e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
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
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.