Supramolecular complexes consisting of a hydrophobic dendrimer host [DAB-dendr-(NHCONH-Ad)64] as well as solubilizing and bioactive guest molecules have been synthesized using a noncovalent approach. The guest - host supramolecular assembly is first preassembled in chloroform and transferred via the neat phase to aqueous solution. The bioactive guest molecules can bind to a natural (serotonin 5-HT3) receptor with nanomolar affinity as well as to the synthetic dendrimer receptor in aqueous solution, going toward a dynamic multivalent supramolecular construct capable of adapting itself to a multimeric receptor motif. © 2010 American Chemical Society.
Galeazzi, S., Hermans, T.M., Paolino, M., Anzini, M., Mennuni, L., Giordani, A., et al. (2010). Multivalent Supramolecular Dendrimer-Based Drugs. BIOMACROMOLECULES, 11(1), 182-186 [10.1021/bm901055a].
Multivalent Supramolecular Dendrimer-Based Drugs
Paolino, Marco;Anzini, Maurizio;Vomero, Salvatore;Cappelli, Andrea
2010-01-01
Abstract
Supramolecular complexes consisting of a hydrophobic dendrimer host [DAB-dendr-(NHCONH-Ad)64] as well as solubilizing and bioactive guest molecules have been synthesized using a noncovalent approach. The guest - host supramolecular assembly is first preassembled in chloroform and transferred via the neat phase to aqueous solution. The bioactive guest molecules can bind to a natural (serotonin 5-HT3) receptor with nanomolar affinity as well as to the synthetic dendrimer receptor in aqueous solution, going toward a dynamic multivalent supramolecular construct capable of adapting itself to a multimeric receptor motif. © 2010 American Chemical Society.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/8639
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