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 |
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