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Clinical evaluation of plasma coagulation parameters in patients with advanced‐stage non‐small cell lung cancer treated with palliative chemotherapy in China.
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- International Journal of Clinical Practice, 2020, v. 74, n. 12, p. 1, doi. 10.1111/ijcp.13619
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- Article
Discovery of a series of novel phenylpiperazine derivatives as EGFR TK inhibitors.
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- Scientific Reports, 2015, p. 13934, doi. 10.1038/srep13934
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- Article
Design, synthesis, and biological evaluation of 2,3‐diphenyl‐cycloalkyl pyrazole derivatives as potential tubulin polymerization inhibitors.
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- Chemical Biology & Drug Design, 2019, v. 94, n. 5, p. 1894, doi. 10.1111/cbdd.13565
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- Article
Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.
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- Chemical Biology & Drug Design, 2018, v. 91, n. 3, p. 681, doi. 10.1111/cbdd.13141
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- Article
Design of potent B‐Raf<sup>V600E</sup> inhibitors by multiple copy simulation search strategy.
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- Chemical Biology & Drug Design, 2018, v. 91, n. 2, p. 567, doi. 10.1111/cbdd.13121
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- Article
Synthesis, molecular docking and biological evaluation of 1-phenylsulphonyl-2-(1-methylindol-3-yl)-benzimidazole derivatives as novel potential tubulin assembling inhibitors.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 1, p. 112, doi. 10.1111/cbdd.12932
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- Article
Design, synthesis, and biological evaluation of chrysin derivatives as potential FabH inhibitors.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 1, p. 136, doi. 10.1111/cbdd.12839
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- Article
Metronidazole containing pyrazole derivatives potently inhibit tyrosyl-tRNA synthetase: design, synthesis, and biological evaluation.
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- Chemical Biology & Drug Design, 2016, v. 88, n. 4, p. 592, doi. 10.1111/cbdd.12793
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- Article
Discovery of New 4-Alkoxyquinazoline-Based Derivatives as Potent VEGFR2 Inhibitors.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 5, p. 1323, doi. 10.1111/cbdd.12596
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- Article
Synthesis, Biological Evaluation, and Docking of Dihydropyrazole Sulfonamide Containing 2-hydroxyphenyl Moiety: A Series of Novel MMP-2 Inhibitors.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 6, p. 1405, doi. 10.1111/cbdd.12604
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- Article
Combined Molecular Docking, 3D- QSAR, and Pharmacophore Model: Design of Novel Tubulin Polymerization Inhibitors by Binding to Colchicine-binding Site.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 731, doi. 10.1111/cbdd.12545
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- Article
Synthesis, Molecular Modeling, and Biological Evaluation of Novel 1, 3-Diphenyl-2-propen-1-one Based Pyrazolines as Anti-inflammatory Agents.
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- Chemical Biology & Drug Design, 2015, v. 85, n. 6, p. 729, doi. 10.1111/cbdd.12457
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- Article
Dihydropyrazole Derivatives Containing Benzo Oxygen Heterocycle and Sulfonamide Moieties Selectively and Potently Inhibit COX-2: Design, Synthesis, and Anti-Colon Cancer Activity Evaluation.
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- Molecules, 2019, v. 24, n. 9, p. 1685, doi. 10.3390/molecules24091685
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- Article
Synthesis and Biological Evaluation of Dithiobisacetamides as Novel Urease Inhibitors.
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- ChemMedChem, 2022, v. 17, n. 2, p. 1, doi. 10.1002/cmdc.202100618
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- Article
Identification and Biological Evaluation of Novel Type II B‐Raf<sup>V600E</sup> Inhibitors.
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- ChemMedChem, 2018, v. 13, n. 23, p. 2558, doi. 10.1002/cmdc.201800574
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- Article
Synthesis, Characterization and Crystal Structures of Four Dinuclear Schiff Base Nickel(II) and Copper(II) Complexes with Versatile Bridging Groups.
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- Zeitschrift für Anorganische und Allgemeine Chemie, 2007, v. 633, n. 9, p. 1480, doi. 10.1002/zaac.200700132
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- Article
Design, Synthesis, and Pharmacological Investigation of Iodined Salicylimines, New Prototypes of Antimicrobial Drug Candidates.
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- Archiv der Pharmazie, 2010, v. 343, n. 5, p. 282, doi. 10.1002/ardp.200900129
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- Article
Design and Synthesis of Fluoroacylshikonin as an Anticancer Agent.
