Abstract
Novel pyrazolyl-2,4-thiazolidinediones were prepared via the reaction of appropriate pyrazolecarboxaldehydes with 2,4-thiazolidinediones and substituted benzyl-2,4-thiazolidinediones. The resultant compounds were first evaluated for their anti-inflammatory and neuroprotective properties in vitro. The active compounds were further studied in vivo by using the formalin-induced paw edema and the turpentine oil-induced granuloma pouch bioassays. We identified four novel compounds that showed protective effects in vitro at non-toxic concentrations, and were also effective in the animal models of acute and sub-acute inflammation. © 2010 Elsevier Ltd. All rights reserved.
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Youssef, A. M., Sydney White, M., Villanueva, E. B., El-Ashmawy, I. M., & Klegeris, A. (2010). Synthesis and biological evaluation of novel pyrazolyl-2,4-thiazolidinediones as anti-inflammatory and neuroprotective agents. Bioorganic and Medicinal Chemistry, 18(5), 2019–2028. https://doi.org/10.1016/j.bmc.2010.01.021
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