Arietis Corp, Boston, MA 02118, United States.
Curr Opin Microbiol. 2011 Oct;14(5):550-5. doi: 10.1016/j.mib.2011.07.026. Epub 2011 Aug 11.
The β-lactams have been among the most successful classes of antibacterial agents for the past half century. However, a disturbing increase in resistance to β-lactams has been noted among Gram-negative bacteria, which is attributable to β-lactamase enzymes not within the spectrum of currently marketed β-lactams or β-lactam/β-lactamase inhibitor combinations. Diazabicyclooctanes (DBOs) were first investigated as β-lactam mimics in the mid-1990s by chemists at Hoechst Marion Roussel (now part of Sanofi-Aventis) and proved to be a rich source of β-lactamase inhibitors (BLI). Two members of this novel series of highly potent, broad spectrum BLIs are now in clinical development and their properties are reviewed here.
β-内酰胺类抗生素在过去半个世纪以来一直是最成功的抗菌药物类别之一。然而,革兰氏阴性菌对β-内酰胺类抗生素的耐药性令人担忧,这归因于β-内酰胺酶不在目前市售的β-内酰胺类抗生素或β-内酰胺/β-内酰胺酶抑制剂组合的范围内。二氮杂双环辛烷(DBO)于 20 世纪 90 年代中期首次由 Hoechst Marion Roussel(现为 Sanofi-Aventis 的一部分)的化学家作为β-内酰胺模拟物进行研究,结果证明是β-内酰胺酶抑制剂(BLI)的丰富来源。该新型高活性、广谱 BLIs 系列中有两个成员目前正在临床开发中,本文对其特性进行了综述。