SYNTHESIS OF NOVEL CHALCONES OF SCHIFF'S BASES AND TO STUDY THEIR EFFECT ON BOVINE SERUM ALBUMIN
Abstract
Objective: Some novel chalcones consisting –unsaturated carbonyl group and C=N bond were synthesized i.e. 1-(4-(benzylideneamino)phenyl)-3-phenylprop-2-en-1-ones and studied the influence of their presence on bovine serum albumin.
Methods: 1-(4-(benzylideneamino)phenyl)-3-phenylprop-2-en-1-ones were synthesized by the reaction of substituted benzaldehydes with 1-((4-benzylideneamino)phenyl)ethanone and in the presence of a base. The structures were confirmed by their IR and 1HNMR spectra. After establishing the structures of 1-(4-(benzylideneamino)phenyl)-3-phenylprop-2-en-1-ones, their effect were observed on BSA in solution.
Results: Out of synthesized chalcones, 1-(4-(4-(3-phenylallylideneamino)phenyl)-3-p-tolylprop-2-en-1-one is most reactive chalcone as it decreased the availability of BSA in solution to maximum extent.
Conclusion: 1-(4-(benzylideneamino)phenyl)-3-phenylprop-2-en-1-ones interact with the bovine serum albumin which is responsible for the transportation of a number of compounds.
Keywords: Bovine serum albumin, interaction studies, chalcones.
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