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Record Information |
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Version | 4.0 |
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Status | Expected but not Quantified |
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Creation Date | 2005-11-16 15:48:42 UTC |
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Update Date | 2020-07-10 15:01:36 UTC |
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HMDB ID | HMDB0001313 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | D-myo-Inositol 4-phosphate |
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Description | D-myo-Inositol 4-phosphate, also known as inositol 4-phosphoric acid, belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. D-myo-Inositol 4-phosphate is an extremely weak basic (essentially neutral) compound (based on its pKa). Within humans, D-myo-inositol 4-phosphate participates in a number of enzymatic reactions. In particular, D-myo-inositol 4-phosphate can be biosynthesized from D-myo-inositol 1,4-bisphosphate through its interaction with the enzyme inositol polyphosphate 1-phosphatase. In addition, D-myo-inositol 4-phosphate can be converted into myo-inositol through its interaction with the enzyme inositol monophosphatase 1. |
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Structure | |
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Synonyms | Value | Source |
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1D-Myo-inositol 4-monophosphate | ChEBI | 1D-Myo-inositol 4-phosphate | Kegg | Inositol 4-phosphate | Kegg | 1D-Myo-inositol 4-monophosphoric acid | Generator | 1D-Myo-inositol 4-phosphoric acid | Generator | Inositol 4-phosphoric acid | Generator | D-Myo-inositol 4-phosphoric acid | Generator | D-Myo-inositol-4-phosphate | HMDB | D-Myoinositol 4-phosphate | HMDB | Myo-inositol 4-phosphate | HMDB | D-Myo-inositol 4-monophosphate | HMDB | Inositol 4-monophosphate | HMDB | D-myo-Inositol 4-phosphate | HMDB |
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Chemical Formula | C6H13O9P |
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Average Molecular Weight | 260.1358 |
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Monoisotopic Molecular Weight | 260.029718526 |
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IUPAC Name | {[(1S,2R,3S,4S,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphonic acid |
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Traditional Name | myo-inositol 4-phosphate |
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CAS Registry Number | 69256-52-6 |
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SMILES | O[C@@H]1[C@H](O)[C@H](O)[C@@H](OP(O)(O)=O)[C@H](O)[C@H]1O |
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InChI Identifier | InChI=1S/C6H13O9P/c7-1-2(8)4(10)6(5(11)3(1)9)15-16(12,13)14/h1-11H,(H2,12,13,14)/t1-,2-,3-,4+,5-,6-/m0/s1 |
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InChI Key | INAPMGSXUVUWAF-CNWJWELYSA-N |
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Chemical Taxonomy |
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Description | belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. |
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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 | Alcohols and polyols |
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Direct Parent | Inositol phosphates |
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Alternative Parents | |
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Substituents | - Inositol phosphate
- Monoalkyl phosphate
- Cyclohexanol
- Alkyl phosphate
- Phosphoric acid ester
- Organic phosphoric acid derivative
- Secondary alcohol
- Polyol
- Organic oxide
- Hydrocarbon derivative
- Aliphatic homomonocyclic compound
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Molecular Framework | Aliphatic homomonocyclic compounds |
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External Descriptors | |
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Ontology |
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Disposition | Source: Biological location: |
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Process | Naturally occurring process: |
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Physical Properties |
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State | Solid |
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Experimental Properties | Property | Value | Reference |
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Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
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Predicted Properties | |
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Spectra |
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| Spectrum Type | Description | Splash Key | View |
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Predicted GC-MS | Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive | splash10-0005-9650000000-12db07845ff78aa5511d | Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - GC-MS (5 TMS) - 70eV, Positive | splash10-0a4i-2611259000-774915a3f6fc15006373 | Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Positive | splash10-03di-2390000000-036684c0736cc37701a9 | Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Positive | splash10-03dl-2290000000-2692f0855292325fd753 | Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Positive | splash10-000w-9600000000-81c4994a2212052d4690 | Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-0a4i-4190000000-f8cff124acad5d21332f | Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-004i-9220000000-2153b6c9b35a97307acb | Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-004i-9000000000-5f386828ffd5102695f3 | Spectrum |
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Biological Properties |
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Cellular Locations | - Cytoplasm (predicted from logP)
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Biospecimen Locations | Not Available |
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Tissue Locations | Not Available |
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Pathways | |
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Normal Concentrations |
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| Not Available |
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Abnormal Concentrations |
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| Not Available |
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Associated Disorders and Diseases |
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Disease References | None |
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Associated OMIM IDs | None |
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External Links |
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DrugBank ID | Not Available |
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Phenol Explorer Compound ID | Not Available |
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FooDB ID | FDB022548 |
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KNApSAcK ID | Not Available |
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Chemspider ID | 17216102 |
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KEGG Compound ID | C03546 |
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BioCyc ID | D-MYO-INOSITOL-4-PHOSPHATE |
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BiGG ID | 42060 |
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Wikipedia Link | Not Available |
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METLIN ID | 6151 |
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PubChem Compound | Not Available |
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PDB ID | Not Available |
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ChEBI ID | 18384 |
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Food Biomarker Ontology | Not Available |
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VMH ID | MI4P_D |
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MarkerDB ID | |
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References |
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Synthesis Reference | Billington, David C.; Baker, Raymond; Kulagowski, Janusz J.; Mawer, Ian M. Synthesis of myo-inositol 1-phosphate and 4-phosphate, and of their individual enantiomers. Journal of the Chemical Society, Chemical Communications (1987), (4), 314-16. |
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Material Safety Data Sheet (MSDS) | Not Available |
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General References | Not Available |
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