New Biginelli derivatives with trifluoro extension as inhibitors of epidermal growth factor receptor tyrosine kinase: molecular docking study in comparison with monastrol
Author:
Funder
Gondwana University, Gadchiroli
Slovenian Research Agency
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
https://link.springer.com/content/pdf/10.1007/s11224-023-02174-4.pdf
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2. Razzaghi-Asl N, Kamrani-Moghadam M, Farhangi B, Vahabpour R, Zabihollahi R, Sepehri S (2019) Design, synthesis and evaluation of cytotoxic, antimicrobial, and anti-HIV-1 activities of new 1,2,3,4-tetrahydropyrimidine derivatives. Res Pharm Sci 14:155–166. https://doi.org/10.4103/1735-5362.253363
3. Matos LHS, Masson FT, Simeoni LA, Homem-deMello M (2018) Biological activity of dihydropyrimidinone (DHPM) derivatives: a systematic review. Eur J Med Chem 143:1779–1789. https://doi.org/10.1016/j.ejmech.2017.10.073
4. Jin T, Zhang S, Li T (2002) p-Toluenesulfonic acid catalyzed efficient synthesis of dihydropyrimidines: improved high yielding protocol for the Biginelli reaction. SyntCommuns 32:1847–1851. https://doi.org/10.1081/SCC-120004068
5. Marques LA, Semprebon SC, Niwa AM, D’Epiro GFR, Sartori D, de Fátima  (2016) Antiproliferative activity of monastrol in human adenocarcinoma (MCF-7) and non-tumor (HB4a) breast cells. Naunyn-Schmiedebergs Arch Pharmacol 389:1279–1288. https://doi.org/10.1007/s00210-016-1292-1299
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