Record Information |
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Version | 5.0 |
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Status | Detected and Quantified |
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Creation Date | 2005-11-16 15:48:42 UTC |
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Update Date | 2023-02-21 17:14:33 UTC |
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HMDB ID | HMDB0000143 |
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Secondary Accession Numbers | - HMDB0005762
- HMDB00143
- HMDB05762
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Metabolite Identification |
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Common Name | D-Galactose |
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Description | D-Galactose (CAS: 59-23-4) is an aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. D-Galactose is an energy-providing nutrient and also a necessary basic substrate for the biosynthesis of many macromolecules in the body. Metabolic pathways for D-galactose are important not only for the provision of these pathways but also for the prevention of D-galactose metabolite accumulation. The main source of D-galactose is lactose in the milk of mammals, but it can also be found in some fruits and vegetables. Utilization of D-galactose in all living cells is initiated by the phosphorylation of the hexose by the enzyme galactokinase (E.C. 2.7.1.6) (GALK) to form D-galactose-1-phosphate. In the presence of D-galactose-1-phosphate uridyltransferase (E.C. 2.7.7.12) (GALT) D-galactose-1-phosphate is exchanged with glucose-1-phosphate in UDP-glucose to form UDP-galactose. Glucose-1-phosphate will then enter the glycolytic pathway for energy production. Deficiency of the enzyme GALT in galactosemic patients leads to the accumulation of D-galactose-1-phosphate. Classic galactosemia, a term that denotes the presence of D-galactose in the blood, is the rare inborn error of D-galactose metabolism, diagnosed by the deficiency of the second enzyme of the D-galactose assimilation pathway, GALT, which, in turn, is caused by mutations at the GALT gene (PMID: 15256214 , 11020650 , 10408771 ). Galactose in the urine is a biomarker for the consumption of milk. |
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Structure | OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6+/m1/s1 |
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Synonyms | Value | Source |
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ALPHA D-GALACTOSE | ChEBI | alpha-D-Gal | ChEBI | Gal-alpha | ChEBI | alpha-D-Galactose | Kegg | a D-GALACTOSE | Generator | Α D-galactose | Generator | a-D-Gal | Generator | Α-D-gal | Generator | Gal-a | Generator | Gal-α | Generator | a-D-Galactose | Generator | Α-D-galactose | Generator | (+)-Galactose | HMDB | 5Abp | HMDB | 8Abp | HMDB | alpha-D-Galactopyranose | HMDB | D-(+)-Galactose | HMDB | D-Hexose | HMDB | GAL | HMDB | Galactose | HMDB | Galactose (NF) | HMDB | GLA | HMDB | GLC | HMDB | Hexose | HMDB | SHU 508 a | MeSH, HMDB | SH-TA-508 | MeSH, HMDB | SHU 508 | MeSH, HMDB | Levovist | MeSH, HMDB | SHU-508 | MeSH, HMDB |
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Chemical Formula | C6H12O6 |
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Average Molecular Weight | 180.1559 |
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Monoisotopic Molecular Weight | 180.063388116 |
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IUPAC Name | (2S,3R,4S,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol |
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Traditional Name | galactose |
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CAS Registry Number | 3646-73-9 |
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SMILES | OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O |
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InChI Identifier | InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6+/m1/s1 |
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InChI Key | WQZGKKKJIJFFOK-PHYPRBDBSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity. |
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Kingdom | Organic compounds |
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Super Class | Organic oxygen compounds |
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Class | Organooxygen compounds |
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Sub Class | Carbohydrates and carbohydrate conjugates |
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Direct Parent | Hexoses |
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Alternative Parents | |
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Substituents | - Hexose monosaccharide
- Oxane
- Secondary alcohol
- Hemiacetal
- Oxacycle
- Organoheterocyclic compound
- Polyol
- Hydrocarbon derivative
- Primary alcohol
- Alcohol
- Aliphatic heteromonocyclic compound
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Molecular Framework | Aliphatic heteromonocyclic compounds |
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External Descriptors | |
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Ontology |
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Not Available | Not Available |
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Physical Properties |
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State | Solid |
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Experimental Molecular Properties | Property | Value | Reference |
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Melting Point | 170 °C | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | 683 mg/mL | Not Available | LogP | Not Available | Not Available |
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Experimental Chromatographic Properties | Experimental Collision Cross SectionsAdduct Type | Data Source | CCS Value (Å2) | Reference |
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[M-H]- | Astarita_neg | 130.0 | 30932474 |
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Predicted Molecular Properties | |
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Retention Times UnderivatizedChromatographic Method | Retention Time | Reference |
