Synthesis of analogues of the O-β-D-Ribofuranosyl nucleoside moiety of liposidomycins. Part 2: Role of the hydroxyl groups upon the inhibition of MraY

Bioorganic and Medicinal Chemistry Letters

Volumn 11, Issue 4, 2001, Pages 533-536

  Dini, C ^a   Drochon, N ^a   Guillot, J C ^a   Mauvais, P ^a   Walter, P ^a   Aszodi, J ^a  

^a SANOFI   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIINFECTIVE AGENT; BACTERIAL ENZYME; CARRIER PROTEIN; ENZYME INHIBITOR; HYDROXYL GROUP; LIPOSIDOMYCIN; O BETA DEXTRO RIBOFURANOSYLNUCLEOSIDE; UNCLASSIFIED DRUG;

ARTICLE; DRUG ACTIVITY; DRUG STRUCTURE; ENZYME INHIBITION; NONHUMAN; PARTIAL DRUG SYNTHESIS;

AMINOGLYCOSIDES; ANTI-BACTERIAL AGENTS; BACTERIAL PROTEINS; STRUCTURE-ACTIVITY RELATIONSHIP; TRANSFERASES;

EID: 0035952292     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(00)00714-9     Document Type: Article

References (13)