| Identification | Back Directory | [Name]
B-PENTASACCHARIDE | [CAS]
72468-43-0 | [Synonyms]
B-PENTA
B-PENTASACCHARIDE
II2FUC,I3FUC-IGBOSE3
BloodGroupBPentasaccharide
B-pentasaccharide from human urine
α-fuc-(1→2)(α-gal-[1→3])-β-gal-(1→4)(α-fuc-[1→3])-glc
ALPHA-FUC-[1->2][ALPHA-GAL-(1->3)]-BETA-GAL-[1->4][ALPHA-FUC-(1->3)]-GLC
D-Glucose, O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-[α-D-galactopyranosyl-(1→3)]-O-β-D-galactopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→3)]-
(2S,3S,4R,5S,6S)-2-[(3R,4R,5R,6R)-2,3-dihydroxy-5-[(2S,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol | [Molecular Formula]
C30H52O24 | [MDL Number]
MFCD01076416 | [MOL File]
72468-43-0.mol | [Molecular Weight]
796.72 |
| Hazard Information | Back Directory | [Uses]
B-Pentasaccharide 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]. | [Definition]
ChEBI: (2S,3S,4R,5S,6S)-2-[(3R,4R,5R,6R)-2,3-Dihydroxy-5-[(2S,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol is an oligosaccharide. | [References]
[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922 |
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