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2. Polyamine derivatives as inhibitors of trypanothione reductase and assessment of their trypanocidal activities. O'Sullivan MC; Zhou Q; Li Z; Durham TB; Rattendi D; Lane S; Bacchi CJ Bioorg Med Chem; 1997 Dec; 5(12):2145-55. PubMed ID: 9459012 [TBL] [Abstract][Full Text] [Related]
3. New spermine and spermidine derivatives as potent inhibitors of Trypanosoma cruzi trypanothione reductase. Bonnet B; Soullez D; Davioud-Charvet E; Landry V; Horvath D; Sergheraert C Bioorg Med Chem; 1997 Jul; 5(7):1249-56. PubMed ID: 9377084 [TBL] [Abstract][Full Text] [Related]
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7. Rationally designed selective inhibitors of trypanothione reductase. Phenothiazines and related tricyclics as lead structures. Benson TJ; McKie JH; Garforth J; Borges A; Fairlamb AH; Douglas KT Biochem J; 1992 Aug; 286 ( Pt 1)(Pt 1):9-11. PubMed ID: 1355650 [TBL] [Abstract][Full Text] [Related]
8. Synthesis and evaluation of substrate analogue inhibitors of trypanothione reductase. Duyzend MH; Clark CT; Simmons SL; Johnson WB; Larson AM; Leconte AM; Wills AW; Ginder-Vogel M; Wilhelm AK; Czechowicz JA; Alberg DG J Enzyme Inhib Med Chem; 2012 Dec; 27(6):784-94. PubMed ID: 22085139 [TBL] [Abstract][Full Text] [Related]
9. Structure-activity relationships in 2-aminodiphenylsulfides against trypanothione reductase from Trypanosoma cruzi. Girault S; Davioud-Charvet E; Salmon L; Berecibar A; Debreu MA; Sergheraert C Bioorg Med Chem Lett; 1998 May; 8(10):1175-80. PubMed ID: 9871730 [TBL] [Abstract][Full Text] [Related]
10. Phenothiazine inhibitors of trypanothione reductase as potential antitrypanosomal and antileishmanial drugs. Chan C; Yin H; Garforth J; McKie JH; Jaouhari R; Speers P; Douglas KT; Rock PJ; Yardley V; Croft SL; Fairlamb AH J Med Chem; 1998 Jan; 41(2):148-56. PubMed ID: 9457238 [TBL] [Abstract][Full Text] [Related]
11. Design, synthesis and biological evaluation of new potent 5-nitrofuryl derivatives as anti-Trypanosoma cruzi agents. Studies of trypanothione binding site of trypanothione reductase as target for rational design. Aguirre G; Cabrera E; Cerecetto H; Di Maio R; González M; Seoane G; Duffaut A; Denicola A; Gil MJ; Martínez-Merino V Eur J Med Chem; 2004 May; 39(5):421-31. PubMed ID: 15110968 [TBL] [Abstract][Full Text] [Related]
12. Crystal structure of Trypanosoma cruzi trypanothione reductase in complex with trypanothione, and the structure-based discovery of new natural product inhibitors. Bond CS; Zhang Y; Berriman M; Cunningham ML; Fairlamb AH; Hunter WN Structure; 1999 Jan; 7(1):81-9. PubMed ID: 10368274 [TBL] [Abstract][Full Text] [Related]
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17. Trypanothione is the primary target for arsenical drugs against African trypanosomes. Fairlamb AH; Henderson GB; Cerami A Proc Natl Acad Sci U S A; 1989 Apr; 86(8):2607-11. PubMed ID: 2704738 [TBL] [Abstract][Full Text] [Related]
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20. Trypanothione reductase from Trypanosoma cruzi. Catalytic properties of the enzyme and inhibition studies with trypanocidal compounds. Jockers-Scherübl MC; Schirmer RH; Krauth-Siegel RL Eur J Biochem; 1989 Mar; 180(2):267-72. PubMed ID: 2647489 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]