1001671-08-4Relevant academic research and scientific papers
Towards new MraY inhibitors: A serine template for uracil and 5-amino-5-deoxyribosyl scaffolding
Le Corre, Laurent,Gravier-Pelletier, Christine,Le Merrer, Yves
, p. 5386 - 5394 (2007)
The bacterial translocase MraY is a good target for the development of new antitbiotics as it is ubiquitous and essential for bacterial growth. The goal of this work was the synthesis of simplified analogues of naturally occurring inhibitors of this enzyme to investigate the essential character of the uridine moiety of these inhibitors with regards to biological activity. Thus, the structure of the targeted enantiomerically pure N-(uracilylpentyl)-β-D-O- (5-amino-5-deoxyribosyl)-L-serine retains uracil and 5-amino-5-deoxyribose parts linked by a serinyl template. The synthetic strategy towards this compound relies on sequential O-glycosylation and N-alkylation by reductive amination of a serine derivative. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
