1-C-phosphonomethyl- and 1-C-difluorophosphonomethyl-1,4-imino-l-arabinitols as Galf transferase inhibitors: A comparison

Abstract The convenient preparation of iminopentitol derivatives, based on a 1,4-dideoxy-1,4-imino- l -arabinitol scaffold carrying β-phosphono(difluoromethyl) or β-phosphonomethyl appendages, as Gal f -1P mimics, is reported. The compounds were tested for their ability to inhibit GlfT2, a vital galactofuranosyltransferase involved in the cell wall biosynthesis of mycobacteria. Interestingly, the Gal f -1P mimics lacking a fluorine atom ( 7 and 8 ) were very poor inhibitors, showing less than 20% inhibition of GlfT2, whereas compounds 2 and 3 , which contains a difluoromethylenephosphonate moiety were more potent inhibitors. Compound 3 that is fully deprotected was the most potent showing a significant IC 50 value (0.9 m m ), despite the absence of the diphosphate linkage present in the parent sugar nucleotide. This study paves the way to the synthesis of more complex β-phosphonomethyl-imino- l -arabinitol derivatives as simplified mimics of UDP-α- d -Gal f .