Chemistry:Epi-Inositol
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| Names | |
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| IUPAC name
epi-Inositol[1]
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| Systematic IUPAC name
(1R,2R,3r,4S,5S,6s)-Cyclohexane-1,2,3,4,5,6-hexol | |
| Identifiers | |
3D model (JSmol)
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| Properties | |
| C6H12O6 | |
| Molar mass | 180.156 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Epi-Inositol is one of the stereoisomers of inositol.[2]
Use in medicine
Epi-inositol has been found to regulate Yeast INO1 Gene Encoding (Inositol-1-P synthase) in animals. During the study with Epi-Inositol, Yeast INO1-expression was measured in northern blots.[3]
See also
- allo-Inositol
- cis-Inositol
- D-chiro-Inositol
- L-chiro-Inositol
- muco-Inositol
- neo-Inositol
- scyllo-Inositol
References
- ↑ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. pp. 1415. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
- ↑ "Inositols". http://ursula.chem.yale.edu/~chem220/chem220js/STUDYAIDS/isomers/RS14272/inositol.html.
- ↑ A., Shaldubina; S., Ju; L., Vaden; D, Ding; Belmaker, R. H; Greenberg, M. L (February 13, 2002). "Epi-inositol regulates expression of the yeast INO1 gene encoding inositol-1-P synthase." (in EN). https://www.sigmaaldrich.com/US/en/tech-docs/paper/594424.
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