Assessing molecular scaffolds for CNS drug discovery

被引:42
|
作者
Mayol-Llinas, Joan [1 ]
Nelson, Adam [1 ]
Farnaby, William [2 ,3 ]
Ayscough, Andrew [2 ]
机构
[1] Univ Leeds, Sch Chem, Leeds LS2 9JT, W Yorkshire, England
[2] Takeda Cambridge, Unit 418, Cambridge Sci Pk,Milton Rd, Cambridge CB4 0PA, England
[3] Univ Dundee, Sch Life Sci, Biol Chem & Drug Discovery, Dundee DD1 5EH, Scotland
基金
英国工程与自然科学研究理事会;
关键词
DESIGN;
D O I
10.1016/j.drudis.2017.01.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
There is a need for high-quality screening collections that maximise hit rate and minimise the time taken in lead optimisation to derive a candidate drug. Identifying and accessing molecules that meet these criteria is a challenge. Within central nervous system (CNS)-focused drug discovery, this challenge is heightened by the requirement for lead compounds to cross the blood-brain barrier. Herein, we demonstrate use of a multiparameter optimisation tool to prioritise the synthesis of molecular scaffolds that, when subsequently decorated, yield screening compounds with experimentally determined properties that align with CNS lead generation needs. Prospective use of this CNS Lead Multiparameter Optimisation (MPO) scoring protocol can guide the further development of novel synthetic methodologies to access CNS-relevant and lead-like chemical space.
引用
收藏
页码:965 / 969
页数:5
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