Bioorganic and Medicinal Chemistry Letters p. 1375 - 1380 (1996)
Update date:2022-08-04
Topics:
Witty, David R.
Walker, Graham
Bateson, John H.
O'Hanlon, Peter J.
Cassels, Robert
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
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