Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/10261/1980
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dc.creatorChiara, José Luis-
dc.creatorStorch, Isabel-
dc.creatorGarcía, Ángela-
dc.creatorBastida, Ágatha-
dc.creatorBobo, Sofía-
dc.creatorMartín-Ortega, María D.-
dc.date2007-11-12T11:11:00Z-
dc.date2007-11-12T11:11:00Z-
dc.date2004-11-08-
dc.date.accessioned2017-01-31T00:58:17Z-
dc.date.available2017-01-31T00:58:17Z-
dc.identifierChemBioChem 6(1): 186-191 (2005)-
dc.identifier10.1002/cbic.200400231-
dc.identifierhttp://hdl.handle.net/10261/1980-
dc.identifier10.1002/cbic.200400231-
dc.identifier.urihttp://dspace.mediu.edu.my:8181/xmlui/handle/10261/1980-
dc.description6 páginas, 2 figuras, 2 esquemas, 2 tablas.-- ChemBioChem Special Issue: EMBO Symposium: Chemistry Meets Biology.-
dc.descriptionA new trehazolin analogue, 1-thiatrehazolin, has been synthesized from carbohydrate precursors by a highly efficient route based on our previously developed ketone/oxime ether reductive carbocyclization reaction for the construction of the cyclitol ring and an intramolecular nucleophilic displacement reaction for the construction of the thiazoline ring. 1-Thiatrehazolin is a very potent, slow, tight-binding trehalase inhibitor. On the basis of the experimental results, a structural model for trehalase inhibition by trehazolin and analogues is proposed, supported by theoretical calculations.-
dc.descriptionFinancial support by the Ministry of Science and Technology of Spain (project BQU2000-1501-C02-01) is gratefully acknowledged.-
dc.descriptionPeer reviewed-
dc.languageeng-
dc.publisherJohn Wiley & Sons-
dc.relationhttp://dx.doi.org/10.1002/cbic.200400231-
dc.rightsopenAccess-
dc.subjectAb initio calculations-
dc.subjectCyclitols-
dc.subjectGlycosidases-
dc.subjectInhibitors-
dc.subjectSulfur heterocycles-
dc.titleSynthesis, inhibition properties and theoretical study of the new nanomolar trehalase inhibitor 1-thiatrehazolin: Towards a structural understanding of trehazolin inhibition-
dc.typeArtículo-
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