Synthesis and biological properties of new 5-nitroindazole derivatives

VJ Arán, C Ochoa, L Boiani, P Buccino… - Bioorganic & medicinal …, 2005 - Elsevier
VJ Arán, C Ochoa, L Boiani, P Buccino, H Cerecetto, A Gerpe, M González, D Montero…
Bioorganic & medicinal chemistry, 2005Elsevier
A series of new 3-alkoxy-or 3-hydroxy-1-[ω-(dialkylamino) alkyl]-5-nitroindazoles have been
synthesized and their trichomonacidal, antichagasic and antineoplastic properties studied.
Five derivatives (5, 6, 8, 9 and 17) showed remarkable trichomonacidal activity against
Trichomonas vaginalis at 10μg/mL concentration. Three compounds (8, 10, 11) exhibited
interesting antichagasic activity and these same compounds moderate antineoplastic activity
against TK-10 and HT-29 cell lines. Unspecific cytotoxicity against macrophages has also …
A series of new 3-alkoxy- or 3-hydroxy-1-[ω-(dialkylamino)alkyl]-5-nitroindazoles have been synthesized and their trichomonacidal, antichagasic and antineoplastic properties studied. Five derivatives (5, 6, 8, 9 and 17) showed remarkable trichomonacidal activity against Trichomonas vaginalis at 10μg/mL concentration. Three compounds (8, 10, 11) exhibited interesting antichagasic activity and these same compounds moderate antineoplastic activity against TK-10 and HT-29 cell lines. Unspecific cytotoxicity against macrophages has also been evaluated and only compounds 9, 10 and 11 resulted cytotoxic at the higher dose evaluated (100μg/mL), loosing cytotoxicity at lower doses. QSAR studies have been carried out. X-ray crystallographic study of compound 8 has been performed.
Elsevier
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