Reversible acylation of elastase by gamma-lactam analogues of beta-lactam inhibitors
The reaction of a monocyclic γ-lactam with the serine protease elastase occurs via reversible formation of a hydrolytically labile acyl-enzyme complex; in contrast analogous β-lactam inhibitors irreversibly react to form a relatively stable acyl-enzyme complex.
Asıl Yazarlar: | Westwood, N, Claridge, T, Edwards, P, Schofield, C |
---|---|
Materyal Türü: | Journal article |
Dil: | English |
Baskı/Yayın Bilgisi: |
1997
|
Benzer Materyaller
-
Inhibition of elastase by N-sulfonylaryl beta-lactams: anatomy of a stable acyl-enzyme complex.
Yazar:: Wilmouth, R, ve diğerleri
Baskı/Yayın Bilgisi: (1998) -
Synthesis of delta-lactam (2-oxopiperazine) inhibitors of elastase
Yazar:: Seibel, J, ve diğerleri
Baskı/Yayın Bilgisi: (2005) -
Synthesis and evaluation of delta-lactams (piperazones) as elastase inhibitors.
Yazar:: Seibel, J, ve diğerleri
Baskı/Yayın Bilgisi: (2003) -
'pH-jump' crystallographic analyses of gamma-lactam-porcine pancreatic elastase complexes.
Yazar:: Wright, P, ve diğerleri
Baskı/Yayın Bilgisi: (2000) -
γ-Lactam analogues of carbapenicillanic acids
Yazar:: Baldwin, J, ve diğerleri
Baskı/Yayın Bilgisi: (1986)