Works matching DE "PHENYLALANINE derivatives"
Results: 32
Hydrogen/deuterium exchange of cross-linkable α-amino acid derivatives in deuterated triflic acid.
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- Bioscience, Biotechnology & Biochemistry, 2014, v. 78, n. 7, p. 1129, doi. 10.1080/09168451.2014.917267
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Morphology Diversity of L‐Phenylalanine‐Based Short Peptide Supramolecular Aggregates and Hydrogels.
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- ChemNanoMat, 2018, v. 4, n. 8, p. 796, doi. 10.1002/cnma.201800202
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Synthesis of D- and L-Phenylalanine Derivatives by Phenylalanine Ammonia Lyases: A Multienzymatic Cascade Process.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 15, p. 4608, doi. 10.1002/anie.201410670
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High flavonoid accompanied with high starch accumulation triggered by nutrient starvation in bioenergy crop duckweed (Landoltia punctata).
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-3559-z
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A Review of Analytical Methods for the Determination of Nateglinide in Pharmaceuticals and Biological Samples.
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- Pharmaceutical Chemistry Journal, 2016, v. 49, n. 12, p. 854, doi. 10.1007/s11094-016-1386-1
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Synthesis of new tetrazolyl derivatives of L- and D-phenylalanine.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 11, p. 1681, doi. 10.1134/S1070428016110221
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Experimental and theoretical NMR studies of interaction between phenylalanine derivative and egg yolk lecithin.
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- Magnetic Resonance in Chemistry, 2014, v. 52, n. 6, p. 298, doi. 10.1002/mrc.4064
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Characterization of the mature cell surface proteinase of Lactobacillus delbrueckii subsp. lactis CRL 581.
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- Applied Microbiology & Biotechnology, 2015, v. 99, n. 10, p. 4277, doi. 10.1007/s00253-014-6258-6
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Design and synthesis of novel organometallic complexes using boronated phenylalanine derivatives as potential anticancer agents.
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- Drug & Chemical Toxicology, 2019, v. 42, n. 4, p. 436, doi. 10.1080/01480545.2018.1504057
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Strong Emissive Nanofibers of Organogels for the Detection of Volatile Acid Vapors.
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- Chemistry - A European Journal, 2015, v. 21, n. 12, p. 4712, doi. 10.1002/chem.201405074
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Synthesis of Both Enantiomers of Chiral Phenylalanine Derivatives Catalyzed by Cinchona Alkaloid Quaternary Ammonium Salts as Asymmetric Phase Transfer Catalysts.
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- Molecules, 2018, v. 23, n. 6, p. 1421, doi. 10.3390/molecules23061421
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fMLP-dependent activation of Akt and ERK1/2 through ROS/Rho A pathways is mediated through restricted activation of the FPRL1 (FPR2) receptor.
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- Inflammation Research, 2018, v. 67, n. 8, p. 711, doi. 10.1007/s00011-018-1163-6
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The Cooperative Effect of Both Molecular and Supramolecular Chirality on Cell Adhesion.
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- Angewandte Chemie, 2018, v. 130, n. 22, p. 6585, doi. 10.1002/ange.201801462
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The identification of elevated urinary kisspeptin-immunoreactivity during pregnancy.
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- Annals of Clinical Biochemistry, 2015, v. 52, n. 3, p. 395, doi. 10.1177/0004563214551612
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Molecular Dynamics Simulation of Tryptophan Hydroxylase-1: Binding Modes and Free Energy Analysis to Phenylalanine Derivative Inhibitors.
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- International Journal of Molecular Sciences, 2013, v. 14, n. 5, p. 9947, doi. 10.3390/ijms14059947
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Eumelanin–PEDOT:PSS Complementing En Route to Mammalian‐Pigment‐Based Electrodes: Design and Fabrication of an ITO‐Free Organic Light‐Emitting Device.
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- Advanced Electronic Materials, 2017, v. 3, n. 5, p. 1, doi. 10.1002/aelm.201600342
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Biosynthesis, physiology, and functions of hydroxycinnamic acid amides in plants.
