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dc.contributor.authorCamarasa Rius, María José 
dc.contributor.authorVelázquez Díaz, Sonsoles
dc.contributor.authorSan Félix García, Ana
dc.contributor.authorPérez Pérez, María Jesús
dc.contributor.authorGago Badenas, Federico 
dc.date.accessioned2009-11-26T11:34:56Z
dc.date.available2009-11-26T11:34:56Z
dc.date.issued2006
dc.identifier.bibliographicCitationAntiviral Research 71 (2006) 260 267en_US
dc.identifier.urihttp://hdl.handle.net/10017/5071
dc.description.abstractThe genome of human immunodeficiency virus type 1 (HIV-1) encodes 15 distinct proteins, three of which provide essential enzymatic functions: a reverse transcriptase (RT), an integrase (IN), and a protease (PR). Since these enzymes are all homodimers, pseudohomodimers or multimers, disruption of protein-protein interactions in these retroviral enzymes may constitute an alternative way to achieve HIV-1 inhibition. A growing number. of dimerization inhibitors for these enzymes is being reported. This mini review summarizes some approaches that have been followed for the development of compounds that inhibit those three enzymes by interfering with the dimerization interfaces between the enzyme subunits. (c) 2006 Elsevier B.V. All rights reserved.en_US
dc.format.mimetypeapplication/pdfen
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.subjectHIV-1en_US
dc.subjectReverse transcriptaseen_US
dc.subjectIntegraseen_US
dc.subjectProteaseen_US
dc.titleDimerization inhibitors of HIV-1 reverse transcriptase, protease and integrase: A single mode of inhibition for the three HIV enzymes?en_US
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaCienciaes_ES
dc.subject.ecienciaFarmacologíaes_ES
dc.subject.ecienciaScienceen
dc.subject.ecienciaPharmacologyen
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Farmacología
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.antiviral.2006.05.021
dc.type.versioninfo:eu-repo/semantics/publishedVersionen_US
dc.identifier.doi10.1016/j.antiviral.2006.05.021
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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