Dr. Witty et al., STRUCTURE-ACTIVITY DEPENDENCY OF NEW BACTERIAL TRYPTOPHANYL TRANSFER-RNA SYNTHETASE INHIBITORS, Bioorganic & medicinal chemistry letters, 6(12), 1996, pp. 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 inhibitor
y potency is related to steric properties and conformational preferenc
es. Copyright (C) 1996 Elsevier Science Ltd