Literature DB >> 16079546

Discovery of N-(3-{4-[(3-fluorobenzyl)oxy]phenoxy}propyl)-2-pyridin-4-ylacetamide as a potent and selective reverse NCX inhibitor.

Takahiro Kuramochi1, Akio Kakefuda, Hiroyoshi Yamada, Takashi Ogiyama, Taku Taguchi, Shuichi Sakamoto.   

Abstract

In the setting of heart failure and myocardial ischemia-reperfusion, the sodium-calcium exchanger (NCX) can lead to calcium overload, which is responsible for contractile dysfunction and arrhythmia. NCX is an attractive target for treatment in heart failure and myocardial ischemia-reperfusion. We have designed and synthesized a series of benzyloxyphenyl derivatives based on compound 3. These derivatives have been evaluated for their inhibitory activity against both the reverse and forward modes of NCX. We have discovered a novel potent and selective reverse NCX inhibitor (12) with an IC50 value of 0.085 microM against reverse NCX.

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Year:  2005        PMID: 16079546     DOI: 10.1248/cpb.53.1043

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Inhibition of beta-cell sodium-calcium exchange enhances glucose-dependent elevations in cytoplasmic calcium and insulin secretion.

Authors:  Kevin S C Hamming; Daniel Soliman; Nicola J Webster; Gavin J Searle; Laura C Matemisz; David A Liknes; Xiao-Qing Dai; Thomas Pulinilkunnil; Michael J Riedel; Jason R B Dyck; Patrick E Macdonald; Peter E Light
Journal:  Diabetes       Date:  2010-04-22       Impact factor: 9.461

  1 in total

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