Title of article :
Synthesis of acyclic galactitol- and lyxitol-aminophosphonates as inhibitors of UDP-galactopyranose mutase
Author/Authors :
Pan، نويسنده , , Weidong and Ansiaux، نويسنده , , Christophe and Vincent، نويسنده , , Stéphane P.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2007
Abstract :
UDP-galactopyranose mutase (UGM) catalyzes the isomerization of UDP-galactopyranose (UDP-Galp) into UDP-galactofuranose (UDP-Galf), an essential step of the mycobacterial cell wall biosynthesis. Acyclic alditol-aminophosphonates in the d-galactose and d-lyxose series were designed as mimics of high energy intermediates of the UGM catalyzed isomerization. Interestingly, the d-lyxitol-aminophosphonate displayed better inhibition properties than the d-galactitol-aminophosphonate.
Keywords :
enzymes , Tuberculosis , galactofuranose , Aminophosphonates
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters