2008
DOI: 10.1016/j.ejmech.2007.05.006
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Synthesis, physicochemical properties and antimicrobial evaluation of new (E)-chalcones

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Cited by 98 publications
(58 citation statements)
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“…Also when heterocyclic chalcones 1a, c, d and f were allowed to react with 2-aminobenzimidazole (10) under the same conditions, afforded 4-(5-methyl-1-phenyl-1H-pyrazol-4-yl)-2-aryl/or heteroaryl benzo [4,5] imidazo[1,2-a] pyrimidine derivatives 11a-d, respectively, and not compounds 12a and b (Chart 2) as elucidated from spectroscopic tools (cf. Experimental).…”
Section: Resultsmentioning
confidence: 99%
“…Also when heterocyclic chalcones 1a, c, d and f were allowed to react with 2-aminobenzimidazole (10) under the same conditions, afforded 4-(5-methyl-1-phenyl-1H-pyrazol-4-yl)-2-aryl/or heteroaryl benzo [4,5] imidazo[1,2-a] pyrimidine derivatives 11a-d, respectively, and not compounds 12a and b (Chart 2) as elucidated from spectroscopic tools (cf. Experimental).…”
Section: Resultsmentioning
confidence: 99%
“…It is well known that the majority of natural or synthetic chalcones are highly biologically active with great pharmaceutical and medicinal applications. For a structurally simple group of compounds, chalcones have been shown to display a diverse array of biological activities among with antimalarial [1,2], antimicrobial [3][4][5], anticancer [6,7], antioxidant [8], antiallergic [9], antihyperglycemic [10], and anti-inflammatory [11,12] activities.…”
Section: Introductionmentioning
confidence: 99%
“…Lahtchev et al reported a mechanistic study on chalcones using various yeast strains (Lahtchev et al, 2008). Nowakowska et al have reported antibacterial and antifungal activities of chalcones (Nowakowska et al, 2008).…”
Section: Introductionmentioning
confidence: 99%