152006-17-2
Chemical Structure
2,3-O-(1-Methylethylidene)-L-lyxonic acid γ-lactone
- CAS No.: 152006-17-2
- Formula:C8H12O5
- Molecular Weight:188.18
IUPAC Name: (3aR,6S,6aR)-6-(hydroxymethyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one
InChIKey: NHHKFJCWLPPNCN-KVQBGUIXSA-N
SMILES: OC[C@H]1[C@]2([H])[C@@](C(O1)=O)([H])OC(C)(O2)C
Biological Activity: 2,3-O-(1-Methylethylidene)-L-lyxonic 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].
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2,3-O-(1-Methylethylidene)-L-lyxonic acid γ-lactone | 2,3-O-(1-Methylethylidene)-L-lyxonic 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. | |||||||||||||||||||||
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