Abstract
A new molecule incorporating nicotinoyl moiety, thiazolidin-4-one ring and 3,5-di-tert-butyl-4-hydroxyphenyl group (a potent antioxidant moiety) was synthesized and evaluated for anti-inflammatory activity in acute as well as chronic phase models of inflammation. The compound exhibited significant anti-inflammatory activity in three experimental models of inflammation, comparable to the positive control drug, ibuprofen (CAS 15687-27-1). It is suggested that besides the hypolipidemic and antioxidant potential of the molecule, its anti-inflammatory action could possibly act as an additional mechanism of its hypothesized anti-atherosclerotic activity.
| Original language | English |
|---|---|
| Pages (from-to) | 616-622 |
| Number of pages | 7 |
| Journal | Arzneimittel-Forschung/Drug Research |
| Volume | 57 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - 2007 |
All Science Journal Classification (ASJC) codes
- Drug Discovery
Fingerprint
Dive into the research topics of 'Synthesis and evaluation of the anti-inflammatory activity of N-[2-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-oxothiazolidin-3-yl]-nicotinamide'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver