Title:Diversified Thiazole Substituted Coumarins and Chromones as Non- Cytotoxic ROS and NO Inhibitors
Volume: 17
Issue: 5
Author(s): Uzma Salar, Khalid Mohammed Khan*, Almas Jabeen, Shafquat Hussain, Aisha Faheem, Farwa Naqvi and Shahnaz Perveen
Affiliation:
- H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi-75270,Pakistan
Keywords:
Coumarin, chromone, thiazole, ROS, nitric oxide, cytotoxicity, antiinflammatory, ibuprofen, structure-activity
relationship.
Abstract: Background: Non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen, aspirin,
indomethacin, flufenamic acid and phenylbutazone are used to treat most of the inflammatory
disorders. These NSAIDs are also associated with serious side effects including gastric ulceration,
nephrotoxicity, and bleeding, mainly due to acidic nature. Hence, there is a need to identify highly
potent and safer treatment for inflammatory disorders.
Methods: Herein, synthetic hydrazinyl thiazole substituted coumarins and chromones 1-48 were
evaluated for ROS inhibitory activity. ROS were generated from zymosan activated whole blood
phagocytes.
Results: Among all tested compounds, compounds 1 (IC50 = 38.3 ± 7.1 μM), 2 (IC50 = 5.7 ±
0.2 μM), 5 (IC50 = 28.3 ± 3.5 μM), 23 (IC50 = 12.5 ± 3.1 μM), 27 (IC50 = 32.8 ± 1.1 μM), 39 (IC50 =
20.2 ± 1.6 μM), and 42 (IC50 = 43.2 ± 3.8 μM) showed potent ROS inhibition as compared to
standard ibuprofen (IC50 = 54.3 ± 1.9 μM). Whereas, compounds 3 (IC50 = 134.7 ± 1.0 μM), 16
(IC50 = 75.4 ± 7.2 μM), 24 (IC50 = 102.4 ± 1.0 μM), and 31 (IC50 = 86.6 ± 1.5 μM) were found to be
moderately active. Compounds 1, 2, 5, 23, 27, 39, and 42, having potent ROS inhibitory activity
were also screened for their nitric oxide (NO) inhibition. Cytotoxicity was also checked for all active
compounds on NIH-3T3 cell line. Cyclohexamide (IC50 = 0.13 ± 0.02 μM) was used as standard.
Conclusion: Identified active compounds from these libraries may serve as lead candidates for future
research in order to obtain a more potent, and safer anti-inflammatory agent.