Antibacterial, Antifungal, Phytotoxic, and Genotoxic Properties of Two Complexes of AgI with Sulfachloropyridazine (SCP): X‐ray Diffraction of [Ag(SCP)]n. Issue 6 (7th May 2014)
- Record Type:
- Journal Article
- Title:
- Antibacterial, Antifungal, Phytotoxic, and Genotoxic Properties of Two Complexes of AgI with Sulfachloropyridazine (SCP): X‐ray Diffraction of [Ag(SCP)]n. Issue 6 (7th May 2014)
- Main Title:
- Antibacterial, Antifungal, Phytotoxic, and Genotoxic Properties of Two Complexes of AgI with Sulfachloropyridazine (SCP): X‐ray Diffraction of [Ag(SCP)]n
- Authors:
- Mosconi, Natalia
Giulidori, Cecilia
Velluti, Francesca
Hure, Estela
Postigo, Agustina
Borthagaray, Graciela
Back, Davi Fernando
Torre, María H.
Rizzotto, Marcela - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>We report the synthesis, characterization, antibacterial and antifungal activities, phytotoxicity, and genotoxicity of two new complexes of silver(I) with sulfachloropyridazine (SCP), one of which is heteroleptic with SCP and SCN<sup>−</sup> ligands (Ag–SCP–SCN), the other of which is homoleptic (Ag–SCP); furthermore, the crystal structure of the homoleptic complex is disclosed. The heterocyclic N atom nearest to the Cl atom and the N<sub>sulfonamide</sub> atom could be coordination sites for the silver ion in the Ag–SCP–SCN complex. The Ag–SCP complex is a polymeric compound with metal–metal bonds, and the heterocyclic and sulfonamide N atoms are points of coordination for Ag<sup>I</sup>. Both complexes showed activity against all the tested bacteria, and in the cases of <italic>Escherichia coli</italic> and <italic>Pseudomonas aeruginosa</italic>, the action was better than that of SCP. In all cases, both silver–SCP complexes showed better antifungal activity than SCP, which was inactive against the tested fungi. Notably, the activity against <italic>P. aeruginosa</italic>, a nosocomial multidrug‐resistant pathogen, was better than that of the reference antibiotic cefotaxim. Both silver–sulfa complexes displayed moderate activity against the tested yeast, especially for <italic>C. neoformans</italic>, which is an important fact considering the incidence of cryptococcosis, mainly in immune‐deficient<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>We report the synthesis, characterization, antibacterial and antifungal activities, phytotoxicity, and genotoxicity of two new complexes of silver(I) with sulfachloropyridazine (SCP), one of which is heteroleptic with SCP and SCN<sup>−</sup> ligands (Ag–SCP–SCN), the other of which is homoleptic (Ag–SCP); furthermore, the crystal structure of the homoleptic complex is disclosed. The heterocyclic N atom nearest to the Cl atom and the N<sub>sulfonamide</sub> atom could be coordination sites for the silver ion in the Ag–SCP–SCN complex. The Ag–SCP complex is a polymeric compound with metal–metal bonds, and the heterocyclic and sulfonamide N atoms are points of coordination for Ag<sup>I</sup>. Both complexes showed activity against all the tested bacteria, and in the cases of <italic>Escherichia coli</italic> and <italic>Pseudomonas aeruginosa</italic>, the action was better than that of SCP. In all cases, both silver–SCP complexes showed better antifungal activity than SCP, which was inactive against the tested fungi. Notably, the activity against <italic>P. aeruginosa</italic>, a nosocomial multidrug‐resistant pathogen, was better than that of the reference antibiotic cefotaxim. Both silver–sulfa complexes displayed moderate activity against the tested yeast, especially for <italic>C. neoformans</italic>, which is an important fact considering the incidence of cryptococcosis, mainly in immune‐deficient patients. No chromosomal aberrations were observed with the <italic>Allium cepa</italic> test, which is auspicious for further study of these complexes as potential drugs.</p> </abstract> … (more)
- Is Part Of:
- ChemMedChem. Volume 9:Issue 6(2014:Jun.)
- Journal:
- ChemMedChem
- Issue:
- Volume 9:Issue 6(2014:Jun.)
- Issue Display:
- Volume 9, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 9
- Issue:
- 6
- Issue Sort Value:
- 2014-0009-0006-0000
- Page Start:
- 1211
- Page End:
- 1220
- Publication Date:
- 2014-05-07
- Subjects:
- Pharmaceutical chemistry -- Periodicals
615.19005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1860-7187 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/110485305 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cmdc.201400071 ↗
- Languages:
- English
- ISSNs:
- 1860-7179
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.254000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3439.xml