862694-88-0
Chemical Structure
L-octaguluronic acid octasodium salt
- CAS No.: 862694-88-0
- Formula:C48H58Na8O49
- Molecular Weight:1602.86
IUPAC Name: sodium (2R,3S,4R,5S,6R)-3-(((2R,3S,4S,5S,6R)-6-carboxylato-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)-6-(((2R,3S,4R,5S,6R)-2-carboxylato-6-(((2R,3S,4R,5S,6R)-2-carboxylato-6-(((2R,3S,4R,5S,6R)-2-carboxylato-6-(((2R,3S,4R,5S,6R)-2-carboxylato-6-(((2R,3S,4R,5S,6R)-2-carboxylato-6-(((2R,3S,4R,5S,6R)-2-carboxylato-4,5,6-trihydroxytetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxytetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxytetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxytetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxytetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxytetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxytetrahydro-2H-pyran-2-carboxylate
InChIKey: ZCRGLNGLIYSWSI-NMARHFQZSA-F
SMILES: O=C([C@H](O[C@H]1O[C@@H]([C@@H]([C@@H]2O)O)[C@@H](O[C@H]2O[C@@H]([C@@H]([C@@H]3O)O)[C@@H](O[C@H]3O[C@@H]([C@@H]([C@@H]4O)O)[C@@H](O[C@H]4O)C(O[Na])=O)C(O[Na])=O)C(O[Na])=O)[C@H]([C@@H]([C@@H]1O)O)O[C@@H]([C@H]([C@H]5O)O)O[C@H]([C@H]5O[C@@H]([C@H]([C@H]6O)O)O[C@H]([C@H]6O[C@@H]([C@H]([C@H]7O)O)O[C@H]([C@H]7O[C@@H]([C@H]([C@H]8O)O)O[C@H]([C@H]8O)C(O[Na])=O)C(O[Na])=O)C(O[Na])=O)C(O[Na])=O)O[Na]
Biological Activity: L-octaguluronic acid octasodium salt is extracted from seaweed. L-octaguluronic acid octasodium salt is the component of the natural biopolymers, alginates[1][2].
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L-octaguluronic acid octasodium salt | L-octaguluronic acid octasodium salt is extracted from seaweed. L-octaguluronic acid octasodium salt is the component of the natural biopolymers, alginates. | |||||||||||||||||||||
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- [1]. Iwamoto M, et, al. Structure-activity relationship of alginate oligosaccharides in the induction of cytokine production from RAW264.7 cells. FEBS Lett. 2005 Aug 15; 579(20): 4423-9. [Content Brief]
- [2]. Plazinski W, et, al. Conformational properties of acidic oligo- and disaccharides and their ability to bind calcium: a molecular modeling study. Carbohydr Res. 2012 Aug 1; 357:111-7. [Content Brief]
Keywords