Lead-Oriented Synthesis: A New Opportunity for Synthetic Chemistry

被引:337
作者
Nadin, Alan [1 ]
Hattotuwagama, Channa [1 ]
Churcher, Ian [1 ]
机构
[1] GlaxoSmithKline Med Res Ctr, Stevenage SG1 2NY, Herts, England
关键词
drug discovery; lipophilicity; medicinal chemistry; molecular diversity; synthetic methods; DRUG DISCOVERY; COMBINATORIAL LIBRARIES; MOLECULAR-PROPERTIES; MEDICINAL CHEMISTS; ORGANIC-SYNTHESIS; ADMET RULES; DIVERSITY; DESIGN; LIPOPHILICITY; CANDIDATES;
D O I
10.1002/anie.201105840
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The pharmaceutical industry remains solely reliant on synthetic chemistry methodology to prepare compounds for small-molecule drug discovery programmes. The importance of the physicochemical properties of these molecules in determining their success in drug development is now well understood but we present here data suggesting that much synthetic methodology is unintentionally predisposed to producing molecules with poorer drug-like properties. This bias may have ramifications to the early hit- and lead-finding phases of the drug discovery process when larger numbers of compounds from array techniques are prepared. To address this issue we describe for the first time the concept of lead-oriented synthesis and the opportunity for its adoption to increase the range and quality of molecules used to develop new medicines.
引用
收藏
页码:1114 / 1122
页数:9
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