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Synthesis, Characterization, and Biological Activity of N (′)-[(Z)-(3-Methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and Its Co(II), Ni(II), and Cu(II) Complexes
Reaction of 1-phenyl-3-methyl-4-benzoyl-pyrazol-5-one and benzoyl hydrazide in refluxing ethanol gave N (′)-[(Z)-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide (HL(1)), which was characterized by NMR spectroscopy and single-crystal X-ray structure study. X-ra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181943/ https://www.ncbi.nlm.nih.gov/pubmed/25332694 http://dx.doi.org/10.1155/2014/718175 |
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author | Asegbeloyin, Jonnie N. Ujam, Oguejiofo T. Okafor, Emmanuel C. Babahan, Ilknur Coban, Esin Poyrazoglu Özmen, Ali Biyik, Halil |
author_facet | Asegbeloyin, Jonnie N. Ujam, Oguejiofo T. Okafor, Emmanuel C. Babahan, Ilknur Coban, Esin Poyrazoglu Özmen, Ali Biyik, Halil |
author_sort | Asegbeloyin, Jonnie N. |
collection | PubMed |
description | Reaction of 1-phenyl-3-methyl-4-benzoyl-pyrazol-5-one and benzoyl hydrazide in refluxing ethanol gave N (′)-[(Z)-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide (HL(1)), which was characterized by NMR spectroscopy and single-crystal X-ray structure study. X-ray diffraction analyses of the crystals revealed a nonplanar molecule, existing in the keto-amine form, with intermolecular hydrogen bonding forming a seven-membered ring system. The reaction of HL(1) with Co(II), Ni(II), and Cu(II) halides gave the corresponding complexes, which were characterized by elemental analysis, molar conductance, magnetic measurements, and infrared and electronic spectral studies. The compounds were screened for their in vitro cytotoxic activity against HL-60 human promyelocytic leukemia cells and antimicrobial activity against some bacteria and yeasts. Results showed that the compounds are potent against HL-60 cells with the IC(50) value ≤5 μM, while some of the compounds were active against few studied Gram-positive bacteria. |
format | Online Article Text |
id | pubmed-4181943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41819432014-10-20 Synthesis, Characterization, and Biological Activity of N (′)-[(Z)-(3-Methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and Its Co(II), Ni(II), and Cu(II) Complexes Asegbeloyin, Jonnie N. Ujam, Oguejiofo T. Okafor, Emmanuel C. Babahan, Ilknur Coban, Esin Poyrazoglu Özmen, Ali Biyik, Halil Bioinorg Chem Appl Research Article Reaction of 1-phenyl-3-methyl-4-benzoyl-pyrazol-5-one and benzoyl hydrazide in refluxing ethanol gave N (′)-[(Z)-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide (HL(1)), which was characterized by NMR spectroscopy and single-crystal X-ray structure study. X-ray diffraction analyses of the crystals revealed a nonplanar molecule, existing in the keto-amine form, with intermolecular hydrogen bonding forming a seven-membered ring system. The reaction of HL(1) with Co(II), Ni(II), and Cu(II) halides gave the corresponding complexes, which were characterized by elemental analysis, molar conductance, magnetic measurements, and infrared and electronic spectral studies. The compounds were screened for their in vitro cytotoxic activity against HL-60 human promyelocytic leukemia cells and antimicrobial activity against some bacteria and yeasts. Results showed that the compounds are potent against HL-60 cells with the IC(50) value ≤5 μM, while some of the compounds were active against few studied Gram-positive bacteria. Hindawi Publishing Corporation 2014 2014-09-15 /pmc/articles/PMC4181943/ /pubmed/25332694 http://dx.doi.org/10.1155/2014/718175 Text en Copyright © 2014 Jonnie N. Asegbeloyin et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Asegbeloyin, Jonnie N. Ujam, Oguejiofo T. Okafor, Emmanuel C. Babahan, Ilknur Coban, Esin Poyrazoglu Özmen, Ali Biyik, Halil Synthesis, Characterization, and Biological Activity of N (′)-[(Z)-(3-Methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and Its Co(II), Ni(II), and Cu(II) Complexes |
title | Synthesis, Characterization, and Biological Activity of N
(′)-[(Z)-(3-Methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and Its Co(II), Ni(II), and Cu(II) Complexes |
title_full | Synthesis, Characterization, and Biological Activity of N
(′)-[(Z)-(3-Methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and Its Co(II), Ni(II), and Cu(II) Complexes |
title_fullStr | Synthesis, Characterization, and Biological Activity of N
(′)-[(Z)-(3-Methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and Its Co(II), Ni(II), and Cu(II) Complexes |
title_full_unstemmed | Synthesis, Characterization, and Biological Activity of N
(′)-[(Z)-(3-Methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and Its Co(II), Ni(II), and Cu(II) Complexes |
title_short | Synthesis, Characterization, and Biological Activity of N
(′)-[(Z)-(3-Methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and Its Co(II), Ni(II), and Cu(II) Complexes |
title_sort | synthesis, characterization, and biological activity of n
(′)-[(z)-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4h-pyrazol-4-ylidene)(phenyl)methyl]benzohydrazide and its co(ii), ni(ii), and cu(ii) complexes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181943/ https://www.ncbi.nlm.nih.gov/pubmed/25332694 http://dx.doi.org/10.1155/2014/718175 |
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