Добірка наукової літератури з теми "Γ Amino Acid"
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Статті в журналах з теми "Γ Amino Acid"
Hettasch, Joann M., Mark G. Bolyard та Susan T. Lord. "The Residues AGDV of Recombinant γ Chains of Human Fibrinogen Must Be Carboxy-Terminal to Support Human Platelet Aggregation". Thrombosis and Haemostasis 68, № 06 (1992): 701–6. http://dx.doi.org/10.1055/s-0038-1646347.
Повний текст джерелаValachová, Dominika, Branislav Ferko, Eva Puchľová, Oľga Caletková, Dušan Berkeš, Andrej Kolarovič та Pavol Jakubec. "Stereoselective Synthesis of syn-γ-Hydroxynorvaline and Related α-Amino Acids". Synthesis 51, № 24 (16 жовтня 2019): 4568–75. http://dx.doi.org/10.1055/s-0039-1690705.
Повний текст джерелаDutta, Arpita, Suven Das, Purak Das, Suvendu Maity, Prasanta Ghosh та Soumya Shankha Biswas. "Unique supramolecular assembly of a synthetic achiral α, γ-hybrid tripeptide". Zeitschrift für Kristallographie - Crystalline Materials 237, № 1-3 (1 березня 2022): 77–81. http://dx.doi.org/10.1515/zkri-2022-0002.
Повний текст джерелаКудрявский, Дмитрий Леонович, Елена Константиновна Фомина, Людмила Юльевна Тычинская, Евгений Доминикович Скаковский та Светлана Евгеньевна Богушевич. "NMR spectroscopy of Cu(II) complexes with acrylamide and sodium acrylate copolymer and ω-amino acids". Journal of the Belarusian State University. Chemistry, № 1 (12 квітня 2021): 85–98. http://dx.doi.org/10.33581/2520-257x-2021-1-85-98.
Повний текст джерелаSperanza, Giovanna, Marco Rabuffetti, Nikolina Vidović та Carlo F. Morelli. "Synthesis of γ-Glutamyl Derivatives of Sulfur-Containing Amino Acids in a Multigram Scale via a Two-Step, One-Pot Procedure". Molbank 2020, № 3 (10 липня 2020): M1147. http://dx.doi.org/10.3390/m1147.
Повний текст джерелаČeřovský, Václav, та Karel Jošt. "Enzymatically catalyzed synthesis of dipeptides of γ-carboxy-L-glutamic acid from benzyloxycarbonyl-γ-carboxy-DL-glutamic acid". Collection of Czechoslovak Chemical Communications 50, № 4 (1985): 878–84. http://dx.doi.org/10.1135/cccc19850878.
Повний текст джерелаZhu, Shaozhou, Cuiyu Gong, Dawei Song, Shuaihua Gao та Guojun Zheng. "Discovery of a Novel (+)-γ-Lactamase from Bradyrhizobium japonicum USDA 6 by Rational Genome Mining". Applied and Environmental Microbiology 78, № 20 (10 серпня 2012): 7492–95. http://dx.doi.org/10.1128/aem.01398-12.
Повний текст джерелаPataj, Zoltán, István Ilisz, Anita Aranyi, Enikő Forró, Ferenc Fülöp, Daniel W. Armstrong та Antal Péter. "LC Separation of γ-Amino Acid Enantiomers". Chromatographia 71, S1 (5 лютого 2010): 13–19. http://dx.doi.org/10.1365/s10337-010-1484-2.
Повний текст джерелаOnozato, Mayu, Kana Kobata, Tatsuya Sakamoto, Hideaki Ichiba, and Takeshi Fukushima. "LC–MS/MS Analysis of Thiol-Containing Amino Acids in Exosomal Fraction of Serum." Journal of Chromatographic Science 58, no. 7 (June 24, 2020): 636–40. http://dx.doi.org/10.1093/chromsci/bmaa028.
Повний текст джерелаAllan, RD, RK Duke, TW Hambley, GAR Johnston, KN Mewett, N. Quickert, and HW Tran. "Synthesis of Unsaturated Analogues of Glutamic Acid: Amination of Trianions From Unsaturated Dicarboxylic Acids With Chloramine." Australian Journal of Chemistry 49, no. 7 (1996): 785. http://dx.doi.org/10.1071/ch9960785.
