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Synthesis, Characterization and in vivo Biological Activity of n-(2-chlorophenyl)-2-(2-methyl-5-nitro-1h-imidazol-1-yl) Acetamide and its Derivatives.
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- Journal of Young Pharmacists, 2024, v. 16, n. 2, p. 252, doi. 10.5530/jyp.2024.16.33
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- Article
Chromatographical fingerprint analysis, in silico investigation, and identification of hepatoprotective active compounds from Capparis decidua Edgwe (Forssk.).
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- Journal of Applied Pharmaceutical Science, 2024, v. 14, n. 8, p. 112, doi. 10.7324/JAPS.2024.174125
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Exploring Benzimidazole Chemistry: Synthesis, Biological activity, and Molecular Docking Studies for Alzheimer's Treatment.
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- Oriental Journal of Chemistry, 2024, v. 40, n. 4, p. 1045, doi. 10.13005/ojc/400415
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The application of chemical similarity measures in an unconventional modeling framework c-RASAR along with dimensionality reduction techniques to a representative hepatotoxicity dataset.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-71892-4
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Exploring the Potential Pharmacological Basis and Mechanism of HJT Activity in the Treatment of CHD Based on UPLC-QE-MS and Network Pharmacology.
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- Natural Product Communications, 2024, v. 19, n. 8, p. 1, doi. 10.1177/1934578X241275005
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基于层状锌铝复合氢氧化物前驱体优化制备 Cu / ZnO / Al<sub>2</sub>O<sub>3</sub> 气相醛加氢催化剂.
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- Journal of China University of Petroleum, 2024, v. 48, n. 4, p. 224, doi. 10.3969/j.issn.1673-5005.2024.04.025
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Biodegradable Schiff bases: a novel approach for the management of pathogenic fungi (Sclerotium rolfsii and Rhizoctonia bataticola) and stored grain insect (Callosobruchus maculatus) in green gram (Vigna radiata).
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- Environmental Science & Pollution Research, 2024, v. 31, n. 39, p. 52540, doi. 10.1007/s11356-024-34713-9
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Alpinia officinarum Hance: a comprehensive review of traditional uses, phytochemistry, pharmacokinetic and pharmacology.
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- Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1414635
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The study progress of zeolite-based membranes for CO<sub>2</sub> separation.
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- Applied Chemical Industry, 2024, v. 53, n. 7, p. 1687
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- Article
Potential Pharmacological Properties of Triterpene Derivatives of Ursolic Acid.
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- Molecules, 2024, v. 29, n. 16, p. 3884, doi. 10.3390/molecules29163884
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Chemical Synthesis and Structure–Activity Relationship Studies of the Coagulation Factor Xa Inhibitor Tick Anticoagulant Peptide from the Hematophagous Parasite Ornithodoros moubata.
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- Biomimetics (2313-7673), 2024, v. 9, n. 8, p. 485, doi. 10.3390/biomimetics9080485
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An Insight into Rational Drug Design: The Development of In-House Azole Compounds with Antimicrobial Activity.
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- Antibiotics (2079-6382), 2024, v. 13, n. 8, p. 763, doi. 10.3390/antibiotics13080763
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Effect of mometasone furoate nasal spray on moderate-to-severe nasal congestion in seasonal allergic rhinitis: A responder analysis.
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- Allergy & Asthma Proceedings, 2019, v. 40, n. 3, p. 173, doi. 10.2500/aap.2019.40.4214
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Pharmacological Properties of Pt(II) and Pt(IV) Complexes with 2,2′-Dipyridylamine; the Comparative In Vitro Thereof.
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- Cell Biochemistry & Biophysics, 2020, v. 78, n. 4, p. 521, doi. 10.1007/s12013-020-00937-y
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Vanadium Compounds as Biocatalyst Models.
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- Biological Trace Element Research, 2020, v. 195, n. 2, p. 725, doi. 10.1007/s12011-019-01874-5
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Synthesis, growth inhibitory activity against tumor cells, and structure-activity relationship of CGK733 and its analogs.
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- Bioscience, Biotechnology & Biochemistry, 2024, v. 88, n. 7, p. 747, doi. 10.1093/bbb/zbae047
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Structure-activity relationship of anti-inflammatory meroterpenoids isolated from Dictyopteris polypodioides in RAW264 cells.
