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Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors
A series of imidazopyrimidine derivatives with the general formula I was synthesized and identified as potent inhibitors of iNOS dimer formation, a prerequisite for proper functioning of the enzyme. Stille and Negishi coupling reactions were used as key steps to form the carbon-carbon bond connectin...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Bentham Open
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788740/ https://www.ncbi.nlm.nih.gov/pubmed/19966921 http://dx.doi.org/10.2174/1874104500903010008 |
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author | Chu, Guo-Hua Le Bourdonnec, Bertrand Gu, Minghua Ajello, Christopher W Leister, Lara K Sellitto, Ian Cassel, Joel A Tuthill, Paul A O’ Hare, Heather DeHaven, Robert N Dolle, Roland E |
author_facet | Chu, Guo-Hua Le Bourdonnec, Bertrand Gu, Minghua Ajello, Christopher W Leister, Lara K Sellitto, Ian Cassel, Joel A Tuthill, Paul A O’ Hare, Heather DeHaven, Robert N Dolle, Roland E |
author_sort | Chu, Guo-Hua |
collection | PubMed |
description | A series of imidazopyrimidine derivatives with the general formula I was synthesized and identified as potent inhibitors of iNOS dimer formation, a prerequisite for proper functioning of the enzyme. Stille and Negishi coupling reactions were used as key steps to form the carbon-carbon bond connecting the imidazopyrimidine core to the central cycloalkenyl, cycloalkyl and phenyl ring templates. |
format | Text |
id | pubmed-2788740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-27887402009-12-04 Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors Chu, Guo-Hua Le Bourdonnec, Bertrand Gu, Minghua Ajello, Christopher W Leister, Lara K Sellitto, Ian Cassel, Joel A Tuthill, Paul A O’ Hare, Heather DeHaven, Robert N Dolle, Roland E Open Med Chem J Article A series of imidazopyrimidine derivatives with the general formula I was synthesized and identified as potent inhibitors of iNOS dimer formation, a prerequisite for proper functioning of the enzyme. Stille and Negishi coupling reactions were used as key steps to form the carbon-carbon bond connecting the imidazopyrimidine core to the central cycloalkenyl, cycloalkyl and phenyl ring templates. Bentham Open 2009-11-18 /pmc/articles/PMC2788740/ /pubmed/19966921 http://dx.doi.org/10.2174/1874104500903010008 Text en © Chu et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/)which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Chu, Guo-Hua Le Bourdonnec, Bertrand Gu, Minghua Ajello, Christopher W Leister, Lara K Sellitto, Ian Cassel, Joel A Tuthill, Paul A O’ Hare, Heather DeHaven, Robert N Dolle, Roland E Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors |
title | Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors |
title_full | Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors |
title_fullStr | Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors |
title_full_unstemmed | Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors |
title_short | Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors |
title_sort | design and synthesis of imidazopyrimidine derivatives as potent inos dimerization inhibitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788740/ https://www.ncbi.nlm.nih.gov/pubmed/19966921 http://dx.doi.org/10.2174/1874104500903010008 |
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