compound can be developed into a robust (lead) series, and second that the leads have the potential to be converted into drug candidates. Such confidence is gained in a stepwise fashion: initially, hit compounds must have their activity confirmed, and second it must be demonstrated that structural modification of the hit can result in changes in biological activity, thus generating a series. Third, members of the series must pass a series of so-called “developability filters,” thus ensuring that there is a high chance of success in the subsequent phase of lead optimization. The hit-to-lead phase is highly important, as chemists are frequently presented with multiple hits from which to identify a small number of series to take forward. Selection at this point will have a direct impact on the success of lead optimization.
Keywords:
hit;
lead;
lead optimization;
fragment;
ligand efficiency