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pubmed-article:21167778pubmed:abstractTextThe renin-angiotensin-system harbours two main receptor subtypes binding angiotensin II which are the AT1-receptor and the AT2-receptor. While the AT1-receptor has been a drug target in cardiovascular disease for many years, the AT2-receptor was only a subject of academic interest. This has changed with the design and synthesis of a first non-peptide, orally active AT2-receptor agonist, compound 21 (C21). First data using C21 revealed tissue protective effects and functional improvement after myocardial infarction and in hypertension-induced end organ damage, notably in a blood-pressure independent way. In all of these models, AT2-receptor mediated anti-inflammation seemed an important underlying mechanism. C21 is awaited to enter a phase I clinical study in 2011.lld:pubmed
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pubmed-article:21167778pubmed:copyrightInfoCopyright © 2010 Elsevier Ltd. All rights reserved.lld:pubmed
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pubmed-article:21167778pubmed:volume11lld:pubmed
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pubmed-article:21167778pubmed:year2011lld:pubmed
pubmed-article:21167778pubmed:articleTitleNon-peptide AT2-receptor agonists.lld:pubmed
pubmed-article:21167778pubmed:affiliationCenter for Cardiovascular Research, Charité-Universitätsmedizin Berlin, Hessische Str. 3-4, 10115 Berlin, Germany. ulrike.steckelings@charite.delld:pubmed
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