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Eur J Med Chem ; 103: 289-301, 2015 Oct 20.
Article in English | MEDLINE | ID: mdl-26363507

ABSTRACT

Alzheimer's disease (AD) is a neurodegenerative disease which has a higher prevalence and incidence in older people. The need for improved AD therapies is unmet. The 5-hydroxytryptamine4 receptor (5-HT4R) partial agonists may be of benefit for both the symptomatic and disease-modifying treatment of cognitive disorders associated with AD. Herein, we report the design, synthesis and SAR of imidazo[1,5-a] pyridine derivatives as 5-HT4R partial agonists. The focused SAR, optimization of ADME properties resulted the discovery of compound 5a as potent, selective, brain penetrant 5-HT4 partial agonist as a lead compound with good ADME properties and efficacy in both symptomatic and disease modifying animal models of cognition.


Subject(s)
Alzheimer Disease/drug therapy , Cognition Disorders/drug therapy , Drug Partial Agonism , Pyridines/chemistry , Pyridines/pharmacology , Receptors, Serotonin, 5-HT4/metabolism , Alzheimer Disease/metabolism , Animals , Cognition Disorders/metabolism , Dogs , Dose-Response Relationship, Drug , Drug Design , Humans , Molecular Structure , Rats , Structure-Activity Relationship
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