1. Structure–activity relationship of novel series of 1,5-disubstituted tetrazoles as cyclooxygenase-2 inhibitors: Design, synthesis, bioassay screening and molecular docking studies.
- Author
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Jawabrah Al-Hourani, Baker, Al-Awaida, Wajdy, Matalka, Khalid Z., El-Barghouthi, Musa I., Alsoubani, Fatima, and Wuest, Frank
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TETRAZOLES , *CYCLOOXYGENASES , *CYCLOOXYGENASE 2 inhibitors , *BIOLOGICAL assay , *MOLECULAR docking , *IN vitro studies , *THERAPEUTICS - Abstract
A novel class of modified 1,5-disubstituted tetrazoles was designed and synthesized, their biological activity as cyclooxygenases inhibitors was screened, and their molecular docking studies were performed. The structural modifications of the first category included the 4-methylsulfonyl phenyl at C-1 of the central moiety and the linkers (–OH, –CH 2 OH, –CH 2 CH 2 OH) with different lengths at the para position of the N-1 phenyl group. For the second category, the 4-methylsulfonyl phenyl group at C-1 was replaced with 4-aminosulfonyl phenyl. While for the third category, a methylene unit was inserted between the C-1 of the tetrazole central ring and the 4-(methylsulfonyl)phenyl group, keeping the same linkers of various extensions at the para position of the N-1 phenyl group. Among the screened compounds, tetrazole 4i showed the best inhibition potency and selectivity values for both COX-2 enzyme (IC 50 = 3 μM, SI > 67) and COX-1 isoenzyme (IC 50 > 200 μM). Compounds 4e , 4h , and 4i , which have the highest inhibition potency toward COX-2 were selected for the molecular docking studies to verify their inhibition and selectivity for COX-2 over COX-1 with their modified structure. The obtained theoretical studies are in agreement with the in vitro bioassay screening results, which supports the importance of the structural modifications for our studied compounds. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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