Повний текст джерелаДисертації з теми "Γ Amino Acid"
Stanovych, Andrii. "Synthèse et études structurales de γ-peptides synthétisés à partir d’acides β,γ-diaminés". Thesis, Paris 11, 2014. http://www.theses.fr/2014PA112310/document.
Повний текст джерелаThe design of a new oligopeptides, capable to mimic the properties of natural proteins, is an important field not only for structural studies but also in the developpement of new efficient drugs. The peptides featuring β-amino acids have been extensively explored, whereas the research in γ-peptides is more recent. The studies of γ-peptides show their ability to adopt stable secondary structures and also to have a promising biological activity. Our laboratory is interested in the synthesis of new β,γ-diaminoacids.The aim of this work is a developpement of new synthetic route starting from different natural α -amino acids and to use obtained β,γ-diaminoacids to access novel unnatural peptides having specific conformational properties.The synthetic strategy, developed and optimized in our laboratory during this work, gives access to diastereomers cis and trans from L-leucine, L- and D-phenylalanine which were used in the synthesis of a new hybrid α/γ-peptides. The structural studies were performed on two series of hybrid α/γ-peptides consisting of β,γ-aminoacid from L-leucine and L- or D-α-amino acids. In the first case, the peptides are able to adopt stable secondary structures stabilized by intramolecular hydrogen bonds involving the nitrogen on the β-position. In addition, we present the synthesis of an analogue of gramicidine S, a naturally occuring antibiotic cyclic peptide. The dipeptide pattern D-Phe-L-Pro has been replaced with the β,γ-diaminoacid synthesized from D-phenylalanine
Bonnel, Clément. "Oligopeptides construits autour du γ-aminoacide ATC : synthèses, analyses structurales et évaluation biologique". Thesis, Montpellier, 2016. http://www.theses.fr/2016MONTT201.
Повний текст джерелаThis manuscript describes the synthesis, the structural study and the biological evaluation of abiotic oligopeptides incorporating the heterocyclic gamma-amino acid ATC (4-Aminomethyl-1,3-Thiazole-5 Carboxylic acid). This original block is built around a thiazole ring and displays two lateral chains. Previous work in our laboratory highlighted that the presence of the thiazole ring between the positions alpha and beta implied that zeta angle was blocked around 0°, thus structuring poly-(S)-ATCs homo-oligomers in a right-handed 9-helix foldamer. First, development of a simple, flexible and enantioselective synthesis on a few grams scale has allowed to get access of a highly diverse ATC library from commercial alpha-amino acids. Introduction of the chemical diversity occurs via two key steps implying a cross-Claisen condensation and a Hantzsch cyclization. Then identification of NMR and FT-IR structural markers of ATC-containing oligomers was used to characterize the folding propensity of hybrid α:ATC oligomers. We demonstrated that 1:1 (L)-alpha:(S)-ATC heterochiral oligomers are structured in solution in a new ribbon-like shape stabilized by a bidentate intramolecular hydrogen bond network forming 9- and 12-membered pseudorings. The distribution of lateral chains along the main skeleton shows a high analogy with alpha-helix thus constituting a major advantage for potential medicinal applications. The last part of this work has focused on the design of amphipathic ATC-containing pseudo-peptides as antimicrobial agents
Wenjie, Lu. "Synthesis and Evaluation of Functionalized Dirhodium(II) Carboxylate Catalysts Bearing Axially Chiral Amino Acid Derivatives." 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225528.
Повний текст джерелаWersinger, Eric. "Inhibition présynaptique et contraste dans la rétine de souris : à la recherche du rôle des dystrophines." Paris 6, 2007. http://www.theses.fr/2007PA066122.
Повний текст джерелаOlszewski, Tomasz Krzysztof. "Original syntheses of new biomolecules : from imidazole and thiazole derivatives of α-aminophosphonic acids and γ-amino-α, β-dihydroxy carboxylic acid derivatives to disaccharide mimics". Montpellier 2, 2006. http://www.theses.fr/2006MON20017.
Повний текст джерелаFlanigan, David L. Jr. "Studies in Rhodium Catalyzed Intramolecular C-H Insertion of Amino Acid Derived α-Diazo-α-(substituted)acetamides and its Application to the Total Synthesis of clasto-Lactacystin β-Lactone". Scholar Commons, 2004. https://scholarcommons.usf.edu/etd/1037.
