CC(C)CCC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCOCC(COC1O[C@H](CO)C(O)C(O)[C@H]1O[C@H]1OC(CO[C@@H]2OC(CO)[C@H](O)C(OS(O)(=O)=O)C2O)[C@@H](O)C(O[C@H]2O[C@@H]([C@H](O)CO)C(O)C2O)C1O)OCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C

InChIKey=VVKQUHPUUNWZNO-BGBLWOPYSA-N

C67H128O26S

1381.8

Organic compounds

Lipids and lipid-like molecules

Glycerolipids

Glycosylglycerols

Not available

Glycosylglycerols

Oligosaccharides Glycosyldialkylglycerols Diterpenoids O-glycosyl compounds Glycerol ethers Sulfuric acid monoesters Alkyl sulfates Oxanes Tetrahydrofurans Secondary alcohols Oxacyclic compounds Acetals Dialkyl ethers Organic oxides Primary alcohols Hydrocarbon derivatives

Aliphatic heteromonocyclic compounds

Oligosaccharide - Diterpenoid - Glycosyldialkylglycerol - Glycosyldiradylglycerol - Glycosylglycerol - Glycosyl compound - O-glycosyl compound - Glycerol ether - Sulfuric acid ester - Alkyl sulfate - Sulfate-ester - Sulfuric acid monoester - Oxane - Tetrahydrofuran - Organic sulfuric acid or derivatives - Secondary alcohol - Organoheterocyclic compound - Dialkyl ether - Ether - Oxacycle - Acetal - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organooxygen compound - Aliphatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as glycosylglycerols. These are glycerolipids structurally characterized by the presence of one or more sugar residues attached to glycerol via a glycosidic linkage.

Not available