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Inhibitors of human mitotic kinesin Eg5: characterization of the 4-phenyl-tetrahydroisoquinoline lead series
Authors:Tarby Christine M  Kaltenbach Robert F  Huynh Tram  Pudzianowski Andrew  Shen Henry  Ortega-Nanos Marie  Sheriff Steven  Newitt John A  McDonnell Patricia A  Burford Neil  Fairchild Craig R  Vaccaro Wayne  Chen Zhong  Borzilleri Robert M  Naglich Joseph  Lombardo Louis J  Gottardis Marco  Trainor George L  Roussell Deborah L
Affiliation:Bristol-Myers Squibb Company, Route 206 and Province Line Road, Princeton, NJ 08543, USA. christine.tarby@bms.com
Abstract:In a high-throughput screening effort, a series of tetrahydroisoquinolines was identified as modest inhibitors of human Eg5. A medicinal chemistry optimization effort led to the identification of R-4-(3-hydroxyphenyl)-N,N-7,8-tetramethyl-3,4-dihydroisoquinoline-2(1H)-carboxamide (32a) as a potent inhibitor of human Eg5 (ATPase IC50 104 nM) with good anti-proliferative activity in A2780 cells (IC50 234 nM).
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