| Record Information |
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| Version | 2.0 |
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| Creation Date | 2015-09-08 17:50:17 -0600 |
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| Update Date | 2015-09-14 16:46:40 -0600 |
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| Secondary Accession Numbers | |
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| Identification |
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| Name: | aldehydo-D-glucuronate |
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| Description | Aldehydo-D-glucuronate is an intermediate in beta-D-glucuronide and D-glucuronate degradation pathway in E.coli. It is a substrate for the enzyme D-glucuronate isomerase which catalyzes the reaction aldehydo-D-glucuronate -> D-fructuronate. It is also a product in the spontaneous reaction D-glucopyranuronate -> aldehydo-D-glucuronate (BioCyc compound: CPD-15530). |
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| Structure | |
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| Synonyms: | - aldehydo-D-Glucuronic acid
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| Chemical Formula: | C6H10O7 |
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| Weight: | Average: 194.1394
Monoisotopic: 194.042652674 |
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| InChI Key: | IAJILQKETJEXLJ-QTBDOELSSA-N |
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| InChI: | InChI=1S/C6H10O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h1-5,8-11H,(H,12,13)/t2-,3+,4-,5-/m0/s1 |
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| CAS number: | Not Available |
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| IUPAC Name: | (2S,3S,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexanoic acid |
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| Traditional IUPAC Name: | aldehydo-D-glucuronic acid |
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| SMILES: | [H][C@](O)(C=O)[C@@]([H])(O)[C@]([H])(O)[C@]([H])(O)C(O)=O |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as glucuronic acid derivatives. Glucuronic acid derivatives are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid. |
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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 | Glucuronic acid derivatives |
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| Alternative Parents | |
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| Substituents | - Glucuronic acid or derivatives
- Hexose monosaccharide
- Medium-chain hydroxy acid
- Medium-chain fatty acid
- Hydroxy fatty acid
- Beta-hydroxy acid
- Fatty acyl
- Fatty acid
- Monosaccharide
- Hydroxy acid
- Beta-hydroxy aldehyde
- Alpha-hydroxy acid
- Alpha-hydroxyaldehyde
- Secondary alcohol
- Polyol
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Organic oxide
- Hydrocarbon derivative
- Carbonyl group
- Aldehyde
- Alcohol
- Aliphatic acyclic compound
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| Molecular Framework | Aliphatic acyclic compounds |
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| External Descriptors | |
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| Physical Properties |
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| State: | Not Available |
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| Charge: | -1 |
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| Melting point: | Not Available |
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| Experimental Properties: | |
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| Predicted Properties | |
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| Biological Properties |
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| Cellular Locations: | Cytoplasm |
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| Reactions: | |
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| SMPDB Pathways: | | hexuronide and hexuronate degradation | PW000834 |    |
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| KEGG Pathways: | Not Available |
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| EcoCyc Pathways: | Not Available |
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| Concentrations |
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| Not Available |
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| Spectra |
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| Spectra: | |
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| References |
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| References: | Not Available |
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| Synthesis Reference: | Not Available |
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| Material Safety Data Sheet (MSDS) | Not Available |
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| Links |
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| External Links: | | Resource | Link |
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| CHEBI ID | 47953 | | HMDB ID | Not Available | | Pubchem Compound ID | 65041 | | Kegg ID | C16245 | | ChemSpider ID | Not Available | | Wikipedia ID | Not Available | | BioCyc ID | Not Available |
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