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- Plant Biotechnology Reports, 2015, v. 9, n. 5, p. 269, doi. 10.1007/s11816-015-0368-1
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ENANTIOSELECTIVE ACYLATION OF β-PHENYLALANINE ACID AND ITS DERIVATIVES CATALYZED BY PENICILLIN G ACYLASE FROM Alcaligenes faecalis.
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- Preparative Biochemistry & Biotechnology, 2013, v. 43, n. 2, p. 207, doi. 10.1080/10826068.2012.719847
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A Phenylalanine Derivative Containing a 4‐Pyridine Group Can Construct Both Single Crystals and a Selective Cu‐Ag Bimetallohydrogel.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 10, p. 1349, doi. 10.1002/ejic.201900078
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New Prenylated Aeruginosin, Microphycin, Anabaenopeptin and Micropeptin Analogues from a Microcystis Bloom Material Collected in Kibbutz Kfar Blum, Israel.
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- Marine Drugs, 2015, v. 13, n. 4, p. 2347, doi. 10.3390/md13042347
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Synthesis of D- and L-Phenylalanine Derivatives by Phenylalanine Ammonia Lyases: A Multienzymatic Cascade Process.
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- Angewandte Chemie, 2015, v. 127, n. 15, p. 4691, doi. 10.1002/ange.201410670
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- Article
Anomalous Nuclear Overhauser Effects in Carbon-Substituted Aziridines: Scalar Cross-Relaxation of the First Kind.
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- Angewandte Chemie, 2015, v. 127, n. 12, p. 3768, doi. 10.1002/ange.201410271
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Control of Three-Dimensional Cell Adhesion by the Chirality of Nanofibers in Hydrogels.
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- Angewandte Chemie, 2014, v. 126, n. 30, p. 7923, doi. 10.1002/ange.201403249
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Mechanically Induced Multicolor Switching Based on a Single Organic Molecule.
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- Angewandte Chemie, 2013, v. 125, n. 47, p. 12494, doi. 10.1002/ange.201306503
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Enantioselective Extraction of Phenylalanine Enantiomers Using Environmentally Friendly Aqueous Two-Phase Systems.
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- Processes, 2018, v. 6, n. 11, p. 212, doi. 10.3390/pr6110212
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Reciprocal moderation by Toxoplasma gondii seropositivity and blood phenylalanine - tyrosine ratio of their associations with trait aggression.
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- Pteridines, 2016, v. 27, n. 3/4, p. 77, doi. 10.1515/pterid-2016-0006
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Effects of Intraduodenal Infusions of L-phenylalanine and L-glutamine on Antropyloroduodenal Motility and Plasma Cholecystokinin in Healthy Men.
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- Journal of Neurogastroenterology & Motility, 2015, v. 21, n. 3, p. 404, doi. 10.5056/jnm14143
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Use of Some Chemical Inducers to Improve Wheat Resistance to Puccinia striiformis f. sp. tritici.
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- Field & Vegetable Crops Research / Ratarstvo i povrtarstvo, 2014, v. 51, n. 2, p. 83, doi. 10.5937/ratpov51-5985
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Efficient Synthesis of Glycosylated Matijin-Su Derivatives via Ultrasonic Irradiation.
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- Chinese Journal of Chemistry, 2016, v. 34, n. 12, p. 1353, doi. 10.1002/cjoc.201600468
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A Redox-Responsive Supramolecular Hydrogel for Controllable Dye Release.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 19, p. 1945, doi. 10.1002/macp.201500210
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Double crosslinked chitosan and gelatin submicronic capsules entrapping aminoacid derivatives with potential antitumoral activity.
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- Journal of Materials Science, 2012, v. 47, n. 23, p. 8223, doi. 10.1007/s10853-012-6719-1
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Design, Synthesis, Biological Evaluation, and Docking Studies of ( S)-Phenylalanine Derivatives with a 2-Cyanopyrrolidine Moiety as Potent Dipeptidyl Peptidase 4 Inhibitors.
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- Chemical Biology & Drug Design, 2013, v. 82, n. 2, p. 140, doi. 10.1111/cbdd.12139
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