Article Id:JPRS-PC-00001626 Title:Synthesis, characterization and antioxidant evaluation of 2-(2-substituted) naphthalene-1,4-dione derivatives Category:Pharmaceutical Chemistry Section:Research Article
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Background: 1,4- naphthoquinone (Lawsone) are widely distributed in nature and have been used since ancient times in traditional medicine. Lawsone has been used as a dye, and both its natural form and synthetic derivatives exhibit antifungal, antibacterial, antitumor, antimalarial, molluscicidal and antioxidant activity. Methods: 1,4- naphthoquinone (Lawsone) was isolated from the leaves of lawsonia inermis by using pH gradient method. A convenient synthesis of 2-substituted amino naphthalene-1,4-dione (3a-e) has been achieved by reaction of isolated 1,4- naphthoquinone with substituted aniline in the presence of ethanol and evaluated for in- vitro antioxidant activity using DPPH model. The structure of the final analogues has been confirmed on the basis of elemental analysis, FTIR, 1H NMR and mass spectra. All the values of elemental analysis, FTIR, 1H NMR and mass spectra were found to be prominent. Results and discussion: The results indicate that synthesized compound 3d having IC50 75.39 ± 4.12 mg/ml showed potent antioxidant activity comparable to standard ascorbic acid (IC50 45.54 ± 3.06 mg/ml). Conclusion: This study suggests that leaves of Lawsonia inermis have bioactive compounds for a new antioxidant drug development.
*1Department of Pharmaceutical Chemistry, Hygia Institute of Pharmaceutical Education and Research, Lucknow-206020,Uttar Pradesh, India. 2Department of Pharmaceutical Chemistry, Acharya Narendra Deo College of Pharmacy, Babhnan, Gonda – 271313, Uttar Pradesh,India.
*Corresponding author. Bhumika Yogi Department of Pharmaceutical Chemistry, Hygia Institute of Pharmaceutical Education and Research, Lucknow-206020, Uttar Pradesh,India.
Received on:28-08-2016; Revised on: 18-09-2016; Accepted on: 13-10-2016