Manganese(II) complexes of the quinolone family member flumequine: Structure, antimicrobial activity and affinity for albumins and calf-thymus DNA. (1st May 2018)
- Record Type:
- Journal Article
- Title:
- Manganese(II) complexes of the quinolone family member flumequine: Structure, antimicrobial activity and affinity for albumins and calf-thymus DNA. (1st May 2018)
- Main Title:
- Manganese(II) complexes of the quinolone family member flumequine: Structure, antimicrobial activity and affinity for albumins and calf-thymus DNA
- Authors:
- Barmpa, Amalia
Frousiou, Olympia
Kalogiannis, Stavros
Perdih, Franc
Turel, Iztok
Psomas, George - Abstract:
- Graphical abstract: Three novel manganese(II)–flumequine complexes exhibit noteworthy antimicrobial activity and bind tightly to albumins and to calf-thymus DNA. Abstract: In the present contribution, the synthesis and the characterization of the manganese(II) complexes with the quinolone antimicrobial agent flumequine (Hflmq) in the absence or presence of the N, N′-donor heterocyclic ligands 1, 10-phenanthroline (phen) and 2, 2′-bipyridylamine (bipyam) are reported. The structure of complex [Mn(flmq)2 (phen)]·2MeOH was also determined by X-ray crystallography. In the novel complexes, the quinolone ligands are bound to manganese(II) in a bidentate manner through a carboxylato oxygen and the pyridone oxygen. The affinity of the complexes to human or bovine serum albumin proteins was investigated by fluorescence emission spectroscopy and the corresponding binding constants exhibit relatively high values. The binding of the complexes to calf-thymus (CT) DNA was studied by UV–Vis spectroscopy and DNA-viscosity measurements. The DNA-binding constants of the complexes were calculated. Intercalation is the most possible DNA-binding mode, and this was verified through the ability of the complexes to displace ethidium bromide (EB) from the EB–DNA conjugate. The antimicrobial activity of the complexes was tested against four different microorganisms ( Escherichia coli, Xanthomonas campestris, Staphylococcus aureus and Bacillus subtilis ) and was found similar or higher than free Hflmq.
- Is Part Of:
- Polyhedron. Volume 145(2018)
- Journal:
- Polyhedron
- Issue:
- Volume 145(2018)
- Issue Display:
- Volume 145, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 145
- Issue:
- 2018
- Issue Sort Value:
- 2018-0145-2018-0000
- Page Start:
- 166
- Page End:
- 175
- Publication Date:
- 2018-05-01
- Subjects:
- B. subtilis Bacillus subtilis ATCC 6633 -- bipyam 2, 2′-bipyridylamine -- BSA bovine serum albumin -- CT calf-thymus -- E. coli Escherichia coli NCTC 29212 -- EB ethidium bromide, 3, 8-diamino-5-ethyl-6-phenylphenanthridinium bromide -- flmq−1 anion of flumequine -- Hflmq flumequine, 6, 7-dihydro-9-fluoro-5-methyl-1-oxo-1H, 5H-[ij]quinolizine-2-carboxylic acid -- HSA human serum albumin -- IC50 half-minimum inhibitory concentration -- K SA-binding constant -- Kb DNA-binding constant -- kq quenching constant -- KSV Stern–Volmer constant -- MIC minimum inhibitory concentration -- phen 1, 10-phenanthroline -- r [complex]/[DNA] or [complex]/[albumin] -- s strong -- S. aureus Staphylococcus aureus ATCC 6538 -- SA serum albumin -- sh shoulder -- vs very strong -- X. campestris Xanthomonas campestris ATCC 1395 -- Δν(CO2) νasym(CO2) − νasym(CO2) -- λem λemission -- λexc λexcitation
Manganese(II) complexes -- Flumequine -- Antimicrobial activity -- Interaction with albumins -- Interaction with DNA
Chemistry, Inorganic -- Periodicals
Chimie inorganique -- Périodiques
Organometaalverbindingen
Anorganische chemie
546.05 - Journal URLs:
- http://www.sciencedirect.com/science/journal/02775387 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.poly.2018.02.006 ↗
- Languages:
- English
- ISSNs:
- 0277-5387
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.690000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19121.xml