Works about GUANIDINE
Results: 679
Asymmetric Carbene Insertion into Se−S Bonds by Synergistic Rh(II)/Guanidine Catalysis Involving Chalcogen‐Bond Assistance.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202417636
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Guanidinium‐Stapled Helical Peptides for Targeting Protein‐Protein Interactions.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202416348
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Decompositions of Urea and Guanidine Nitrates.
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- Journal of Energetic Materials, 2009, v. 27, n. 1, p. 17, doi. 10.1080/07370650802328814
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Accumulation of AC E Inhibitory Tripeptides, Val-Pro-Pro and Ile-Pro-Pro, in Vascular Endothelial Cells.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 9, p. 1792, doi. 10.1271/bbb.120299
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High-Casein Diet Suppresses Guanidinoacetic Acid-Induced Hyperhomocysteinemia and Potentiates the Hypohomocysteinemic Effect of Serine in Rats.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 12, p. 3258, doi. 10.1271/bbb.80543
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Super Agonist Actions of Clothianidin and Related Compounds on the SADβ2 Nicotinic Acetylcholine Receptor Expressed in Xenopus laevis Oocytes.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 3, p. 761, doi. 10.1271/bbb.68.761
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Anchoring Guanidine Polymer onto Sesbania Gum to Endow Excellent Antibacterial Function.
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- Macromolecular Chemistry & Physics, 2023, v. 224, n. 7, p. 1, doi. 10.1002/macp.202200430
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Redox‐Induced Aromatic Substitution: A Study on Guanidino‐Functionalized Aromatics.
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- Chemistry - A European Journal, 2024, v. 30, n. 72, p. 1, doi. 10.1002/chem.202403080
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Modular Synthesis of Azines Bearing a Guanidine Core from N‐Heterocyclic Carbene (NHC)‐Derived Selenoureas and Diazo Reagents.
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- Chemistry - A European Journal, 2024, v. 30, n. 53, p. 1, doi. 10.1002/chem.202401816
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Formation, Selective Encapsulation, and Tautomerization Control of Isoindolone Utilizing Guanidinium Sulfonate Frameworks.
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- Chemistry - A European Journal, 2024, v. 30, n. 33, p. 1, doi. 10.1002/chem.202400957
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Intramolecular Through‐Space Double‐Electron Transfer Between A Pair of Redox‐Active Guanidine Units Aligned by Dithiolate Bridges.
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- Chemistry - A European Journal, 2023, v. 29, n. 64, p. 1, doi. 10.1002/chem.202302418
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Unlocking The Role of Guanidinium Salts in Interface Engineering for Boosted Performance of Inverted Perovskite Solar Cells.
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- Chemistry - A European Journal, 2023, v. 29, n. 47, p. 1, doi. 10.1002/chem.202301214
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Rhodium‐Catalyzed Acrylate Synthesis from Carbon Dioxide and Ethylene by using a Guanidine‐Based Pincer Ligand: Perturbing Occupied d‐Orbitals by pπ‐dπ Repulsion Makes a Difference.
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- Chemistry - A European Journal, 2022, v. 28, n. 58, p. 1, doi. 10.1002/chem.202201870
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Reactive Oxygen Species (ROS) Activated Liposomal Cell Delivery using a Boronate‐Caged Guanidine Lipid.
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- Chemistry - A European Journal, 2022, v. 28, n. 46, p. 1, doi. 10.1002/chem.202201057
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Bicyclic Guanidine Promoted Mechanistically Divergent Depolymerization and Recycling of a Biobased Polycarbonate.
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- Angewandte Chemie, 2023, v. 135, n. 51, p. 1, doi. 10.1002/ange.202314659
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Guanidine Additive Enabled Intermolecular ortho‐Phthalaldehyde‐Amine‐Thiol Three‐Component Reactions for Modular Constructions.
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- Angewandte Chemie, 2023, v. 135, n. 10, p. 1, doi. 10.1002/ange.202217150
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Carbamoylated Guanidine‐Containing Polymers for Non‐Covalent Functional Protein Delivery in Serum‐Containing Media.
