2011
DOI: 10.1111/j.1747-0285.2011.01231.x
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Synthesis and Antibacterial Activity of Aromatic and Heteroaromatic Amino Alcohols

Abstract: Two series of aromatic and heteroaromatic amino alcohols were synthesized from alcohols and aldehydes and evaluated for their antibacterial activities. All the octylated compounds displayed a better activity against the four bacteria tested when evaluated by the agar diffusion method and were selected for the evaluation of minimal inhibitory concentration. The best results were obtained for p-octyloxybenzyl derivatives against Staphylococcus epidermidis (minimal inhibitory concentrations = 32 μm).

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Cited by 17 publications
(8 citation statements)
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“…All the synthesized rac ‐ and meso ‐compounds ( 7, 8, 10, 17, 18 , and 19 ) were examined for their antimicrobial activity by the well‐diffusion method against six Gram‐negative bacteria ( S. typhi H, E. coli, E. aerogenes sp., K. pneumoniae, P. vulgaris , and P. putida ), four Gram‐positive bacteria ( S. aureus, S. epidermis, M. luteus, B. cereus ), and one yeast ( C. albicans ). For the detection of antimicrobial activity, the well‐diffusion method was used …”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…All the synthesized rac ‐ and meso ‐compounds ( 7, 8, 10, 17, 18 , and 19 ) were examined for their antimicrobial activity by the well‐diffusion method against six Gram‐negative bacteria ( S. typhi H, E. coli, E. aerogenes sp., K. pneumoniae, P. vulgaris , and P. putida ), four Gram‐positive bacteria ( S. aureus, S. epidermis, M. luteus, B. cereus ), and one yeast ( C. albicans ). For the detection of antimicrobial activity, the well‐diffusion method was used …”
Section: Methodsmentioning
confidence: 99%
“…In the last stage, the plates were incubated for 24 hr at 37°C in an incubator. On completion of the incubation period, the mean value obtained for the two wells was used to calculate the zone of growth inhibition of each sample . The pathogenic bacterial cultures and yeast were tested for resistance to five antibiotics produced by Oxoid Ltd., Basingstoke, UK.…”
Section: Methodsmentioning
confidence: 99%
“…Glycidyl furfuryl etherwas prepared according to the procedure proposed by de Almeida [18]. In order to synthesize the 2Ph2Epo DA adduct (Scheme 1), 1,1'methylenedi-4,1-phenylene-bismaleimmide (31.1 mmol) was dissolved in chloroform (10 -12 ml) in a 250 ml round-bottom flask equipped with a condenser.…”
Section: Synthesis and Materialsmentioning
confidence: 99%
“…A number of artemisinin derivatives showed highly potent cytotoxicity against several cancer cell lines [6][7][8], antiviral [9], and immunosuppressive properties [10]. Besides that, functionalized β-aminopropanols are not only part of biologically active agents [11][12][13][14], but also important intermediates or precursors in the chemical synthesis of therapeutically or biologically relevant compounds [15]. The introduction of β-aminopropanol into C-10 side chain of artemisinin led to a new type of water soluble artemisinin derivatives 2 (Fig.…”
mentioning
confidence: 99%