The antimicrobial natural product chuangxinmycin and some synthetic analogues are potent and selective inhibitors of bacterial tryptophanyl tRNA synthetase

…, RL Jarvest, L Mensah, PH Milner, PJ O'Hanlon…

文献索引：Brown, Murray J.; Carter, Paul S.; Fenwick, Ashley E.; Fosberry, Andrew P.; Hamprecht, Dieter W.; Hibbs, Martin J.; Jarvest, Richard L.; Mensah, Lucy; Milner, Peter H.; O'Hanlon, Peter J.; Pope, Andrew J.; Richardson, Christine M.; West, Andrew; Witty, David R. Bioorganic and Medicinal Chemistry Letters, 2002 , vol. 12, # 21 p. 3171 - 3174

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被引用次数: 71

摘要

The antimicrobial natural product chuangxinmycin has been found to be a potent and selective inhibitor of bacterial tryptophanyl tRNA synthetase (WRS). A number of analogues have been synthesised. The interaction with WRS appears to be highly constrained, as only sterically smaller analogues afforded significant inhibition. The only analogue to show inhibition comparable to chuangxinmycin also had antibacterial activity. WRS inhibition ...