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Session ID: b21391bd0602c302e3e237cb3a6c4fce

Search Type: metabolite

Started at: 2010-02-17 03:42:13

Finished at: 2010-02-17 03:43:41

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Field Result Source
Name
glucose External
HMDB ID
HMDB00122 HMDB
Bigg ID
Not Available Not Applicable
Description
Aldohexose sugars have four chiral centers, giving 24 = 16 stereoisomers. These are split into two groups, L and D, with eight sugars in each. Glucose is one of these sugars, and L-glucose and D-glucose are two of the stereoisomers. Only seven of these are found in living organisms, of which D-glucose (Glu), D-galactose (Gal) and D-mannose (Man) are the most important. These eight isomers (including glucose itself) are related as diastereoisomers and belong to the D series. Wikipedia
Because glucose is a basic necessity of many organisms, a correct understanding of its chemical makeup and structure contributed greatly to a general advancement in organic chemistry. This understanding occurred largely as a result of the investigations of Emil Fischer, a German chemist who received the 1902 Nobel Prize in Chemistry as a result of his findings. The synthesis of glucose established the structure of organic material and consequently formed the first definitive validation of Jacobus Henricus van't Hoff's theories of chemical kinetics and the arrangements of chemical bonds in carbon-bearing molecules. Between 1891 and 1894, Fischer established the stereochemical configuration of all the known sugars and correctly predicted the possible isomers, applying van't Hoff's theory of asymmetrical carbon atoms. Wikipedia
Glucose (C6H12O6) contains six carbon atoms, one of which is part of an aldehyde group. Therefore glucose is an aldohexose. In solution, the glucose molecule can exist in an open-chain (acyclic) form and a ring (cyclic) form (in equilibrium). The cyclic form is the result of a covalent bond between the aldehyde C atom and the C-5 hydroxyl group to form a six-membered cyclic hemiacetal. At pH 7 the cyclic form is predominant. In the solid phase, glucose assumes the cyclic form. Because the ring contains five carbon atoms and one oxygen atom (like pyran), the cyclic form of glucose is also referred to as glucopyranose. In this ring, each carbon is linked to a hydroxyl side group with the exception of the fifth atom, which links to a sixth carbon atom outside the ring, forming a CH2OH group. Glucose is commonly available in the form of a white powder or as a solid crystal. It can also be dissolved in water as an aqueous solution. Its solubility level is very high. Wikipedia
Glucose (Glc), a monosaccharide (or simple sugar) also known as grape sugar, blood sugar, or corn sugar, is a very important carbohydrate in biology. The living cell uses it as a source of energy and metabolic intermediate. Glucose is one of the main products of photosynthesis and starts cellular respiration in both prokaryotes (bacteria and archaea) and eukaryotes (animals, plants, fungi, and protists). Wikipedia
Glucose is a monosaccharide containing six carbon atoms and an aldehyde group and is therefore referred to as an aldohexose. The glucose molecule can exist in an open-chain (acyclic) and ring (cyclic) form, the latter being the result of an intramolecular reaction between the aldehyde C atom and the C-5 hydroxyl group to form an intramolecular hemiacetal. In water solution both forms are in equilibrium and at pH 7 the cyclic one is the predominant. Glucose is a primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. In animals glucose arises from the breakdown of glycogen in a process known as glycogenolysis. Glucose is synthesized in the liver and kidneys from non-carbohydrate intermediates, such as pyruvate and glycerol, by a process known as gluconeogenesis. HMDB
