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International Journal of Advanced Chemistry Research
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Vol. 7, Issue 11, Part B (2025)

Design, Synthesis, and Biological Assessment of Pyridyl Azo Dyes and Their Palladium Complexes with Antioxidant and Anticancer Potential

Author(s):

Anand Mohan Jha

Abstract:

Herein, we describe the preparation and characterization of a novel azo dye of pyridyl, namely, (E)-N-(4-hydroxy-3-(pyridin-3-yldiazenyl)phenyl)acetamide (EHPYPA) and its palladium complex. The palladium complex bears the formulation a[Pd(EHPYPA)Cl], which is supported by electrospray ionization mass spectrometry, CHN analysis, FT-IR, UV-Vis, 1HNMR spectroscopies, molecular docking and simulation. The synthesis and structural properties of the azo dye and a palladium complex are reported. The EHPYPA ligand showed important changes in the colours and spectra at different values of acidity which permit to use of it as an indicator in analytical chemistry. The EHPYPA ligand behaves as N, O-bidentate donor ligand forming chelates. The ligand and palladium complex have been screened against the SKOV-3 cell line using the MTT method. Furthermore, the docking results indicate favourable docking with scores were -7.3, -7.8 and -11.2 kcal/mol for the ligand, palladium complex and Co-crystal. RMSD values for the prepared compounds indicate stability while PSA, MolSA and SASA values indicate favorable drug-like potentials for the ligands. The palladium complex has been investigated as an anticancer agent where the activity data had shown that the palladium metal complex has to be a more potent anticancer than the parent azo ligand, suggesting that metalation increases the anticancer activity of the azo ligand of pyridyl.

Pages: 74-83  |  197 Views  101 Downloads


International Journal of Advanced Chemistry Research
How to cite this article:
Anand Mohan Jha. Design, Synthesis, and Biological Assessment of Pyridyl Azo Dyes and Their Palladium Complexes with Antioxidant and Anticancer Potential. Int. J. Adv. Chem. Res. 2025;7(11):74-83. DOI: 10.33545/26646781.2025.v7.i11b.334
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