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Preparation, Characterization and In Vitro Biological Activities of New Diphenylsulphone Derived Schiff Base Ligands and Their Co(II) Complexes

The present work describes the chemical preparation of Schiff bases derived from 4,4′-diaminodiphenyl sulfone (L(1)–L(5)) and their Co(II) metal complexes. The evaluation of antimicrobial and anticancer activities against MCF-7 cell line and human lung cancer cell line A-549 was performed. The afore...

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Detalles Bibliográficos
Autores principales: Gaikwad, Kundalkesha D., Ubale, Panchsheela, Khobragade, Rahul, Deodware, Sachin, Dhale, Pratibha, Asabe, Mahadev R., Ovhal, Rekha M., Singh, Pranav, Vishwanath, Prashant, Shivamallu, Chandan, Achar, Raghu Ram, Silina, Ekaterina, Stupin, Victor, Manturova, Natalia, Shati, Ali A., Alfaifi, Mohammad Y., Elbehairi, Serag Eldin I., Gaikwad, Shashikant H., Kollur, Shiva Prasad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741402/
https://www.ncbi.nlm.nih.gov/pubmed/36500665
http://dx.doi.org/10.3390/molecules27238576
Descripción
Sumario:The present work describes the chemical preparation of Schiff bases derived from 4,4′-diaminodiphenyl sulfone (L(1)–L(5)) and their Co(II) metal complexes. The evaluation of antimicrobial and anticancer activities against MCF-7 cell line and human lung cancer cell line A-549 was performed. The aforementioned synthesized compounds are characterized by spectroscopic techniques and elemental analysis confirms successful synthesis. The results from the above analytical techniques revealed that the complexes are in an octahedral geometry. The antimicrobial activity of the synthesized Schiff base ligands and their metal complexes under study was carried out by using the agar well diffusion method. The ligand and complex interactions for biological targets were predicted using molecular docking and high binding affinities. Further, the anticancer properties of the synthesized compounds are performed against the MCF-7 cell line and human lung cancer cell line A-549 using adriamycin as the standard drug.