A Convenient Synthesis and Biological Research of Novel 5,6,7,8-Tetrahydro-1,6-naphthyridin-2(1H)-one Derivatives Hydrochloride as Cytotoxic Agents
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Qing-jie Ding | Bin Sun | Yu-qin Jiang | Gui-qing Xu | L. Mao | Yuan Gao | Lizeng Peng
[1] J. Joubert,et al. Design, synthesis and evaluation of indole derivatives as multifunctional agents against Alzheimer's disease. , 2018, MedChemComm.
[2] S. Suzen. Recent Studies and Biological Aspects of Substantial Indole Derivatives with Anti-cancer Activity , 2017 .
[3] F. J. Luque,et al. Design, synthesis and multitarget biological profiling of second-generation anti-Alzheimer rhein-huprine hybrids. , 2017, Future medicinal chemistry.
[4] P. A. Suchetan,et al. Synthesis, crystal structure and molecular docking studies of novel 2-(4-(4-substitutedphenylsulfonyl)piperazin-1-yl)quinolone-3-carbaldehyde derivatives , 2017, Research on Chemical Intermediates.
[5] R. C.-Gaudreault,et al. Synthesis of novel substituted pyrimidine derivatives bearing a sulfamide group and their in vitro cancer growth inhibition activity. , 2017, Bioorganic & medicinal chemistry letters.
[6] Yuechao Ma,et al. Synchronization for complex dynamical networks with mixed mode-dependent time delays , 2016 .
[7] B. Hu,et al. Long noncoding RNA AK126698 inhibits proliferation and migration of non-small cell lung cancer cells by targeting Frizzled-8 and suppressing Wnt/β-catenin signaling pathway , 2016, OncoTargets and therapy.
[8] S. Knapp,et al. Structure-Based Design of an in Vivo Active Selective BRD9 Inhibitor , 2016, Journal of medicinal chemistry.
[9] Huanfeng Jiang,et al. Ruthenium-Catalyzed Straightforward Synthesis of 1,2,3,4-Tetrahydronaphthyridines via Selective Transfer Hydrogenation of Pyridyl Ring with Alcohols. , 2015, Organic letters.
[10] Fu-xian Wan,et al. Synthesis and antibacterial activity of novel ethyl 2-alkoxyimino-2-benzimidazol-2-yl acetates bearing a morpholine group , 2015, Research on Chemical Intermediates.
[11] Y. Pommier,et al. 4-Amino-1-hydroxy-2-oxo-1,8-naphthyridine-Containing Compounds Having High Potency against Raltegravir-Resistant Integrase Mutants of HIV-1 , 2014, Journal of medicinal chemistry.
[12] K. Muthusamy,et al. Pharmacophore modeling, 3D-QSAR, and molecular docking study on naphthyridine derivatives as inhibitors of 3-phosphoinositide-dependent protein kinase-1 , 2013, Medicinal Chemistry Research.
[13] Maninder Kaur,et al. Exploring the Role of Water Molecules for Docking and Receptor Guided 3D-QSAR Analysis of Naphthyridine Derivatives as Spleen Tyrosine Kinase (Syk) Inhibitors , 2012, J. Chem. Inf. Model..
[14] M. Doble,et al. QSAR studies on substituted 3- or 4-phenyl-1,8-naphthyridine derivatives as antimicrobial agents , 2012, Medicinal Chemistry Research.
[15] Lin Jiang,et al. Synthesis and phytotoxic activity of novel acylthiourea and 2H-1,2,4-thiadiazolo[2,3-α]pyrimidine derivatives , 2012 .
[16] Y. Pommier,et al. Design, synthesis, and evaluation of dibenzo[c,h][1,6]naphthyridines as topoisomerase I inhibitors and potential anticancer agents. , 2010, Journal of medicinal chemistry.
[17] Mingliang Liu,et al. Synthesis and in vitro antibacterial activity of 7-(4-alkoxyimino-3-amino-3-methylpiperidin-1-yl)fluoroquinolone derivatives. , 2009, European journal of medicinal chemistry.
[18] D. Boschelli,et al. Discovery of dibenzo[c,f][2,7]naphthyridines as potent and selective 3-phosphoinositide-dependent kinase-1 inhibitors. , 2007, Journal of medicinal chemistry.
[19] P. Coleman,et al. Non-peptide αvβ3 antagonists. Part 7: 3-Substituted tetrahydro-[1,8]naphthyridine derivatives , 2004 .
[20] K. Fujishige,et al. 1,7- and 2,7-naphthyridine derivatives as potent and highly specific PDE5 inhibitors. , 2003, Bioorganic & medicinal chemistry letters.
[21] M. Kozlowski,et al. Convenient preparation of naphthyridines from halopyridines: sequential Heck coupling and cyclization , 2001 .
[22] G. Mele,et al. Synthesis and Evaluation of Pyrido[2,3‐d]pyrimidine and 1,8‐Naphthyridine Derivatives as Potential Antitumor Agents , 2017 .