Fragment and Structure-Based Drug Discovery for a Class C GPCR: Discovery of the mGlu<sub>5</sub> Negative Allosteric Modulator HTL14242 (3-Chloro-5-[6-(5-fluoropyridin-2-yl)pyrimidin-4-yl]benzonitrile)
作者:John A. Christopher、Sarah J. Aves、Kirstie A. Bennett、Andrew S. Doré、James C. Errey、Ali Jazayeri、Fiona H. Marshall、Krzysztof Okrasa、Maria J. Serrano-Vega、Benjamin G. Tehan、Giselle R. Wiggin、Miles Congreve
DOI:10.1021/acs.jmedchem.5b00892
日期:2015.8.27
Fragmentscreening of a thermostabilized mGlu5 receptor using a high-concentration radioligand binding assay enabled the identification of moderate affinity, high ligand efficiency (LE) pyrimidine hit 5. Subsequent optimization using structure-based drug discoverymethods led to the selection of 25, HTL14242, as an advanced lead compound for further development. Structures of the stabilized mGlu5 receptor
The disclosures herein relate to novel compounds of formula wherein R
1
, R
2
, R
3
and R
4
and n are defined here, and their use in treating, preventing, ameliorating, controlling or reducing the risk of inflammation, neurological or psychiatric disorders associated with modulating mGlu5 receptor function.
The disclosures herein relate to novel compounds of formula wherein R1, R2, R3 and R4 and n are defined herein, and their use in treating, preventing, ameliorating, controlling or reducing the risk of inflammation, neurological or psychiatric disorders associated with modulating mGlu5 receptor function.
本文公开的内容涉及式中 R1、R2、R3 和 R4 以及 n 在本文中定义的新型化合物,以及它们在治疗、预防、改善、控制或降低与调节 mGlu5 受体功能相关的炎症、神经或精神疾病风险方面的用途。