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- Bioscience, Biotechnology & Biochemistry, 2024, v. 88, n. 6, p. 594, doi. 10.1093/bbb/zbae038
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(E)-7-phenyl-2-heptene-4,6-diyn-1-ol from Bidens pilosa as a repellent against isopods.
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- Bioscience, Biotechnology & Biochemistry, 2023, v. 87, n. 8, p. 833, doi. 10.1093/bbb/zbad060
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Synthesis of aglycones, structure-activity relationships, and mode of action of lycosides as inhibitors of the asexual reproduction of Phytophthora.
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- Bioscience, Biotechnology & Biochemistry, 2023, v. 87, n. 2, p. 208, doi. 10.1093/bbb/zbac179
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Synthesis and structure-activity relationship study of aldose reductase inhibiting marine alkaloid lukianol A and its derivatives.
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- Bioscience, Biotechnology & Biochemistry, 2023, v. 87, n. 2, p. 148, doi. 10.1093/bbb/zbac193
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Enantioselective total syntheses of (S)-phosphonothrixin and unexpected cyclic derivative (S)-cyclic phosphonothrixin via enzymatic resolution.
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- Bioscience, Biotechnology & Biochemistry, 2023, v. 87, n. 2, p. 138, doi. 10.1093/bbb/zbac188
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Structure-activity relationship in advanced glycation end products formation inhibitory activity of phlorotannins.
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- Bioscience, Biotechnology & Biochemistry, 2022, v. 86, n. 9, p. 1207, doi. 10.1093/bbb/zbac106
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A yeast-based screening system identified bakkenolide B contained in Petasites japonicus as an inhibitor of interleukin-2 production in a human T cell line.
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- Bioscience, Biotechnology & Biochemistry, 2021, v. 85, n. 10, p. 2153, doi. 10.1093/bbb/zbab130
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Structure–activity relationships of antityrosinase and antioxidant activities of cinnamic acid and its derivatives.
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- Bioscience, Biotechnology & Biochemistry, 2021, v. 85, n. 7, p. 1697, doi. 10.1093/bbb/zbab084
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N-terminal [Glu]<sub>3</sub> moiety of γ-glutamyl peptides contributes largely to the activation of human calcium-sensing receptor, a kokumi receptor.
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- Bioscience, Biotechnology & Biochemistry, 2020, v. 84, n. 7, p. 1497, doi. 10.1080/09168451.2020.1743169
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4-O-methylascochlorin stabilizes hypoxia-inducible factor-1 in a manner different from hydroxylase inhibition by iron chelating or substrate competition.
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- Bioscience, Biotechnology & Biochemistry, 2019, v. 83, n. 12, p. 2244, doi. 10.1080/09168451.2019.1651626
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Effect of O -methylated and glucuronosylated flavonoids from Tamarix gallica on α-glucosidase inhibitory activity: structure–activity relationship and synergistic potential.
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- Bioscience, Biotechnology & Biochemistry, 2017, v. 81, n. 3, p. 445, doi. 10.1080/09168451.2016.1254538
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Theoretical Study and Virtual Screening of Nitrogen‐Containing Corrosion Inhibitors Based on Quantitative Structure–Activity Relationship.
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- Chemical Engineering & Technology, 2024, v. 47, n. 5, p. 851, doi. 10.1002/ceat.202300188
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Unexpected Correlation Between Boron Chain Condensation and Hydrogen Evolution Reaction (HER) Activity in Highly Active Vanadium Borides: Enabling Predictions.
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- Angewandte Chemie, 2020, v. 132, n. 29, p. 11872, doi. 10.1002/ange.202000154
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Covalent‐Allosteric Inhibitors to Achieve Akt Isoform‐Selectivity.
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- Angewandte Chemie, 2019, v. 131, n. 52, p. 18999, doi. 10.1002/ange.201909857
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Reordering d Orbital Energies of Single‐Site Catalysts for CO<sub>2</sub> Electroreduction.
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- Angewandte Chemie, 2019, v. 131, n. 36, p. 12841, doi. 10.1002/ange.201907399
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Halogen Bonding Increases the Potency and Isozyme Selectivity of Protein Arginine Deiminase 1 Inhibitors.
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- Angewandte Chemie, 2019, v. 131, n. 36, p. 12606, doi. 10.1002/ange.201906334
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A Selection Rule for Hydrofluoroether Electrolyte Cosolvent: Establishing a Linear Free‐Energy Relationship in Lithium–Sulfur Batteries.
