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New synthetic procedure for the antiviral sulfonate carbosilane dendrimer G2-S16 and its fluorescein-labelled derivative for biological studies
Authors:Carlos Gutié  rrez-Ulloa,Cornelia E. Peñ  a-Gonzá  lez,Andrea Barrios-Gumiel,Rafael Ceñ  a-Dí  ez,M. Jesú  s Serramí  a-Lobera,M. Á  ngeles Muñ  oz-Ferná  ndez,F. Javier de la Mata,Javier Sá  nchez-Nieves,Rafael Gó  mez
Abstract:The anionic carbosilane (CBS) dendrimer with sulfonate groups G2-S16 is a promising compound for the preparation of a microbicide gel to prevent HIV infection. However, until now its synthesis required aggressive conditions. Hence, a reliable synthetic procedure is very important to face GMP conditions and clinical trials. In this study, G2-S16 has been prepared by a new approach that involves the addition of an amine-terminated dendrimer to ethenesulfonyl fluoride (C2H3SO3F, ESF) and then transformation to the sulfonate dendrimer by treatment with a base. This strategy also makes feasible the synthesis of a labelled sulfonate dendrimer (G2-S16-FITC) to be used as a molecular probe for in vivo experiments. Interestingly, G2-S16-FITC enters into human peripheral blood mononuclear cells (PBMCs).

Ethenesulfonyl fluoride (ESF) is a useful reagent to prepare sulfonate carbosilane dendrimers with antiviral properties and labelled dendrimers for biological studies.
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