| Record Information |
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| Version | 2.0 |
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| Creation Date | 2012-10-10 12:15:02 -0600 |
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| Update Date | 2015-06-03 17:25:52 -0600 |
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| Secondary Accession Numbers | |
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| Identification |
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| Name: | L-Rhamnonate |
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| Description | L-Rhamnoate (6-deoxy-L-mannonate) is a mono-acid sugar. It is the preferred substrate for the E. coli enzyme called L-Rhamnoate dehydratase (YfaW). L-Rhamnonate, L-mannonate, and L-lyxonate share the same configurations at carbons-2, -3, and -4; D-gulonate differs from L-rhamnonate and L-mannonate by the configuration of carbon-5. |
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| Structure | |
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| Synonyms: | - 6-Deoxy-L-mannonate
- 6-Deoxy-L-mannonic acid
- L-Rhamnonic acid
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| Chemical Formula: | C6H12O6 |
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| Weight: | Average: 180.1559
Monoisotopic: 180.063388116 |
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| InChI Key: | NBFWIISVIFCMDK-QMKXCQHVSA-N |
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| InChI: | InChI=1S/C6H12O6/c1-2(7)3(8)4(9)5(10)6(11)12/h2-5,7-10H,1H3,(H,11,12)/t2-,3-,4+,5+/m0/s1 |
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| CAS number: | Not Available |
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| IUPAC Name: | (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanoic acid |
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| Traditional IUPAC Name: | L-rhamnonic acid |
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| SMILES: | [H][C@@](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 medium-chain hydroxy acids and derivatives. These are hydroxy acids with a 6 to 12 carbon atoms long side chain. |
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| Kingdom | Organic compounds |
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| Super Class | Organic acids and derivatives |
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| Class | Hydroxy acids and derivatives |
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| Sub Class | Medium-chain hydroxy acids and derivatives |
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| Direct Parent | Medium-chain hydroxy acids and derivatives |
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| Alternative Parents | |
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| Substituents | - Medium-chain hydroxy acid
- Medium-chain fatty acid
- Beta-hydroxy acid
- Hydroxy fatty acid
- Alpha-hydroxy acid
- Monosaccharide
- Fatty acyl
- Fatty acid
- Secondary alcohol
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Polyol
- Organooxygen compound
- Hydrocarbon derivative
- Organic oxide
- Carbonyl group
- Alcohol
- Organic oxygen compound
- 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: | Not Available |
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| KEGG Pathways: | - Fructose and mannose metabolism ec00051
- Microbial metabolism in diverse environments ec01120
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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 | 17357 | | HMDB ID | Not Available | | Pubchem Compound ID | 6602429 | | Kegg ID | C01934 | | ChemSpider ID | Not Available | | Wikipedia ID | Not Available | | BioCyc ID | Not Available |
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