One‐Pot Three‐Component Synthesis of Some 6‐Methoxy‐2‐Naphthyl Pyrimidinones with Molecular Docking and Biological Activities Studies

Abstract A new series of 6‐methoxy‐2‐naphthalene based pyrimidinones were synthesized via one pot‐three component synthetic reaction of aryl aldehydes, 6‐methoxy‐2‐acetonapthone and urea in the presence of nano zinc ferrite catalyst under conventional method. The synthesized compounds were characterized by their spectral techniques including FT‐IR, H 1 , C 13 NMR, LCMS, and analysis of elements. Molecular docking analysis was also performed to identify the protein‐ligand interactions and binding energy of synthesized compounds. Biological studies of all synthesized pyrimidinone compounds have been measured against bacterial and fungal strains by calculating the zone of inhibition.

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Journal
ChemistrySelect
Published
2024-10-01
DOI
https://doi.org/10.1002/slct.202402276
Citations
1
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.25

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One‐Pot Three‐Component Synthesis of Some 6‐Methoxy‐2‐Naphthyl Pyrimidinones with Molecular Docking and Biological Activities Studies

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1 citations
ChemistrySelect
Synthesis and biological activity
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article

One‐Pot Three‐Component Synthesis of Some 6‐Methoxy‐2‐Naphthyl Pyrimidinones with Molecular Docking and Biological Activities Studies

Ganesamoorthy Thirunarayanan, Jaganathan Divya, I. Muthuvel, P. Gayathri, S. Suguna
article en
1 citations

Abstract

Abstract A new series of 6‐methoxy‐2‐naphthalene based pyrimidinones were synthesized via one pot‐three component synthetic reaction of aryl aldehydes, 6‐methoxy‐2‐acetonapthone and urea in the presence of nano zinc ferrite catalyst under conventional method. The synthesized compounds were characterized by their spectral techniques including FT‐IR, H 1 , C 13 NMR, LCMS, and analysis of elements. Molecular docking analysis was also performed to identify the protein‐ligand interactions and binding energy of synthesized compounds. Biological studies of all synthesized pyrimidinone compounds have been measured against bacterial and fungal strains by calculating the zone of inhibition.

ChemistrySelectVol. 9(38)
Annamalai University (IN)
Department of Science and Technology, Ministry of Science and Technology, India
Affordable and clean energy
Openalex Percentile: Top 48%
Synthesis and biological activity
0.25
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