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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>16</Volume><Issue>1</Issue></Journal><ArticleTitle>Synthesis and antitubercular activity of new N,N-diaryl-4-(4,5-dichloroimidazole-2-yl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxamides</ArticleTitle><FirstPage>9</FirstPage><LastPage>12</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Amini M.</LastName></Author><Author><FirstName></FirstName><LastName>Navidpour L.</LastName></Author><Author><FirstName></FirstName><LastName>Shafiee A.</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>Background and the purpose of the study: Dihydropyridines having carboxamides in 3 and 5 positions show anti-tuberculosis activity. The purpose of the present study was to synthesize new DHPs having possible anti-tuberculosis activity. Methods: 4,5-Dichloroimidazole-2-carboxaldehyde was condensed with N-arylaceto-acetamides and ammonium acetate in methanol to give N,N-diaryl-4-(4,5-dichloroimid-azole-2-yl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxamides. All compounds were screened for their antitubercular activity against Mycobacterium tuberculosis (H37Rv). Results and major conclusion: Some of the new synthesized compounds exhibited a moderate activity in comparison to rifampicin.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/336</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/336/336</pdf_url></Article></Articles>
