94697-68-4
Chemical Structure
5,6-Isopropylidene-L-gulonic acid γ-lactone
- CAS No.: 94697-68-4
- Formula:C9H14O6
- Molecular Weight:218.20
IUPAC Name: (3S,4R,5S)-5-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-3,4-dihydroxydihydrofuran-2(3H)-one
InChIKey: JNTPPVKRHGNFKM-BNHYGAARSA-N
SMILES: O[C@H]1[C@@](OC([C@H]1O)=O)([H])[C@]2([H])COC(C)(O2)C
Biological Activity: 5,6-Isopropylidene-L-gulonic acid γ-lactone is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
5,6-Isopropylidene-L-gulonic acid γ-lactone | 5,6-Isopropylidene-L-gulonic acid γ-lactone is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
