Disclosed herein is 10-α/β-D-Arabinofuranosylundecenes of general Formula (II) or pharmaceutically acceptable
N salts thereof as anti-mycobacterial agents in vitro; (II) wherein R, R1 and R″ are as defined herein in the specification. The present invention also discloses a simple stereoselective synthesis 10-α/β-D-Arabinofuranosylundecenes of Formula (II) to target enzymes involved in the biosynthesis of cell wall of
Mycobacterium
and thus useful as inhibitors in the
Mycobacterium tuberculosis
drug development.
本文披露了一种通式(II)或其药学上可接受的N盐,作为体外抗分枝杆菌药物的10-α/β-D-阿拉伯
呋喃糖基十一烯类化合物;其中R,R1和R″的定义如本规范中所述。本发明还披露了一种简单的立体选择性合成方法,用于制备通式(II)的10-α/β-D-阿拉伯
呋喃糖基十一烯类化合物,以靶向参与分枝杆菌细胞壁
生物合成的酶,并因此在结核分枝杆菌药物开发中作为
抑制剂有用。