<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE Articles SYSTEM "HBI_DTD">
<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>10</Volume><Issue>3</Issue></Journal><ArticleTitle>"Synthesis and smooth muscle Calcium channel antagonist effects of new derivatives of 1,4-Dihydropyridine containing Nitroimidazol substituent "</ArticleTitle><FirstPage>130</FirstPage><LastPage>136</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Miri R</LastName></Author><Author><FirstName></FirstName><LastName>Niknahad H</LastName></Author><Author><FirstName></FirstName><LastName>Vazin A</LastName></Author><Author><FirstName></FirstName><LastName>Azarpira A</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>A group of racemic 3-[(2-hydroxyethyl), (2-Methoxyethyl), (2-acetylethyl) or (2-cyanoethyl)], 5- methyl, ethyl or isopropyl-1, 4-dihydro-2, 6-dimethyl-4-(1-methyl-5-nitro-2-imidazolyl)-3, 5-pyridinedicarboxylates [XIV-XXV] were prepared by the reaction of 1-methyl-5-nitroimidazol-2-carboxaldehyde [X] with acetoacetic esters [VI-IX] and alkys 3-aminocrotonate [XI-XIII]. In vitro calcium channel antagonist activities of the tested compounds were determined by their effects on contraction of Guinea Pig Ileal Longitudinal Smooth Muscle (GPILSM) which was induced by carbacol (1.67 &amp;#967; 10^-7 M). All compounds exhibited calcium channel antagonist activity (IC50=10^-12 to 10^-13 M range) comparable to nifedipine as reference drug (IC50=1.07±0.12x 10^-11 M).</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/153</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/153/153</pdf_url></Article></Articles>
