Arylfurans as potential Trypanosoma cruzi trypanothione reductase inhibitors
Mem. Inst. Oswaldo Cruz
; 101(2): 169-173, Mar. 2006. ilus
Article
in English
| LILACS
| ID: lil-430894
Responsible library:
BR1.1
RESUMO
The natural lignans veraguensin and grandisin have been reported to be active against Trypanosoma cruzi bloodstream forms. Aiming at the total synthesis of these and related compounds, we prepared three 2-arylfurans and eight 2,5-diarylfurans. They were evaluated for their potential as T. cruzi trypanothione reductase (TR) inhibitors as well against the parasite's intracellular (amastigote) and bloodstream (trypomastigote) forms. Compound 12 was the most effective against TR with an IC50 of 48.5 æM while 7 and 14 were active against amastigotes, inhibiting the parasite development by 60 percent at 20 æg/ml (59 and 90 æM, respectively). On the other hand, none of the compounds was significantly active against the parasite bloodstream forms even at 250 æg/ml (0.6-1.5 mM).
Full text:
Available
Collection:
International databases
Database:
LILACS
Main subject:
Trypanocidal Agents
/
Trypanosoma cruzi
/
Enzyme Inhibitors
/
Furans
/
NADH, NADPH Oxidoreductases
Limits:
Animals
Language:
English
Journal:
Mem. Inst. Oswaldo Cruz
Journal subject:
Tropical Medicine
/
Parasitology
Year:
2006
Document type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Fundação Oswaldo Cruz/BR
/
Universidade Federal de Minas Gerais/BR