Literature DB >> 6120232

Inhibition of inosinic acid dehydrogenase by 8-substituted purine nucleotides.

E B Skibo, R B Meyer.   

Abstract

A series of 8-substituted derivatives of adenosine monophosphate (AMP) and inosine monophosphate (IMP) were synthesized and examined for their ability to inhibit Escherichia coli IMP dehydrogenase. All compounds studied were competitive inhibitors in IMP-dependent competition studies and lacked substrate activity. In oxidized nicotinamide adenine dinucleotide dependent studies, 8-(p-NO2PhCH2S)-IMP was noncompetitive and 8-(p-NO2PhCH2S)-AMP showed mixed inhibition. Multiple regression analysis showed that for the series of 8-(para-substituted-benzylthio)-AMPs and -IMPs, the electron-withdrawing ability of the para substituent on the benzylthio moiety correlated best with log Ki of the analogues.

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Year:  1981        PMID: 6120232     DOI: 10.1021/jm00142a007

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

Review 1.  IMP dehydrogenase: structure, mechanism, and inhibition.

Authors:  Lizbeth Hedstrom
Journal:  Chem Rev       Date:  2009-07       Impact factor: 60.622

2.  Synthesis and anti-Hantaan virus activity of N(1)-3-fluorophenyl-inosine.

Authors:  Dong-Hoon Chung; J Jacob Strouse; Yanjie Sun; Jeffrey B Arterburn; William B Parker; Colleen B Jonsson
Journal:  Antiviral Res       Date:  2009-04-02       Impact factor: 5.970

  2 in total

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