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Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives
4-Oxo-4H-quinolizine-3-carboxylic acid derivatives bearing sulfamido, carboxylamido, benzimidazole and benzothiazole substituents have been designed and synthesized. The structures of these new compounds were confirmed by (1)H-NMR, (13)C- NMR, IR and ESI (or HRMS) spectra. Compounds were screened fo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254011/ https://www.ncbi.nlm.nih.gov/pubmed/19255545 http://dx.doi.org/10.3390/molecules14020868 |
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author | Xu, Yi-Sheng Zeng, Cheng-Chu Jiao, Zi-Guo Hu, Li-Ming Zhong, Ru-gang |
author_facet | Xu, Yi-Sheng Zeng, Cheng-Chu Jiao, Zi-Guo Hu, Li-Ming Zhong, Ru-gang |
author_sort | Xu, Yi-Sheng |
collection | PubMed |
description | 4-Oxo-4H-quinolizine-3-carboxylic acid derivatives bearing sulfamido, carboxylamido, benzimidazole and benzothiazole substituents have been designed and synthesized. The structures of these new compounds were confirmed by (1)H-NMR, (13)C- NMR, IR and ESI (or HRMS) spectra. Compounds were screened for possible HIV integrase inhibitory activity. |
format | Online Article Text |
id | pubmed-6254011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-62540112018-11-30 Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives Xu, Yi-Sheng Zeng, Cheng-Chu Jiao, Zi-Guo Hu, Li-Ming Zhong, Ru-gang Molecules Article 4-Oxo-4H-quinolizine-3-carboxylic acid derivatives bearing sulfamido, carboxylamido, benzimidazole and benzothiazole substituents have been designed and synthesized. The structures of these new compounds were confirmed by (1)H-NMR, (13)C- NMR, IR and ESI (or HRMS) spectra. Compounds were screened for possible HIV integrase inhibitory activity. Molecular Diversity Preservation International 2009-01-19 /pmc/articles/PMC6254011/ /pubmed/19255545 http://dx.doi.org/10.3390/molecules14020868 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Xu, Yi-Sheng Zeng, Cheng-Chu Jiao, Zi-Guo Hu, Li-Ming Zhong, Ru-gang Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives |
title | Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives |
title_full | Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives |
title_fullStr | Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives |
title_full_unstemmed | Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives |
title_short | Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives |
title_sort | design, synthesis and anti-hiv integrase evaluation of 4-oxo-4h-quinolizine-3-carboxylic acid derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254011/ https://www.ncbi.nlm.nih.gov/pubmed/19255545 http://dx.doi.org/10.3390/molecules14020868 |
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