Glucose is a primary source of energy for the brain, and hence its availability influences psychological processes. When glucose is low, psychological processes requiring mental effort (e.g., self-control, effortful decision-making) are impaired. Wikipedia
Glucose is a ubiquitous fuel in biology. It is used as an energy source in most organisms, from bacteria to humans. Use of glucose may be by either aerobic respiration, anaerobic respiration, or fermentation. Carbohydrates are the human body's key source of energy, through aerobic respiration, providing approximately 3.75 kilocalories (16 kilojoules) of food energy per gram. Breakdown of carbohydrates (e.g. starch) yields mono- and disaccharides, most of which is glucose. Through glycolysis and later in the reactions of the citric acid cycle (TCAC), glucose is oxidized to eventually form CO2 and water, yielding energy sources, mostly in the form of ATP. The insulin reaction, and other mechanisms, regulate the concentration of glucose in the blood. A high fasting blood sugar level is an indication of prediabetic and diabetic conditions. Wikipedia
Glucose is used as a precursor for the synthesis of several important substances. Starch, cellulose, and glycogen ("animal starch") are common glucose polymers (polysaccharides). Lactose, the predominant sugar in milk, is a glucose-galactose disaccharide. In sucrose, another important disaccharide, glucose is joined to fructose. These synthesis processes also rely on the phosphorylation of glucose through the first step of glycolysis. Wikipedia
Two stereoisomers of the aldohexose sugars are known as glucose, only one of which (D-glucose) is biologically active. This form (D-glucose) is often referred to as dextrose monohydrate, or, especially in the food industry, simply dextrose (from dextrorotatory glucose). This article deals with the D-form of glucose. The mirror-image of the molecule, L-glucose, cannot be metabolized by cells in the biochemical process known as glycolysis. Wikipedia
Chemical Kingdom
Organic BioSpider
Chemical Class
Carbohydrates HMDB
Chemical Species
1,2-diol Checkmol
aldehyde Checkmol
hemiacetal HMDB
heterocyclic compound HMDB
primary alcohol Checkmol
secondary alcohol Checkmol
Synonym
α-d-glucose NIST
(+)-glucose HMDB
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal Pubchem
Allose Pubchem
Alpha-d-glucopyranose Pubchem
Altrose Pubchem
Anhydrous dextrose HMDB
Blood sugar NIST
CPC hydrate HMDB
Candex NIST
Cartose NIST
Cartose cerelose Pubchem
Cerebrose Pubchem
Cerelose HMDB
Cerelose 2001 HMDB
Clearsweet 95 HMDB
Clintose l HMDB
Corn sugar HMDB
D(+)-glucose HMDB
D-(+)-allose Pubchem
D-(+)-altrose Pubchem
D-(+)-dextrose Pubchem
D-(+)-galactose Pubchem
D-(+)-glucose NIST
D-(+)-glucose, acs Pubchem
D-(+)-mannose Pubchem
D-(+)-sorbose Pubchem
D-(-)-gulose Pubchem
D-altropyranose Pubchem
D-altrose Pubchem
D-glucopyranose Pubchem
D-glucose NIST
D-glucose in linear form Pubchem
D-glucose, anhydrous NIST
D-glucose-ring Pubchem
D-mannose Pubchem
Dextropur HMDB
Dextrose HMDB
Dextrose monohydrate NIST
Dextrose solution Pubchem
Dextrose, anhydrous NIST
Dextrosol HMDB
Emdex NIST
Flolys NIST
GLC Pubchem
GLC-ring Pubchem
Glucan Pubchem
Glucodin HMDB
Glucolin HMDB
Glucopyranose, d- Pubchem
Glucose (JP15) Pubchem
Glucose (d) NIST
Glucose liquid NIST
Glucose solution Pubchem
Glucose, anhydrous NIST
Glucose, liquid NCI
Glucosteril Pubchem
Goldsugar HMDB
Grape sugar HMDB
Hexose NIST
L -mannopyranose Pubchem
L-(+)-gulose Pubchem
L-(-)-mannose Pubchem
L-(-)-talose Pubchem
L-galactose Pubchem
L-glucose Pubchem
MAN Pubchem
Maxim energy gel Pubchem
Meritose HMDB
Meritose 200 Pubchem
Roferose NIST
Roferose ST HMDB
Seminose Pubchem
Sirup Pubchem
Staleydex 111 HMDB
Staleydex 130 Pubchem
Staleydex 333 Pubchem
Staleydex 95M HMDB
Sugar, grape NIST
Tabfine 097(HS) HMDB
Traubenzucker Pubchem
UNII-5SL0G7R0OK Pubchem
Vadex HMDB
hexose (ACD/Name 4.0) NCI
CAS
50-99-7 NIST
InChI Identifier
