Design and NMR-Based Screening of LEF, a Library of Chemical Fragments with Different Local Environment of Fluorine

被引:96
作者
Vulpetti, Anna [1 ]
Hommel, Ulrich [1 ]
Landrum, Gregory [1 ]
Lewis, Richard [1 ]
Dalvit, Claudio [1 ,2 ]
机构
[1] Novartis Pharma AG, Novartis Inst Biomed Res, CH-4002 Basel, Switzerland
[2] Italian Inst Technol, I-16163 Genoa, Italy
关键词
LEAD GENERATION; DRUG DISCOVERY; MOLECULAR FRAGMENTS; LIGAND EFFICIENCY; PROTEIN NMR; BINDING; SHIFTS; SPECTROSCOPY; SAR; OPTIMIZATION;
D O I
10.1021/ja905207t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel strategy for the design of a fluorinated fragment library that takes into account the local environment of fluorine is described. The procedure, based on a fluorine fingerprints descriptor, and the criteria used in the design, selection, and construction of the library are presented. The library, named LEF (Local Environment of Fluorine), combined with F-19 NMR ligand-based screening experiments represents an efficient and sensitive approach for the initial fragment identification within a fragment-based drug discovery project and for probing the presence of fluorophilic protein environments. Proper setup of the method, according to described theoretical simulations, allows the detection of very weak-affinity ligands and the detection of multiple ligands present within the same tested mixture, thus capturing all the potential fragments interacting with the receptor. These NMR hits are then used in the FAXS experiments for the fragment optimization process and for the follow-up screening aimed at identifying other chemical scaffolds relevant for the binding to the receptor.
引用
收藏
页码:12949 / 12959
页数:11
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