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Synthesis and DNA binding selectivity of pyrrole-amidine oligopeptides.

Frederico Arcamone

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Abstract

A class of DNA binding antibiotics endowed with antiviral and antitumor properties is reviewed. Starting from the original natural products, namely distamycin and netropsin, new compounds have been recently synthesized with the aim to obtain agents with specific affinity for defined DNA sequences and with different interaction mechanism (reversible or irreversible).

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A class of DNA binding antibiotics endowed with antiviral and antitumor properties is reviewed. Starting from the original natural products, namely distamycin and netropsin, new compounds have been recently synthesized with the aim to obtain agents with specific affinity for defined DNA sequences and with different interaction mechanism (reversible or irreversible).

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Available abstract

A class of DNA binding antibiotics endowed with antiviral and antitumor properties is reviewed. Starting from the original natural products, namely distamycin and netropsin, new compounds have been recently synthesized with the aim to obtain agents with specific affinity for defined DNA sequences and with different interaction mechanism (reversible or irreversible).

Key concepts: Netropsin, Amidine, Chemistry, DNA, Oligopeptide, Stereochemistry, Selectivity, Chemical synthesis

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Synthesis and DNA binding selectivity of pyrrole-amidine oligopeptides. — Research Paper | ScholarLens