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- Angewandte Chemie, 2019, v. 131, n. 31, p. 10701, doi. 10.1002/ange.201904240
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Ovatodiolides: Scalable Protection‐Free Syntheses, Configuration Determination, and Biological Evaluation against Hepatic Cancer Stem Cells.
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- Angewandte Chemie, 2019, v. 131, n. 31, p. 10697, doi. 10.1002/ange.201904096
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Divergent Synthesis of Chiral Covalent Organic Frameworks.
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- Angewandte Chemie, 2019, v. 131, n. 28, p. 9543, doi. 10.1002/ange.201903534
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Integrated Transmission Electron and Single-Molecule Fluorescence Microscopy Correlates Reactivity with Ultrastructure in a Single Catalyst Particle.
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- Angewandte Chemie, 2018, v. 130, n. 1, p. 263, doi. 10.1002/ange.201709723
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Discovery of a Highly Selective Cell-Active Inhibitor of the Histone Lysine Demethylases KDM2/7.
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- Angewandte Chemie, 2017, v. 129, n. 49, p. 15761, doi. 10.1002/ange.201706788
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Total Synthesis of (−)-Spiroleucettadine.
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- Angewandte Chemie, 2017, v. 129, n. 46, p. 14855, doi. 10.1002/ange.201708110
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Inhibition of Ras Signaling by Blocking Ras-Effector Interactions with Cyclic Peptides.
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- Angewandte Chemie, 2015, v. 127, n. 26, p. 7712, doi. 10.1002/ange.201502763
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CH Activation Generates Period-Shortening Molecules That Target Cryptochrome in the Mammalian Circadian Clock.
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- Angewandte Chemie, 2015, v. 127, n. 24, p. 7299, doi. 10.1002/ange.201502942
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Stereodivergent Total Synthesis of Δ<sup>9</sup>-Tetrahydrocannabinols.
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- Angewandte Chemie, 2014, v. 126, n. 50, p. 14118, doi. 10.1002/ange.201408380
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Structure–activity relationship of thermal interaction between arylmalonamide[70]fullerocyclopropane stabilizer and nitrocellulose.
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- Cellulose, 2022, v. 29, n. 12, p. 6579, doi. 10.1007/s10570-022-04669-5
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Understanding the effect of an anionic side-chain on the nuclear spin dynamics of a polysaccharide.
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- Cellulose, 2022, v. 29, n. 3, p. 1381, doi. 10.1007/s10570-021-04394-5
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Structure-activity relationships of organosulfur compounds as inhibitors of cytochrome P450 1-mediated activation of benzo[a]pyrene in a human cell model.
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- Biotechnology Letters, 2002, v. 24, n. 24, p. 2041, doi. 10.1023/A:1021315320245
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Inhibition of benzo[a]pyrene-induced cytotoxicity and cytochrome P450 1A activity by dietary flavonoids in human liver cell model: structure-activity relationship.
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- Biotechnology Letters, 2000, v. 22, n. 24, p. 1941, doi. 10.1023/A:1026749606363
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A study of structure–activity relationship and anion-controlled quinolinyl Ag(I) complexes as antimicrobial and antioxidant agents as well as their interaction with macromolecules.
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- BioMetals, 2022, v. 35, n. 2, p. 363, doi. 10.1007/s10534-022-00377-6
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Surface modifications based on the cyanobacterial siderophore anachelin: from structure to functional biomaterials design.
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- BioMetals, 2009, v. 22, n. 4, p. 595, doi. 10.1007/s10534-009-9234-3
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Siderophores as drug delivery agents: application of the “Trojan Horse” strategy.
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- BioMetals, 2009, v. 22, n. 4, p. 615, doi. 10.1007/s10534-009-9219-2
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Structure–function relationships in the bifunctional ferrisiderophore FpvA receptor from Pseudomonas aeruginosa.
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- BioMetals, 2009, v. 22, n. 4, p. 671, doi. 10.1007/s10534-008-9203-2
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Single and multiple inhibitors of the biosynthesis of 5‐, 12‐, 15‐lipoxygenase products derived from cinnamyl‐3,4‐dihydroxy‐α‐cyanocinnamate: Synthesis and structure–activity relationship.
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- Drug Development Research, 2024, v. 85, n. 3, p. 1, doi. 10.1002/ddr.22181
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