Novel hydroxamic acid compounds of Formula (I) are disclosed. These hydroxamates inhibit peptide deformylase (PDF), an enzyme present in prokaryotes and are therefore useful as antimicrobials and antibiotics. Methods of synthesis and use of the compounds are also disclosed.
本发明揭示了
化学式(I)的新型羟
肟酸化合物。这些羟
肟酸盐可以抑制肽变形酶(PDF)的活性,该酶存在于原核
生物中,因此可用作抗微
生物和抗生素。本发明还揭示了这些化合物的合成方法和使用方法。