CHEBI:63518 - 3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl α-D-galactosyl-(1→4)-β-D-galactoside

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl α-D-galactosyl-(1→4)-β-D-galactoside
ChEBI ID CHEBI:63518
ChEBI ASCII Name 3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl alpha-D-galactosyl-(1->4)-beta-D-galactoside
Definition A glycoside that consists of α-D-galactosyl-(1→4)-β-D-galactose where the hydrogen of the anomeric OH group is substituted by a 3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C48H94O15S2
Net Charge 0
Average Mass 975.38100
Monoisotopic Mass 974.60341
InChI InChI=1S/C48H94O15S2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-64(56,57)36-38(37-65(58,59)32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)35-60-47-45(55)43(53)46(40(34-50)62-47)63-48-44(54)42(52)41(51)39(33-49)61-48/h38-55H,3-37H2,1-2H3/t39-,40-,41+,42+,43-,44-,45-,46+,47-,48-/m1/s1
InChIKey ZJEIXRMBHAATLQ-FYINUOHNSA-N
SMILES CCCCCCCCCCCCCCCCS(=O)(=O)CC(CO[C@@H]1O[C@H](CO)[C@H](O[C@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O)CS(=O)(=O)CCCCCCCCCCCCCCCC
ChEBI Ontology
Outgoing 3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl α-D-galactosyl-(1→4)-β-D-galactoside (CHEBI:63518) is a disaccharide derivative (CHEBI:63353)
3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl α-D-galactosyl-(1→4)-β-D-galactoside (CHEBI:63518) is a glycoside (CHEBI:24400)
3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl α-D-galactosyl-(1→4)-β-D-galactoside (CHEBI:63518) is a sulfone (CHEBI:35850)
IUPAC Name
3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl α-D-galactopyranosyl-(1→4)-β-D-galactopyranoside
Synonyms Sources
3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propyl 4-O-α-D--galactopyranosyl-β-D--galactopyranoside IUPAC
Gal2-bisulfone ChEBI
Registry Number Type Source
4229107 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
10023770 PubMed citation Europe PMC
Last Modified
20 September 2012