Identification |
---|
YMDB ID | YMDB00792 |
---|
Name | Myo-inositol 1-phosphate |
---|
Species | Saccharomyces cerevisiae |
---|
Strain | Baker's yeast |
---|
Description | D-myo-Inositol 3-phosphate, also known as inositol 3-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 3-phosphate exists in all living species, ranging from bacteria to plants to humans. Based on a literature review a significant number of articles have been published on D-myo-Inositol 3-phosphate. |
---|
Structure | |
---|
Synonyms | - 1-(dihydrogen phosphate) DL-myo-Inositol
- 1-(dihydrogen phosphate) myo-Inositol
- DL-myo-Inositol 1-phosphate
- myo-Inositol 1-monophosphate
- myo-Inositol 1-phosphate
- myo-Inositol-1-phosphate
- Myoinositol 1-phosphate
- Myoinositol 1-phosphic acid
- 1D-Myo-inositol 3-monophosphate
- 1l-Myo-inositol 1-phosphate
- D-Myo-inositol 3-monophosphate
- Inositol 3-phosphate
- L-Myo-inositol 1-phosphate
- Myoinositol 3-phosphate
- Myo-inositol 3-phosphate
- Myo-inositol 3-monophosphate
- Inositol 3-monophosphate
- 1D-Myo-inositol 3-monophosphoric acid
- 1l-Myo-inositol 1-phosphoric acid
- D-Myo-inositol 3-monophosphoric acid
- Inositol 3-phosphoric acid
- L-Myo-inositol 1-phosphoric acid
- Myoinositol 3-phosphoric acid
- Myo-inositol 3-phosphoric acid
- Myo-inositol 3-monophosphoric acid
- Inositol 3-monophosphoric acid
- D-Myo-inositol 3-phosphoric acid
- Myo-inositol 1-phosphoric acid
- 1D-Myo-inositol 1-phosphoric acid
- D-myo-Inositol 3-phosphate
|
---|
CAS number | 573-35-3 |
---|
Weight | Average: 260.1358 Monoisotopic: 260.029718526 |
---|
InChI Key | INAPMGSXUVUWAF-PTQMNWPWSA-N |
---|
InChI | 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 |
---|
IUPAC Name | {[(1R,2S,3R,4R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphonic acid |
---|
Traditional IUPAC Name | myo-inositol 1-phosphate |
---|
Chemical Formula | C6H13O9P |
---|
SMILES | [H]O[C@@]1([H])[C@]([H])(O[H])[C@]([H])(O[H])[C@]([H])(OP(=O)(O[H])O[H])[C@@]([H])(O[H])[C@]1([H])O[H] |
---|
Chemical Taxonomy |
---|
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. |
---|
Kingdom | Organic compounds |
---|
Super Class | Organic oxygen compounds |
---|
Class | Organooxygen compounds |
---|
Sub Class | Alcohols and polyols |
---|
Direct Parent | Inositol phosphates |
---|
Alternative Parents | |
---|
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
|
---|
Molecular Framework | Aliphatic homomonocyclic compounds |
---|
External Descriptors | |
---|
Physical Properties |
---|
State | Solid |
---|
Charge | 0 |
---|
Melting point | 195 °C |
---|
Experimental Properties | Property | Value | Reference |
---|
Water Solubility | 333 mg/mL [MERCK INDEX (1996)] | PhysProp | LogP | Not Available | PhysProp |
|
---|
Predicted Properties | |
---|
Biological Properties |
---|
Cellular Locations | Not Available |
---|
Organoleptic Properties | Not Available |
---|
SMPDB Pathways | |
---|
KEGG Pathways | Inositol phosphate metabolism | ec00562 |  |
|
---|
SMPDB Reactions | Not Available |
---|
KEGG Reactions | Not Available |
---|
Concentrations |
---|
Intracellular Concentrations | Not Available |
---|
Extracellular Concentrations | Not Available |
---|
Spectra |
---|
Spectra | Spectrum Type | Description | Splash Key | View |
---|
