Design, synthesis and study of quinoxaline-2- carboxamide 1,4-DI-N-Oxide derivatives as anti-tuberculosis agents
The experimental work presented in this memory is based on the hypothesis that quinoxalines di-N-oxide, considered to be the core of the structure, which present a carboxamide moiety on position two and aliphatic linker between this group and an aromatic system, can be proposed as potent anti-tuberc...
| Main Authors: | , , |
|---|---|
| Format: | info:eu-repo/semantics/doctoralThesis |
| Language: | eng |
| Published: |
Servicio de Publicaciones de la Universidad de Navarra
2013
|
| Subjects: | |
| Online Access: | https://hdl.handle.net/10171/34367 |
| _version_ | 1793400543692980224 |
|---|---|
| author | Moreno-de-Viguri, E. (Elsa) Pérez-Silanes, S. (Silvia) Monge, A. (Antonio) |
| author_facet | Moreno-de-Viguri, E. (Elsa) Pérez-Silanes, S. (Silvia) Monge, A. (Antonio) |
| author_sort | Moreno-de-Viguri, E. (Elsa) |
| collection | DSpace |
| description | The experimental work presented in this memory is based on the hypothesis that quinoxalines di-N-oxide, considered to be the core of the structure, which present a carboxamide moiety on position two and aliphatic linker between this group and an aromatic system, can be proposed as potent anti-tuberculosis agents. The main purpose of this project is the synthesis of new quinoxaline di-N-oxide derivatives as anti-tuberculosis agents. The strategy consists of the design and synthesis of several derivatives of each series, and their in vitro biological evaluation against M.tb. Some compounds will be selected, based on their structural variability and biological results, for an in depth study of the physicochemical properties and electrochemical behavior of this family of derivatives.
A series of specific objectives are proposed in order to achieve the main purpose of this project:
1. Bibliographic review: state of the art.
2. Design of new quinoxaline di-N-oxide derivatives.
3. Synthesis of the designed compounds.
4. Characterization of the synthesized compounds.
5. In vitro biological evaluation of the synthesized derivatives.
6. Study of the lipophilicity of quinoxaline di-N-oxide derivatives.
7. Study of the electrochemical behavior of quinoxaline di-N-oxide derivatives.
8. Study of possible structure-property and structure-activity relationships (SPR, SAR).
9. Search of new lead compounds and design of future work plans. |
| format | info:eu-repo/semantics/doctoralThesis |
| id | oai:dadun.unav.edu:10171-34367 |
| institution | Universidad de Navarra |
| language | eng |
| publishDate | 2013 |
| publisher | Servicio de Publicaciones de la Universidad de Navarra |
| record_format | dspace |
| spelling | oai:dadun.unav.edu:10171-343672020-03-03T10:40:42Z Design, synthesis and study of quinoxaline-2- carboxamide 1,4-DI-N-Oxide derivatives as anti-tuberculosis agents Moreno-de-Viguri, E. (Elsa) Pérez-Silanes, S. (Silvia) Monge, A. (Antonio) Materias Investigacion::Farmacia The experimental work presented in this memory is based on the hypothesis that quinoxalines di-N-oxide, considered to be the core of the structure, which present a carboxamide moiety on position two and aliphatic linker between this group and an aromatic system, can be proposed as potent anti-tuberculosis agents. The main purpose of this project is the synthesis of new quinoxaline di-N-oxide derivatives as anti-tuberculosis agents. The strategy consists of the design and synthesis of several derivatives of each series, and their in vitro biological evaluation against M.tb. Some compounds will be selected, based on their structural variability and biological results, for an in depth study of the physicochemical properties and electrochemical behavior of this family of derivatives. A series of specific objectives are proposed in order to achieve the main purpose of this project: 1. Bibliographic review: state of the art. 2. Design of new quinoxaline di-N-oxide derivatives. 3. Synthesis of the designed compounds. 4. Characterization of the synthesized compounds. 5. In vitro biological evaluation of the synthesized derivatives. 6. Study of the lipophilicity of quinoxaline di-N-oxide derivatives. 7. Study of the electrochemical behavior of quinoxaline di-N-oxide derivatives. 8. Study of possible structure-property and structure-activity relationships (SPR, SAR). 9. Search of new lead compounds and design of future work plans. 2013-11-06T08:45:17Z 2013-11-06T08:45:17Z 2013 2011-06-17 info:eu-repo/semantics/doctoralThesis https://hdl.handle.net/10171/34367 eng info:eu-repo/semantics/openAccess application/pdf Servicio de Publicaciones de la Universidad de Navarra |
| spellingShingle | Materias Investigacion::Farmacia Moreno-de-Viguri, E. (Elsa) Pérez-Silanes, S. (Silvia) Monge, A. (Antonio) Design, synthesis and study of quinoxaline-2- carboxamide 1,4-DI-N-Oxide derivatives as anti-tuberculosis agents |
| title | Design, synthesis and study of quinoxaline-2- carboxamide 1,4-DI-N-Oxide derivatives as anti-tuberculosis agents |
| title_full | Design, synthesis and study of quinoxaline-2- carboxamide 1,4-DI-N-Oxide derivatives as anti-tuberculosis agents |
| title_fullStr | Design, synthesis and study of quinoxaline-2- carboxamide 1,4-DI-N-Oxide derivatives as anti-tuberculosis agents |
| title_full_unstemmed | Design, synthesis and study of quinoxaline-2- carboxamide 1,4-DI-N-Oxide derivatives as anti-tuberculosis agents |
| title_short | Design, synthesis and study of quinoxaline-2- carboxamide 1,4-DI-N-Oxide derivatives as anti-tuberculosis agents |
| title_sort | design, synthesis and study of quinoxaline-2- carboxamide 1,4-di-n-oxide derivatives as anti-tuberculosis agents |
| topic | Materias Investigacion::Farmacia |
| url | https://hdl.handle.net/10171/34367 |
| work_keys_str_mv | AT morenodevigurieelsa designsynthesisandstudyofquinoxaline2carboxamide14dinoxidederivativesasantituberculosisagents AT perezsilanesssilvia designsynthesisandstudyofquinoxaline2carboxamide14dinoxidederivativesasantituberculosisagents AT mongeaantonio designsynthesisandstudyofquinoxaline2carboxamide14dinoxidederivativesasantituberculosisagents |