Synthesis of methyl 5-S-alkyl-5-thio-d-arabinofuranosides and evaluation of their antimycobacterial activity

The emergence of drug resistant tuberculosis necessitates a search for new antimycobacterial compounds. The antigen 85 (ag85) complex is a family of mycolyl transferases involved in the synthesis of trehalose-6,6′-dimycolate and the mycolated hexasaccharide motif found at the terminus of the arabinogalactan in mycobacterium. Enzymes involved in the synthesis of cell wall structures like these are potential targets for the development of new antiinfectives. To potentially inhibit the ag85 complex, methyl 5-S-alkyl-5-thio-arabinofuranoside analogues were designed based on docking studies with ag85C derived from Mycobacterium tuberculosis. The target arabinofuranosides were then synthesized and the antibacterial activity evaluated against Mycobacterium smegmatis ATCC 14468. Two of the compounds, 5-S-octyl-5-thio-α-d-arabinofuranoside (8) and 5-S-octyl-5-thio-β-d-arabinofuranoside (11), showed MICs of 256 and 512 μg/mL, respectively. Attempts to directly evaluate acyltransferase inhibitory activity of the arabinofuranosides against ag85C are also described. In conclusion, a new class of antimycobacterial arabinofuranosides has been discovered.

Methyl 5-S-alkyl-5-thio-d-arabinofuranosides were synthesized as potential inhibitors of mycobacterial antigen 85 complex. The most potent compounds 8 and 11 showed MICs of 256 and 512 μg/mL, respectively, against Mycobacterium smegmatis ATCC 14468.Figure optionsDownload as PowerPoint slide