Supplemental material
Journal of Enzyme Inhibition and Medicinal Chemistry
Volume 34, 2019 - Issue 1
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ERK-mediated phosphorylation regulates SOX10 sumoylation and targets expression in mutant BRAF melanoma.
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Biomedical Importance of Indoles
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NAD+ analog reveals PARP-1 substrate-blocking mechanism and allosteric communication from catalytic center to DNA-binding domains.
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The discovery of antibacterial agents using diversity-oriented synthesis
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Design, synthesis and biological evaluation of indole derivatives as novel inhibitors targeting B-Raf kinase
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Computer-aided molecular design: An introduction and review of tools, applications, and solution techniques
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Discovery of AZ0108, an orally bioavailable phthalazinone PARP inhibitor that blocks centrosome clustering
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DataWarrior: An Open-Source Program For Chemistry Aware Data Visualization And Analysis
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Novel Structural Insight into Inhibitors of Heme Oxygenase-1 (HO-1) by New Imidazole-Based Compounds: Biochemical and In Vitro Anticancer Activity Evaluation.
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Repurposing strategies on pyridazinone-based series by pharmacophore- and structure-driven screening.
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Veliparib and Temozolomide in mCRC
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Navigating chemical space for biology and medicine
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Synthesis and Biological Evaluation of N-Alkoxyphenyl-3-hydroxynaphthalene-2-carboxanilides
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Inverse Virtual Screening allows the discovery of the biological activity of natural compounds.
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Non-oxime inhibitors of B-Raf(V600E) kinase.
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Impact of high-throughput screening in biomedical research
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Diversity-oriented synthesis; a spectrum of approaches and results
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Diversity-oriented synthesis; a challenge for synthetic chemists
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Dasatinib inhibits c-src phosphorylation and prevents the proliferation of Triple-Negative Breast Cancer (TNBC) cells which overexpress Syndecan-Binding Protein (SDCBP).
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Synthesis and biological evaluation of novel N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives as PTP1B inhibitors
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New inhibitors of poly(ADP-ribose) polymerase and their potential therapeutic targets
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Diversity-oriented synthesis of macrocyclic peptidomimetics.
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Synthesis of unprecedented scaffold diversity.
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Synthesis, Biological Evaluation and 2D-QSAR Study of Halophenyl Bis-Hydrazones as Antimicrobial and Antitubercular Agents
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Design and synthesis of 2-(4,5,6,7-tetrahydrothienopyridin-2-yl)-benzoimidazole carboxamides as novel orally efficacious Poly(ADP-ribose)polymerase (PARP) inhibitors.
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Ligand efficiency indices as guideposts for drug discovery.
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