Works matching DE "TRIAZINE derivatives"
Results: 512
ABSTRACTS.
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- AATCC Review, 2024, v. 24, n. 1, p. 37
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Yellow Triazine as an Efficient Photoinitiator for Polymerization and 3D Printing under LEDs.
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- Macromolecular Chemistry & Physics, 2019, v. 220, n. 18, p. N.PAG, doi. 10.1002/macp.201900315
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Yellow Triazine as an Efficient Photoinitiator for Polymerization and 3D Printing under LEDs.
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- Macromolecular Chemistry & Physics, 2019, v. 220, n. 18, p. N.PAG, doi. 10.1002/macp.201900315
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Triazine-Based Type-II Photoinitiating System for Free Radical Photopolymerization: Mechanism, Efficiency, and Modeling.
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- Macromolecular Chemistry & Physics, 2017, v. 218, n. 18, p. n/a, doi. 10.1002/macp.201600597
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Contents: Macromol. Chem. Phys. 18/2017.
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- Macromolecular Chemistry & Physics, 2017, v. 218, n. 18, p. n/a, doi. 10.1002/macp.201770057
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Optimization of the Lead Compound NVP‐BHG712 as a Colorectal Cancer Inhibitor.
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- Chemistry - A European Journal, 2023, v. 29, n. 23, p. 1, doi. 10.1002/chem.202203967
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A Gold(I)–Acetylene Complex Synthesised using Single‐Crystal Reactivity.
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- Angewandte Chemie, 2024, v. 136, n. 30, p. 1, doi. 10.1002/ange.202404264
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A Semisynthesis Platform for the Efficient Production and Exploration of Didemnin‐Based Drugs.
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- Angewandte Chemie, 2024, v. 136, n. 12, p. 1, doi. 10.1002/ange.202318784
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Necroptosis Induced by Ruthenium(II) Complexes as Dual Catalytic Inhibitors of Topoisomerase I/II.
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- Angewandte Chemie, 2020, v. 132, n. 38, p. 16774, doi. 10.1002/ange.202006089
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Innentitelbild: Controlling the Product Platform of Carbon Dioxide Reduction: Adaptive Catalytic Hydrosilylation of CO<sub>2</sub> Using a Molecular Cobalt(II) Triazine Complex (Angew. Chem. 36/2020).
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- Angewandte Chemie, 2020, v. 132, n. 36, p. 15382, doi. 10.1002/ange.202010500
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Controlling the Product Platform of Carbon Dioxide Reduction: Adaptive Catalytic Hydrosilylation of CO<sub>2</sub> Using a Molecular Cobalt(II) Triazine Complex.
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- Angewandte Chemie, 2020, v. 132, n. 36, p. 15804, doi. 10.1002/ange.202004463
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Tunable Reduction of 2,4,6‐Tri(4‐pyridyl)‐1,3,5‐Triazine: From Radical Anion to Diradical Dianion to Radical Metal–Organic Framework.
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- Angewandte Chemie, 2019, v. 131, n. 50, p. 18392, doi. 10.1002/ange.201910468
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The pressure effects and vibrational properties of energetic material: Hexahydro‐1,3,5‐trinitro‐1,3,5‐triazine (α‐RDX).
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- Journal of Raman Spectroscopy, 2019, v. 50, n. 6, p. 889, doi. 10.1002/jrs.5589
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CRYSTALLOGRAPHIC ANALYSIS OF A SAMARIUM(III) COMPLEX WITH 1,3,5-TRIS(1-IMIDAZOLYL)BENZENE.
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- Journal of Structural Chemistry, 2020, v. 61, n. 12, p. 1945, doi. 10.1134/S0022476620120124
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TWO MIXED-LIGAND Cu(II)-BASED COORDINATION POLYMERS: CRYSTAL STRUCTURES AND TREATMENT ACTIVITY ON CHILD ACUTE PANCREATITIS WITH PERITONITIS BY INHIBITING THE BACTERIAL SURVIVAL.
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- Journal of Structural Chemistry, 2020, v. 61, n. 8, p. 1281, doi. 10.1134/S0022476620080144
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Sustainable metal-free leather manufacture via synergistic effects of triazine derivative and vegetable tannins.