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Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022. | 0.47 minutes | 32390414 | Predicted by Siyang on May 30, 2022 | 9.6866 minutes | 33406817 | Predicted by Siyang using ReTip algorithm on June 8, 2022 | 6.01 minutes | 32390414 | AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid | 302.0 seconds | 40023050 | Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid | 634.4 seconds | 40023050 | Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid | 309.4 seconds | 40023050 | Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid | 33.2 seconds | 40023050 | Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid | 183.4 seconds | 40023050 | RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid | 76.7 seconds | 40023050 | Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid | 293.2 seconds | 40023050 | BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid | 226.3 seconds | 40023050 | HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate) | 703.6 seconds | 40023050 | UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid | 577.8 seconds | 40023050 | BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid | 42.0 seconds | 40023050 | UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid | 785.4 seconds | 40023050 | SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid | 196.6 seconds | 40023050 | RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid | 260.1 seconds | 40023050 | MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate | 650.8 seconds | 40023050 | KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA | 366.5 seconds | 40023050 | Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water | 323.2 seconds | 40023050 |
Predicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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D-Galactose,1TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O | 1738.4 | Semi standard non polar | 33892256 | D-Galactose,1TMS,isomer #2 | C[Si](C)(C)O[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O | 1673.8 | Semi standard non polar | 33892256 | D-Galactose,1TMS,isomer #3 | C[Si](C)(C)O[C@H]1[C@@H](O)O[C@H](CO)[C@H](O)[C@@H]1O | 1683.6 | Semi standard non polar | 33892256 | D-Galactose,1TMS,isomer #4 | C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@H](O)[C@@H]1O | 1688.3 | Semi standard non polar | 33892256 | D-Galactose,1TMS,isomer #5 | C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O | 1678.0 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O | 1722.4 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #10 | C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C | 1681.6 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #2 | C[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O | 1737.0 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #3 | C[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O | 1742.6 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #4 | C[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C | 1712.2 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #5 | C[Si](C)(C)O[C@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O | 1701.4 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #6 | C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H]1O | 1703.5 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #7 | C[Si](C)(C)O[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C | 1679.6 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #8 | C[Si](C)(C)O[C@H]1[C@@H](O)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O | 1697.1 | Semi standard non polar | 33892256 | D-Galactose,2TMS,isomer #9 | C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@H](O)[C@@H]1O[Si](C)(C)C | 1692.2 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O | 1703.6 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #10 | C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]1CO | 1736.7 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #2 | C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O | 1753.4 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #3 | C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C | 1717.5 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #4 | C[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O | 1748.2 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #5 | C[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C | 1766.0 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #6 | C[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C | 1701.0 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #7 | C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C | 1739.0 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #8 | C[Si](C)(C)O[C@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C | 1733.4 | Semi standard non polar | 33892256 | D-Galactose,3TMS,isomer #9 | C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C | 1725.4 | Semi standard non polar | 33892256 | D-Galactose,4TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O | 1815.5 | Semi standard non polar | 33892256 | D-Galactose,4TMS,isomer #2 | C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C | 1815.2 | Semi standard non polar | 33892256 | D-Galactose,4TMS,isomer #3 | C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C | 1820.5 | Semi standard non polar | 33892256 | D-Galactose,4TMS,isomer #4 | C[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C | 1819.4 | Semi standard non polar | 33892256 | D-Galactose,4TMS,isomer #5 | C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]1CO | 1800.9 | Semi standard non polar | 33892256 | D-Galactose,5TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C | 1877.4 | Semi standard non polar | 33892256 | D-Galactose,1TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O | 2002.6 | Semi standard non polar | 33892256 | D-Galactose,1TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O | 1940.1 | Semi standard non polar | 33892256 | D-Galactose,1TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)O[C@H](CO)[C@H](O)[C@@H]1O | 1940.5 | Semi standard non polar | 33892256 | D-Galactose,1TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@H](O)[C@@H]1O | 1947.1 | Semi standard non polar | 33892256 | D-Galactose,1TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O | 1943.8 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O | 2208.7 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #10 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 2181.6 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O | 2210.9 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O | 2219.8 