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- Angewandte Chemie, 2022, v. 134, n. 12, p. 1, doi. 10.1002/ange.202116722
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Microporosity of a Guanidinium Organodisulfonate Hydrogen‐Bonded Framework.
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- Angewandte Chemie, 2020, v. 132, n. 5, p. 2013, doi. 10.1002/ange.201911861
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Surface Attachment Enhances the Thermodynamic Stability of Protein L.
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- Angewandte Chemie, 2019, v. 131, n. 6, p. 1728, doi. 10.1002/ange.201812231
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Divergent Synthesis of Natural Derivatives of (+)‐Saxitoxin Including 11‐Saxitoxinethanoic Acid.
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- Angewandte Chemie, 2019, v. 131, n. 6, p. 1703, doi. 10.1002/ange.201811717
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Insights into the Biosynthesis of Cyclic Guanidine Alkaloids from Crambeidae Marine Sponges.
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- Angewandte Chemie, 2019, v. 131, n. 2, p. 530, doi. 10.1002/ange.201809539
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Raman spectroscopic and quantum chemical investigation of the effects of trimethylamine N‐oxide on hydrated guanidinium and hydrogen‐bonded water networks.
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- Journal of Raman Spectroscopy, 2021, v. 52, n. 4, p. 788, doi. 10.1002/jrs.6061
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Transmission electron microscopy comparison of methods for collecting in situ formed enamel pellicle.
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- Clinical Oral Investigations, 2005, v. 9, n. 1, p. 30, doi. 10.1007/s00784-004-0284-1
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Effect of N-[Imino(1-Piperidinyl)Methyl]Guanidine on Free-Radical Processes and Antioxidant-Enzyme Activity in Kidneys of Rats with Experimental Type 2 Diabetes Mellitus.
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- Pharmaceutical Chemistry Journal, 2018, v. 52, n. 3, p. 191, doi. 10.1007/s11094-018-1788-3
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Influence of auxiliary components on the physicochemical properties of aqueous solutions of guanidine antiseptics.
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- Pharmaceutical Chemistry Journal, 2006, v. 40, n. 7, p. 394, doi. 10.1007/s11094-006-0136-1
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The Properties of Protease C in Complexes with Poly(Hexamethylene Guanidine).
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- Pharmaceutical Chemistry Journal, 2003, v. 37, n. 12, p. 667, doi. 10.1023/B:PHAC.0000022087.13639.56
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Stereochemistry of the citrate anion in compounds containing guanidinium and citrate ions.
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- Journal of Structural Chemistry, 2015, v. 56, n. 1, p. 134, doi. 10.1134/S0022476615010199
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Crystal structure of the N,N′,N″-triphenyl-guanidinium- bis-[η-π-(3)-dicarbollide]Ni(III) complex.
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- Journal of Structural Chemistry, 2013, v. 54, n. 3, p. 547, doi. 10.1134/S0022476613030116
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Probing of some compounds as anti-aggregatory additives in the protein refolding process from Escherichia coli inclusion bodies.
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- Biotechnology & Applied Biochemistry, 2011, v. 58, n. 4, p. 277, doi. 10.1002/bab.40
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New Metal Complexes Derived from Guanidine-Containing Dialdehyde Cellulose.
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- Fibre Chemistry, 2018, v. 49, n. 6, p. 437, doi. 10.1007/s10692-018-9916-0
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Xylanase II from Trichoderma reesei QM 9414: conformational and catalytic stability to Chaotropes, Trifluoroethanol, and pH changes.
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- Journal of Industrial Microbiology & Biotechnology, 2011, v. 38, n. 1, p. 113, doi. 10.1007/s10295-010-0836-0
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Application of guanidine and its salts in multicomponent reactions.
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- Turkish Journal of Chemistry, 2014, v. 38, n. 3, p. 345, doi. 10.3906/kim-1307-38
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Guanidine thiocyanate solution facilitates sample collection for plant rhizosphere microbiome analysis.
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.6440
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Surface Treatment of Perovskite Layer with Guanidinium Iodide Leads to Enhanced Moisture Stability and Improved Efficiency of Perovskite Solar Cells.
