2014
DOI: 10.1016/j.bmcl.2014.04.084
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Synthesis, cytotoxicity, antimicrobial and anti-biofilm activities of novel pyrazolo[3,4-b]pyridine and pyrimidine functionalized 1,2,3-triazole derivatives

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Cited by 89 publications
(43 citation statements)
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“…Afterwards, synthesized target compounds were characterized by various spectral techniques like FTIR, 1 H NMR, 13 C NMR spectroscopy and HRMS. In FTIR spectra, C-H stretching of triazole ring absorbed in the region at 3154-3137 cm -1 .…”
Section: Resultsmentioning
confidence: 99%
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“…Afterwards, synthesized target compounds were characterized by various spectral techniques like FTIR, 1 H NMR, 13 C NMR spectroscopy and HRMS. In FTIR spectra, C-H stretching of triazole ring absorbed in the region at 3154-3137 cm -1 .…”
Section: Resultsmentioning
confidence: 99%
“…The progress of reaction was monitored by readymade silica gel plates (SIL G/UV254, ALUGRAM) and visualization was carried out with ultraviolet lamp. The 1 H NMR spectra and 13 C NMR spectra were recorded on BRUKER AVANCE II 400 MHz spectrometer at 400 MHz and 100 MHz respectively in CDCl3/DMSO-d6. Values of coupling constant (J) were given in Hz.…”
Section: Methodsmentioning
confidence: 99%
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“…Pyridines form a class of compounds exhibiting potential activities against a wide range of biological targets [18][19][20]. Its derivatives have been designed and synthesized as therapeutic agents [21][22][23][24], as herbicides, fungicides, pesticides and as fluorescent dyes [25,26].…”
Section: Pyridines Dihydropyridines Piperidinesmentioning
confidence: 99%
“…Biofilm Inhibitory Assay Inhibition of bacterial biofilm formation was screened using method, described previously, 39) with some modification. Eight hospital isolates of methicillinresistant and two standard strains of Staphylococcus epidermidis (ATC C 12228, ATC C 35984) were cultured overnight in Tryptone Soy Broth with 0,5% glucose.…”
Section: Biologymentioning
confidence: 99%