Synthesis and Evaluation of Analgesic andAnti-inflammatory Activities of Most Active FreeRadical Scavenging Derivatives of Mangiferin

摘要

In the present study, structural modification of mangiferin was carried out for structure activity relationship studies. One new compound and three known derivatives were prepared from mangiferin. All these compounds were synthesized and purified by standard procedures, identified by using physical and spectral (IR, ~(1)H NMR, ~(13)C NMR and MS) properties. The synthesized mangiferin derivatives were tested for In vitro antioxidant properties. Benzyl and methyl substituted mangiferin showed poor antioxidant activity than mangiferin. However, mangiferin derivatives substituted with acetyl and benzoyl groups were showed potent antioxidant activity than mangiferin in lipid peroxidation, p-NDA, deoxyribose and alkaline DMSO methods. But both the compounds failed to show potent analgesic and anti-inflammatory activities. In all these methods, standard drugs showed better activity than mangiferin and its derivatives.