A series of hydrolytically-stable aza analogs of arabinofuranose was p
repared and evaluated against Mycobacterium tuberculosis and M avium.
The compounds were designed to mimic the putative arabinose donor invo
lved in biogenesis of the essential cell wall polysaccharide, arabinog
alactan. Though most compounds displayed little activity in cell cultu
re, one compound showed significant activity in infected macrophage mo
dels. (C) 1998 Elsevier Science Ltd. All rights reserved.