申请人:——
公开号:US20020115863A1
公开(公告)日:2002-08-22
Novel hydroxamic acid compounds are disclosed. These hydroxamates inhibit peptidyl deformylase (PDF), an enzyme present in prokaryotes. The hydroxymates are useful as antimicrobials and antibiotics. The compounds of the invention display selective inhibition of peptidyl deformylase versus other metalloproteinases such as matrix metalloproteinases (MMPs). Methods of synthesis and of use of the compounds are also disclosed.
揭示了一种新型羟羧酸化合物。这些羟羧酸酯抑制肽变形酶(PDF),这是一种存在于原核生物中的酶。这些羟羧酸酯可用作抗微生物和抗生素。该发明的化合物表现出对肽变形酶的选择性抑制,而不影响其他金属蛋白酶如基质金属蛋白酶(MMPs)。该文还揭示了这些化合物的合成方法和使用方法。