Title of article
Synthesis of analogues of the O-β- -Ribofuranosyl Nucleoside Moiety of Liposidomycins. Part 1: contribution of the amino group and the Uracil Moiety upon the inhibition of MraY
Author/Authors
C. Dini، نويسنده , , N. Drochon، نويسنده , , S. Feteanu، نويسنده , , J. C. Guillot، نويسنده , , C. Peixoto، نويسنده , , J. Aszodi، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2001
Pages
3
From page
529
To page
531
Abstract
The O-β- -ribofuranosyl nucleoside I is the minimal structural entity of liposidomycins maintaining enzyme inhibitory activity. Modifications performed on both the primary amine and the uracil moieties clearly demonstrate their major contribution to the inhibition of the bacterial translocase (MraY).
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
2001
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
800387
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