Structure-based design, synthesis, biological evaluation, and molecular docking of novel 10-methoxy dibenzo[b,h][1,6]naphthyridinecarboxamides
Author:
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics
Link
https://link.springer.com/content/pdf/10.1007/s00044-020-02645-x.pdf
Reference42 articles.
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2. Feng BB, Lu L, Li C, Wang XS. Iodine-catalyzed synthesis of dibenzo[b,h][1,6]naphthyridine-11-carboxamides via a domino reaction involving double elimination of hydrogen bromide. Org Biomol Chem. 2016;14:2774–9. https://doi.org/10.1039/c5ob02620b.
3. Eweas AF, Khalifa NM, Ismail NS, Al-Omar MA, Soliman AM. Synthesis, molecular docking of novel 1,8-naphthyridine derivatives and their cytotoxic activity against HepG2 cell lines. Med Chem Res. 2014;23:76–86. https://doi.org/10.1007/s00044-013-0604-6.
4. Zeng LF, Wang Y, Kazemi R, Xu S, Xu ZL, Sanchez TW, et al. Repositioning HIV-1 integrase inhibitors for cancer therapeutics: 1,6-naphthyridine-7-carboxamide as a promising scaffold with drug-like properties. J Med Chem. 2012;55:9492–509. https://doi.org/10.1021/jm300667v.
5. Bedard J, May S, L’Heureux L, Stamminger T, Copsey A, Drach J. Antiviral properties of a series of 1,6-naphthyridine and 7, 8-dihydroisoquinoline derivatives exhibiting potent activity against human cytomegalovirus. Antimicrob Agents Chemother. 2000;44:929–37.
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