BindingDB logo
myBDB logout

BindingDB Data by Journal

PMIDDataArticle TitleCitationOrganizationSD Files Download
2764355928Further investigation of inhibitors of MRSA pyruvate kinase: Towards the conception of novel antimicrobial agents.EBIEur J Med Chem 125: 1-13 (2017)Simon Fraser University2D 3D TSV
276620311Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities.EBIEur J Med Chem 125: 143-189 (2017)Hamdard University2D 3D TSV
2766203233Design, synthesis and evaluation of novel 2-amino-3-(naphth-2-yl)propanoic acid derivatives as potent inhibitors of platelet aggregation.EBIEur J Med Chem 125: 197-209 (2017)China Pharmaceutical University2D 3D TSV
2768818050Design and discovery of 4-anilinoquinazoline-urea derivatives as dual TK inhibitors of EGFR and VEGFR-2.EBIEur J Med Chem 125: 245-254 (2017)China Pharmaceutical University2D 3D TSV
2768818140Synthesis and evaluation of C9 alkoxy analogues of (-)-stepholidine as dopamine receptor ligands.EBIEur J Med Chem 125: 255-268 (2017)City University of New York2D 3D TSV
2768818429New azepino[4,3-b]indole derivatives as nanomolar selective inhibitors of human butyrylcholinesterase showing protective effects against NMDA-induced neurotoxicity.EBIEur J Med Chem 125: 288-298 (2017)University of Bari"A. Moro"2D 3D TSV
2768818915Synthesis and in vitro characterization of novel fluorinated derivatives of the translocator protein 18 kDa ligand CfO-DPA-714.EBIEur J Med Chem 125: 346-359 (2017)France; Inserm/CEA/Universit£ Paris Sud2D 3D TSV
2768972689Repurposing N,N'-bis-(arylamidino)-1,4-piperazinedicarboxamidines: An unexpected class of potent inhibitors of cholinesterases.EBIEur J Med Chem 125: 430-434 (2017)Martin-Luther University Halle-Wittenberg2D 3D TSV
2768972746Synthesis, biological evaluation and molecular modeling of 1-oxa-4-thiaspiro- and 1,4-dithiaspiro[4.5]decane derivatives as potent and selective 5-HTEBIEur J Med Chem 125: 435-452 (2017)Universit£ degli Studi di Modena e Reggio Emilia2D 3D TSV
2771847440Synthesis and evaluation of N-substituted 2-amino-4,5-diarylpyrimidines as selective adenosine AEBIEur J Med Chem 125: 586-602 (2017)Leiden University2D 3D TSV
2772115318Design, synthesis and biological evaluation of new phthalimide and saccharin derivatives with alicyclic amines targeting cholinesterases, beta-secretase and amyloid beta aggregation.EBIEur J Med Chem 125: 676-695 (2017)Jagiellonian University Medical College2D 3D TSV
2772115732Design, synthesis, in-silico and biological evaluation of novel donepezil derivatives as multi-target-directed ligands for the treatment of Alzheimer's disease.EBIEur J Med Chem 125: 736-750 (2017)University of Delhi2D 3D TSV
277690323Design of a doxorubicin-peptidomimetic conjugate that targets HER2-positive cancer cells.EBIEur J Med Chem 125: 914-924 (2017)University of Louisiana at Monroe2D 3D TSV
2776903616Green fluorescent protein chromophore derivatives as a new class of aldose reductase inhibitors.EBIEur J Med Chem 125: 965-974 (2017)Toho University2D 3D TSV
2785535915Discovery of benzimidazole derivatives as modulators of mitochondrial function: A potential treatment for Alzheimer's disease.EBIEur J Med Chem 125: 1172-1192 (2017)Korea Institute of Science and Technology2D 3D TSV
278710386Imidazopyridine-fused [1,3]-diazepinones part 2: Structure-activity relationships and antiproliferative activity against melanoma cells.EBIEur J Med Chem 125: 1225-1234 (2017)Universit£ de Montpellier2D 3D TSV
2788654515Design, synthesis, docking studies and biological evaluation of novel dihydro-1,3,5-triazines as human DHFR inhibitors.EBIEur J Med Chem 125: 1279-1288 (2017)Shanghai Institute of Pharmaceutical Industry2D 3D TSV