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DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF 3-[4-(7-CHLORO-QUINOLIN-4-YL)-PIPERAZIN-1-YL]-PROPIONIC ACID HYDRAZONES AS ANTIPROTOZOAL AGENTS.
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Abstract
N-Acylhydrazones derived from 7-chloro-4-piperazin-1-yl-quinoline were synthesized and biologically
evaluated for blood-stage of Plasmodium falciparum and Entamoeba histolytica trophozoites. N-Acylhydrazone
F12 was found to inhibit the P. falciparum growth as well as its life cycle with good selectivity,
which was achieved by inhibiting hematin formation. Compound F24 showed better IC50 value than the
amoebicidal drug metronidazole
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