The search for potential inhibitors that target so far unexplored bacterial enzyme mono-N-succinyl-L,Ldiaminopimelic acid desuccinylase (DapE) has stimulated a development of methodology for quick and efficient preparation of mono-N-acylated 2,6-diaminopimelic acid (DAP) derivatives bearing the different carboxyl groups or lipophilic moieties on their amino group.
对尚未被广泛探索的细菌酶单-N-琥珀酰-L,L-二
氨基
庚二酸去琥珀酰酶(DAPE)潜在
抑制剂的搜索,促进了快速高效制备具有不同羧基或疏
水基团的单-N-酰基-
2,6-二氨基庚二酸(DAP)衍
生物的方法发展。