Am Ende, C.W., S.E. Knudson, N. Liu, J. Childs and T.J. Sullivan et al., 2008. Synthesis and in vitro antimycobacterial activity of b-ring modified diaryl ether inha inhibitors. Bioorg. Med. Chem. Lett., 18: 3029-3033. CrossRef | Bonnac, L., G. Gao, L. Chen, K. Felczak and E.M. Bennett et al., 2007. Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against Enoyl-ACP Reductase (InhA) of Mycobacterium tuberculosis. Bioorg. Med. Chem. Lett., 17: 4588-4591. Direct Link | Kruh, N.A., J.G. Borgaro, B.P. Ruzsicska, H. Xu and P.J. Tonge, 2008. A novel interaction linking the FAS-II and PDIM biosynthetic pathways. J. Biol. Chem., 283: 31719-31725. Direct Link | Li, J., H. Xu and Y. Zhang, 2005. Metallic samarium and iodine promoted facile and efficient syntheses of trisubstituted alkenes from the acetates of baylis–hillman adducts. Tetrahedron Lett., 46: 1931-1934. CrossRef | Ni, S., Y. Pan, P. Wu, Y. Chen, C. Fu and H. Xu, 2004. Analysis of volatile oil from Lygodium japonicum by GC-MS. Chinese Pharmaceutical J., 39: 99-100. Direct Link | Tremblay, L.W., H. Xu and J.S. Blanchard, 2010. Structures of the Michaelis complex (1.2 Å) and the covalent acyl intermediate (2.0 Å) of cefamandole bound in the active sites of the Mycobacterium tuberculosis β-lactamase K73A and E166A mutants. Biochemistry, 49: 9685-9687. Direct Link | Xu, H., S.S. Hegde and J.S. Blanchard, 2011. Reversible Acetylation and Inactivation of Mycobacterium tuberculosis acetyl-CoA synthetase is dependent on cAMP. Biochemistry, 50: 5883-5892. CrossRef | Xu, H., T.J. Sullivan, J. Sekiguchi, T. Kirikae and I. Ojima et al., 2008. Mechanism and inhibition of saFabI, the enoyl reductase from Staphylococcus aureus. Biochemistry, 47: 4228-4236. PubMed | Direct Link |
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