Universidad Complutense de Madrid
E-Prints Complutense

Diseño, síntesis y estudio de 1,3,4-tiadiazoles como inhibidores de la enoil-ACP-reductasa (InhA) de M. tuberculosis

Impacto

Descargas

Último año



Fernández Menéndez, Raquel (2017) Diseño, síntesis y estudio de 1,3,4-tiadiazoles como inhibidores de la enoil-ACP-reductasa (InhA) de M. tuberculosis. [Tesis]

[img]
Vista previa
PDF
7MB


Resumen

The work described in this report has been developed in the DDW (Diseases of the Developing World) GlaxoSmithKline center in Tres Cantos (Madrid) under the direction of Dra. Julia Castro Pichel and Dra. Esther Fernández Velando. This work was done in collaboration with the GATB (Global Alliance for Tuberculosis) organization. The main objective of this research program has been to identify new InhA inhibitors within the family of thiadiazoles, these molecules should be active against TB-MDR strains and TB-XDR type. These new compounds would be administered in combination, replacing one or more of the drugs used in current regimens of directly observed therapy. The identified compounds should be able to be administered orally, well tolerated and show low generation frequency of resistance. In the development of this research project the design and synthesis of new modifications in the overall structure of GSK1, hit of the thiadiazole series, have been carried out with the aim of improving the enzymatic activity as well as the whole cell potency and physicochemical profile of the new compounds. Molecules result of the proposed modifications were evaluated in the appropriate biological studies, assessing their potential as anti-TB drugs. After the biological evaluation exercise and SAR study of the series compound 106 was identified as the most promising structure. This compound has been progressed to the Pre-Candidate and is currently in combination studies, contributing that way to the identification of a novel direct inhibitor of the well validated enzyme InhA.


Tipo de documento:Tesis
Información Adicional:

Tesis inédita de la Universidad Complutense de Madrid, Facultad de Ciencias Químicas, Departamento de Química Orgánica I, leída el 15/01/2016

Directores (o tutores):
NombreEmail del director (o tutor)
Castro Pichel, Julia
Fernández Velando, Esther
Palabras clave:Química orgánica, fármacos antituberculosos, Tuberculosis, Inhibidores de InhA, Tiadiazoles
Palabras clave (otros idiomas):Organic chemistry, Anti-TB drugs, Tuberculosis, InhA inhibitors, Thiadiazoles
Materias:Ciencias > Química > Química orgánica
Ciencias Biomédicas > Farmacia > Farmacología
Código ID:42684
Depositado:11 May 2017 11:05
Última Modificación:11 May 2017 11:05

Descargas en el último año

Sólo personal del repositorio: página de control del artículo