Literature DB >> 26818858

The Recent Development of α7 Nicotinic Acetylcholine Receptor (nAChR) Ligands as Therapeutic Candidates for the Treatment of Central Nervous System (CNS) Diseases.

Corinne Beinat, Samuel D Banister, Marco Herrera, Michael Kassiou1.   

Abstract

Homomeric α7 nicotinic acetylcholine receptors (nAChRs) are implicated in the regulation of cognitive processes such as memory and attention and have potential as therapeutic targets for the treatment of the cognitive deficits associated with schizophrenia. Though numerous α7 nAChR agonists have been developed, and several have progressed to clinical trials, these are derived from few common chemotypes. Consequently, many of these α7 nAChR clinical candidates share unfavorable side-effect profile. SEN12333 represents a novel chemotype for the development of α7 nAChR agonists, and exploration of this scaffold has produced structurally diverse ligands with promising pharmacological properties. This review will summarize structure-affinity and -activity relationships surrounding analogs of SEN12333.

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Year:  2016        PMID: 26818858     DOI: 10.2174/1381612822666160127114125

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  1 in total

1.  Brain PET Imaging of α7-nAChR with [18F]ASEM: Reproducibility, Occupancy, Receptor Density, and Changes in Schizophrenia.

Authors:  Dean F Wong; Hiroto Kuwabara; Andrew G Horti; Joshua M Roberts; Ayon Nandi; Nicola Cascella; James Brasic; Elise M Weerts; Kelly Kitzmiller; Jenny A Phan; Lorena Gapasin; Akira Sawa; Heather Valentine; Gary Wand; Chakradhar Mishra; Noble George; Michael McDonald; Wojtek Lesniak; Daniel P Holt; Babak B Azad; Robert F Dannals; William Kem; Robert Freedman; Albert Gjedde
Journal:  Int J Neuropsychopharmacol       Date:  2018-07-01       Impact factor: 5.176

  1 in total

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