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Synthesis, spectroscopic characterizations, and biological evalution of some substituted 1-ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carbohydrazide and their copper complexes.
Author(s):
1. Farah Deeba: Center for environmental protection studies, PCSIR Laboratories Complex,Lahore,Pakistan
2. Misbahul Ain Khan: Institute of Chemistry, University of the Punjab University Lahore.
3. Naeem Abbas: Center for environmental protection studies, PCSIR Laboratories Complex,Lahore,Pakistan
4. Rauf Ahmad Khan: Center for environmental protection studies, PCSIR Laboratories Complex, Lahore Pakistan.
5. Muhammad Muneeb Ahsan: COMSAT, institute of Information technology,Lahore,Pakistan
Abstract:
Summary: Different analogs of 1-ethyl-1, 4-dihydro-7-methyH-4-oxo-1, 8-naphthyridine-3carbohydrazide (carbonyl hydrazone derivatives of Nalidixic acid, H 1-10) and their copper complexes have been synthesized from reaction of Nalidixic acid hydrazide with substituted benzaldehyde. These are characterized on the basis of IR spectra, 1H-NMR spectra, Mass spectra, elemental and AAS studies for metals. Copper complexes were prepared from CuCl2.2H2O and these ligands, the metal ligand ratio was found to be 1:1 and found to be bidentate. The antibacterial, antifungal and antioxidant activities of these hydrazone ligands and their copper complexes have also been evaluated. Copper complexes possess antibacterial and antifungal activities better than the parent hydrazone ligands while they have better antioxidant activity with DPPH radical than copper complexes. Nalidixic acid have maximum of all biological activities, but H-6 showed slightly better antioxidant activity than Nalidixic acid and other activities were close to it.
Page(s): 419-428
DOI: DOI not available
Published: Journal: Journal of Chemical Society of Pakistan, Volume: 39, Issue: 3, Year: 2017
Keywords:
synthesis , 1HNMR spectra , IR spectra , Biologic evaluation
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