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pubmed-article:14684323pubmed:abstractTextInhibition of the sodium hydrogen exchanger isoform-1 (NHE-1) has been shown to limit damage to the myocardium under ischemic conditions in animals. While most known NHE-1 inhibitors are acylguanidines, this report describes the design and synthesis of a series of heterocyclic inhibitors of NHE-1 including aminoimidazoles with undiminished in vitro activity and oral bioavailability.lld:pubmed
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pubmed-article:14684323pubmed:articleTitleAminoimidazoles as bioisosteres of acylguanidines: novel, potent, selective and orally bioavailable inhibitors of the sodium hydrogen exchanger isoform-1.lld:pubmed
pubmed-article:14684323pubmed:affiliationBristol-Myers Squibb Pharmaceutical Research Institute, PO Box 4000, Princeton, NJ 08543, USA. saleem.ahmad@bms.comlld:pubmed
pubmed-article:14684323pubmed:publicationTypeJournal Articlelld:pubmed
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