Bioorganic and medicinal chemistry letters p. 2221 - 2224 (2002)
Update date:2022-08-11
Topics:
Valdez, Juan
Cedillo, Roberto
Hernandez-Campos, Alicia
Yepez, Lilian
Hernandez-Luis, Francisco
Navarrete-Vazquez, Gabriel
Tapia, Amparo
Cortes, Rafael
Hernandez, Manuel
Castillo, Rafael
Compounds 1-18 have been synthesized and tested in vitro against the protozoa Giardia lamblia, Entamoeba histolytica and the helminth Trichinella spiralis. Inhibition of rat brain tubulin polymerization was also measured and compared for each compound. Results indicate that most of the compounds tested were more active as antiprotozoal agents than Metronidazole and Albendazole. None of the compounds was as active as Albendazole against T. spiralis. Although only compounds 3, 9 and 15 (2-methoxycarbonylamino derivatives) inhibited tubulin polymerization, these were not the most potent antiparasitic compounds.
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