Structure-activity dependency of new bacterial tryptophanyl tRNA synthetase inhibitors

…, G Walker, JH Bateson, PJ O'Hanlon, R Cassels

Index: Witty, David R.; Walker, Graham; Bateson, John H.; O'Hanlon, Peter J.; Cassels, Robert Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 12 p. 1375 - 1380

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Citation Number: 12

Abstract

Analogues of the aminoacyl tRNA synthetase inhibitor, indolmycin, have been synthesised in which the side chain methyl group is replaced by a wide range of substituents. Their antibacterial and enzyme inhibitory potency is related to steric properties and conformational preferences.