| Literature DB >> 26363507 |
Ramakrishna Nirogi1, Abdul Rasheed Mohammed2, Anil K Shinde2, Narsimha Bogaraju2, Shankar Reddy Gagginapalli2, Srinivasa Rao Ravella2, Laxman Kota2, Gopinadh Bhyrapuneni2, Nageswara Rao Muddana2, Vijay Benade2, Raghava Chowdary Palacharla2, Pradeep Jayarajan2, Ramkumar Subramanian2, Vinod Kumar Goyal2.
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.Entities:
Keywords: 5-HT(4) receptor; Alzheimer's disease; Cognitive impairment; Disease modifying; Imidazo[1,5-a]pyridines; sAPPα
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Year: 2015 PMID: 26363507 DOI: 10.1016/j.ejmech.2015.08.051
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514