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1
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0029874716
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Preliminary biological results for some of these compounds were presented as part of the 13th Forum in Microbiology
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17
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0026737589
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11. For another example of I-homologated sugars as transferase inhibitors, see: Noort, D.; van Straten, N. C. R.; Boons, G. J. P. H.; van der Marel, G. A.; Bossuyt, X.; Blanckaert, N.; Mulder, G, J.; van boom, J. H. Bioorg. Med. Chem. Lett. 1992, 2, 583.
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18
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0010635752
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note
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4 and concentrated to yield 1.53 g (74%) crude, protected sulfone. This material was deblocked in two steps as for 9 to afford 13a.
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23
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0010543539
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note
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2-6), 4.66 (bs, 1H, OH-6), 4.98 (d, 1H, OH-3), 5.08 (d, 1H, OH-4), 7.65 (m, 2H, H-3′ & H-5′), 7.75 (m, 1H, H-4′), 7.90 (m, 2H, H-2′ & H-6′).
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24
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0000080763
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26
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0010579154
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note
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25
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27
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0010615582
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note
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27
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28
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0010576191
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note
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6 Erdman. Four hours later monolayers were washed to remove extracellular bacteria, then incubated for eight days in the presence of a series of dilutions of 11e. Monolayers were lysed and plated on 7H11 agar for three weeks. A TNF response was also performed.
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30
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0001916119
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Antimycobacterial agents: In vitro susceptibility testing, spectra of activity, mechanisms of resistance, and assays for activity in biological fluids
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Lorian, V., ed.; Williams and Wilkins; Baltimore
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Nash, K.A.2
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31
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0010541394
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In preparation
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23. Reynolds, R. C.; Bansal, N.; Comber, R. N.; Friedrich, J. A.; Rose, J. D.; Suling, W. J.; Maddry, J. A. Ethambutol Derivatives as Putative Inhibitors of Mycobacterial Glycosyltransferases. In preparation.
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Ethambutol Derivatives as Putative Inhibitors of Mycobacterial Glycosyltransferases
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Bansal, N.2
Comber, R.N.3
Friedrich, J.A.4
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Maddry, J.A.7
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32
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0029094682
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