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- Advanced Materials Interfaces, 2020, v. 7, n. 14, p. 1, doi. 10.1002/admi.202000105
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Comparison of the enzyme-hydrolyzed casein, guanidination, and isotope dilution methods for determining ileal endogenous protein flow in the growing rat and pig.
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- Journal of Animal Science, 2003, v. 81, n. 10, p. 2525, doi. 10.2527/2003.81102525x
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Evaluation of the homoarginine technique for measuring true ileal amino acid digestibilities in pigs fed a barley-canola meal-based diet.
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- Journal of Animal Science, 2002, v. 80, n. 2, p. 440, doi. 10.2527/2002.802440x
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Novel Nano-Size Inorganic-Bioorganic Hybrids Based on Graphene Oxide and Arginine-Derived Ionic Liquids (GO@Mono-Arg Malonate and GO@di-Arg Malonate): Versatile Catalysts to Prepare Spiro[Indeno[1,2-d]Pyrimidineindoline]Ones, Spiro[Indoline-Pyrimido[4,5-d]Pyrimidine]Ones, and Dihydro-Spiro[Indoline-Pyrimidine]-Carboxylates under Solvent-Free Conditions
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 10, p. 6589, doi. 10.1080/10406638.2023.2281467
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2-((1H-Benzo[d]imidazol-2-yl)amino)benzo[d]thiazole-6-sulphonamides: a class of carbonic anhydrase II and VII-selective inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2174981
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Design, synthesis, and biological evaluation of bifunctional thyrointegrin inhibitors: new anti-angiogenesis analogs.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2011, v. 26, n. 6, p. 871, doi. 10.3109/14756366.2011.557023
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Synthesis and antiproliferative activity of some diaryldiazepines and diarylpyrimidines.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2007, v. 22, n. 6, p. 716, doi. 10.1080/14756360701306073
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The Inhibition Mechanism of Guanidine Hydrochloride on the Catalytic Activity of Recombinant Human Protein Disulfide Isomerase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2003, v. 18, n. 1, p. 47, doi. 10.1080/1475636021000049212
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AGAT knockout mice provide an opportunity to titrate tissue creatine content.
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- Journal of Physiology, 2013, v. 591, n. 2, p. 393, doi. 10.1113/jphysiol.2012.247924
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Longitudinal long term follow up investigation on the carcinogenic impact of polyhexamethylene guanidine phosphate in rat models.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-57605-x
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Guanidine Hydrochloride/ZnI<sub>2</sub> as Heterogeneous Catalyst for Conversion of CO<sub>2</sub> and Epoxides to Cyclic Carbonates under Mild Conditions.
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- Catalysts (2073-4344), 2015, v. 5, n. 1, p. 119, doi. 10.3390/catal5010119
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Comprehensive Virtual Screening of the Antiviral Potentialities of Marine Polycyclic Guanidine Alkaloids against SARS-CoV-2 (COVID-19).
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- Biomolecules (2218-273X), 2021, v. 11, n. 3, p. 460, doi. 10.3390/biom11030460
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The Guanidine Pseudoalkaloids 10-Methoxy-Leonurine and Leonurine Act as Competitive Inhibitors of Tyrosinase.
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- Biomolecules (2218-273X), 2020, v. 10, n. 2, p. 174, doi. 10.3390/biom10020174
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FAILURE OF STILBAMIDINE TO ARREST EXPERIMENTAL BLASTOMYCOSIS IN MICE.
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- British Journal of Dermatology, 1954, v. 66, n. 7, p. 274
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In vitro penetration of bleaching agents into the pulp chamber.
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- International Endodontic Journal, 2004, v. 37, n. 2, p. 120, doi. 10.1111/j.0143-2885.2004.00761.x
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A New Antisense Phosphoryl Guanidine Oligo-2′-O-Methylribonucleotide Penetrates Into Intracellular Mycobacteria and Suppresses Target Gene Expression.
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- Frontiers in Pharmacology, 2019, p. 1, doi. 10.3389/fphar.2019.01049
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Thermal and guanidine hydrochloride-induced denaturation of human cystatin C.
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- European Biophysics Journal, 2004, v. 33, n. 5, p. 454, doi. 10.1007/s00249-003-0384-x
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