7333-33-7
7333-33-7
Chemical Structure
UDP-β-D-glucose disodium
- CAS No.: 7333-33-7
- Formula:C15H22N2Na2O17P2
- Molecular Weight:610.27
InChIKey: PKJQEQVCYGYYMM-BYFFMYLLSA-L
SMILES: O[C@H]1[C@H](O)[C@@H](O)[C@H](O[P](O[P](OC[C@@H]2[C@@H](O)[C@@H](O)[C@H](N3C=CC(NC3=O)=O)O2)(O[Na])=O)(O[Na])=O)O[C@@H]1CO
Biological Activity: UDP-β-D-glucose disodium acts as a glycosyl donor and biosynthetic intermediate, and is also a stereoisomer of UDP-α-D-glucose[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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UDP-β-D-glucose disodium | 99.9% | UDP-β-D-glucose disodium acts as a glycosyl donor and biosynthetic intermediate, and is also a stereoisomer of UDP-α-D-glucose. | ||||||||||||||||||||
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References
- [1]. Sato S, et al. Complete In Vitro Reconstitution of the Apramycin Biosynthetic Pathway Demonstrates the Unusual Incorporation of a β-d-Sugar Nucleotide in the Final Glycosylation Step. J Am Chem Soc. 2024;146(14):10103-10114. [Content Brief]
- [2]. Sang S, et al. The chemistry and biotransformation of tea constituents. Pharmacol Res. 2011;64(2):87-99. [Content Brief]
- [3]. Hundt K, et al. Transformation of triclosan by Trametes versicolor and Pycnoporus cinnabarinus. Appl Environ Microbiol. 2000;66(9):4157-4160. [Content Brief]
Keywords
