Biological activity and DNA Sequence Specificity of Synthetic Carbamoyl Analogues of Distamycin

A new penta(N-methylpyrrole carboxamide) analogue of the antibiotic distamycin has been synthesized in which the N-terminal formylamino group was replaced by a carbamoyl moiety. It was substantially more stable than distamycin in aqueous solution and bound to DNA with about the same affinity constan...

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Veröffentlicht in:Antiviral chemistry & chemotherapy 1997-06, Vol.8 (3), p.243-254
Hauptverfasser: Alfieri, A, Animati, F, Arcamone, F, Bailly, C, Crisanti, A, Dentini, M, Felicetti, P, lafrate, E, Lombardi, P, Manzini, S, Rossi, C, Waring, MJ
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