Journal article
Synthesis, structure-activity relationships and brain uptake of a novel series of benzopyran inhibitors of insulin-regulated aminopeptidase
SJ Mountford, AL Albiston, WN Charman, L Ng, JK Holien, MW Parker, JA Nicolazzo, PE Thompson, SY Chai
Journal of Medicinal Chemistry | Published : 2014
DOI: 10.1021/jm401540f
Abstract
Peptide inhibitors of insulin-regulated aminopeptidase (IRAP) enhance fear avoidance and spatial memory and accelerate spatial learning in a number of memory paradigms. Using a virtual screening approach, a series of benzopyran compounds was identified that inhibited the catalytic activity of IRAP, ultimately resulting in the identification of potent and specific inhibitors. The present study describes the medicinal chemistry campaign that led to the development of the lead candidate, 3, highlighting the key structural features considered as critical for binding. Furthermore, the in vivo pharmacokinetics and brain uptake of compounds (1 and 3) were assessed in rats and were complemented with..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
This work was supported by grants from the National Health and Medical Research Council of Australia (NHMRC), Neurosciences Victoria, and AJzheimer's Drug Discovery Foundation/Institute for the Study of Aging, USA. Funding was also obtained from the Victorian Government Operational Infrastructure Support Scheme to St. Vincent's Institute. M.W.P. is an NHMRC Senior Principal Research Fellow, S.Y.C. is an NHMRC Senior Research Fellow, and J.K.H. is a joint Cure Cancer/Leukemia Foundation Post-Doctoral Fellow. We acknowledge the contribution of Dr. Keith Watson in the design some of the analogues of 1.