CAS 209977-55-9
:2-Deoxy-4-O-β-D-galactopyranosyl-2-[[(2-propen-1-yloxy)carbonyl]amino]-D-glucose
Description:
2-Deoxy-4-O-β-D-galactopyranosyl-2-[[(2-propen-1-yloxy)carbonyl]amino]-D-glucose, with CAS number 209977-55-9, is a synthetic carbohydrate derivative that features a complex structure combining elements of both sugar and amine functionalities. This compound is characterized by the presence of a deoxy sugar moiety, specifically 2-deoxy-D-glucose, which contributes to its biological activity and potential applications in medicinal chemistry. The β-D-galactopyranosyl group indicates that it has a galactose unit linked via a glycosidic bond, enhancing its solubility and interaction with biological systems. The incorporation of a propenyl group suggests potential reactivity, making it suitable for further chemical modifications or conjugations. This compound may exhibit interesting properties such as selective binding to specific receptors or enzymes, which could be leveraged in drug design or as a biochemical probe. Overall, its unique structural features position it as a candidate for research in glycoscience and therapeutic applications.
Formula:C16H27NO12
InChI:InChI=1S/C16H27NO12/c1-2-3-27-16(26)17-7(4-18)10(22)14(8(21)5-19)29-15-13(25)12(24)11(23)9(6-20)28-15/h2,4,7-15,19-25H,1,3,5-6H2,(H,17,26)/t7-,8+,9+,10+,11-,12-,13+,14+,15-/m0/s1
InChI key:InChIKey=ZDCLIFMVPIQKMV-BINQEVQLSA-N
SMILES:O([C@@H]([C@@H]([C@@H](NC(OCC=C)=O)C=O)O)[C@@H](CO)O)[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O
Synonyms:- D-Glucose, 2-deoxy-4-O-β-D-galactopyranosyl-2-[[(2-propenyloxy)carbonyl]amino]-
- 2-Deoxy-4-O-β-D-galactopyranosyl-2-[[(2-propen-1-yloxy)carbonyl]amino]-D-glucose
- D-Glucose, 2-deoxy-4-O-β-D-galactopyranosyl-2-[[(2-propen-1-yloxy)carbonyl]amino]-
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Found 5 products.
N-Allyloxycarbonyl-β-lactosamine
CAS:Controlled ProductFormula:C16H27NO12Color and Shape:NeatMolecular weight:425.39N-Allyloxycarbonyl-b-lactosamine
CAS:<p>The linker N-Allyloxycarbonyl-b-lactosamine (NALB) is a bifunctional molecule that can be used to form triplexes with DNA. The NALB has been shown to inhibit the growth of gram-negative bacteria such as Escherichia coli and Haemophilus influenzae by binding to the bacterial cell wall and disrupting its permeability. The linker is synthesized by solid phase synthesis. This process involves the stepwise addition of building blocks in a sequence that is predetermined. The residues are usually protected with protecting groups, which are then removed at the end of the synthesis process.</p>Formula:C16H27NO12Purity:Min. 95%Molecular weight:425.38 g/mol




