GREEN SYNTHESIS OF NEW SULFANYL DERIVATIVES OF AMPYRONE AND PREDICTION OF THEIR ANTI-INFLAMMATORY ACTIVITY
DOI:
https://doi.org/10.1007/5472Keywords:
sulfanyl-substituted ampyrones, anti-inflammatory activity prediction, green chemistry, molecular docking, multicomponent reactions.Abstract
A selective method was developed for the synthesis of acyclic sulfanyl derivatives of ampyrone by thiomethylation reaction of 4-amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one with formaldehyde and thiols in aqueous medium under various conditions (room temperature, 80°C, ultrasonication or microwave irradiation). A series of the synthesized sulfanyl derivatives of ampyrone were characterized with regard to their anti-inflammatory activity by molecular docking method using the AutoDock 4.2 and AutoDock Vina software. The steric complementarity with the active sites of cyclooxygenase isoforms (COX-1 and COX-2) was explored.
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Published
2020-04-30
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Section
Original Papers