Page Michael I
Department of Chemical and Biological Sciences, University of Huddersfield, Queensgate, Huddersfield HD1 3DH, UK.
Acc Chem Res. 2004 May;37(5):297-303. doi: 10.1021/ar0200899.
beta-Sultams are reactive sulfonyl analogues of beta-lactams and show enormous rate enhancements over analogous reactions of sulfonamides. N-Acyl beta-sultams undergo S-N rather than C-N fission, although alpha-alkenyl substituents direct nucleophilic attack to the acyl center. They also inactivate serine enzymes such as elastase and beta-lactamase by sulfonylation of the active site serine. Structure-activity relationships are used to identify differences in transition state structures.
β-磺内酰胺是β-内酰胺的活性磺酰类似物,与磺酰胺的类似反应相比,反应速率有极大提高。N-酰基β-磺内酰胺发生S-N而非C-N裂解,尽管α-烯基取代基会引导亲核进攻酰基中心。它们还通过使活性位点丝氨酸磺酰化来使弹性蛋白酶和β-内酰胺酶等丝氨酸酶失活。结构-活性关系用于识别过渡态结构的差异。