Record Information |
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Version | 2.0 |
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Creation Date | 2012-05-31 14:50:31 -0600 |
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Update Date | 2015-06-07 12:23:21 -0600 |
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Secondary Accession Numbers | |
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Identification |
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Name: | Fructoselysine |
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Description | Fructoselysine is a member of the chemical class known as Alpha Amino Acids and Derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).Fructoselysine is invovled in Fructoselysine degradation. Escherichia coli was found to grow on fructoselysine as an energetic substrate at a rate of about one-third of that observed with glucose. (PMID:12147680) |
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Structure | |
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Synonyms: | - Fructoselysine
- Psicoselysine
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Chemical Formula: | C12H22N2O7 |
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Weight: | Average: 306.3123 Monoisotopic: 306.142701068 |
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InChI Key: | ZRMPOBPOYIGDMF-UHFFFAOYSA-N |
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InChI: | InChI=1S/C12H22N2O7/c13-6(12(19)20)3-1-2-4-14-11-10(18)9(17)8(16)7(5-15)21-11/h6-9,11,14-17H,1-5,13H2,(H,19,20) |
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CAS number: | Not Available |
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IUPAC Name: | 2-amino-6-{[4,5-dihydroxy-6-(hydroxymethyl)-3-oxooxan-2-yl]amino}hexanoic acid |
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Traditional IUPAC Name: | 2-amino-6-{[4,5-dihydroxy-6-(hydroxymethyl)-3-oxooxan-2-yl]amino}hexanoic acid |
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SMILES: | NC(CCCCNC1OC(CO)C(O)C(O)C1=O)C(O)=O |
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Chemical Taxonomy |
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Description | belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). |
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Kingdom | Organic compounds |
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Super Class | Organic acids and derivatives |
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Class | Carboxylic acids and derivatives |
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Sub Class | Amino acids, peptides, and analogues |
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Direct Parent | Alpha amino acids |
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Alternative Parents | |
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Substituents | - Alpha-amino acid
- Medium-chain fatty acid
- Amino fatty acid
- Heterocyclic fatty acid
- Hydroxy fatty acid
- Monosaccharide
- Oxane
- Fatty acid
- Fatty acyl
- Ketone
- Cyclic ketone
- Amino acid
- Secondary alcohol
- Oxacycle
- Carboxylic acid
- Secondary aliphatic amine
- Organoheterocyclic compound
- Monocarboxylic acid or derivatives
- Secondary amine
- Alcohol
- Organic oxygen compound
- Primary aliphatic amine
- Organic nitrogen compound
- Organic oxide
- Organopnictogen compound
- Amine
- Hydrocarbon derivative
- Organonitrogen compound
- Organooxygen compound
- Primary alcohol
- Primary amine
- Carbonyl group
- Aliphatic heteromonocyclic compound
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Molecular Framework | Aliphatic heteromonocyclic compounds |
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External Descriptors | Not Available |
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Physical Properties |
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State: | Not Available |
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Charge: | 0 |
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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: | Fructoselysine and Psicoselysine Degradation | PW002049 | |
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KEGG Pathways: | Not Available |
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EcoCyc Pathways: | - fructoselysine and psicoselysine degradation PWY0-521
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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: | - Keseler, I. M., Collado-Vides, J., Santos-Zavaleta, A., Peralta-Gil, M., Gama-Castro, S., Muniz-Rascado, L., Bonavides-Martinez, C., Paley, S., Krummenacker, M., Altman, T., Kaipa, P., Spaulding, A., Pacheco, J., Latendresse, M., Fulcher, C., Sarker, M., Shearer, A. G., Mackie, A., Paulsen, I., Gunsalus, R. P., Karp, P. D. (2011). "EcoCyc: a comprehensive database of Escherichia coli biology." Nucleic Acids Res 39:D583-D590. Pubmed: 21097882
- van der Werf, M. J., Overkamp, K. M., Muilwijk, B., Coulier, L., Hankemeier, T. (2007). "Microbial metabolomics: toward a platform with full metabolome coverage." Anal Biochem 370:17-25. Pubmed: 17765195
- Winder, C. L., Dunn, W. B., Schuler, S., Broadhurst, D., Jarvis, R., Stephens, G. M., Goodacre, R. (2008). "Global metabolic profiling of Escherichia coli cultures: an evaluation of methods for quenching and extraction of intracellular metabolites." Anal Chem 80:2939-2948. Pubmed: 18331064
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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: | |
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