2005
DOI: 10.21608/bfsa.2005.65235
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Synthesis of Some Quinoline Thiosemicarbazone Derivatives of Potential Antimicrobial Activity

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Cited by 10 publications
(2 citation statements)
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References 12 publications
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“…FTIR spectrophotometer from Shimadzu (model 8101) In KBr pellets, Fourier transform infrared (FT-IR) spectra between 400 and 4000 cm −1 were recorded. A Bruker 400 MHz spectrometer was used to record the 1 H and 13 C NMR spectra in DMSO-d 6 , with tetra methyl silane (TMS) serving as an internal standard. The electron ionization method was utilized to record mass spectra at 70 eV on an HP MS-5988 GS-MS. UV-visible spectra were recorded using a Shimadzu UV mini-1240 spectrophotometer.…”
Section: Characterizationmentioning
confidence: 99%
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“…FTIR spectrophotometer from Shimadzu (model 8101) In KBr pellets, Fourier transform infrared (FT-IR) spectra between 400 and 4000 cm −1 were recorded. A Bruker 400 MHz spectrometer was used to record the 1 H and 13 C NMR spectra in DMSO-d 6 , with tetra methyl silane (TMS) serving as an internal standard. The electron ionization method was utilized to record mass spectra at 70 eV on an HP MS-5988 GS-MS. UV-visible spectra were recorded using a Shimadzu UV mini-1240 spectrophotometer.…”
Section: Characterizationmentioning
confidence: 99%
“…Due to the presence of oxygen and nitrogen atoms, the 8-hydroxy quinoline (Q) molecule has a strong chelating effect on metal ions. The Q compounds have a variety of pharmacologically advantageous effects, including antibacterial [13], antioxidant, anticancer, and anti-inflammatory effects [14].…”
Section: Introductionmentioning
confidence: 99%