Different cell death pathways induced by drugs in Trypanosoma cruzi: an ultrastructural study.
Menna-Barreto, Rubem F S; Salomão, Kelly; Dantas, Andréia P; Santa-Rita, Ricardo M; Soares, Maurilio J; Barbosa, Helene S; de Castro, Solange L.
; 40(2): 157-68, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18849169
New imidazolidine derivatives as anti-Trypanosoma cruzi agents: structure-activity relationships.
TrypanocidalActivity of Natural Sesquiterpenoids Involves Mitochondrial Dysfunction, ROS Production and Autophagic Phenotype in Trypanosomacruzi.
Quantitative Structure-Activity Relationships for Structurally Diverse Chemotypes Having Anti-<i>Trypanosoma cruzi</i> Activity.
Antiparasitic evaluation of betulinic acid derivatives reveals effective and selective anti-Trypanosoma cruzi inhibitors.
Physalins B and F, seco-steroids isolated from Physalis angulata L., strongly inhibit proliferation, ultrastructure and infectivity of Trypanosoma cruzi.
Initial studies on mechanism of action and cell death of active N-oxide-containing heterocycles in Trypanosoma cruzi epimastigotes in vitro.
In vitro activities of adamantylidene-substituted alkylphosphocholine TCAN26 against Trypanosoma cruzi: Antiproliferative and ultrastructural effects.
In vitro and in vivo activity of the chloroaryl-substituted imidazole viniconazole against Trypanosoma cruzi.
Synthesis of Xylitan Derivatives and Preliminary Evaluation of in Vitro Trypanocidal Activity.
Biological factors that impinge on Chagas disease drug development.