Повний текст джерелаWan, Yang. "Synthesis of β,γ-diamino acids and their use to design new analogues of the antimicrobial peptide Gramicidin Septide antimicrobien, la Gramicidine S". Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS407/document.
Повний текст джерелаIn our group, we are interested in developing peptides containing β,γ-diamino acids . Along with many other peptides containing unnatural amino acids, they have shown the ability to possess stable conformations and/or interesting biological activities. Moreover, those peptides are usually more resistant to proteolysis. In order to synthesize stereopure γ-amino acids, we have developed a synthetic route using Blaise reaction and subsequent diastereoselective reduction as key reactions. Through applying this method, we have synthesized β,γ-diamino acids derived from D-phenylalanine and L-glutamic acid. The former β,γ-diamino acid was used for designing antimicrobial peptide gramicidin S analogues. Compared with mother molecule, the analogues exerted much less host cell cytotoxicity while remaining interesting antibacterial activity. Meanwhile, it gave us more knowledge for further developing analogues of gramicidin S as well as other antimicrobial peptides. We also paid lots of effort to efficiently synthesize cyclic β,γ-diamino acids starting from L-glutamic acid. Interestingly, when oligomers incorporating this β,γ-diamino acids and α-amino acids, they have shown the potential to adopt stable conformations. The following studies will be continuously investigated
Zammit, Charlotte Maria. "Asymmetric synthesis of β- and γ- amino acids". Thesis, University of Oxford, 2015. http://ora.ox.ac.uk/objects/uuid:35138286-c217-4d28-990b-941149b5daa5.
Повний текст джерелаHallinan, Keith Oliver. "Synthetic and metabolic studies on β,γ-unsaturated α-amino acids". Thesis, University of Warwick, 1992. http://wrap.warwick.ac.uk/110385/.
Повний текст джерелаKerres, Sabine Martha [Verfasser], та Oliver [Akademischer Betreuer] Reiser. "Synthesis of γ-cyclobutane amino acids via visible light / Sabine Martha Kerres ; Betreuer: Oliver Reiser". Regensburg : Universitätsbibliothek Regensburg, 2019. http://d-nb.info/1196873410/34.
Повний текст джерелаКниги з теми "Γ Amino Acid"
Pearl, Phillip L., and William P. Welch. Pediatric Neurotransmitter Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0059.
Повний текст джерелаЧастини книг з теми "Γ Amino Acid"
Hanrahan, Jane R., and Graham A. R. Johnston. "Synthesis of γ-Aminobutyric Acid Analogs." In Amino Acids, Peptides and Proteins in Organic Chemistry, 573–689. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527631766.ch14.
Повний текст джерелаffrench-Constant, R. H., H. G. Zhang, and M. B. Jackson. "Biophysical Analysis of a Single Amino Acid Replacement in the Resistance to Dieldrin γ-Aminobutyric Acid Receptor." In ACS Symposium Series, 192–204. Washington, DC: American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0591.ch012.
Повний текст джерелаTung, Roger D., Chong-Qing Sun, Don Deyo, and Daniel H. Rich. "Asymmetric syntheses of β-OH and β-OH, γ-alkyl α-amino acids: Analogs of the unusual cyclosporin amino acid MeBmt." In Peptides, 149–51. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-010-9595-2_43.
Повний текст джерелаKumar, Antul, Anuj Choudhary, Harmanjot Kaur, Mohammed Javed, and Sahil Mehta. "Plant Performance and Defensive Role of γ-Gamma Amino Butyric Acid Under Environmental Stress." In Plant Performance Under Environmental Stress, 277–99. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-78521-5_11.
Повний текст джерелаLangford, Marlyn P., Thomas B. Redens, and Donald E. Texada. "Excitatory Amino Acid Transporters, Xc− Antiporter, γ-Glutamyl Transpeptidase, Glutamine Synthetase, and Glutathione in Human Corneal Epithelial Cells." In Oxidative Stress in Applied Basic Research and Clinical Practice, 67–82. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1935-2_4.
Повний текст джерелаFurukawa, Tadayasu, and Takahiro Hara. "Potential of γ-L-glutamyl-L-glutamine as an L-glutamine-containing dipeptide for parenteral nutrition." In Amino Acids, 1114–18. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_140.
