4319-56-6
Chemical Structure
Deoxycorticosterone 21-glucoside
- CAS No.: 4319-56-6
- Formula:C27H40O8
- Molecular Weight:492.60
IUPAC Name: (8S,9S,10R,13S,14S,17S)-10,13-dimethyl-17-(2-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)acetyl)-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopenta[a]phenanthren-3-one
InChIKey: SMSMUZPFFJLROV-LARVYCNESA-N
SMILES: C[C@@]12[C@](CC[C@@H]2C(CO[C@@H]3O[C@@H]([C@H]([C@@H]([C@H]3O)O)O)CO)=O)([H])[C@@]4([H])[C@@](CC1)([H])[C@@]5(C(CC4)=CC(CC5)=O)C
Biological Activity: Deoxycorticosterone 21-glucoside 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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Deoxycorticosterone 21-glucoside | Deoxycorticosterone 21-glucoside 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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Keywords
