Analysis of myo-inositol phosphates by 2D 1H-n.m.r. spectroscopy
✍ Scribed by Charlotta Johansson; Johan Kördel; Torbjörn Drakenberg
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 494 KB
- Volume
- 207
- Category
- Article
- ISSN
- 0008-6215
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✦ Synopsis
2D 'H-N.m.r. spectroscopy applied to phosphorylated myo-inositols can indicate the number and the sites of phosphorylation, and up to three isomers can be completely analyzed simultaneously. The resonance of the sole equatorial proton (H-2) is shifted furthest downfield (to -4.7 p.p.m.) when C-2 is phosphorylated; when C-5 is unphosphorylated, the H-5 resonance has the lowest chemical shift (N 3.3 p,p.m,). The number of sites of phosphorylation can be determined from the sum of the chemical shifts for the resonances in a given myo-inositol phosphate and, based on the data presented, an algorithm can be constructed that will identify any myo-inositol phosphate on the basis of the chemical shifts.
📜 SIMILAR VOLUMES
Models of the trisaccharide, 1-kestose [beta-D-fructofuranosyl-(2----1)-beta-D-fructofuranosyl-(2 in equilibrium with 1)-alpha-D -glucopyranoside], were analyzed with the molecular mechanics computer program MM2(87) to ascertain their inter-ring torsion angles, primary alcohol side-group orientation