GC-MS | GC-MS Spectrum - GC-MS (7 TMS) | splash10-014i-1559000000-8a2b9550f104f28e0f7d | JSpectraViewer | MoNA | GC-MS | GC-MS Spectrum - GC-MS (7 TMS) | splash10-014i-0149000000-db7a2abef248fd1db09b | JSpectraViewer | MoNA | GC-MS | GC-MS Spectrum - GC-MS (Non-derivatized) | splash10-014i-1559000000-8a2b9550f104f28e0f7d | JSpectraViewer | MoNA | GC-MS | GC-MS Spectrum - GC-MS (Non-derivatized) | splash10-014i-0149000000-db7a2abef248fd1db09b | JSpectraViewer | MoNA | Predicted GC-MS | Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive | splash10-0005-9650000000-12db07845ff78aa5511d | JSpectraViewer | Predicted GC-MS | Predicted GC-MS Spectrum - GC-MS (5 TMS) - 70eV, Positive | splash10-0a4i-2601259000-2775d0992be57f9b2782 | JSpectraViewer | Predicted GC-MS | Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive | Not Available | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Positive | splash10-03di-2390000000-872b3b8044fff0ad80a9 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Positive | splash10-03dl-2290000000-122539b694f8b31100a9 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Positive | splash10-0002-9700000000-bed069cf85feb1dc4ab8 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-0a4i-4190000000-ea44c00eea91f419e692 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-004i-9220000000-d6c08f18832b9de73a53 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-004i-9000000000-3c92a73868c327380526 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-0a4i-0090000000-05d6010bb4bbf2b0c228 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-0a6s-9280000000-69bd06f4ab8866ad9db1 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-004j-9000000000-f3e6675946c65f8f8f07 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Positive | splash10-03di-0090000000-89fa9427c518aa95bbd0 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Positive | splash10-03di-0190000000-fa4c1ecfe995d290a153 | JSpectraViewer | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Positive | splash10-0002-9100000000-fc4055901243469636ad | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 13C NMR Spectrum | Not Available | JSpectraViewer | 1D NMR | 1H NMR Spectrum | Not Available | JSpectraViewer |
|
---|
References |
---|
References: | - Scheer, M., Grote, A., Chang, A., Schomburg, I., Munaretto, C., Rother, M., Sohngen, C., Stelzer, M., Thiele, J., Schomburg, D. (2011). "BRENDA, the enzyme information system in 2011." Nucleic Acids Res 39:D670-D676.21062828
- Albuquerque, C. P., Smolka, M. B., Payne, S. H., Bafna, V., Eng, J., Zhou, H. (2008). "A multidimensional chromatography technology for in-depth phosphoproteome analysis." Mol Cell Proteomics 7:1389-1396.18407956
- Smolka, M. B., Albuquerque, C. P., Chen, S. H., Zhou, H. (2007). "Proteome-wide identification of in vivo targets of DNA damage checkpoint kinases." Proc Natl Acad Sci U S A 104:10364-10369.17563356
- Murray, M., Greenberg, M. L. (2000). "Expression of yeast INM1 encoding inositol monophosphatase is regulated by inositol, carbon source and growth stage and is decreased by lithium and valproate." Mol Microbiol 36:651-661.10844654
- Funato, K., Vallee, B., Riezman, H. (2002). "Biosynthesis and trafficking of sphingolipids in the yeast Saccharomyces cerevisiae." Biochemistry 41:15105-15114.12484746
- Reggiori, F., Conzelmann, A. (1998). "Biosynthesis of inositol phosphoceramides and remodeling of glycosylphosphatidylinositol anchors in Saccharomyces cerevisiae are mediated by different enzymes." J Biol Chem 273:30550-30559.9804825
|
---|
Synthesis Reference: | Klyashchitskii, B. A.; Pimenova, V. V.; Shvets, V. I.; Sokolov, S. D.; Preobrazhenskii, N. A. Total synthesis of sn-myoinositol 1-phosphate. Zhurnal Obshchei Khimii (1969), 39(10), 2373. |
---|
External Links: | |
---|