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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>9</Volume><Issue>3-4</Issue></Journal><ArticleTitle>"Synthesis and smooth muscle Calcium channel antagonist effect of Alkyl, Aminoalkyl 1,4-Dihydro-2,6-Dimethyl-4-Nitroimidazole-3,5 Pyridine Dicarboxylates "</ArticleTitle><FirstPage>40</FirstPage><LastPage>45</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Miri R</LastName></Author><Author><FirstName></FirstName><LastName>Dehpour AR</LastName></Author><Author><FirstName></FirstName><LastName>Azimi M</LastName></Author><Author><FirstName></FirstName><LastName>Shafiei A</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>The discovery that 1,4-dihydropyridine (DHP) class of calcium channel antagonist inhibits the Ca+² influx represented a major therapeutic advance in the treatment of cardiovascular diseases such as hypertension, angina pectoris and other spastic smooth muscle disorders. A novel class of calcium channel antagonist of flunarizine containing arylpiperazinyl moiety has recently been reported. It was therefore of interest to determine the effect that selected C-3 substituents contained amino alkyl and arylpiperazine, in conjunction with a C-4 1-methyl-5-nitro-2-imidazolyl substituents on calcium channel antagonist activity. The unsymmetrical analogues were prepared by a procedure reported by Meyer in which 1-methyl-5-nitro-imidazol-2-carboxaldehyde was reacted with acetoacetic esters and alkyl 3-aminocrotonate. In vitro calcium channel antagonist activities were determined by the use of high K+ contraction of guinea pig ileal longitudinal smooth muscle. All compounds exhibited comparable calcium channel antagonist activity (IC50=10^-9 to 10^-11 M) against reference drug nifedipine (IC50=2.75±0.36 x 10^-10 M).</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/128</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/128/128</pdf_url></Article></Articles>
