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Change in optical rotation of a chiral substance due to interconversion of anomers
In stereochemistry, mutarotation is the change in optical rotation of a chiral material in a solution due to a change in proportion of the two constituent
Mutarotation
Naturally produced monosaccharide
yield the 4-fold ester α-D-glucofuranose-1,2:3,5-bis(p-tolylboronate). Mutarotation consists of a temporary reversal of the ring-forming reaction, resulting
Glucose
Form of stereoisomerism in carbohydrates
For the reducing sugars present in biology, this process is known as mutarotation, catalyzed by dilute acid or base. Because they have different three-dimensional
Anomer
Simple sugars such as glucose and fructose
The molecule can change between these two forms by a process called mutarotation, that consists in a reversal of the ring-forming reaction followed by
Monosaccharide
Chemical compound
glycosidic bond.[citation needed] Maltose in aqueous solution exhibits mutarotation, because the α and β isomers that are formed by the different conformations
Maltose
Organic compound of the general form C(H2O)
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Carbohydrate
Chemical compound
through a metabolic process termed sulfoglycolysis. The half-life for mutarotation of sulfoquinovose at pD 7.5 and 26C is 299 minutes. Sulfolipid Sulfoglycolysis
Sulfoquinovose
Polysaccharide gum used as a food additive and thickener
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Xanthan_gum
Edible mixture of glucose and fructose, obtained from sucrose hydrolysis
Mutarotation: The α-anomer of glucose (left) interconverts into its β-anomer (right)
Inverted_sugar_syrup
6-carbon simple sugar
and then closing in the opposite configuration. This process is called mutarotation. Although all hexoses have similar structures and share some general
Hexose
Cyclic carbohydrate
an l-configuration furanose. Typically, the anomeric carbon undergoes mutarotation in solution, and the result is an equilibrium mixture of α and β configurations
Furanose
Sweet-tasting, water-soluble carbohydrates
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Sugar
Long-chain polymer of a N-acetylglucosamine
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Chitin
Long carbohydrate polymers such as starch, glycogen, cellulose, and chitin
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Polysaccharide
Rearrangement reaction
mix of D-glucose, D-fructose and D-mannose. Sugar Chemistry: Explains mutarotation and interconversion of Glucose ↔ Fructose ↔ Mannose. Food Chemistry:
Lobry de Bruyn–Van Ekenstein transformation
Lobry_de_Bruyn–Van_Ekenstein_transformation
Carbohydrate
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Lactose
Metabolic pathway for the catabolism of D-galactose
converts the D-glucose 1-phosphate to D-glucose 6-phosphate. Anomer Mutarotation Epimer Epimerase Trucco, R.E.; Caputto, R; Leloir, L.F.; Mittelman, N
Leloir_pathway
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Allulose
Covalent bond joining a sugar molecule to another group
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Glycosidic_bond
Treatment for constipation and hepatic encephalopathy
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Lactulose
Polysaccharide of glucose
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Maltodextrin
Polysaccharide
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Oat_beta-glucan
Monosaccharide sugar
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Galactose
Class of chemical compounds
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Beta-glucan
American chemist
Hudson, C. S. (1903). "Uber die Multirotation des Milchzuckers (On the Mutarotation of Milk Sugar)". Z. Phys. Chem. 44: 487–494. doi:10.1515/zpch-1903-4421
Claude_Hudson
Glycoside hydrolase enzymes that cleave the glycosidic linkages of neuraminic acids
step is the formation of Neu5Ac initially as the α-anomer, and then mutarotation and release as the more thermodynamically stable β-Neu5Ac. Neuraminidase
Neuraminidase
Polysaccharide from crustacean shells
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Chitosan
Class of saccharide compounds structured as a 5-carbon, 1-oxygen ring
configuration of each of the hydroxyl groups around the ring. Furanose Mutarotation Monosaccharide Carbohydrate conformation Robyt, J.F. (1998). Essentials
Pyranose
Enzyme inhibition
however he lacked noting the importance of hydrogen ion concentration and mutarotation of glucose. The goal of Henri's thesis was to compare his knowledge of
Non-competitive_inhibition
Catabolic process in wide variety of organisms
Sulfoglycolysis is a catabolic process in primary metabolism in which sulfoquinovose (6-deoxy-6-sulfonato-glucose) is metabolized to produce energy and
Sulfoglycolysis
Natural plant polysaccharides
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Inulin
Disaccharide made of glucose and fructose
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Sucrose
Glucose polymer used as energy store in plants
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Starch
Polymer of glucose and structural component of cell wall of plants and green algae
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Cellulose
Glucose polymer used as energy store in animals
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Glycogen
Chemical compound
gov. Shriner, R. L.; Shotton, J. A.; Sutherland, H. (1938). "Anomalous Mutarotation of Salts of Reychler's Acid. VI. Synthesis and Structure of the Sultam
Camphorsultam
Saccharide polymer
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Oligosaccharide
Mixture of short-chain carbohydrates
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Isomaltooligosaccharide
Structural carbohydrate in the cell walls of land plants and some algae
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Pectin
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Trehalose
