BIOMAT Database Logo BIOMAT Database Logo

Polymorphism in the crystal structure of the cellulose fragment analogue methyl 4-O-methyl-beta-D-glucopyranosyl-(1-4)-beta-D-glucopyranoside. 2002

Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
CERMAV-CNRS, 601 rue de la Chimie, BP 53, 38041 Grenoble cedex 9, France.

UI MeSH Term Description Entries
D008958 Models, Molecular Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures. Molecular Models,Model, Molecular,Molecular Model
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
D009844 Oligosaccharides Carbohydrates consisting of between two (DISACCHARIDES) and ten MONOSACCHARIDES connected by either an alpha- or beta-glycosidic link. They are found throughout nature in both the free and bound form. Oligosaccharide
D002475 Cellobiose A disaccharide consisting of two glucose units in beta (1-4) glycosidic linkage. Obtained from the partial hydrolysis of cellulose. 4-O-beta-D-Glucopyranosyl-D-glucopyranose,4 O beta D Glucopyranosyl D glucopyranose
D002482 Cellulose A polysaccharide with glucose units linked as in CELLOBIOSE. It is the chief constituent of plant fibers, cotton being the purest natural form of the substance. As a raw material, it forms the basis for many derivatives used in chromatography, ion exchange materials, explosives manufacturing, and pharmaceutical preparations. Alphacel,Avicel,Heweten,Polyanhydroglucuronic Acid,Rayophane,Sulfite Cellulose,alpha-Cellulose,Acid, Polyanhydroglucuronic,alpha Cellulose
D003198 Computer Simulation Computer-based representation of physical systems and phenomena such as chemical processes. Computational Modeling,Computational Modelling,Computer Models,In silico Modeling,In silico Models,In silico Simulation,Models, Computer,Computerized Models,Computer Model,Computer Simulations,Computerized Model,In silico Model,Model, Computer,Model, Computerized,Model, In silico,Modeling, Computational,Modeling, In silico,Modelling, Computational,Simulation, Computer,Simulation, In silico,Simulations, Computer
D003460 Crystallization The formation of crystalline substances from solutions or melts. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Crystalline Polymorphs,Polymorphism, Crystallization,Crystal Growth,Polymorphic Crystals,Crystal, Polymorphic,Crystalline Polymorph,Crystallization Polymorphism,Crystallization Polymorphisms,Crystals, Polymorphic,Growth, Crystal,Polymorph, Crystalline,Polymorphic Crystal,Polymorphisms, Crystallization,Polymorphs, Crystalline
D006027 Glycosides Any compound that contains a constituent sugar, in which the hydroxyl group attached to the first carbon is substituted by an alcoholic, phenolic, or other group. They are named specifically for the sugar contained, such as glucoside (glucose), pentoside (pentose), fructoside (fructose), etc. Upon hydrolysis, a sugar and nonsugar component (aglycone) are formed. (From Dorland, 28th ed; From Miall's Dictionary of Chemistry, 5th ed) Glycoside
D006860 Hydrogen Bonding A low-energy attractive force between hydrogen and another element. It plays a major role in determining the properties of water, proteins, and other compounds. Hydrogen Bonds,Bond, Hydrogen,Hydrogen Bond
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular

Related Publications

Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Crystal and molecular structure of methyl 4-O-methyl-beta-D-glucopyranosyl-(1-->4)-beta-D-glucopyranoside.
February 2002, Carbohydrate research,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Crystal structure of methyl 3-O-beta-D-glucopyranosyl-beta-D-glucopyranoside (methyl beta-D-laminarabioside) monohydrate.
December 1992, Carbohydrate research,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Synthesis of oxidized methyl 4-O-methyl-beta-D-glucopyranoside and methyl beta-D-glucopyranosyl-(1-->4)-beta-D-glucopyranoside derivatives as substrates for fluorescence labeling reactions.
April 2002, Carbohydrate research,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Synthesis of methyl O-(2-O-methyl-beta-D-galactopyranosyl)-(1----4)-O-(2- acetamido-2-deoxy-beta-D-glucopyranosyl)-(1----3)-beta-D- galactopyranoside and 4-nitrophenyl O-beta-D-galactopyranosyl-(1----4)-O-(2-acetamido-2-deoxy-beta-D- glucopyranosyl)-(1----3)-beta-D-galactopyranoside.
August 1990, Carbohydrate research,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Synthesis of oligosaccharins: a chemical synthesis of propyl O-beta-D-galactopyranosyl-(1----2)-O-alpha-D-xylopyranosyl-(1----6)- O-beta-D-glucopyranosyl-(1----4)-beta-D-glucopyranoside.
September 1990, Carbohydrate research,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Methyl 4-O-beta-D-galactopyranosyl alpha-D-glucopyranoside (methyl alpha-lactoside).
December 2005, Acta crystallographica. Section C, Crystal structure communications,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Synthesis of 4-O-beta-D-glucopyranosyl-D-xylose. 4-O-beta-D-glucopyranosyl-D-arabinose, 4-O-beta-D-glucopyranosyl-2-deoxy-D-glucose, 4-O-beta-D-glucopyranosyl-D-mannose, and 4-O-beta-D-glucopyranosyl-D-glucosamine by cellobiose phosphorylase from Clostridium thermocellum.
February 1968, Archives of biochemistry and biophysics,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Methyl 4-O-beta-L-galactopyranosyl-beta-D-glucopyranoside (methyl beta-L-lactoside).
February 2006, Acta crystallographica. Section C, Crystal structure communications,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Vomifoliol 9-O-beta-D-glucopyranosyl-4-O-beta-D-xylopyranosyl-6-O-beta-D- glucopyranoside: a trisaccharide glycoside from apple fruit.
March 1992, Phytochemistry,
Anna Rencurosi, and Jürgen Röhrling, and Jutta Pauli, and Antje Potthast, and Christian Jäger, and Serge Pérez, and Paul Kosma, and Anne Imberty
Molecular and crystal structure of (2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-(1-->3)- [2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl-(1-->6)]- (2,4-di-O-acetyl-beta-D-glucopyranosyl)- (1-->3)-1,2,4,6-tetra-O-acetyl-beta-D-glucopyranose.
May 1994, Carbohydrate research,
Copied contents to your clipboard!