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dc.contributor.authorLlanos Gargallo, Ana
dc.contributor.otherCarda Usó, Pedro Miguel
dc.contributor.otherUniversitat Jaume I. Departament de Química Inorgànica i Orgànica
dc.date.accessioned2018-10-02T10:32:58Z
dc.date.available2018-10-02T10:32:58Z
dc.date.issued2018-07
dc.identifier.urihttp://hdl.handle.net/10234/176456
dc.descriptionTreball Final de Grau en Química. Codi: QU0943. Curs acadèmic: 2017/2018ca_CA
dc.description.abstractImidazole is an important nucleus that can be found in Nature and it is present in many biomolecules. Compounds including an imidazole are used as new drugs in medicinal chemistry, including anti-cancer reagents. However, there is still the need to improve of already used drugs and the search for new and more effective drugs. Thus, the aims of the current study are twofold, by one hand the synthesis of 1-benzyl-4- phenyl-1H-imidazole and derivatives and by the other hand their biological evaluation as c-MYC gene and PD-L1 inhibitors. The more specific objectives of this study were: 1. The synthesis of 1-arylmethyl-4-fenil-1H-imidazoles whose general structure is shown in the following figure. 2. The biological evaluation of the above mentioned compounds as regards: • Their antiproliferative activity. • Their interaction with PD-L1 protein. • Their activity on the inhibition of c-MYC gene and PD-L1 protein.ca_CA
dc.format.extent73 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherUniversitat Jaume Ica_CA
dc.rights.urihttp://rightsstatements.org/vocab/CNE/1.0/*
dc.subjectGrau en Químicaca_CA
dc.subjectGrado en Químicaca_CA
dc.subjectBachelor's Degree in Chemistryca_CA
dc.titleSynthesis and biological evaluation of anticancer compoundsca_CA
dc.typeinfo:eu-repo/semantics/bachelorThesisca_CA
dc.educationLevelEstudios de Gradoca_CA
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA


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