The chemical substance known as (3beta,5beta,6beta,8xi,9beta,14beta,15alpha)-3,6,8,15-tetrahydroxycholestan-24-yl alpha-L-arabinofuranoside, with the CAS number 88191-35-9, is a glycosylated sterol derivative. This compound features a cholestane backbone, characterized by multiple hydroxyl groups at specific positions, which contribute to its hydrophilicity and potential biological activity. The presence of the alpha-L-arabinofuranoside moiety indicates that it is a glycoside, which may enhance its solubility and interaction with biological systems. Such compounds often exhibit various pharmacological properties, including potential roles in cell signaling, membrane structure, and as precursors in the synthesis of more complex biomolecules. The stereochemistry of the hydroxyl groups and the glycosidic linkage is crucial for its biological function and interaction with receptors or enzymes. Overall, this compound represents a complex structure that may have implications in biochemistry and medicinal chemistry, particularly in the study of sterols and their derivatives.

(3beta,5beta,6beta,8xi,9beta,14beta,15alpha)-3,6,8,15-tetrahydroxycholestan-24-yl alpha-L-arabinofuranoside

88191-35-9: The chemical substance known as (3beta,5beta,6beta,8xi,9beta,14beta,15alpha)-3,6,8,15-tetrahydroxycholestan-24-yl alpha-L-arabinofuranoside, with the CAS number 88191-35-9, is a glycosylated sterol derivative. This compound features a cholestane backbone, characterized by multiple hydroxyl groups at specific positions, which contribute to its hydrophilicity and potential biological activity. The presence of the alpha-L-arabinofuranoside moiety indicates that it is a glycoside, which may enhance its solubility and interaction with biological systems. Such compounds often exhibit various pharmacological properties, including potential roles in cell signaling, membrane structure, and as precursors in the synthesis of more complex biomolecules. The stereochemistry of the hydroxyl groups and the glycosidic linkage is crucial for its biological function and interaction with receptors or enzymes. Overall, this compound represents a complex structure that may have implications in biochemistry and medicinal chemistry, particularly in the study of sterols and their derivatives.

(3S,5R,6R,9S,10R,13R,14R,15S,17R)-17-[(2R)-5-[(2R,3R,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-methyl-heptan-2-yl]-10,13-dimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,6,8,15-tetrol

CAS 88191-35-9

(3beta,5beta,6beta,8xi,9beta,14beta,15alpha)-3,6,8,15-tetrahydroxycholestan-24-yl alpha-L-arabinofuranoside

(3S,5R,6R,9S,10R,13R,14R,15S,17R)-17-[(2R)-5-[(2R,3R,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-methyl-heptan-2-yl]-10,13-dimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,6,8,15-tetrol

Ref: IN-DA004C67