2012
DOI: 10.1016/j.jfluchem.2012.06.021
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Facile synthesis of novel fluorine containing pyrazole based thiazole derivatives and evaluation of antimicrobial activity

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Cited by 91 publications
(40 citation statements)
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“…The model reaction and yields are shown in Scheme 1 and Table 1. Eight candidates such as trypsin from porcine pancreas (PPT), α-amylase from hog pancreas, diastase from Aspergillus oryzae, α-amylase from Aspergillus oryzae, lipase AT30, Amano lipase M from Mucor javanicus, and bovine serum albumin (BSA) were screened ( Table 1, entries [1][2][3][4][5][6][7][8]. The yield of product was the monitored parameter to evaluate the catalytic activity of enzymes.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The model reaction and yields are shown in Scheme 1 and Table 1. Eight candidates such as trypsin from porcine pancreas (PPT), α-amylase from hog pancreas, diastase from Aspergillus oryzae, α-amylase from Aspergillus oryzae, lipase AT30, Amano lipase M from Mucor javanicus, and bovine serum albumin (BSA) were screened ( Table 1, entries [1][2][3][4][5][6][7][8]. The yield of product was the monitored parameter to evaluate the catalytic activity of enzymes.…”
Section: Resultsmentioning
confidence: 99%
“…Thiazoles and their derivatives are an important class of heterocyclic compounds which possess broad biological activities, such as antimicrobial [1], antipyretic [2], antiparasitic [3], antihistaminic [4], and antiviral properties [5]. Aryl-substituted thiazoles are also important functional materials in applications such as fluorescent dyes and liquid crystals [6].…”
Section: Introductionmentioning
confidence: 99%
“…Compounds bearing thiazole and pyrazole nuclei are found to have various antimicrobial activities such as antibacterial, antifungal and antitumor [1][2][3][4][5][6][7]. The asymmetric unit (cf.…”
Section: Discussionmentioning
confidence: 99%
“…3-(4-nitrophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde (1) was prepared according to the literature method [34].…”
Section: Synthesis Of 3-(4-nitrophenyl)-1-phenyl-1h-pyrazole-4-carbalmentioning
confidence: 99%