Publication | Open Access
Synthesis, antioxidant activity, and α‐glucosidase enzyme inhibition of α‐aminophosphonate derivatives bearing piperazine‐1,2,3‐triazole moiety
23
Citations
35
References
2020
Year
Piperazine‐1,2,3‐triazole Bearing DimethylMedicinal Chemistryα‐Aminophosphonate DerivativesDerivativesDiversity Oriented SynthesisBiochemistryNatural Sciencesα‐Glucosidase Enzyme InhibitionClick ReactionMedicineAntioxidant ActivityOrganic ChemistryPhosphonate DerivativesHeterocycle ChemistryPharmacologyPharmaceutical ChemistryDrug DiscoveryNatural Product Synthesis
Abstract A novel series of piperazine‐1,2,3‐triazole bearing dimethyl(((2‐(4‐((1H‐1,2,3‐triazole‐4‐yl)methyl)piperazin‐1‐yl)ethylamino)(2‐hydroxyaryl)methyl)phosphonate derivatives have been prepared via copper‐catalyzed azide‐alkyne 1,3‐dipolar cycloaddition (CuAAC) (Click Reaction) and Schiff base reactions. The synthesized compounds were confirmed by spectral characterization ( 1 H, 13 C and 31 P NMR, and mass). The title compounds were evaluated for in vitro alpha glucosidase enzyme inhibition and in vitro antioxidant activity using DPPH and H 2 O 2 methods.
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