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- Chirality, 2013, v. 25, n. 11, p. 757, doi. 10.1002/chir.22209
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- Article
Corrigendum: An Activatable and Switchable Nanoaggregate Probe for Detecting H<sub>2</sub>S and Its Application in Mice Brains.
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- 2021
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- Correction Notice
An Activatable and Switchable Nanoaggregate Probe for Detecting H<sub>2</sub>S and Its Application in Mice Brains.
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- Chemistry - An Asian Journal, 2020, v. 15, n. 21, p. 3551, doi. 10.1002/asia.202000964
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- Article
Discovery of novel indole‐1,2,4‐triazole derivatives as tubulin polymerization inhibitors.
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- Drug Development Research, 2021, v. 82, n. 7, p. 1008, doi. 10.1002/ddr.21805
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- Article
Imaging Dynamic Peroxynitrite Fluxes in Epileptic Brains with a Near‐Infrared Fluorescent Probe.
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- Advanced Science, 2019, v. 6, n. 15, p. N.PAG, doi. 10.1002/advs.201900341
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- Article
Synthesis, Characterization and Antibacterial Activity of New 5-( o-Chlorophenyl)-3-( o, p-dichlorophenyl)-4,5-dihydropyrazol-1-yl Oxime Ester Derivatives.
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- Chinese Journal of Chemistry, 2008, v. 26, n. 3, p. 505, doi. 10.1002/cjoc.200890095
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- Article
Syntheses, Crystal Structures and Cytotoxities of Silver (I) Complexes of 2,2′-Bipyridines and 1,10-Phenanthroline.
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- Chinese Journal of Chemistry, 2001, v. 19, n. 3, p. 263, doi. 10.1002/cjoc.20010190310
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- Article
Modification, Biological Evaluation and 3D QSAR Studies of Novel 2-(1,3-Diaryl- 4,5-Dihydro-1<i>H-</i>Pyrazol-5-yl)Phenol Derivatives as Inhibitors of B-Raf Kinase.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0095702
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- Article
Optimization of Substituted 6-Salicyl-4-Anilinoquinazoline Derivatives as Dual EGFR/HER2 Tyrosine Kinase Inhibitors.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0069427
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- Article
Synthesis, Structure and Antibacterial Activity of Potent DNA Gyrase Inhibitors: N′-Benzoyl-3-(4-Bromophenyl)-1<i>H</i>-Pyrazole-5-Carbohydrazide Derivatives.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069751
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- Article
Supramolecular Architecture of Two 4-(Methylsulfonyl) Benzaldehyde Schiff Bases.
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- Journal of Chemical Crystallography, 2012, v. 42, n. 6, p. 611, doi. 10.1007/s10870-012-0290-0
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- Article
Structure and Antibacterial Activity of 3-(3,4-Dimethoxyphenyl)furan-2(5 H)-ones.
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- Journal of Chemical Crystallography, 2012, v. 42, n. 4, p. 323, doi. 10.1007/s10870-011-0246-9
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- Article
Synthesis, Characterization and Bioactivity Research of a Derivative of Secnidazole: 1-(2-Chloropropyl)-2-methyl-5-nitro-1 H-imidazole.
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- Journal of Chemical Crystallography, 2011, v. 41, n. 9, p. 1360, doi. 10.1007/s10870-011-0104-9
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- Article
Crystal structures of azido or thiocyanato-coordinated nickel(II) complexes with tridentate Schiff bases.
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- Journal of Structural Chemistry, 2013, v. 54, n. 5, p. 926, doi. 10.1134/S0022476613050120
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- Article
Design, biological evaluation and 3D QSAR studies of novel dioxin-containing pyrazoline derivatives with thiourea skeleton as selective HER-2 inhibitors.
- Published in:
- Scientific Reports, 2016, p. 27571, doi. 10.1038/srep27571
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- Article
Design, Synthesis and Antitumor Activity of Novel link-bridge and B-Ring Modified Combretastatin A-4 (CA-4) Analogues as Potent Antitubulin Agents.
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- Scientific Reports, 2016, p. 25387, doi. 10.1038/srep25387
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- Article
Synthesis and Biological Evaluation of Glycyrrhetic Acid Derivatives as Potential VEGFR2 Inhibitors.
