| Record Information |
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| Version | 2.0 |
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| Creation Date | 2012-10-10 12:14:40 -0600 |
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| Update Date | 2015-06-03 17:25:51 -0600 |
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| Secondary Accession Numbers | |
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| Identification |
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| Name: | L-Tagatose-6-phosphate |
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| Description | L-Tagatose-6-phosphate is a substrate for galactitol-1-phosphate 5-dehydrogenase. Specifically this enzyme converts galactitol 1-phosphate to tagatose 6-phosphate. Galactitol (dulcitol) is a sugar alcohol and is actually the reduction product of galactose. L-tagatose 6-phosphate is an intermediate in galactose metabolism Tagatose is a naturally occurring monosaccharide, specifically a hexose. It is often found in dairy products, and is very similar in texture to sucrose (table sugar). E. coli can use tagatose and galactose as a carbon source. |
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| Structure | |
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| Synonyms: | - (2S,3S,4R)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-ylmethyl dihydrogen phosphate
- (2S,3S,4R)-3,4,5-Trihydroxy-5-(hydroxymethyl)oxolan-2-ylmethyl dihydrogen phosphoric acid
- 6-O-Phosphono-L-tagatofuranose
- L-Tagatose 6-phosphate
- L-Tagatose 6-phosphoric acid
- L-Tagatose-6-phosphoric acid
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| Chemical Formula: | C6H13O9P |
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| Weight: | Average: 260.1358
Monoisotopic: 260.029718526 |
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| InChI Key: | BGWGXPAPYGQALX-JMSAOHGTSA-N |
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| InChI: | InChI=1S/C6H13O9P/c7-2-6(10)5(9)4(8)3(15-6)1-14-16(11,12)13/h3-5,7-10H,1-2H2,(H2,11,12,13)/t3-,4+,5+,6?/m0/s1 |
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| CAS number: | Not Available |
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| IUPAC Name: | {[(2S,3S,4R)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methoxy}phosphonic acid |
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| Traditional IUPAC Name: | L-tagatose 6-phosphate |
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| SMILES: | [H][C@@]1(O)[C@]([H])(COP(O)(O)=O)OC(O)(CO)[C@]1([H])O |
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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
- C-glycosyl compound
- Glycosyl compound
- Monosaccharide phosphate
- Monoalkyl phosphate
- Phosphoric acid ester
- Organic phosphoric acid derivative
- Alkyl phosphate
- Tetrahydrofuran
- Secondary alcohol
- Hemiacetal
- Polyol
- Organoheterocyclic compound
- Oxacycle
- Primary alcohol
- Alcohol
- Hydrocarbon derivative
- Organic oxide
- 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: | -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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| SMPDB Pathways: | |
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| KEGG Pathways: | |
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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 | 6307 | | HMDB ID | Not Available | | Pubchem Compound ID | 440970 | | Kegg ID | C06312 | | ChemSpider ID | Not Available | | Wikipedia ID | Not Available | | BioCyc ID | Not Available |
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