2016
DOI: 10.1248/bpb.b15-00586
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Novel Pyrazolo[3,4-<i>b</i>]pyridine Derivatives: Synthesis, Characterization, Antimicrobial and Antiproliferative Profile

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Cited by 67 publications
(37 citation statements)
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“…Following overnight incubation at 37°C for 24 h (bacterial strains) or at 25°C for 4-10 days (fungal strains), the tubes are examined for the presence of visible microbial growth by turbidity. The lowest concentration of the antimicrobial agent where the growth was completely inhibited (no turbidity) represents the MIC (Salem and Ali 2016). The precision of broth macrodilution was considered to be plus/minus one twofold dilution concentration, due to the manual preparation of the dilutions (CLSI 2018b).…”
Section: Broth Macrodilutionmentioning
confidence: 99%
“…Following overnight incubation at 37°C for 24 h (bacterial strains) or at 25°C for 4-10 days (fungal strains), the tubes are examined for the presence of visible microbial growth by turbidity. The lowest concentration of the antimicrobial agent where the growth was completely inhibited (no turbidity) represents the MIC (Salem and Ali 2016). The precision of broth macrodilution was considered to be plus/minus one twofold dilution concentration, due to the manual preparation of the dilutions (CLSI 2018b).…”
Section: Broth Macrodilutionmentioning
confidence: 99%
“…In continuation of our previous work, the present work aims at utilization of the reactivity of 2‐thioxo‐1,2‐dihydrobenzo[d][1,3]thiazin‐4‐one ( 1 ) toward different electrophilic and nucleophilic reagents to design and construct new fused and nonfused heterocyclic systems and evaluate them for antitumor activity.…”
Section: Resultsmentioning
confidence: 99%
“…Pyrazolopyridines represent a well-known organic scaffold in various bioactive derivatives and have various pharmacological properties. These compounds exhibit significant biological properties, including anti-bacterial [1,2], anti-microbial [3,4], anti-fungal [5], anti-tumor [6], anti-virus [7], anti-Leishmania [8], HIF 1-a-prolyl hydroxylase inhibitors [9], B-Raf V600E3 inhibitors [10], protein kinase inhibitors [11], PDE4B inhibitors [12], dopaminergic properties [13] and cancer cell lines growth inhabitation activities [14]. The main problems for the synthesis of pyrazolopyridine compounds are long reaction times, utilization of non-reusable and toxic catalyst and use of particular conditions.…”
Section: Introductionmentioning
confidence: 99%