Abstract
A focused library of novel bis-heterocycles encompassing 2-mercapto benzothiazole and 1,2,3-triazoles were synthesized using click chemistry approach. The synthesized compounds have been tested for their anti-inflammatory activity by using biochemical cyclooxygenase (COX) activity assays and carrageenan-induced hind paw edema. Among the tested compounds, compound 4d demonstrated a potent selective COX-2 inhibition with COX-2/COX-1 ratio of 0.44. Results from carrageenan-induced hind paw edema showed that compounds 4a, 4d, 4e and 4f posses significant anti-inflammatory activity as compared to the standard drug Ibuprofen. The compounds showing significant activity were further subjected to anti-nociceptive activity by writhing test. These four compounds have shown comparable activity with the standard Ibuprofen. Further ulcerogenic studies shows that none of these compounds causing gastric ulceration. © 2012 Elsevier Masson SAS. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
Shafi, S., Mahboob Alam, M., Mulakayala, N., Mulakayala, C., Vanaja, G., Kalle, A. M., … Alam, M. S. (2012). Synthesis of novel 2-mercapto benzothiazole and 1,2,3-triazole based bis-heterocycles: Their anti-inflammatory and anti-nociceptive activities. European Journal of Medicinal Chemistry, 49, 324–333. https://doi.org/10.1016/j.ejmech.2012.01.032
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.