Synthesis of N-benzyloxycarbonyl-l-cysteinylglycine 3-dimethylaminopropylamide disulfide: A cheap and convenient new assay for trypanothione reductase

Abdussalam El-Waer, Kenneth T. Douglas, Keith Smith, Alan H. Fairlamb

    Research output: Contribution to journalArticlepeer-review

    44 Citations (Scopus)

    Abstract

    Trypanothione disulfide [N1,N8-bis(glutathionyl)-spermidine], the physiological substrate for the chemotherapeutic target enzyme trypanothione reductase, is difficult to isolate, expensive to buy, and awkward to synthesize. Here we describe the straightforward synthesis of N,N′-bis(benzyloxycarbonyl)-l-cysteinylglycyl-3-dimethylaminopropylamide disulfide, which is shown to be a good alternative substrate for the trypanothione reductases from Crithidia fasciculata and Trypanosoma cruzi.

    Original languageEnglish
    Pages (from-to)212-216
    Number of pages5
    JournalAnalytical Biochemistry
    Volume198
    Issue number1
    DOIs
    Publication statusPublished - Oct 1991

    ASJC Scopus subject areas

    • Biophysics
    • Biochemistry
    • Molecular Biology
    • Cell Biology

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