Cargando…
C-3 Substituted Lawsonemonoximates of Holmium(III): Synthesis, Characterization, and Antimicrobial Activity
A series of five new metal complexes of Ho(III) with C-3 substituted derivatives of lawsonemonexime (2-hydroxy-1,4-naphthalenediene-1-oxime) were synthesized. The compounds were characterized by melting point, elemental analysis, IR spectroscopy and magnetic susceptibility. The antimicrobial activit...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2000
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365214/ https://www.ncbi.nlm.nih.gov/pubmed/18475938 http://dx.doi.org/10.1155/MBD.2000.147 |
_version_ | 1782154114229075968 |
---|---|
author | Jagtap, S. B. Joshi, S. G. Litake, G. M. Ghole, V. S. Kulkarni, B. A. |
author_facet | Jagtap, S. B. Joshi, S. G. Litake, G. M. Ghole, V. S. Kulkarni, B. A. |
author_sort | Jagtap, S. B. |
collection | PubMed |
description | A series of five new metal complexes of Ho(III) with C-3 substituted derivatives of lawsonemonexime (2-hydroxy-1,4-naphthalenediene-1-oxime) were synthesized. The compounds were characterized by melting point, elemental analysis, IR spectroscopy and magnetic susceptibility. The antimicrobial activity of the compounds were determined by disk diffusion method and broth micro-dilution techniques using Mueller Hinton medium against the following organisms: S. aureus ATCC 6538P, Klebsiella pneumoniae, NCTC 418, Pseudomonas aeruginosa ATCC 27833, Salmonella typhimurium ATCC 23564, E. coli U 1777, E. coli HB101, Proteus morganii NCIM 2860, Providencia stuartii NCIM 2799 and Acinetobacter baumannii U 24. The chelates of Ho(III) with lawsonemonoxime and Ho(III) with 3-bromolawsonemonoxime showed a variable antimicrobial activity against all organisms tested except Pseudomonas and Klebsiella spp. S. aureus was found more sensitive to all ligands and chelates tested; but the MIC values of chelates were considerably less; thus having more antimicrobial effect. |
format | Text |
id | pubmed-2365214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-23652142008-05-12 C-3 Substituted Lawsonemonoximates of Holmium(III): Synthesis, Characterization, and Antimicrobial Activity Jagtap, S. B. Joshi, S. G. Litake, G. M. Ghole, V. S. Kulkarni, B. A. Met Based Drugs Research Article A series of five new metal complexes of Ho(III) with C-3 substituted derivatives of lawsonemonexime (2-hydroxy-1,4-naphthalenediene-1-oxime) were synthesized. The compounds were characterized by melting point, elemental analysis, IR spectroscopy and magnetic susceptibility. The antimicrobial activity of the compounds were determined by disk diffusion method and broth micro-dilution techniques using Mueller Hinton medium against the following organisms: S. aureus ATCC 6538P, Klebsiella pneumoniae, NCTC 418, Pseudomonas aeruginosa ATCC 27833, Salmonella typhimurium ATCC 23564, E. coli U 1777, E. coli HB101, Proteus morganii NCIM 2860, Providencia stuartii NCIM 2799 and Acinetobacter baumannii U 24. The chelates of Ho(III) with lawsonemonoxime and Ho(III) with 3-bromolawsonemonoxime showed a variable antimicrobial activity against all organisms tested except Pseudomonas and Klebsiella spp. S. aureus was found more sensitive to all ligands and chelates tested; but the MIC values of chelates were considerably less; thus having more antimicrobial effect. Hindawi Publishing Corporation 2000 /pmc/articles/PMC2365214/ /pubmed/18475938 http://dx.doi.org/10.1155/MBD.2000.147 Text en Copyright © 2000 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ 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 Jagtap, S. B. Joshi, S. G. Litake, G. M. Ghole, V. S. Kulkarni, B. A. C-3 Substituted Lawsonemonoximates of Holmium(III): Synthesis, Characterization, and Antimicrobial Activity |
title | C-3 Substituted Lawsonemonoximates of Holmium(III): Synthesis, Characterization, and Antimicrobial Activity |
title_full | C-3 Substituted Lawsonemonoximates of Holmium(III): Synthesis, Characterization, and Antimicrobial Activity |
title_fullStr | C-3 Substituted Lawsonemonoximates of Holmium(III): Synthesis, Characterization, and Antimicrobial Activity |
title_full_unstemmed | C-3 Substituted Lawsonemonoximates of Holmium(III): Synthesis, Characterization, and Antimicrobial Activity |
title_short | C-3 Substituted Lawsonemonoximates of Holmium(III): Synthesis, Characterization, and Antimicrobial Activity |
title_sort | c-3 substituted lawsonemonoximates of holmium(iii): synthesis, characterization, and antimicrobial activity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365214/ https://www.ncbi.nlm.nih.gov/pubmed/18475938 http://dx.doi.org/10.1155/MBD.2000.147 |
work_keys_str_mv | AT jagtapsb c3substitutedlawsonemonoximatesofholmiumiiisynthesischaracterizationandantimicrobialactivity AT joshisg c3substitutedlawsonemonoximatesofholmiumiiisynthesischaracterizationandantimicrobialactivity AT litakegm c3substitutedlawsonemonoximatesofholmiumiiisynthesischaracterizationandantimicrobialactivity AT gholevs c3substitutedlawsonemonoximatesofholmiumiiisynthesischaracterizationandantimicrobialactivity AT kulkarniba c3substitutedlawsonemonoximatesofholmiumiiisynthesischaracterizationandantimicrobialactivity |