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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>8</Volume><Issue>3-4</Issue></Journal><ArticleTitle>Synthesis and Calcium channel antagonist activity of Nifedipine analogues with Chloroindolyl substituent</ArticleTitle><FirstPage>32</FirstPage><LastPage>36</LastPage><AuthorList><Author><FirstName></FirstName><LastName>"Shafiei A</LastName></Author><Author><FirstName></FirstName><LastName>Dehpour AR</LastName></Author><Author><FirstName></FirstName><LastName>Hadizadeh F</LastName></Author><Author><FirstName></FirstName><LastName>Rezaei B "</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>Various diester analogues of nifedipine in which the ortho nitrophenyl group at position 4 were replaced by 3-chloro-1H-2-indolyl substituent, were synthesized and evaluated as calcium antagonists on guinea-pig ileal smooth muscle. Nifedipine was used as a standard. Compound 6f was found to be the most active.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/108</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/108/108</pdf_url></Article></Articles>
