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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>10</Volume><Issue>1</Issue></Journal><ArticleTitle>"Synthesis and antifungal activity of some new 1,2,4-Triazolo [3,4-b] [1,3,4] Thiadiazines "</ArticleTitle><FirstPage>34</FirstPage><LastPage>37</LastPage><AuthorList><Author><FirstName></FirstName><LastName>"Foroumadi AR</LastName></Author><Author><FirstName></FirstName><LastName>Mirzaei M</LastName></Author><Author><FirstName></FirstName><LastName>Emami S</LastName></Author><Author><FirstName></FirstName><LastName>Salari P</LastName></Author><Author><FirstName></FirstName><LastName>Ghaffari F</LastName></Author><Author><FirstName></FirstName><LastName>Amini 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>A new series of 5-aryl - 3 - (2 - furyl) - (7H) - s - triazolo [3, 4 - b] [1 , 3 , 4 ] thiadiazines were prepared by the reaction of 4-amino - 5 - ( 2 - furyl) - 2 , 4 - dihydro - 3H - 1 , 2 , 4 - triazole - 3 - thione with &amp;alpha;- halocarbonyl compounds in refluxing ethanolic potassium hydroxid. The compounds were tested against a variery of fungal strains in comparison to clotrimazole. Some compounds exhibited moderate activity against candida albicans and some of the fungi.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/137</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/137/137</pdf_url></Article></Articles>
