Expeditious synthesis and biological evaluation of new C-6 1,2,3-triazole adenosine derivatives A1 receptor antagonists or agonists.

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Title: Expeditious synthesis and biological evaluation of new C-6 1,2,3-triazole adenosine derivatives A1 receptor antagonists or agonists.
Authors: Mathew SC; Aix-Marseille Université, Institut des Sciences Moléculaires de Marseille, iSm2-UMR CNRS 6263, Centre Saint Jérôme, Service 532, 13397, Marseille Cedex 20, France., By Y, Berthault A, Virolleaud MA, Carrega L, Chouraqui G, Commeiras L, Condo J, Attolini M, Gaudel-Siri A, Ruf J, Rodriguez J, Parrain JL, Guieu R
Source: Organic & biomolecular chemistry [Org Biomol Chem] 2010 Sep 07; Vol. 8 (17), pp. 3874-81. Date of Electronic Publication: 2010 Jul 09.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101154995 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-0539 (Electronic) Linking ISSN: 14770520 NLM ISO Abbreviation: Org Biomol Chem Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Expeditious synthesis and biological evaluation of new C-6 1,2,3-triazole adenosine derivatives A1 receptor antagonists or agonists.
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  Data: <searchLink fieldCode="AU" term="%22Mathew+SC%22">Mathew SC</searchLink>; Aix-Marseille Université, Institut des Sciences Moléculaires de Marseille, iSm2-UMR CNRS 6263, Centre Saint Jérôme, Service 532, 13397, Marseille Cedex 20, France.<br /><searchLink fieldCode="AU" term="%22By+Y%22">By Y</searchLink><br /><searchLink fieldCode="AU" term="%22Berthault+A%22">Berthault A</searchLink><br /><searchLink fieldCode="AU" term="%22Virolleaud+MA%22">Virolleaud MA</searchLink><br /><searchLink fieldCode="AU" term="%22Carrega+L%22">Carrega L</searchLink><br /><searchLink fieldCode="AU" term="%22Chouraqui+G%22">Chouraqui G</searchLink><br /><searchLink fieldCode="AU" term="%22Commeiras+L%22">Commeiras L</searchLink><br /><searchLink fieldCode="AU" term="%22Condo+J%22">Condo J</searchLink><br /><searchLink fieldCode="AU" term="%22Attolini+M%22">Attolini M</searchLink><br /><searchLink fieldCode="AU" term="%22Gaudel-Siri+A%22">Gaudel-Siri A</searchLink><br /><searchLink fieldCode="AU" term="%22Ruf+J%22">Ruf J</searchLink><br /><searchLink fieldCode="AU" term="%22Rodriguez+J%22">Rodriguez J</searchLink><br /><searchLink fieldCode="AU" term="%22Parrain+JL%22">Parrain JL</searchLink><br /><searchLink fieldCode="AU" term="%22Guieu+R%22">Guieu R</searchLink>
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  Data: <searchLink fieldCode="JN" term="%22101154995%22">Organic & biomolecular chemistry</searchLink> [Org Biomol Chem] 2010 Sep 07; Vol. 8 (17), pp. 3874-81. <i>Date of Electronic Publication: </i>2010 Jul 09.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Royal+Society+of+Chemistry%22">Royal Society of Chemistry </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101154995 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1477-0539 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214770520%22">14770520 </searchLink><i>NLM ISO Abbreviation: </i>Org Biomol Chem <i>Subsets: </i>MEDLINE
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        Value: 10.1039/c0ob00017e
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        Text: English
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              Text: 2010 Sep 07
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