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dc.contributor.authorLatorre, Antonio
dc.contributor.authorRodríguez, Santiago
dc.contributor.authorGonzález, Florenci
dc.contributor.authorFlorea, Bogdan I.
dc.contributor.authorOverkleeft, Herman S.
dc.date.accessioned2016-04-14T10:46:49Z
dc.date.available2016-04-14T10:46:49Z
dc.date.issued2015-07
dc.identifier.citationLATORRE, Antonio, et al. Synthetic Studies on the Preparation of Alanyl Epoxysulfones as Cathepsin Cysteine Protease Electrophilic Traps. The Journal of organic chemistry, 2015, vol. 80, no 15, p. 7752-7756.ca_CA
dc.identifier.urihttp://hdl.handle.net/10234/158585
dc.description.abstractA Darzens reaction between tert-butoxycarbonyl alaninal and chloromethyl phenyl sulfone afforded chlorohydrins, which were converted into epoxysulfones by reaction with sodium tert-butoxide. Epoxysulfone 10 and chloroketone 14 derived from chlorohydrins by oxidation proved to be inhibitors of cathepsins H, S, and C as determined by competitive activity-based protein profiling.ca_CA
dc.format.extent4 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherAmerican Chemical Societyca_CA
dc.relation.isPartOfJ. Org. Chem., 2015, 80 (15)ca_CA
dc.rightsCopyright © 2015, American Chemical Societyca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectCysteine Proteasesca_CA
dc.subjectEpoxysulfonesca_CA
dc.subjectAlanineca_CA
dc.subjectChloromethylca_CA
dc.subjectCathepsinca_CA
dc.titleSynthetic studies on the preparation of alanyl epoxysulfones as cathepsin cysteine protease electrophilic trapsca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1021/acs.joc.5b01013
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://pubs.acs.org/doi/abs/10.1021/acs.joc.5b01013ca_CA


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