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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 | PAMDB003512 |
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Identification |
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| Name: |
1-Deoxy-L-glycero-tetrulose 4-phosphate |
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| Description: | 1-deoxy-L-glycero-tetrulose 4-phosphate is an intermediate in the synthesis of riboflavin. It is a substrate for the enzyme 6,7-dimethyl-8-ribityllumazine synthase (RibE) which catalyzes the formation of 6,7-dimethyl-8 ribityllumazine by condensation of 5-amino-6-(D-ribitylamino)uracil with 1-deoxy-L-glycero-tetrulose 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin. |
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Structure |
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| Synonyms: | - (2-hydroxy-3-oxobutyl) dihydrogen phosphate
- (2-Hydroxy-3-oxobutyl) dihydrogen phosphoric acid
- 1-Deoxy-L-glycero-tetrulose 4-phosphoric acid
- 2-Hydroxy-3-oxobutyl dihydrogen phosphate
- 2-Hydroxy-3-oxobutyl dihydrogen phosphoric acid
- 2-Hydroxy-3-oxobutyl phosphate
- 2-Hydroxy-3-oxobutyl phosphoric acid
- 3,4-Dihydroxy-2-butanone 4-phosphate
- 3,4-Dihydroxy-2-butanone 4-phosphoric acid
- L-3,4-Dihydroxybutan-2-one 4-phosphate
- L-3,4-Dihydroxybutan-2-one 4-phosphoric acid
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Chemical Formula: |
C4H9O6P |
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| Average Molecular Weight: |
184.0844 |
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| Monoisotopic Molecular
Weight: |
184.013674532 |
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| InChI Key: |
OKYHYXLCTGGOLM-UHFFFAOYSA-N |
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| InChI: | InChI=1S/C4H9O6P/c1-3(5)4(6)2-10-11(7,8)9/h4,6H,2H2,1H3,(H2,7,8,9) |
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| CAS
number: |
Not Available |
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| IUPAC Name: | (2-hydroxy-3-oxobutoxy)phosphonic acid |
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Traditional IUPAC Name: |
2-hydroxy-3-oxobutyl phosphate |
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| SMILES: | CC(=O)C(O)COP(O)(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 monoalkyl phosphates. These are organic compounds containing a phosphate group that is linked to exactly one alkyl chain. |
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Kingdom |
Organic compounds |
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| Super Class | Organophosphorus compounds |
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Class |
Organic phosphoric acids and derivatives |
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| Sub Class | Phosphate esters |
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Direct Parent |
Monoalkyl phosphates |
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| Alternative Parents |
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| Substituents |
- Monoalkyl phosphate
- Organic phosphate
- Monosaccharide
- Beta-ketoaldehyde
- Acyloin
- Alpha-hydroxy ketone
- Secondary alcohol
- Ketone
- Hydrocarbon derivative
- Organooxygen compound
- Carbonyl group
- Alcohol
- Aliphatic acyclic compound
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| Molecular Framework |
Aliphatic acyclic 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: | -2 |
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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: |
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 | 50608 | | HMDB ID | Not Available | | Pubchem Compound ID | 669 | | Kegg ID | C15556 | | ChemSpider ID | 649 | | Wikipedia ID | Not Available | | BioCyc ID | Not Available |
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