2009
DOI: 10.2174/157340609789117804
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Synthesis, DNA Binding, Docking and Photoclevage Studies of Novel Benzo[b][1,8]naphthyridines

Abstract: The synthesis and docking studies of novel benzo[b][1,8]naphthyridines is discribed. The docking studies show that the derivatives prefer to bind the AT-rich region of double stranded DNA (ds-DNA). The maximum binding energy -7.16 (kcal/mol) was observed for benzo[b][1,8]naphthyridine-5-thiol 5a and it is a better candidate as an enantioselective binder to ds-DNA than the other derivatives of benzo[b][1,8]naphthyridines. When photoirradiated at 365 nm, benzo[1,8]-naphthyridines have been found to promote the p… Show more

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Cited by 15 publications
(6 citation statements)
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“…On the other hand, a pleasant experience will make consumers have a high tolerance for the company so that consumers feel satisfied even though the service provided is considered unsatisfactory. This is supported by studies which state that service quality has a positive and significant effect on customer satisfaction in the retail context [7,8].…”
Section: Introductionmentioning
confidence: 71%
See 1 more Smart Citation
“…On the other hand, a pleasant experience will make consumers have a high tolerance for the company so that consumers feel satisfied even though the service provided is considered unsatisfactory. This is supported by studies which state that service quality has a positive and significant effect on customer satisfaction in the retail context [7,8].…”
Section: Introductionmentioning
confidence: 71%
“…This study is inspired by studies [6,7,9,[16][17][18]. This study emphasizes the empirical analysis of the relationship of service quality, image, customer satisfaction and customer loyalty in the retail industry in Yogyakarta.…”
Section: Research Modelmentioning
confidence: 99%
“…In view of the above biological importance and in continuation of our previous work 26–28, we demonstrate a new strategy to introduce oxadiazole or thiadiazole or triazole rings into macrocycles employing the novel precursors 1 , 2 and 3 (Fig. 1) without using high dilution conditions.…”
Section: Introductionmentioning
confidence: 80%
“…Several organic compounds, bearing quite diverse structures, have been identified as DNA photocleavaging agents. These include [1,2,4]−triazolo−[4,3−a]quinoxalines (33), quinoxalin−4(5 H )−ones (34), enediynes (35,36), pyrrolecarboxamide conjugated 4′−bromo−acetophenones (37), halophenyl sulfonamide derivatives of poly N −methylimidazoles (38), naphthalimides, (39–41) nitrobenzamido amino‐acridine derivatives (42,43), benzo[ b ][1,8]naphthyridines (44) and quinolones (45–47), N −phenylhydroxylamine derivatives (48), O −acyl (49–53), O −sulphonyl (54,55) and O ‐carbamoyl (56) oximes, β−carbolines (57,58), pyrazole derivatives (59,60), azido carbonyl compounds (61), etc.…”
Section: Introductionmentioning
confidence: 99%