Structure-activity dependency of new bacterial tryptophanyl tRNA synthetase inhibitors
作者:David R. Witty、Graham Walker、John H. Bateson、Peter J. O'Hanlon、Robert Cassels
DOI:10.1016/0960-894x(96)00237-5
日期:1996.6
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. Copyright (C) 1996 Elsevier Science Ltd