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CAS 153153-62-9

:

O-6-Deoxy-α-L-galactopyranosyl-(1→3)-O-[3-O-sulfo-β-D-galactopyranosyl-(1→4)]-2-(acetylamino)-2-deoxy-D-glucose

Description:
O-6-Deoxy-α-L-galactopyranosyl-(1→3)-O-[3-O-sulfo-β-D-galactopyranosyl-(1→4)]-2-(acetylamino)-2-deoxy-D-glucose, with CAS number 153153-62-9, is a complex glycosylated compound characterized by its intricate structure comprising multiple sugar units and functional groups. This substance features a deoxy sugar backbone, specifically 2-deoxy-D-glucose, which is modified with an acetylamino group, enhancing its solubility and biological activity. The presence of sulfo groups indicates that it is likely to exhibit strong ionic interactions, which can influence its solubility and reactivity in biological systems. The glycosidic linkages (1→3 and 1→4) suggest that it may play a role in cellular recognition processes, potentially serving as a ligand for specific receptors. Such compounds are often studied for their biological significance, including their roles in cell signaling, immune response, and as potential therapeutic agents. Overall, the structural complexity and functional modifications of this compound contribute to its unique chemical properties and potential applications in biochemistry and pharmacology.
Formula:C20H35NO18S
InChI:InChI=1S/C20H35NO18S/c1-6-11(27)13(29)14(30)19(35-6)37-16(8(3-22)21-7(2)25)17(9(26)4-23)38-20-15(31)18(39-40(32,33)34)12(28)10(5-24)36-20/h3,6,8-20,23-24,26-31H,4-5H2,1-2H3,(H,21,25)(H,32,33,34)/t6-,8-,9+,10+,11+,12-,13+,14-,15+,16+,17+,18-,19-,20-/m0/s1
InChI key:InChIKey=GZLPVBNMMGOTCD-ZWLGTYGBSA-N
SMILES:[C@H]([C@H](O[C@H]1[C@H](O)[C@@H](OS(=O)(=O)O)[C@@H](O)[C@@H](CO)O1)[C@@H](CO)O)([C@@H](NC(C)=O)C=O)O[C@H]2[C@@H](O)[C@H](O)[C@H](O)[C@H](C)O2
Synonyms:
  • O-6-Deoxy-α-L-galactopyranosyl-(1→3)-O-[3-O-sulfo-β-D-galactopyranosyl-(1→4)]-2-(acetylamino)-2-deoxy-D-glucose
  • Sulfated Lex tri
  • 3′-Sulfatyl Lewis X
  • D-Glucose, O-6-deoxy-α-L-galactopyranosyl-(1→3)-O-[3-O-sulfo-β-D-galactopyranosyl-(1→4)]-2-(acetylamino)-2-deoxy-
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