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- Collagen & Leather, 2023, v. 5, n. 1, p. 1, doi. 10.1186/s42825-022-00108-0
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SYNTHESIS OF PYRAZOLO[1,5-a][1,3,5]TRIAZINE AND OXAZOLO[4,5-d]PYRIMIDINE DERIVATIVES AND STUDY OF THEIR VASODILATOR ACTIVITY.
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- Issues of Chemistry & Chemical Technology / Voprosy Khimii & Khimicheskoi Tekhnologii, 2023, n. 2, p. 51, doi. 10.32434/0321-4095-2023-147-2-51-60
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短碳氟链缩合剂的绿色合成与应用.
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- China Surfactant Detergent & Cosmetics (1001-1803), 2021, v. 51, n. 4, p. 288, doi. 10.3969/j.issn.1001-1803.2021.04.004
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New protocols for the synthesis of 5-amino-7-(4-phenyl)-4,7-dihydro-[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate esters using an efficient additive.
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- Turkish Journal of Chemistry, 2020, v. 44, n. 4, p. 1100, doi. 10.3906/kim-2005-6
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Potentiometric study of equilibrium constants of a novel triazine-thione derivative and its stability constants with Hg<sup>2+</sup>, Cu<sup>2+</sup>, Ni<sup>2+</sup>, Pb<sup>2+</sup>, and Zn<sup>2+</sup> metal ions in ethanol and water mixed.
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- Turkish Journal of Chemistry, 2013, v. 37, n. 3, p. 439, doi. 10.3906/kim-1207-55
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The activity of pyrazolo[4,3-e][1,2,4]triazine and pyrazolo[4,3-e]tetrazolo[1,5-b][1,2,4]triazine sulphonamide derivatives in monolayer and spheroid breast cancer cell cultures.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2024, v. 39, n. 1, p. 1, doi. 10.1080/14756366.2024.2343352
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Design, synthesis, docking, ADMET studies, and anticancer evaluation of new 3-methylquinoxaline derivatives as VEGFR-2 inhibitors and apoptosis inducers.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 1760, doi. 10.1080/14756366.2021.1956488
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Design, synthesis, anticancer evaluation, and molecular modelling studies of novel tolmetin derivatives as potential VEGFR-2 inhibitors and apoptosis inducers.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 922, doi. 10.1080/14756366.2021.1901089
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Exploration of novel heterofused 1,2,4-triazine derivative in colorectal cancer.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 535, doi. 10.1080/14756366.2021.1879803
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Synthesis and biological evaluation of new 3(2H)-pyridazinone derivatives as non-toxic anti-proliferative compounds against human colon carcinoma HCT116 cells.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 1100, doi. 10.1080/14756366.2020.1755670
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Synthesis and biological evaluation of (3/4-(pyrimidin-2-ylamino)benzoyl)-based hydrazine-1-carboxamide/carbothioamide derivatives as novel RXRα antagonists.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 880, doi. 10.1080/14756366.2020.1740692
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Discovery and evaluation of novel synthetic 5-alkyl-4-oxo-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoxaline-1-carbox-amide derivatives as anti-inflammatory agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 85, doi. 10.1080/14756366.2019.1680658
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Binding investigation and preliminary optimisation of the 3-amino-1,2,4-triazin-5(2H)-one core for the development of new Fyn inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 956, doi. 10.1080/14756366.2018.1469017
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Synthesis of chiral pyrazolo[4,3- e ][1,2,4]triazine sulfonamides with tyrosinase and urease inhibitory activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 99, doi. 10.1080/14756366.2016.1238362
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Structure-based design, synthesis, molecular docking study and biological evaluation of 1,2,4-triazine derivatives acting as COX/15-LOX inhibitors with anti-oxidant activities.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1602, doi. 10.3109/14756366.2016.1158713
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Identification of Mycobacterium tuberculosis leucyl-tRNA synthetase (LeuRS) inhibitors among the derivatives of 5-phenylamino-2H-[1,2,4]triazin-3-one.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 201, doi. 10.1080/14756366.2016.1190712
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Design, synthesis, antimicrobial activity and anti-HIV activity evaluation of novel hybrid quinazoline-triazine derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 1, p. 100, doi. 10.3109/14756366.2012.755622
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Characterization of the Ohmyungsamycin Biosynthetic Pathway and Generation of Derivatives with Improved Antituberculosis Activity.
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- Biomolecules (2218-273X), 2019, v. 9, n. 11, p. 672, doi. 10.3390/biom9110672
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Modified Epoxy with Chitosan Triazine Dihydrazide Derivatives for Mechanical and Corrosion Protection of Steel.
