Carbocyclic analogues 2 and 3 of the "trimannosyl structure 1", methyl 3,6-bis(5a-carba-a-Dmannopyranosyl)-3,6-dideoxy-a-D-mannopyranosides bonded by way of respective ether and imino linkages, were synthesized. The ether 2 had no inhibitory activity against a-D-mannosidase; in contrast, the imino c
A reinvestigation towards the conformation of methyl α-d-mannopyranosyl-(1 → 6)-α-d-mannopyranoside by a combined ROE and molecular dynamics analysis
✍ Scribed by Bertina A. Spronk; Alfonso Rivera-Sagredo; Johannis P. Kamerling; Johannes F.G. Vliegenthart
- Book ID
- 102990512
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 638 KB
- Volume
- 273
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
✦ Synopsis
Conformational analysis of a-D-Manp-(1 ~ 6)-a-D-Manpl-OMe, by a combination of extensive molecular dynamics calculations in water and ROE buildup series, afforded two main minima, namely, ~b/~/, = 95/-178 and q~/~b = 140/-185. Transitions between these minima are observed, which have not previously been demonstrated using other approaches. In contrast to literature data for the glycosidic linkage, describing equal populations of both the gg and the gt rotamers, it was found that the gg conformer is present to ca. 96%. The non-reducing mannosyl unit showed approximately a 1:1 ratio for the gg:gt equilibrium, in accordance with earlier reports.
📜 SIMILAR VOLUMES
Proton-proton cross-relaxation rates have been measured for the trisaccharide beta-D-Glcp-(l --> 2)[beta-D-Glcp-(1 --> 3)]alpha-D-Glcp-OMe in D2O as well as in D2O/[D6]DMSO 7:3 solution at 30 degrees C by means of one-dimensional NMR pulsed field gradient 1H,1H NOESY and TROESY experiments. Interato