150399-99-8
Chemical Structure
α-D-Glucose-1-phosphate disodium tetrahydrate
- CAS No.: 150399-99-8
- Formula:C6H19Na2O13P
- Molecular Weight:376.16
IUPAC Name: (S)-2,5-diaminopentanoic-1,2-13C2 acid hydrochloride
InChIKey: INXMOHFFQYLBED-CXWKFSMRSA-L
SMILES: O=P(O[Na])(O[Na])O[C@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CO.O.O.O.O
Biological Activity: α-D-Glucose-1-phosphate disodium tetrahydrate is a derivative of D-glucose (HY-B0389). α-D-Glucose-1-phosphate disodium tetrahydrate serves as a starting material for glucuronic acid synthesis. Glucuronic acid acts as a Ca2+ chelator and also functions as a biosynthetic substrate for the production of linear maltooligosaccharides or α,α-trehalose. α-D-Glucose-1-phosphate disodium tetrahydrate can be used as a cytostatic compound, Antibiotic, and immunosuppressant essential for heart disease management. α-D-Glucose-1-phosphate disodium tetrahydrate is applicable to the research of heart disease[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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α-D-Glucose-1-phosphate disodium tetrahydrate | 98.0% | α-D-Glucose-1-phosphate disodium tetrahydrate is a derivative of D-glucose (HY-B0389). α-D-Glucose-1-phosphate disodium tetrahydrate serves as a starting material for glucuronic acid synthesis. Glucuronic acid acts as a Ca2+ chelator and also functions as a biosynthetic substrate for the production of linear maltooligosaccharides or α,α-trehalose. α-D-Glucose-1-phosphate disodium tetrahydrate can be used as a cytostatic compound, Antibiotic, and immunosuppressant essential for heart disease management. α-D-Glucose-1-phosphate disodium tetrahydrate is applicable to the research of heart disease. | ||||||||||||||||||||
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- [1]. Nihira T, et al. 2-O-α-D-glucosylglycerol phosphorylase from Bacillus selenitireducens MLS10 possessing hydrolytic activity on β-D-glucose 1-phosphate. PLoS One. 2014;9(1):e86548. Published 2014 Jan 22. [Content Brief]
- [2]. Shin, H., et al. Formation of α-D-glucose-1-phosphate by thermophilic α-1,4-D-glucan phosphorylase. J Ind Microbiol Biotech 24, 89–93 (2000).