InChI=1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-
,4+,5+,6+/m0/s1
NIST
IUPAC
(3R,4R,5S,6S)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol HMDB
Chemical Formula
C6H12O6 HMDB
Chemical Structure
Chemical Structure HMDB
Average Molecular Weight (g/mol)
180.155880 BioSpider
Monoisotopic Molecular Weight (g/mol)
180.063390 BioSpider
SMILES (Isomeric)
OC1C(O)C(OC(O)C1O)CO
ChemSpider
SMILES (Canonical)
OCC1OC(O)C(O)C(O)C1O
HMDB
Kegg Compound
C00293 ChEBI
Pubchem Compound ID
24749 PubChem
Pubchem Substance ID
148583 HMDB
206675 HMDB
29215341 Pubchem
29291798 Pubchem
32050275 Pubchem
3333 HMDB
3587 Kegg
36519352 Pubchem
36519419 Pubchem
36519560 Pubchem
36519561 Pubchem
36519585 Pubchem
36519591 Pubchem
36519606 Pubchem
36519638 Pubchem
36519650 Pubchem
36519902 Pubchem
36519983 Pubchem
36525732 Pubchem
36525957 Pubchem
36525997 Pubchem
36526005 Pubchem
36526431 Pubchem
36526718 Pubchem
36527198 Pubchem
36527203 Pubchem
36527829 Pubchem
36528756 Pubchem
36529036 Pubchem
36529085 Pubchem
36529752 Pubchem
36529792 Pubchem
36533809 Pubchem
36535696 Pubchem
36535735 Pubchem
36536592 Pubchem
36536609 Pubchem
36536690 Pubchem
36536744 Pubchem
36536782 Pubchem
36536893 Pubchem
36537607 Pubchem
36537957 Pubchem
36539404 Pubchem
36541402 Pubchem
36541485 Pubchem
37904349 Pubchem
37905768 Pubchem
37905930 Pubchem
37905965 Pubchem
37906016 Pubchem
37906037 Pubchem
37908061 Pubchem
37909438 Pubchem
37910891 Pubchem
37911023 Pubchem
37911036 Pubchem
37911046 Pubchem
37911972 Pubchem
37912028 Pubchem
37912032 Pubchem
37912038 Pubchem
37912040 Pubchem
37912045 Pubchem
37912190 Pubchem
37912191 Pubchem
37912298 Pubchem
37912302 Pubchem
37912317 Pubchem
37912330 Pubchem
37912347 Pubchem
37912349 Pubchem
37912413 Pubchem
37912421 Pubchem
37912765 Pubchem
37912867 Pubchem
37912956 Pubchem
37913835 Pubchem
37914011 Pubchem
37914018 Pubchem
3885805 HMDB
46507147 Pubchem
50073927 Pubchem
50077668 Pubchem
57392797 Pubchem
6435762 HMDB
74723209 Pubchem
7847077 HMDB
8023353 HMDB
819111 HMDB
823016 HMDB
823057 HMDB
833240 HMDB
83549171 Pubchem
838951 HMDB
841535 HMDB
85083497 Pubchem
85083510 Pubchem
85085240 Pubchem
85085241 Pubchem
85086266 Pubchem
85086267 Pubchem
85086268 Pubchem
85086335 Pubchem
85086336 Pubchem
85086337 Pubchem
85086338 Pubchem
85086547 Pubchem
85086548 Pubchem
85087455 Pubchem
85087457 Pubchem
85087458 Pubchem
85089511 Pubchem
85089693 Pubchem
OMIM ID
232200 HMDB
606777 HMDB
606824 HMDB
ChEBI
17234 Chebi
BioCyc
GLC HMDB
Wikipedia
Dextrose HMDB
Melting Point
146-150 oC HMDB
Charge
Not Available Not Applicable
State
Solid HMDB
MSDS Link
1266403405.pdf www.sciencelab.com
1266403407.pdf HMDB
Experimental Water Solubility
1200 mg/mL at 30 oC [MULLIN,JW (1972)] PhysProp
Predicted Water Solubility
261 mg/mL [Predicted by ALOGPS] Alogps
Experimental LogP
-3.24 [SANGSTER (1994)] PhysProp
Predicted LogP
-2.41 [Predicted by ALOGPS] Alogps
-2.57 [Predicted by ALOGPS] HMDB
pKa
12.9 PhysProp
SDF File
1266403362.sdf Pubchem
Mol File
1266403389.mol Molconvert
Pdb File
1266403390.pdb Molconvert
Mass Spec File
1266403409.gif HMDB
Associated Disorder
2-ketoglutarate dehydrogenase complex deficiency Metagene
21-hydroxylase deficiency (CYP21) Metagene
3-beta-hydroxysteroid dehydrogenase deficiency Metagene
3-hydroxy-3-methylglutaryl-coa lyase deficiency Metagene
3-methyl-crotonyl-glycinuria Metagene
3-methylglutaconic aciduria (type I) Metagene
Acth deficiency, isolated Metagene
Adrenal hypoplasia. addison disease, x-linked Metagene
Asphyxia [DD] Metagene
Beckwith-wiedemann syndrome. exomphalos-makroglossia-gigantism syndrome Metagene
Beta-ketothiolase deficiency Metagene
Carnitine deficiency, myopathic Metagene
Carnitine palmitoyl transferase deficiency (I) Metagene
Carnitine palmitoyl transferase deficiency (II) Metagene
Carnitine transporter defect. primary systemic carnitine deficiency Metagene
Carnitine-acylcarnitine translocase deficiency Metagene
