Literature DB >> 9377084

New spermine and spermidine derivatives as potent inhibitors of Trypanosoma cruzi trypanothione reductase.

B Bonnet1, D Soullez, E Davioud-Charvet, V Landry, D Horvath, C Sergheraert.   

Abstract

Several spermine and spermidine derivatives containing 2-amino diphenylsulfide substituents were prepared and tested for their inhibiting effects on Trypanosoma cruzi trypanothione reductase. IC50 values were assessed between 0.3 and 3 microM. Compound 32 (Ki = 0.4 microM) is the most potent TR inhibitor described so far.

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Year:  1997        PMID: 9377084     DOI: 10.1016/s0968-0896(97)00070-9

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  5 in total

Review 1.  Parasite-specific trypanothione reductase as a drug target molecule.

Authors:  R Luise Krauth-Siegel; Oliver Inhoff
Journal:  Parasitol Res       Date:  2003-04-23       Impact factor: 2.289

2.  The regulation of autophagy differentially affects Trypanosoma cruzi metacyclogenesis.

Authors:  María Cristina Vanrell; Antonella Denisse Losinno; Juan Agustín Cueto; Darío Balcazar; Laura Virginia Fraccaroli; Carolina Carrillo; Patricia Silvia Romano
Journal:  PLoS Negl Trop Dis       Date:  2017-11-01

Review 3.  Advances in preclinical approaches to Chagas disease drug discovery.

Authors:  Fernando Villalta; Girish Rachakonda
Journal:  Expert Opin Drug Discov       Date:  2019-08-14       Impact factor: 6.098

4.  Improved tricyclic inhibitors of trypanothione reductase by screening and chemical synthesis.

Authors:  John L Richardson; Isabelle R E Nett; Deuan C Jones; Mohamed H Abdille; Ian H Gilbert; Alan H Fairlamb
Journal:  ChemMedChem       Date:  2009-08       Impact factor: 3.466

Review 5.  Mitochondrial Ca2+ and Reactive Oxygen Species in Trypanosomatids.

Authors:  Roberto Docampo; Aníbal Eugénio Vercesi
Journal:  Antioxid Redox Signal       Date:  2021-09-17       Impact factor: 7.468

  5 in total

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