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

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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

Fingerprint

Dive into the research topics of 'Synthesis of N-benzyloxycarbonyl-l-cysteinylglycine 3-dimethylaminopropylamide disulfide: A cheap and convenient new assay for trypanothione reductase'. Together they form a unique fingerprint.

Cite this