Inhibition of penicillin biosynthesis by δ-(L-α-amino-δ-adipyl)-L-cysteinylglycine. Evidence for initial β-lactam ring formation
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1984/C3/C39840000902
Cited by 26 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Structural Studies on the Reaction of Isopenicillin N Synthase with the Truncated Substrate Analogues δ-(l-α-aminoadipoyl)-l-cysteinyl-glycine and δ-(l-α-aminoadipoyl)-l-cysteinyl-d-alanine,;Biochemistry;2005-04-08
2. Enzymatic Synthesis of Penicillins;Comprehensive Natural Products Chemistry;1999
3. Isopenicilin N synthase: a new mode of reactivity;Tetrahedron;1992-01
4. Isopenicillin N synthase: a new mode of reactivity;Journal of the Chemical Society, Chemical Communications;1991
5. Further evidence for the involvement of a monocyclic β-lactam in the enzymatic conversion of δ-L-α-aminoadipoyl-L-cysteinyl-D-valine into isopenicillin N.;Tetrahedron;1991-01
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