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Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction
Results from our group showed benzyl salicylate to be a moderate inhibitor of the CD81-LEL–HCV-E2 interaction. To increase the biological activity, heterocyclic substituted benzoic acids were coupled to amino acid esters via microwave assisted DCC-reaction. The prepared compounds were tested for the...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Bentham Open
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709478/ https://www.ncbi.nlm.nih.gov/pubmed/19662141 http://dx.doi.org/10.2174/1874104500802010021 |
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author | Holzer, Marcel Ziegler, Sigrid Kronenberger, Bernd Klein, Christian D Hartmann, Rolf W |
author_facet | Holzer, Marcel Ziegler, Sigrid Kronenberger, Bernd Klein, Christian D Hartmann, Rolf W |
author_sort | Holzer, Marcel |
collection | PubMed |
description | Results from our group showed benzyl salicylate to be a moderate inhibitor of the CD81-LEL–HCV-E2 interaction. To increase the biological activity, heterocyclic substituted benzoic acids were coupled to amino acid esters via microwave assisted DCC-reaction. The prepared compounds were tested for their inhibitory potency by means of a fluorescence labeled antibody assay system using HUH7.5 cells. |
format | Text |
id | pubmed-2709478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-27094782009-08-06 Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction Holzer, Marcel Ziegler, Sigrid Kronenberger, Bernd Klein, Christian D Hartmann, Rolf W Open Med Chem J Article Results from our group showed benzyl salicylate to be a moderate inhibitor of the CD81-LEL–HCV-E2 interaction. To increase the biological activity, heterocyclic substituted benzoic acids were coupled to amino acid esters via microwave assisted DCC-reaction. The prepared compounds were tested for their inhibitory potency by means of a fluorescence labeled antibody assay system using HUH7.5 cells. Bentham Open 2008-04-15 /pmc/articles/PMC2709478/ /pubmed/19662141 http://dx.doi.org/10.2174/1874104500802010021 Text en © Holzer et al.; Licensee Bentham Open http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Holzer, Marcel Ziegler, Sigrid Kronenberger, Bernd Klein, Christian D Hartmann, Rolf W Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction |
title | Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction |
title_full | Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction |
title_fullStr | Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction |
title_full_unstemmed | Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction |
title_short | Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction |
title_sort | microwave-assisted syntheses of amino acid ester substituted benzoic acid amides: potential inhibitors of human cd81-receptor hcv-e2 interaction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709478/ https://www.ncbi.nlm.nih.gov/pubmed/19662141 http://dx.doi.org/10.2174/1874104500802010021 |
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