| Record Information |
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| Version | 2.0 |
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| Creation Date | 2015-06-05 11:08:45 -0600 |
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| Update Date | 2015-09-14 16:46:23 -0600 |
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| Secondary Accession Numbers | |
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| Identification |
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| Name: | alpha-D-Ribose 1-methylphosphonate 5-triphosphate |
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| Description | In E. coli, alpha-D-Ribose 1-methylphosphonate 5-triphosphate is an intermediate in the transformation of Phosphonates to Phosphate. The enzyme alpha-D-ribose 1-methylphosphonate 5-triphosphate synthase (EC 2.7.8.37) catalyses the reaction ATP + methylphosphonate <=> alpha-D-ribose 1-methylphosphonate 5-triphosphate + adenine (PMID: 22089136). |
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| Structure | |
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| Synonyms: | - a-D-Ribose 1-methylphosphonate 5-triphosphate
- a-D-Ribose 1-methylphosphonic acid 5-triphosphoric acid
- alpha-D-Ribose 1-methylphosphonic acid 5-triphosphoric acid
- α-D-Ribose 1-methylphosphonate 5-triphosphate
- α-D-Ribose 1-methylphosphonic acid 5-triphosphoric acid
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| Chemical Formula: | C6H16O16P4 |
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| Weight: | Average: 468.073
Monoisotopic: 467.938882427 |
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| InChI Key: | UXNHAIRVTPGNPL-KVTDHHQDSA-N |
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| InChI: | InChI=1S/C6H16O16P4/c1-23(9,10)20-6-5(8)4(7)3(19-6)2-18-25(14,15)22-26(16,17)21-24(11,12)13/h3-8H,2H2,1H3,(H,9,10)(H,14,15)(H,16,17)(H2,11,12,13)/t3-,4-,5-,6-/m1/s1 |
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| CAS number: | Not Available |
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| IUPAC Name: | ({[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-{[hydroxy(methyl)phosphoryl]oxy}oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)phosphonic acid |
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| Traditional IUPAC Name: | ({[(2R,3S,4R,5R)-3,4-dihydroxy-5-{[hydroxy(methyl)phosphoryl]oxy}oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxyphosphonic acid |
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| SMILES: | CP(O)(=O)O[C@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as pentose phosphates. These are carbohydrate derivatives containing a pentose substituted by one or more phosphate groups. |
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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 | Pentose phosphates |
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| Alternative Parents | |
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| Substituents | - Pentose phosphate
- Pentose-5-phosphate
- Monosaccharide phosphate
- Monoalkyl phosphate
- Organic phosphoric acid derivative
- Phosphoric acid ester
- Phosphonic acid ester
- Alkyl phosphate
- Organophosphonic acid derivative
- Organophosphonic acid
- Tetrahydrofuran
- Secondary alcohol
- 1,2-diol
- Oxacycle
- Organoheterocyclic compound
- Alcohol
- Hydrocarbon derivative
- Organic oxide
- Organophosphorus compound
- Organopnictogen compound
- Aliphatic heteromonocyclic compound
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| Molecular Framework | Aliphatic heteromonocyclic 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: | -4 |
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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: | |
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| KEGG Pathways: | - Phosphonate and phosphinate metabolism ec00440
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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 | 68824 | | HMDB ID | Not Available | | Pubchem Compound ID | 70678978 | | Kegg ID | C20422 | | ChemSpider ID | Not Available | | Wikipedia ID | Not Available | | BioCyc ID | Not Available |
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