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Merck
  • Synthesis of new sugar derivatives and evaluation of their antibacterial activities against Mycobacterium tuberculosis.

Synthesis of new sugar derivatives and evaluation of their antibacterial activities against Mycobacterium tuberculosis.

Bioorganic & medicinal chemistry letters (2009-10-16)
Yasuhiro Horita, Takemasa Takii, Taku Chiba, Ryuji Kuroishi, Yasuhiro Maeda, Yukihisa Kurono, Emi Inagaki, Kenji Nishimura, Yoshifumi Yamamoto, Chiyoji Abe, Masami Mori, Kikuo Onozaki
摘要

A series of sugar derivatives (1-13) were synthesized and evaluated for antibacterial activity against Mycobacteriumtuberculosis (MTB), especially multi-drug resistant (MDR) MTB, and the structure-activity relationships of these compounds were studied. The results showed that the compound OCT313 (2-acetamido-2deoxy-beta-D-glucopyranosyl N,N-dimethyldithiocarbamate) (4) exhibited significant in vitro bactericidal activity, and that the dithiocarbamate group at C-1 position of the glucopyranoside ring was requisite for the antibacterial activity.

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Sigma-Aldrich
利福平, ≥95% (HPLC), powder or crystals
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二甲胺 溶液, 40 wt. % in H2O
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二甲胺 溶液, 2.0 M in THF
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二甲胺 盐酸盐, 99%
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二甲胺, anhydrous, ≥99%
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利福平, suitable for plant cell culture, BioReagent, ≥95% (HPLC), powder or crystals
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二甲胺 溶液, 2.0 M in methanol
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异烟肼, analytical standard, ≥99% (TLC)
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二甲胺 溶液, purum, 33% in absolute ethanol (~5.6 M)
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二甲胺 盐酸盐, purum, ≥98.0% (AT)