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- Coatings (2079-6412), 2020, v. 10, n. 12, p. 1256, doi. 10.3390/coatings10121256
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Fabrication of Cotton Fabric with Superoleophilic/Superhydrophobic Characteristic on the Modified Surface by Using Fluoroalkylated Oligomeric Silica/Triazine Derivative Nanocomposites.
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- Coatings (2079-6412), 2020, v. 10, n. 2, p. 174, doi. 10.3390/coatings10020174
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The influence of the chemical structure on the dielectric behavior of triazine derivative-based polyurethane–urea elastomers.
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- Designed Monomers & Polymers, 2013, v. 16, n. 1, p. 47, doi. 10.1080/15685551.2012.705489
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Modulation of H2O2- Induced Neurite Outgrowth Impairment and Apoptosis in PC12 Cells by a 1,2,4-Triazine Derivative.
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- Basic & Clinical Neuroscience, 2012, v. 3, n. 5, p. 49
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A Novel Centrosymmetric Fe(III) Complex with Anionic Bis -pyrazolyl- s -triazine Ligand; Synthesis, Structural Investigations and Antimicrobial Evaluations.
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- Symmetry (20738994), 2021, v. 13, n. 7, p. 1247, doi. 10.3390/sym13071247
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Synthesis and Characterisation of a Boron-Rich Symmetric Triazine Bearing a Hypoxia-Targeting Nitroimidazole Moiety.
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- Symmetry (20738994), 2021, v. 13, n. 2, p. 202, doi. 10.3390/sym13020202
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Label-free quantitative proteomic analysis of ethanamizuril-resistant versus -sensitive strains of Eimeria tenella.
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- Parasites & Vectors, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13071-022-05412-6
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Bioaccumulation kinetics of the conventional energetics TNT and RDX relative to insensitive munitions constituents DNAN and NTO in Rana pipiens tadpoles.
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- Environmental Toxicology & Chemistry, 2015, v. 34, n. 4, p. 880, doi. 10.1002/etc.2863
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Toxicity of the conventional energetics TNT and RDX relative to new insensitive munitions constituents DNAN and NTO in Rana pipiens tadpoles.
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- Environmental Toxicology & Chemistry, 2015, v. 34, n. 4, p. 873, doi. 10.1002/etc.2890
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DFT study of structural, electronic, and absorption properties of crystalline β-RDX under pressures.
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- Canadian Journal of Chemistry, 2013, v. 91, n. 10, p. 968, doi. 10.1139/cjc-2013-0174
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The Determination of Ammeline by Differential Pulse Polarography /Application to Milk.
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- Gazi University Journal of Science, 2016, v. 29, n. 3, p. 549
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Identification and Design of a Next-Generation Multi Epitopes Bases Peptide Vaccine Candidate Against Prostate Cancer: An In Silico Approach.
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- Cell Biochemistry & Biophysics, 2020, v. 78, n. 4, p. 495, doi. 10.1007/s12013-020-00912-7
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The critical role of residues Phe120 and Val161 of (2 R,3 R)‑2,3‑butanediol dehydrogenase from Neisseria gonorrhoeae as probed by molecular docking and site‐directed mutagenesis.
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- Journal of Basic Microbiology, 2024, v. 64, n. 6, p. 1, doi. 10.1002/jobm.202300751
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Design, synthesis and application of chiral tetraoxacalix[2]arene[2]triazine‐based organocatalysts in asymmetric Michael addition reactions.
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- Chirality, 2019, v. 31, n. 4, p. 293, doi. 10.1002/chir.23055
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Genomogenesis of the Plague Bacteria Yersinia pestis as a Process of Mosaic Evolution.
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- Russian Journal of Genetics, 2021, v. 57, n. 2, p. 139, doi. 10.1134/S1022795421020113
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Docking studies to evaluate the biological activities of the Co(II) and Ni(II) complexes containing the triazine unit: supported by structural, spectral, and theoretical studies.
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- Journal of Coordination Chemistry, 2018, v. 71, n. 23, p. 3893, doi. 10.1080/00958972.2018.1543871
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Cloud-point extraction preconcentration of sym-triazine herbicides to determination by gas chromatography.
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- Journal of Analytical Chemistry, 2015, v. 70, n. 2, p. 119, doi. 10.1134/S106193481412003X
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