Literature DB >> 6381100

alpha-Allenyl putrescine, an enzyme-activated irreversible inhibitor of bacterial and mammalian ornithine decarboxylases.

C Danzin, P Casara.   

Abstract

alpha-Allenyl putrescine (5,6-heptadiene-1,4-diamine) was designed as a new potential enzyme-activated irreversible inhibitor of ornithine decarboxylase (ODC). This compound, and more specifically its (R)-enantiomer, produced time-dependent inhibitions of E. coli and rat liver ODC. The inhibitions exhibit saturation kinetics and were not relieved by prolonged dialysis of the inactivated enzyme. Selective inactivation of the two types of ODC by the (R)-enantiomer is in agreement with the stereochemistry reported for ornithine decarboxylation by the enzyme. Kinetic constants of E. coli ODC inactivation by alpha-(R)-allenyl putrescine compare favorably with other irreversible inhibitors of this enzyme.

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Year:  1984        PMID: 6381100     DOI: 10.1016/0014-5793(84)81172-2

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  1 in total

Review 1.  Designing the next generation of proton-exchange membrane fuel cells.

Authors:  Kui Jiao; Jin Xuan; Qing Du; Zhiming Bao; Biao Xie; Bowen Wang; Yan Zhao; Linhao Fan; Huizhi Wang; Zhongjun Hou; Sen Huo; Nigel P Brandon; Yan Yin; Michael D Guiver
Journal:  Nature       Date:  2021-07-14       Impact factor: 49.962

  1 in total

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