Paper
Anticancer and anti-inflammatory activities of 1,8-naphthyridine-3-carboxamide derivatives.
Published Dec 1, 2007 · S. Srivastava, M. Jaggi, Anu T. Singh
Bioorganic & medicinal chemistry letters
Q2 SJR score
37
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
In Vitro StudyStudy Snapshot
1,8-naphthyridine-3-carboxamide derivatives show potential anticancer and anti-inflammatory activities, with compounds 12 showing high cytotoxicity in breast cancer cells and compounds 17 and 22 showing high cytotoxicity in oral and colon cancer cell lines, respectively.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
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Citations
One pot synthesis of 4-iodo-3-phenylbenzo[ b ][1,6]naphthyridine via imino iodization-cyclization of alkynylquinoline-3-carbaldehydes
This one-pot strategy efficiently synthesizes 4-iodo-3-phenylbenzo[b][1,6]naphthyridine from alkynylquinoline-3-carbaldehydes, providing valuable iodine for further reactions and new organic compounds.
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MnO2-catalyzed ligand-free synthesis of (E)-6,7-dihydrodibenzo[b,j][1,7]phenanthrolines and (E)-1,2,3,4-tetrahydrobenzo[b][1,6]n
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Accessing 1,8-Naphthyridone-3-carboxylic Acid Derivatives and Application to the Synthesis of Amfonelic Acid.
This study presents a practical synthesis of diverse 1,8-naphthyridone-3-carboxylic acid derivatives using readily available nicotinic acid derivatives, leading to the first synthesis of amfonelic acid.
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Synthesis of 1, 8-Naphthyridine-3-Carbonitriles under solvent-free conditions using ceric ammonium nitrate
This study presents a solvent-free, one-pot method for synthesizing 1,8-naphthyridine-3-carbonitriles using ceric ammonium nitrate, offering promising factors like shorter reaction duration, excellent yields, and straightforward extraction.
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