Oligopeptide-like derivatives structurally related to the antitumor agent tallimustine, where one or two pyrrole rings were replaced by pyrazole or thiazole rings and beating benzoyl nitrogen mustard or bromoacryloyl moieties were synthesized and evaluated in vitro and in vivo against L1210 murine leukemia. Compounds 9 and 12 showed antitumor activity higher than or comparable with that of tallimustine.

Structure-activity relationship of novel tallimustine derivatives: Synthesis and antitumor activity

BARALDI, Pier Giovanni;CACCIARI, Barbara;ROMAGNOLI, Romeo;
1996

Abstract

Oligopeptide-like derivatives structurally related to the antitumor agent tallimustine, where one or two pyrrole rings were replaced by pyrazole or thiazole rings and beating benzoyl nitrogen mustard or bromoacryloyl moieties were synthesized and evaluated in vitro and in vivo against L1210 murine leukemia. Compounds 9 and 12 showed antitumor activity higher than or comparable with that of tallimustine.
1996
Baraldi, Pier Giovanni; Beria, I; Cacciari, Barbara; Capolongo, L; Cozzi, P; Mongelli, N; Romagnoli, Romeo; Spalluto, G.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/516481
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