Повний текст джерелаMolnár, László, Gábor Kiszler, Edit Pollák, and László Deres. "Distribution pattern of γ-amino butyric acid immunoreactive neural structures in the central and peripheral nervous system of the tubificid worm, Limnodrilus hoffmeisteri." In Aquatic Oligochaete Biology IX, 33–43. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-5368-1_4.
Повний текст джерелаGrübler, G., S. Stoeva, H. Echner, and W. Voelter. "A convenient, straightforward solid phase synthesis of γ-endorphin on polystyrene matrix,grafted with polyoxyethylene spacer arms, using Fmoc amino acid N-carboxy anhydrides." In Peptides, 51–53. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_10.
Повний текст джерелаTrabocchi, Andrea, Gloria Menchi, and Antonio Guarna. "Synthesis of γ- and δ-Amino Acids." In Amino Acids, Peptides and Proteins in Organic Chemistry, 527–71. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527631766.ch13.
Повний текст джерелаBlaskovich, M. A., A. W. Wong, and G. A. Lajoie. "Synthesis of optically enriched β,γ-unsaturated α-amino acids." In Peptides 1994, 205–6. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_85.
Повний текст джерелаТези доповідей конференцій з теми "Γ Amino Acid"
"Computational study of CO2 solubility in amino acid-based ionic liquids using COSMO-RS." In Sustainable Processes and Clean Energy Transition. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902516-33.
Повний текст джерелаTerukina, S., M. Matsuda, N. Yoshida, K. Yamazumi, Y. Takeda та T. Takano. "TWO ABNORMAL FIBRINOGENS DESIGNATED AS OSAKA II AND MORIOKA WITH A HITHERTO UNIDENTIFIED AMINO ACID SUBSTITUTION; γARG-275 BY CYS". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644701.
Повний текст джерелаYoshida, N., S. Terukina, M. Matsuda, M. Moroi, M. Okuma та N. Aoki. "FIBRINOGENS KYOTO AND TOCHIGI, EACH WITH AN APPARENT ABNORMAL MOL. WT. γ CHAIN, ARE CHARACTERIZED BY REPLACEMENT OF γ ASN-308 BY LYS AND γ ARG-275 BY CYS, RESPECTIVELY". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644702.
Повний текст джерелаAndrieux, A., M. H. Charon, G. Hudry-Clergeon, and G. Marguerie. "FIBRINOGEN SEQUENCES INTERACTING WITH PLATELET GPIIbIIIa." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643519.
Повний текст джерелаStenflo, J., A.-K. öhlin, Å. Lundvall та B. Dahlback. "β-HYDROXY ASPARTIC ACID AND ft-HYDROXYASPARAGINE IN THEEGF-HOMOLOGY REGIONS OF PROTEIN C AND PROTEINS". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643995.
Повний текст джерелаWilhelm, O., A. Henschen, R. Hafter, and H. Graeff. "TUMOR-ASSOCIATED FIBRINOLYSIS IN OVARIAN CARCINOMA - HPLC AND N-TERMINAL AMINO ACID ANALYSIS REVEAL THE PATHWAY OF DEGRADATION OF CROSSLINKED FIBRIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643189.
Повний текст джерелаKostić, Marina, Vera Divac, and Sven Mangelinckx. "SYNTHESIS AND CHARACTERIZATION OF PALLADIUM (II)–2- (AZIDOMETHYL)CYCLOPROPANE-1,1-DICARBOXYLIC ACID COMPLEX." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.297k.
Повний текст джерелаJorgensen, M. J., MJ Rabiet, A. B. Cantor, B. Furie, C. L. Brown, C. B. Shoemaker та B. C. Furie. "VITAMIN K-DEPENDENT γ-CARBOXYLATION OF FACTOR IX REQUIRES A RECOGNITION SITE CONTAINED WITHIN THE PROPEPTIDE". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643564.
Повний текст джерелаGoretzki, L., E. Miller, and A. Henschen. "CLEAVAGE PATHWAY,AND SPECIFICITY OF LEUCOCYTE ELASTASE AS COMPARED TO PLASMIN DURING FIBRINOGEN DEGRADATION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643897.
Повний текст джерелаSuttie, W. J., A. Cheung, and M. G. Wood. "ENZYMOLOGY OF THE VITAMIN K-DEPENDENT CARBOXYLASE: CURRENT STATUS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643991.
Повний текст джерела