Oligosaccharide fructans
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Fructooligosaccharide
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Sorbose
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
List_of_sugars
Sugar containing three carbon atoms
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Triose
5-Carbon simple sugar
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Pentose
Sugars that contain free OH group at the anomeric carbon atom
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Reducing_sugar
Subtype of carbohydrates
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Deoxy_sugar
Polysaccharides formed from mannose
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Mannans
Polysaccharides found in animal tissue
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Glycosaminoglycan
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Galactose-α-1,3-galactose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Mannose
French chemist (1797–1881)
Lille, 1 September 1797 – Paris, 7 October 1881) was a French chemist. Mutarotation was discovered by Dubrunfaut in 1844, when he noticed that the specific
Augustin-Pierre_Dubrunfaut
Complex sugar
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Disaccharide
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Isomaltulose
Class of keto acid sugars
JR, Leech A, Williamson D, Wilson KS, Thomas GH (2008). "Sialic acid mutarotation is catalyzed by the Escherichia coli beta-propeller protein YjhT". J
Sialic_acid
Sugar
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Xylose
Monosaccharides with one >C=O group per molecule
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Ketose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Amylose
Class of organic compounds
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Glucan
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Deoxyribose
Low-molecular-weight carbohydrates
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Dextrin
Portion of plant-derived food that cannot be completely digested
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Dietary_fiber
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Acarbose
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Chitin-glucan_complex
Simple ketonic monosaccharide found in many plants
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Fructose
Fructose polymer
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Fructan
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Arabinose
Enzyme involved in glucose metabolism
(1960). "Mutarotase from Penicillium notatum. II. The mechanism of the mutarotation reaction" (PDF). J. Biol. Chem. 235 (5): 1225–1233. doi:10.1016/S0021-9258(18)69389-5
Aldose_1-epimerase
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Amylopectin
French pharmacist and chemist
notably studied the chemistry of sugars, reporting his observations of the mutarotation of glucose in 1895. He also identified quebrachitol in 1887 from the
Charles_Joseph_Tanret
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Xylulose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Tagatose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Glyceraldehyde
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Galactan
Monosaccharide with four carbon atoms
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Tetrose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Dihydroxyacetone
Group of simple sugar and carbohydrate compounds
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Ribose
Class of monosaccharides
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Aldose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Dextran
Class of plant cell wall polysaccharides
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Hemicellulose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Rhamnose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Fucose
Structures of cyclohexane
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Cyclohexane_conformation
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Erythrose
Monosaccharide with five carbon atoms and a ketone functional group
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Ribulose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Neuraminic_acid
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Raffinose
Devising names for a class of carbohydrates
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Oligosaccharide_nomenclature
N-acetylneuraminate Mutarotation Severi E, Müller A, Potts JR, Leech A, Williamson D, Wilson KS, Thomas GH (February 2008). "Sialic acid mutarotation is catalyzed
N-acetylneuraminate_epimerase
Class of prebiotics
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Galactooligosaccharide
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Lentinan
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Erythrulose
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Cellobiose
Class of carbohydrate
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Heptose
Type of sugar molecule
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Amino_sugar
Polysaccharide with four sugar units
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Tetrasaccharide
Chemical compound
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Talose
Protein domain
JR, Leech A, Williamson D, Wilson KS, Thomas GH (2008). "Sialic acid mutarotation is catalyzed by the Escherichia coli beta-propeller protein YjhT". J
Kelch_motif
Chemical reaction
1002/anie.197201311 Organische und biologische Chemie Mechanismus der Mutarotation von 5,6-Dibromcholestan C.A. Grob, S. Winstein Helvetica Chimica Acta
Dyotropic_reaction
Set of all sugars, free or bound, in an organism
Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Dioses Aldodiose Glycolaldehyde Trioses Aldotriose Glyceraldehyde
Glycome
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MUTAROTATION
MUTAROTATION
MUTAROTATION
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