Chronic progressive external ophthalmoplegia and kearns-sayre syndrom Metagene
Cystic fibrosis (CF) Metagene
Cystinosis Metagene
Diabetes mellitus (mody), non-insulin-dependent Metagene
Diabetes mellitus, insulin-dependent Metagene
Diabetes, fetal effects from maternal Metagene
Dicarboxylic aminoaciduria. glutamate-aspartate transport defect Metagene
Exercise-induced-hyperinsulinsm [eihi] Metagene
Familial hyperinsulinemia and hyperproinsulineamia with mild diabetes Metagene
Friedreich ataxia Metagene
Fructose intolerance, hereditary Metagene
Fructose-1,6-diphosphatase deficiency Metagene
Galactosemia Metagene
Glucagon deficiency Metagene
Glucocorticoid deficiency, familial isolated. migeon syndrome Metagene
Glucoglycinuria Metagene
Glucose-galactose malabsorption Metagene
Glut-1 deficiency syndrome Metagene
Glutaric aciduria II Metagene
Glycerol intolerance syndrom Metagene
Glycerol kinase deficiency Metagene
Glycogen synthetase deficiency Metagene
Glycogenosis, type IA. von gierke disease Metagene
Glycogenosis, type IB Metagene
Glycogenosis, type IC Metagene
Glycogenosis, type III. cori disease, debrancher glycogenosis Metagene
Glycogenosis, type IV. amylopectinosis, anderson disease Metagene
Glycogenosis, type VI. hers disease Metagene
Human growth hormone deficiency Metagene
Hypoadrenocorticism, familial Metagene
Hypoglycemia, familial neonatal Metagene
Isovaleric acidemia Metagene
Ketotic hypoglycemia Metagene
Long chain acyl-coa dehydrogenase deficiency (lcad) Metagene
Long-chain-3-hydroxyacyl-coa dehydrogenase deficiency (lchad) Metagene
Malonyl-coa decarboxylase deficiency Metagene
Maple syrup urine disease. branched-chain alpha-keto acid dehydrogenase deficiency (msud) Metagene
Medium chain acyl-coa dehydrogenase deficiency (mcad) Metagene
Methylmalonic aciduria, cbla type Metagene
Neonatal hemochromatosis Metagene
Oculocerebrorenal syndrome of lowe Metagene
Persistant hyperinsulinemic hypoglycemia of infancy, phhi Metagene
Phosphoenolpyruvate carboxykinase deficiency 2 (pepck2) Metagene
Propionic acidemia. ketotic hyperglycinemia (pa) Metagene
Pyruvate carboxylase deficiency Metagene
Pyruvate dehydrogenase deficiency (e3) Metagene
Renal fanconi syndrome Metagene
Renal glycosuria Metagene
Respiratory chain deficiencies Metagene
Reye syndrome Metagene
Reye syndrome like manifestations Metagene
S-adenosylhomocysteine hydrolase deficiency Metagene
Short chain acyl-coa dehydrogenase deficiency (scad) Metagene
Short-chain 3-hydroxyacyl-coa dehydrogenase deficiency (schad) Metagene
Trifunctional protein deficiency Metagene
Tyrosinemia I Metagene
Very-long-chain acyl coa dehydrogenase deficiency (vlcad) Metagene
Wolfram syndrome, didmoad Metagene
Pathway
Not Available Not Applicable
Enzymes
O43280
[ UniProt | Analyze ]
HMDB
O43451
[ UniProt | Analyze ]
HMDB
O60909
[ UniProt | Analyze ]
HMDB
P00709
[ UniProt | Analyze ]
HMDB
P04062
[ UniProt | Analyze ]
HMDB
P06280
[ UniProt | Analyze ]
HMDB
P06744
[ UniProt | Analyze ]
HMDB
P09848
[ UniProt | Analyze ]
HMDB
P11166
[ UniProt | Analyze ]
HMDB
P14410
[ UniProt | Analyze ]
HMDB
P15291
[ UniProt | Analyze ]
HMDB
P19367
[ UniProt | Analyze ]
HMDB
P35557
[ UniProt | Analyze ]
HMDB
P35573
[ UniProt | Analyze ]
HMDB
P35575
[ UniProt | Analyze ]
HMDB
P36871
[ UniProt | Analyze ]
HMDB
P52789
[ UniProt | Analyze ]
HMDB
P52790
[ UniProt | Analyze ]
HMDB
Q14397
[ UniProt | Analyze ]
HMDB
Q14697
[ UniProt | Analyze ]
HMDB
Q8TET4
[ UniProt | Analyze ]
HMDB
Q9BRR6
[ UniProt | Analyze ]
HMDB
Q9H227
[ UniProt | Analyze ]
HMDB
Q9NQR9
[ UniProt | Analyze ]
HMDB
Compartments
Not Available Not Applicable
Reaction (query compound consumed)
Not Available Not Applicable
Reaction (query compound produced)
Not Available Not Applicable
Reaction, reversible (query compound neither consumed nor produced)
Not Available Not Applicable
Reaction (query compound is transported across a membrane)
Not Available Not Applicable