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

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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 μM against reverse NCX. © 2005 Pharmaceutical Society of Japan.

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APA

Kuramochi, T., Kakefuda, A., Yamada, H., Ogiyama, T., Taguchi, T., & Sakamoto, S. (2005). Discovery of N-(3-{4-[(3-fluorobenzyl)oxy]phenoxy}propyl)-2-pyridin-4- ylacetamide as a potent and selective reverse NCX inhibitor. Chemical and Pharmaceutical Bulletin, 53(8), 1043–1047. https://doi.org/10.1248/cpb.53.1043

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