2023
DOI: 10.1007/s00203-023-03584-y
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Chalcone Schiff bases disrupt cell membrane integrity of Saccharomyces cerevisiae and Candida albicans cells

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Cited by 4 publications
(2 citation statements)
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“…Schiff bases have numerous applications including coordination chemistry [23], catalysis [24], chemosensors [25] and intermediates in synthesis [26,27]. They also exhibit a variety of biological applications: antibacterial [28][29][30][31][32][33][34], antifungal [34][35][36], antiviral [37,38], antimalarial [39,40], antituberculosis [41][42][43], anthelmintic [44,45], urease inhibitors [46][47][48], anticancer [49][50][51], antidyslipidemic [52], antidiabetic [53,54], antidepressant Schiff bases are compounds with the structure R'N=CR 2 (R' ̸ = H) [22], traditionally formed in the reaction of alkyl/aryl aldehydes or ketones with primary amines [23]. Many considered them to be synonymous with azomethines (RN=CR 2 , R ̸ = H), both being a particular case of imines (RN=CR 2 , R = H, hydrocarbonyl) [22].…”
Section: Introductionmentioning
confidence: 99%
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“…Schiff bases have numerous applications including coordination chemistry [23], catalysis [24], chemosensors [25] and intermediates in synthesis [26,27]. They also exhibit a variety of biological applications: antibacterial [28][29][30][31][32][33][34], antifungal [34][35][36], antiviral [37,38], antimalarial [39,40], antituberculosis [41][42][43], anthelmintic [44,45], urease inhibitors [46][47][48], anticancer [49][50][51], antidyslipidemic [52], antidiabetic [53,54], antidepressant Schiff bases are compounds with the structure R'N=CR 2 (R' ̸ = H) [22], traditionally formed in the reaction of alkyl/aryl aldehydes or ketones with primary amines [23]. Many considered them to be synonymous with azomethines (RN=CR 2 , R ̸ = H), both being a particular case of imines (RN=CR 2 , R = H, hydrocarbonyl) [22].…”
Section: Introductionmentioning
confidence: 99%
“…Schiff bases have numerous applications including coordination chemistry [23], catalysis [24], chemosensors [25] and intermediates in synthesis [26,27]. They also exhibit a variety of biological applications: antibacterial [28][29][30][31][32][33][34], antifungal [34][35][36], antiviral [37,38], antimalarial [39,40], antituberculosis [41][42][43], anthelmintic [44,45], urease inhibitors [46][47][48], anticancer [49][50][51], antidyslipidemic [52], antidiabetic [53,54], antidepressant [55][56][57], anticonvulsant [58,59], neurodegenerative disorder treatment [60,61], anti-inflammatory [62] and antioxidant [53,54].…”
Section: Introductionmentioning
confidence: 99%