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- ChemMedChem, 2017, v. 12, n. 13, p. 1087, doi. 10.1002/cmdc.201700271
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- Article
Synthesis and Biological Evaluation of 1-Methyl-1H-indole–Pyrazoline Hybrids as Potential Tubulin Polymerization Inhibitors
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- ChemMedChem, 2016, v. 11, n. 13, p. 1446, doi. 10.1002/cmdc.201600137
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- Article
Novel Schiff-Base-Derived FabH Inhibitors with Dioxygenated Rings as Antibiotic Agents.
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- ChemMedChem, 2013, v. 8, n. 3, p. 433, doi. 10.1002/cmdc.201200587
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- Article
Synthesis and Antimicrobial Activities of Oximes Derived from O-Benzylhydroxylamine as FabH Inhibitors.
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- ChemMedChem, 2012, v. 7, n. 9, p. 1587, doi. 10.1002/cmdc.201200225
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- Article
Synthesis, Crystal Structure and Immunosuppressive Activity of Acylamide Derivatives Containing 1,4-Benzodioxan.
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- ChemMedChem, 2009, v. 4, n. 9, p. 1421, doi. 10.1002/cmdc.200900167
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- Article
Synthesis, Antiproliferative Evaluation, and Structure-Activity Relationships of 3-Arylquinolines.
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- ChemMedChem, 2008, v. 3, n. 10, p. 1516, doi. 10.1002/cmdc.200800160
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- Article
Synthesis, Antiproliferative Activity, and Structure-Activity Relationships of 3-Aryl-1 H-quinolin-4-ones.
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- ChemMedChem, 2008, v. 3, n. 7, p. 1077, doi. 10.1002/cmdc.200800057
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- Publication type:
- Article
Metronidazole-Flavonoid Derivatives as Anti- Helicobacter pylori Agents with Potent Inhibitory Activity against HPE-Induced Interleukin-8 Production by AGS Cells.
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- ChemMedChem, 2007, v. 2, n. 9, p. 1361, doi. 10.1002/cmdc.200700097
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- Article
Adsorption of disperse blue 2BLN by microwave activated red mud.
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- Environmental Progress & Sustainable Energy, 2011, v. 30, n. 4, p. 558, doi. 10.1002/ep.10506
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- Article
Synthesis, Crystal Structures, Molecular Docking, and Urease Inhibitory Activities of Transition-Metal Complexes with a 1,2,4-Triazolecarboxylic Acid Derived Ligand.
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- European Journal of Inorganic Chemistry, 2015, v. 2015, n. 12, p. 2076, doi. 10.1002/ejic.201500050
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- Article
Recent Research on Methods to Improve Tumor Hypoxia Environment.
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- Oxidative Medicine & Cellular Longevity, 2020, p. 1, doi. 10.1155/2020/5721258
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- Article
Strategies to Build High‐Rate Cathode Materials for Na‐Ion Batteries.
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- ChemNanoMat, 2019, v. 5, n. 10, p. 1253, doi. 10.1002/cnma.201900254
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- Article
Multifunctional Protein Hybrid Nanoplatform for Synergetic Photodynamic‐Chemotherapy of Malignant Carcinoma by Homologous Targeting Combined with Oxygen Transport.
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- Advanced Science, 2023, v. 10, n. 5, p. 1, doi. 10.1002/advs.202203742
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- Article
Synthesis of 1 H-pyrazolo[1,2- b]phthalazine-5,10-dione derivatives: assessment of their antimicrobial, antituberculosis and antioxidant activity.
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- Research on Chemical Intermediates, 2016, v. 42, n. 3, p. 2101, doi. 10.1007/s11164-015-2138-7
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- Article
Design, synthesis, and antibacterial evaluation of new Schiff's base derivatives bearing nitroimidazole and pyrazole nuclei as potent E. coli FabH inhibitors.
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- Research on Chemical Intermediates, 2015, v. 41, n. 12, p. 10137, doi. 10.1007/s11164-015-2018-1
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- Article
Synthesis of Resveratrol Analogues, and Evaluation of Their Cytotoxic and Xanthine Oxidase Inhibitory Activities.
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- Chemistry & Biodiversity, 2008, v. 5, n. 4, p. 636, doi. 10.1002/cbdv.200890059
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- Article
Synthesis and Cytotoxic Evaluation of Substituted Urea Derivatives as Inhibitors of Human-Leukemia K562 Cells.
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- Chemistry & Biodiversity, 2007, v. 4, n. 5, p. 881, doi. 10.1002/cbdv.200790075
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- Article