906364-48-5
Chemical Structure
epi-Sancycline hydrochloride
- CAS No.: 906364-48-5
- Formula:C21H23ClN2O7
- Molecular Weight:450.87
IUPAC Name: (4R,4aS,5aR,12aS)-4-(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloride
InChIKey: NHHHLWBNBLFCSB-XWKXWCHHSA-N
SMILES: O[C@]12[C@](C[C@@]3([H])C(C(C4=C(O)C=CC=C4C3)=O)=C2O)([H])[C@H](C(O)=C(C1=O)C(N)=O)N(C)C.Cl
Biological Activity: epi-Sancycline (hydrochloride) is a class of biochemical reagents used for glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
epi-Sancycline hydrochloride | epi-Sancycline (hydrochloride) is a class of biochemical reagents used for glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
Keywords
