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A switch in enantiomer preference between mitochondrial F1F0-ATPase chemotypes
Authors:Bisaha Sharon N  Malley Mary F  Pudzianowski Andrew  Monshizadegan Hossain  Wang Paulina  Madsen Cort S  Gougoutas Jack Z  Stein Philip D
Affiliation:Department of Discovery Chemistry, Bristol-Myers Squibb, Pharmaceutical Research Institute, Princeton, NJ 08543-4000, USA.
Abstract:The preferred absolute configuration of two series of F(1)F(0)-ATP synthase inhibitors was determined. Although the configuration of the active enantiomer in each series is different, each series presents the same 'triaryl' pharmacophore to the enzyme binding site.
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