Gotowa bibliografia na temat „Glycosidic bonds”
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Artykuły w czasopismach na temat "Glycosidic bonds"
Wang, Qian, Chao Gao, Nan Yang i Katsuyoshi Nishinari. "Effect of simulated saliva components on the in vitro digestion of peanut oil body emulsion". RSC Advances 11, nr 49 (2021): 30520–31. http://dx.doi.org/10.1039/d1ra03274g.
Pełny tekst źródłaJoseleau, Jean-Paul, i Rachid Kesraoui. "Glycosidic Bonds between Lignin and Carbohydrates". Holzforschung 40, nr 3 (styczeń 1986): 163–68. http://dx.doi.org/10.1515/hfsg.1986.40.3.163.
Pełny tekst źródłaJohnson, Glenn P., Luis Petersen, Alfred D. French i Peter J. Reilly. "Twisting of glycosidic bonds by hydrolases". Carbohydrate Research 344, nr 16 (listopad 2009): 2157–66. http://dx.doi.org/10.1016/j.carres.2009.08.011.
Pełny tekst źródłaKhalilova, Gulnoza Abduvakhobovna, Abbaskhan Sabirkhanovich Turaev, Bahtiyor Ikromovich Muhitdinov, Albina Vasilevna Filatova, Saidakhon Bokijonovna Haytmetova i Nodirali Sokhobatalievich Normakhamatov. "Research On The Composition And Structure Of Β -Glucans Isolated From Basidiomycete Raw Materials Inonotus Hispidus". American Journal of Applied sciences 03, nr 01 (19.01.2021): 9–17. http://dx.doi.org/10.37547/tajas/volume03issue01-03.
Pełny tekst źródłaWeignerová, Lenka, Yukio Suzuki, Zdenka Huňková, Petr Sedmera, Vladimír Havlíček, Radek Marek i Vladimír Křen. "Pyridoxine as a Substrate for Screening Synthetic Potential of Glycosidases". Collection of Czechoslovak Chemical Communications 64, nr 8 (1999): 1325–34. http://dx.doi.org/10.1135/cccc19991325.
Pełny tekst źródłaKobayashi, Hirokazu, Yusuke Suzuki, Takuya Sagawa, Kyoichi Kuroki, Jun-ya Hasegawa i Atsushi Fukuoka. "Impact of tensile and compressive forces on the hydrolysis of cellulose and chitin". Physical Chemistry Chemical Physics 23, nr 30 (2021): 15908–16. http://dx.doi.org/10.1039/d1cp01650d.
Pełny tekst źródłaFrański, R., P. Bednarek, D. Siatkowska, P. Wojtaszek i M. Stobiecki. "Application of mass spectrometry to structural identification of flavonoid monoglycosides isolated from shoot of lupin (Lupinus luteus L.)." Acta Biochimica Polonica 46, nr 2 (30.06.1999): 459–73. http://dx.doi.org/10.18388/abp.1999_4177.
Pełny tekst źródłaHe, Xingxing, Fuyuan Zhang, Jifeng Liu, Guozhen Fang i Shuo Wang. "Homogenous graphene oxide-peptide nanofiber hybrid hydrogel as biomimetic polysaccharide hydrolase". Nanoscale 9, nr 45 (2017): 18066–74. http://dx.doi.org/10.1039/c7nr06525f.
Pełny tekst źródłaDavies, Gideon J., Simon J. Charnock i Bernard Henrissat. "The Enzymatic Synthesis of Glycosidic Bonds: "Glycosynthases" and Glycosyltransferases." Trends in Glycoscience and Glycotechnology 13, nr 70 (2001): 105–20. http://dx.doi.org/10.4052/tigg.13.105.
Pełny tekst źródłaIbatullin, Farid M., Alexander M. Golubev, Leonid M. Firsov i Kirill N. Neustroev. "A model for cleavage ofO-glycosidic bonds in glycoproteins". Glycoconjugate Journal 10, nr 3 (czerwiec 1993): 214–18. http://dx.doi.org/10.1007/bf00702202.
Pełny tekst źródłaRozprawy doktorskie na temat "Glycosidic bonds"
Baker, Anne. "The chemo-enzymatic synthesis of glycosidic bonds". Thesis, University of Exeter, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294484.
Pełny tekst źródłaWebberley, Matthew Christian. "The stereospecific synthesis of glycosidic bonds using glycosidases". Thesis, University of Exeter, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303771.
