Design, synthesis, and X-ray crystallographic studies of α-aryl substituted fosmidomycin analogues as inhibitors of mycobacterium tuberculosis 1-deoxy-d-xylulose 5-phosphate reductoisomerase

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作者： Andaloussi, M. ^[1] ; Henriksson, L.M. ^[2] ; Wi?ckowska, A. ^[3] ; Lindh, M. ; Bj?rkelid, C. ; Larsson, A.M. ; Suresh, S. ; Iyer, H. ; Srinivasa, B.R. ; Bergfors, T. ; Unge, T. ; Mowbray, S.L. ; Larhed, M. ; Jones, T.A. ; Karlén, A.

作者单位： Department of Cell and Molecular Biology, Uppsala University, Biomedical Center, SE-751 24 Uppsala, Sweden ^[1] AstraZeneca India Private Limited, Bellary Road, Hebbal, Bangalore 560024, India ^[2] Department of Medicinal Chemistry, Biomedical Center, Uppsala University, SE-751 23 Uppsala, Sweden ^[3]

发布时间 2013-11-20

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Journal of Medicinal Chemistry

2011年54卷14期

4964-4976页

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Design, synthesis, and X-ray crystallographic studies of α-aryl substituted fosmidomycin analogues as inhibitors of mycobacterium tuberculosis 1-deoxy-d-xylulose 5-phosphate reductoisomerase

Journal of Medicinal Chemistry

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Journal of Medicinal Chemistry

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Design, synthesis, and X-ray crystallographic studies of α-aryl substituted fosmidomycin analogues as inhibitors of mycobacterium tuberculosis 1-deoxy-d-xylulose 5-phosphate reductoisomerase

Journal of Medicinal Chemistry

相似文献

Journal of Medicinal Chemistry

相关期刊

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