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Record Information |
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| Version |
1.0 |
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| Update Date |
1/22/2018 11:54:54 AM |
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Metabolite ID | PAMDB000943 |
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Identification |
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| Name: |
4-Phospho-D-erythronate |
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| Description: | 4-phospho-D-erythronate is a member of the chemical class known as Beta Hydroxy Acids and Derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom. To establish a possible role of E4PDH in pyridoxal 5'-phosphate biosynthesis, we showed that 4-phosphoerythronate is a likely substrate for the 2-hydroxy-acid dehydrogenase encoded by the pdxB gene. (PMID 7751290) |
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Structure |
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| Synonyms: | - (2R,3S)-2,3-dihydroxy-4-phosphonooxybutanoate
- (2R,3S)-2,3-dihydroxy-4-phosphonooxybutanoic acid
- 2,3-Dihydroxy-4-phosphonooxybutanoate
- 2,3-Dihydroxy-4-phosphonooxybutanoic acid
- 4-Phospho-D-erythronate
- 4-Phospho-D-erythronic acid
- 4-Phosphoerythronate
- 4-Phosphoerythronic acid
- D-4-Phosphoerythronate
- D-4-Phosphoerythronic Acid
- D-Erythronate-4-phosphate
- D-Erythronate-4P
- D-Erythronic acid-4-phosphoric acid
- D-Erythronic acid-4P
- Ery4P
- Erythronate-4P
- Erythronic acid-4P
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Chemical Formula: |
C4H9O8P |
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| Average Molecular Weight: |
216.0832 |
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| Monoisotopic Molecular
Weight: |
216.003503776 |
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| InChI Key: |
ZCZXOHUILRHRQJ-PWNYCUMCSA-N |
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| InChI: | InChI=1S/C4H9O8P/c5-2(3(6)4(7)8)1-12-13(9,10)11/h2-3,5-6H,1H2,(H,7,8)(H2,9,10,11)/t2-,3-/m1/s1 |
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| CAS
number: |
Not Available |
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| IUPAC Name: | (2R,3R)-2,3-dihydroxy-4-(phosphonooxy)butanoic acid |
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Traditional IUPAC Name: |
4-phospho-D-erythronic acid |
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| SMILES: | [H][C@@](O)(COP(O)(O)=O)[C@@]([H])(O)C(O)=O |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphated group linked to the carbohydrate unit. |
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Kingdom |
Organic compounds |
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| Super Class | Organooxygen compounds |
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Class |
Carbohydrates and carbohydrate conjugates |
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| Sub Class | Monosaccharides |
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Direct Parent |
Monosaccharide phosphates |
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| Alternative Parents |
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| Substituents |
- Monosaccharide phosphate
- Monoalkyl phosphate
- Sugar acid
- Short-chain hydroxy acid
- Beta-hydroxy acid
- Fatty acid
- Alkyl phosphate
- Phosphoric acid ester
- Organic phosphoric acid derivative
- Organic phosphate
- Hydroxy acid
- Alpha-hydroxy acid
- Secondary alcohol
- 1,2-diol
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Hydrocarbon derivative
- Carbonyl group
- 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: | -3 |
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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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Pathways: |
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Spectra |
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| Spectra: |
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References |
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| References: |
- Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., Tanabe, M. (2012). "KEGG for integration and interpretation of large-scale molecular data sets." Nucleic Acids Res 40:D109-D114. Pubmed: 22080510
- 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
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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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