Pełny tekst źródłaHenderson, Margaret Esther. "Mechanisms of alkaline glycosidic bond cleavage in 1,5-anhydro-4-O-". Diss., Georgia Institute of Technology, 1986. http://hdl.handle.net/1853/5744.
Pełny tekst źródłaDeshpande, Sagar Nandkumar. "Pre-hydrolysis of the Phenyl Glycosidic Bond in a Model Compound". Fogler Library, University of Maine, 2008. http://www.library.umaine.edu/theses/pdf/DeshpandeSN2008.pdf.
Pełny tekst źródłaTennant-Eyles, Richard J. "Peptide templated oligosaccharide synthesis : a novel strategy for glycosidic bond formation". Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365751.
Pełny tekst źródłaCollins, James P. "Prebiotic Synthesis of Pyrimidine Nucleosides". Thesis, Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/14095.
Pełny tekst źródłaMolinarolo, William E. "The high temperature alkaline degradation of phenyl β-D-glucopyranoside". Diss., Georgia Institute of Technology, 1989. http://hdl.handle.net/1853/5753.
Pełny tekst źródłaCallam, Christopher Stephen. "Experimental and Theoretical Studies of: Methyl 4a-carba-D-arabinofuranosides and 2,3-Anydrosugars in Glycoside Bond Synthesis". The Ohio State University, 2003. http://rave.ohiolink.edu/etdc/view?acc_num=osu1048691172.
Pełny tekst źródłaMendoza, Muñoz María Fernanda. "Estudios teóricos y computacionales para la síntesis enzimática del enlace glicosídico". Doctoral thesis, Universitat Autònoma de Barcelona, 2016. http://hdl.handle.net/10803/400072.
Pełny tekst źródłaIn the present thesis the catalytic mechanism of retaining glycosyltransferases has been investigated by means of hybrid quantum mechanics/molecular mechanics (QM/MM) and molecular dynamics (MD) simulations. The research is focused on the evaluation of the mechanistic proposals, as well as the identification of the main factors that contribute to the catalytic efficiency. For that we use two enzymes, α1,4-N-Acetylhexosaminyltransferase (EXTL2) and Mycobacterium Tuberculosis Glucosyl-3-phosphoglycerate Synthase (GpgS). Moreover, further simulations using in silico models built based on the native or mutant enzymes were carried out to unveil the roles of the residues located in one of the faces of the transferable substrate (β-face of the sugar). The results for GpgS are exposed in Chapter 4 and the results for EXTL2 are presented through Chapters 5 and 6. In Chapter 7, two other retaining glycosyltransferases investigated in a previous thesis of the group (LgtC and α3GalT), along with EXTL2 and GpgS are studied and compared to further analyse the structural features in the β-face of the sugar and its implications on the catalytic mechanism. A general discussion around the main factors modulating the catalytic efficiency in each enzyme is also included in this Chapter, providing in this way a more complete and general picture about the catalytic strategies performed by retaining glycosyltransferases. Finally, the general conclusions of this work are outlined in Chapter 8. Part of the results presented in this thesis is already published and can be found in the following papers: • Albesa-Jove, D.; Mendoza, F.; Rodrigo-Unzueta, A.; Gomollon-Bel, F.; Cifuente, J. O.; Urresti, S.; Comino, N.; Gómez, H.; Romero-Garcia, J.; Lluch, J. M.; Sancho-Vaello, E.; Biarnes, X.; Planas, A.; Merino, P.; Masgrau, L.; Guerin, M. E. Angew. Chem. Int. Ed. 2015, 54, 9898-9902. • Gómez, H.; Mendoza, F.; Lluch, J. M.; Masgrau, L. Advances in protein chemistry and structural biology 2015, 100, 225-254. • Mendoza, F.; Gómez, H.; Lluch, J. M.; Masgrau, L. Acs Catalysis 2016, 6, 2577-2589.
Bruneau, Alexandre. "Développement de nouvelles réactions métallo-catalysées pour la création de liaisons C-C et C-hétéroatomes : Application à la synthèse d’inhibiteurs de la Hsp90 et aux ligands de la lectine A". Thesis, Université Paris-Saclay (ComUE), 2015. http://www.theses.fr/2015SACLS138.
