Discovery of Potent Positive Allosteric Modulators of the α3β2 Nicotinic Acetylcholine Receptor by a Chemical Space Walk in ChEMBL

被引:18
作者
Buergi, Justus J. [1 ]
Awale, Mahendra [1 ]
Boss, Silvan D. [1 ]
Schaer, Tifany [2 ]
Marger, Fabrice [2 ]
Viveros-Paredes, Juan M. [3 ]
Bertrand, Sonia [2 ]
Gertsch, Juerg [4 ]
Bertrand, Daniel [2 ]
Reymond, Jean-Louis [1 ]
机构
[1] Univ Bern, NCCR TransCure, Dept Chem & Biochem, CH-3012 Bern, Switzerland
[2] HiQScreen, CH-1222 Geneva, Switzerland
[3] Univ Guadalajara, Dept Farmacobiol CUCEI, Guadalajara 44430, Jalisco, Mexico
[4] Univ Bern, Inst Biochem & Mol Med, CH-3012 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
MOLECULAR QUANTUM NUMBERS; UNIVERSE DATABASE GDB-17; ORGANIC SMALL MOLECULES; DRUG DISCOVERY; VISUALIZATION; AGONISTS; PUBCHEM; DESIGN; SYSTEM; ART;
D O I
10.1021/cn4002297
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While a plethora of ligands are known for the well studied alpha 7 and alpha 4 beta 2 nicotinic acetylcholine receptor (nAChR), only very few ligands address the related alpha 3 beta 2 nAChR expressed in the central nervous system and at the neuromuscular junction. Starting with the public database ChEMBL organized in the chemical space of Molecular Quantum Numbers (MQN, a series of 42 integer value descriptors of molecular structure), a visual survey of nearest neighbors of the alpha 7 nAChR partial agonist N-(3R)-1-azabicyclo[2.2.2] oct-3-yl-4-chlorobenzamide (PNU-282,987) pointed to N-(2-halobenzyl)-3-aminoquinuclidines as possible nAChR modulators. This simple "chemical space walk" was performed using a web-browser available at www.gdb.unibe. ch. Electrophysiological recordings revealed that these ligands represent a new and to date most potent class of positive allosteric significant effects in vivo. The present discovery highlights the value within public databases to uncover new pharmacology. modulators (PAMs) of the alpha 3 beta 2 nAChR, which also exert of surveying chemical space neighbors of known drugs within public databases to uncover new pharmacology. [GRAPHIS]
引用
收藏
页码:346 / 359
页数:14
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