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Updated: Jul 11, 2026

Nucleocapsid Annealing-Mediated Electrophoresis (NAME) Assay Allows the Rapid Identification of HIV-1 Nucleocapsid Inhibitors
Published on: January 19, 2015
Synthesis of a neamine dimer targeting the dimerization initiation site of HIV-1 RNA
Anne Bodlenner1, Aurélien Alix, Jean-Marc Weibel
1Laboratoire de synthèse et réactivité organique, Institut de Chimie, Université Louis Pasteur, 4 rue Blaise Pascal, 67070 Strasbourg, France.
Abstract:
A neamine dimer designed to bind to a specific sequence of HIV-1 RNA has been synthesized. Starting from neomycin B (1), a five-step synthesis efficiently provided a key protected neamine monomer 6 (28%). From the latter, coupling reactions with activated diacids gave dimers. After deprotection, a neamine dimer was obtained as the hexachlorohydrate salt 15 with 13% overall yield over nine steps.
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