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dc.contributor.authorLuis, Santiago V.
dc.contributor.authorAlfonso Rodríguez, Ignacio
dc.date.accessioned2015-07-01T09:31:38Z
dc.date.available2015-07-01T09:31:38Z
dc.date.issued2014
dc.identifier.citationLUIS LAFUENTE, S. V.; ALFONSO RODRÍGUEZ, I. Bioinspired Chemistry Based on Minimalistic Pseudopeptides. Accounts of Chemical Research, v. 47, n. 1 (2014), pp. 112-124ca_CA
dc.identifier.urihttp://hdl.handle.net/10234/125625
dc.description.abstractFor years researchers have tried to understand the molecular behavior of complex biomolecules through the development of small molecules that can partially mimic their function. Now researchers are implementing the reverse approach: using the structural and mechanistic knowledge obtained from those complex systems to design small molecules with defined properties and for specific applications. One successful strategy for constructing bioinspired, minimalistic molecules is to combine natural building blocks that provide functional elements with abiotic fragments that serve as structural scaffolds. Therefore pseudopeptidic compounds, most of them based on C2 symmetric structures, represent a unique opportunity to explore and evaluate this approach. Some of these molecules are as simple as two amino acids connected by a diamino spacer. The results in this Account show how bioinspired minimalistic pseudopeptides can form ordered structures, participate in the recognition and transcription of information events in molecular devices, and catalyze reactions. This strategy allows researchers to design and prepare a variety of open-chain and macrocyclic compounds leading to systems that can self-aggregate to form hierarchically ordered micro- and nanostructures. In addition, small changes in the molecule or external stimuli can regulate the self-aggregation pattern. In the same way, researchers can also tune the molecular movements of simple pseudopeptides through environmental factors, providing a means to control new molecular devices. In addition, some of the prepared model compounds have shown interesting properties in molecular recognition and even as sensors for several targets of interest. Finally we have observed remarkable catalytic activities from these types of molecules, although those results are still far from the efficiency shown by natural peptides. This family of pseudopeptidic compounds offers the opportunity for the more elaborate design of relatively simple abiotic but bioinspired systems that display specific properties. In addition, the results can provide additional information that will increase the molecular understanding of the basic principles that underlie the extraordinary behavior of natural systems.ca_CA
dc.format.extent13 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherACS Publicationsca_CA
dc.relation.isPartOfAccounts of Chemical Research, v. 47, n. 1 (2014)ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/CNE/1.0/*
dc.subjectComplex biomoleculesca_CA
dc.subjectSmall moleculesca_CA
dc.subjectPseudopeptidic compoundsca_CA
dc.subjectC2 symmetric structuresca_CA
dc.subjectBioinspired minimalistic pseudopeptidesca_CA
dc.subjectOpen-chain and macrocyclic compoundsca_CA
dc.titleBioinspired Chemistry Based on Minimalistic Pseudopeptidesca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1021/ar400085p
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://pubs.acs.org/doi/abs/10.1021/ar400085pca_CA


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