2014
DOI: 10.1016/j.saa.2014.01.108
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Exploring DNA binding and nucleolytic activity of few 4-aminoantipyrine based amino acid Schiff base complexes: A comparative approach

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Cited by 47 publications
(19 citation statements)
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“…So it seems worthwhile to compare the antibacterial properties of 1 with copper complexes derived from quinolones. The activity of complex 1 was found to be even higher than some reported 3-carboxy-4-quinolone copper complexes against the same bacterial strain P. aeruginosa (100 lg/mL) [35] but less compared to copper complexes derived from norfloxacin (0.99 lg/mL) [34].…”
Section: Antibacterial Activitycontrasting
confidence: 58%
“…So it seems worthwhile to compare the antibacterial properties of 1 with copper complexes derived from quinolones. The activity of complex 1 was found to be even higher than some reported 3-carboxy-4-quinolone copper complexes against the same bacterial strain P. aeruginosa (100 lg/mL) [35] but less compared to copper complexes derived from norfloxacin (0.99 lg/mL) [34].…”
Section: Antibacterial Activitycontrasting
confidence: 58%
“…Therefore, for improving the quality of life, antioxidant activity is important for preventing the formation of free radicals in human body. According to previous reports in the literature, few metal complexes may able to exhibit the free radical scavenging activity. Hence, it is tried to assess whether the synthesized metal (II) complexes have the free radical scavenging activity.…”
Section: Resultsmentioning
confidence: 86%
“…4-Aminoantipyrine administration caused a significant decrease in the contracture of myometrium, while the cervix did not reveal significant change [16]. Binding studies of 4-aminoantipyrine with human serum albumin and DNA have already been explored [17,18]. 4-Aminoantipyrine derivatives are well recognized for their clinical and sensor abilities, however no attempt has been made to investigate their anticancer activity against cervical cancer.…”
Section: Introductionmentioning
confidence: 99%
“…This study thus aims at assessing the effectiveness and plausible mode of action of compounds belonging to the class of 4AAP derivatives in HPV positive cervical cancer cells. As an effective receptor to design target based drug design, we selectively chose HPV16 E7 protein [18] and the designing and synthesizing of 4-aminoantipyrine derivatives became one of our major goals.…”
Section: Introductionmentioning
confidence: 99%