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 2197.5 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O | 2193.9 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #6 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O | 2195.0 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #7 | CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 2180.7 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #8 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O | 2190.8 | Semi standard non polar | 33892256 | D-Galactose,2TBDMS,isomer #9 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C | 2192.8 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O | 2441.4 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #10 | CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]1CO | 2455.2 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O | 2449.6 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 2445.1 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O | 2466.7 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 2468.7 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #6 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C | 2439.7 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #7 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 2451.2 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #8 | CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 2451.3 | Semi standard non polar | 33892256 | D-Galactose,3TBDMS,isomer #9 | CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C | 2454.9 | Semi standard non polar | 33892256 | D-Galactose,4TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O | 2671.4 | Semi standard non polar | 33892256 | D-Galactose,4TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 2668.4 | Semi standard non polar | 33892256 | D-Galactose,4TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C | 2664.4 | Semi standard non polar | 33892256 | D-Galactose,4TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C | 2681.0 | Semi standard non polar | 33892256 | D-Galactose,4TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)O[C@@H]1CO | 2669.4 | Semi standard non polar | 33892256 | D-Galactose,5TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C | 2890.3 | Semi standard non polar | 33892256 |
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Disease References | Galactose-1-phosphate uridyltransferase deficiency |
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- Ning C, Segal S: Plasma galactose and galactitol concentration in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia: determination by gas chromatography/mass spectrometry. Metabolism. 2000 Nov;49(11):1460-6. [PubMed:11092512 ]
| Galactosemia type 1 |
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- Ning C, Segal S: Plasma galactose and galactitol concentration in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia: determination by gas chromatography/mass spectrometry. Metabolism. 2000 Nov;49(11):1460-6. [PubMed:11092512 ]
| Patent Ductus Venosus |
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- Sakura N, Mizoguchi N, Eguchi T, Ono H, Mawatari H, Naitou K, Ito K: Elevated plasma bile acids in hypergalactosaemic neonates: a diagnostic clue to portosystemic shunts. Eur J Pediatr. 1997 Sep;156(9):716-8. [PubMed:9296537 ]
| Galactosemia |
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- Chen J, Yager C, Reynolds R, Palmieri M, Segal S: Erythrocyte galactose 1-phosphate quantified by isotope-dilution gas chromatography-mass spectrometry. Clin Chem. 2002;48(4):604-12. [PubMed:11901058 ]
| Colorectal cancer |
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- Brown DG, Rao S, Weir TL, O'Malia J, Bazan M, Brown RJ, Ryan EP: Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer Metab. 2016 Jun 6;4:11. doi: 10.1186/s40170-016-0151-y. eCollection 2016. [PubMed:27275383 ]
- Sinha R, Ahn J, Sampson JN, Shi J, Yu G, Xiong X, Hayes RB, Goedert JJ: Fecal Microbiota, Fecal Metabolome, and Colorectal Cancer Interrelations. PLoS One. 2016 Mar 25;11(3):e0152126. doi: 10.1371/journal.pone.0152126. eCollection 2016. [PubMed:27015276 ]
- Goedert JJ, Sampson JN, Moore SC, Xiao Q, Xiong X, Hayes RB, Ahn J, Shi J, Sinha R: Fecal metabolomics: assay performance and association with colorectal cancer. Carcinogenesis. 2014 Sep;35(9):2089-96. doi: 10.1093/carcin/bgu131. Epub 2014 Jul 18. [PubMed:25037050 ]
| Eosinophilic esophagitis |
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- Slae, M., Huynh, H., Wishart, D.S. (2014). Analysis of 30 normal pediatric urine samples via NMR spectroscopy (unpublished work). NA.
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- Ning C, Reynolds R, Chen J, Yager C, Berry GT, McNamara PD, Leslie N, Segal S: Galactose metabolism by the mouse with galactose-1-phosphate uridyltransferase deficiency. Pediatr Res. 2000 Aug;48(2):211-7. [PubMed:10926297 ]
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- van den Nieuwenhof IM, Renardel de Lavalette C, Diaz N, van Die I, van den Berg TK: Differential galactosylation of neuronal and haematopoietic signal regulatory protein-alpha determines its cellular binding-specificity. J Cell Sci. 2001 Apr;114(Pt 7):1321-9. [PubMed:11256998 ]
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- Tamamori A, Fujimoto A, Okano Y, Kobayashi K, Saheki T, Tagami Y, Takei H, Shigematsu Y, Hata I, Ozaki H, Tokuhara D, Nishimura Y, Yorifuji T, Igarashi N, Ohura T, Shimizu T, Inui K, Sakai N, Abukawa D, Miyakawa T, Matsumori M, Ban K, Kaneko H, Yamano T: Effects of citrin deficiency in the perinatal period: feasibility of newborn mass screening for citrin deficiency. Pediatr Res. 2004 Oct;56(4):608-14. Epub 2004 Aug 4. [PubMed:15295082 ]
- Wang ZJ, Berry GT, Dreha SF, Zhao H, Segal S, Zimmerman RA: Proton magnetic resonance spectroscopy of brain metabolites in galactosemia. Ann Neurol. 2001 Aug;50(2):266-9. [PubMed:11506413 ]
- Niebroj-Dobosz I, Janik P, Jamrozik Z, Kwiecinski H: Immunochemical quantification of glycoconjugates in serum and cerebrospinal fluid of amyotrophic lateral sclerosis patients. Eur J Neurol. 1999 May;6(3):335-40. [PubMed:10210915 ]
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- Mizoguchi N, Ono H, Eguchi T, Sakura N: Galactose metabolites in blood from neonates with and without hypergalactosaemia detected by mass screening. Eur J Pediatr. 2000 Nov;159(11):851-3. [PubMed:11079200 ]
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