Pełny tekst źródłaThe work reported in this dissertation concerns the development of new metal-catalyzed reactions for the creation of carbon-heteroatom and carbon-carbon bonds as well as their applications to the synthesis of biologically active products.The first part of this manuscript is devoted to the study of the reactivity of sugars as nucleophiles in organometallic couplings. Conditions were developed for the creation of the C-S bond between glycosyl thiols and aryl partners. Moreover, the creation of the nitrogen carbon bond of glycosyl amine with boronic acids was studied. The products synthesized in this first part have been evaluated for their potential to inhibit the lectin A, in Pseudomonas aeruginosa related lung infections.The second part of this work is dedicated to the creation of a new series of 6BrCaQ analogues as Hsp90 inhibitors and their biological evaluation. This new series was synthetized through a new CH activation methodology. The antitumoral potential was evaluated and will be presented in this manuscript
Książki na temat "Glycosidic bonds"
Henderson, Margaret Esther. Mechanisms of alkaline glycosidic bond cleavage in 1,5-anhydro-4-O- -mannopyranosyl-D-mannitol. 1986.
Znajdź pełny tekst źródłaCzęści książek na temat "Glycosidic bonds"
Monti, Daniela, i Sergio Riva. "Hydrolysis and Formation of Glycosidic Bonds". W Enzyme Catalysis in Organic Synthesis, 417–66. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639861.ch10.
Pełny tekst źródłaPinto, José-Henrique Q., Zin-Eddine Dadach, Alain Lemoyne i Serge Kaliaguine. "Acid Hydrolysis of Glycosidic Bonds in Polysaccharides: Modelling and Stochastic Simulation". W Advances in Thermochemical Biomass Conversion, 1583–97. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1336-6_129.
Pełny tekst źródłaGooch, Jan W. "Glycosidic Bond". W Encyclopedic Dictionary of Polymers, 896. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13849.
Pełny tekst źródłaPengelly, Andrew. "Glycosides." W The constituents of medicinal plants, 59–72. Wyd. 3. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0004.
Pełny tekst źródłaMiljković, Momčilo. "Chemistry of the Glycosidic Bond". W Carbohydrates, 323–421. New York, NY: Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-92265-2_12.
Pełny tekst źródłaAharoni, Amir, i Stephen G. Withers. "Screening Methodologies for Glycosidic Bond Formation". W Protein Engineering Handbook, 605–20. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634026.ch25.
Pełny tekst źródłaYe, Xin-Shan, i Weigang Lu. "GENERAL ASPECTS IN O-GLYCOSIDIC BOND FORMATION". W Glycochemical Synthesis, 69–95. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119006435.ch3.
Pełny tekst źródłaMiljkovic, Momcilo. "Armed-Disarmed Concept in the Synthesis of Glycosidic Bond". W Electrostatic and Stereoelectronic Effects in Carbohydrate Chemistry, 117–79. Boston, MA: Springer US, 2013. http://dx.doi.org/10.1007/978-1-4614-8268-0_5.
Pełny tekst źródłaSchmidt, Richard R., Simon Jonke i Ke-gang Liu. "New Aspects of Glycoside Bond Formation: Solid-Phase Oligosaccharide Synthesis". W ACS Symposium Series, 209–36. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0960.ch013.
Pełny tekst źródłaPriebe, Waldemar, Piotr Skibicki, Oscar Varela, Nouri Neamati, Marcos Sznaidman, Krzysztof Dziewiszek, Grzegorz Grynkiewicz i in. "Non-Cross-Resistant Anthracyclines with Reduced Basicity and Increased Stability of the Glycosidic Bond". W ACS Symposium Series, 14–46. Washington, DC: American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1995-0574.ch002.
Pełny tekst źródłaStreszczenia konferencji na temat "Glycosidic bonds"
Withers, Stephen G. "ENZYMATIC CLEAVAGE AND FORMATION OF GLYCOSIDIC BONDS: FROM GLYCOSIDASES AND LYASES TO TRANSFERASES AND GLYCOSYNTHASES". W XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.355.
Pełny tekst źródłaRodgers, M., Jos Oomens, Giel Berden, Chase Leslie, Erik Soley, Harrison Roy, Zachary Devereaux i in. "INFLUENCE OF NATURALLY-OCCURRING AND SYNTHETIC MODIFICATIONS ON THE STRUCTURES AND GLYCOSIDIC BOND STABILITIES OF DNA AND RNA NUCLEOSIDES". W 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.ma02.
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