18749-71-8

Basic information

• Product Name: Sitosteryl (6'-O-palmitoyl)-3-β-D-glucopyranoside
• Synonyms: Stigmast-5-en-3beta-O-(6-O-hexadecanoyl-beta-D-glucopyranoside);(24R)-3β-(6-O-Palmitoyl-β-D-glucopyranosyloxy)-24-ethylcholesta-5-ene;3β-(6-O-Palmitoyl-β-D-glucopyranosyloxy)stigmasta-5-ene;Sitoindoside I;Sitosteryl (6'-O-palmitoyl)-3-β-D-glucopyranoside;Stigmast-5-en-3β-yl 6-O-hexadecanoyl-β-D-glucopyranoside;Stigmast-5-en-3β-yl 6-O-palmitoyl-β-D-glucopyranoside;beta-Sitosterol glucoside 6'-O-monopalmitate
• CAS NO: 18749-71-8
• Molecular Formula: C₅₁H₉₀O₇
• Molecular Weight: 815.27
• Mol File: 18749-71-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Sitosteryl (6'-O-palmitoyl)-3-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Sitosteryl (6'-O-palmitoyl)-3-β-D-glucopyranoside(18749-71-8)
• EPA Substance Registry System: Sitosteryl (6'-O-palmitoyl)-3-β-D-glucopyranoside(18749-71-8)

Safety Data

• Hazardous Substances Data: 18749-71-8(Hazardous Substances Data)

Usage

Uses

Sitoindoside I was isolated as a potent cytotoxic agent from latex and soybeans and showed in vitro inhibitory effects on proliferation of various cancer cell lines.

Upstream product

• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 83-46-5 β-sitosterol 
• 474-58-8 Daucosterol 
• 112-67-4 n-hexadecanoyl chloride 

Downstream Products

• 83-46-5 β-sitosterol 
• 112-39-0 hexadecanoic acid methyl ester 
• 57-10-3 1-hexadecylcarboxylic acid 

Relevant articles and documents

Suppressors of cancer cell proliferation from fig (Ficus carica) resin: Isolation and structure elucidation

A mixture of 6-O-acyl-β-D-glucosyl-β-sitosterols, the acyl moeity being primarily palmitoyl and linoleyl with minor amounts of stearyl and oleyl, has been isolated as a potent cytotoxic agent from fig (Ficus carica) latex and soybeans. Identity was established by spectroscopic methods (NMR, MS) and confirmed by chemical synthesis. Both the natural and the synthetic compounds showed in vitro inhibitory effects on proliferation of various cancer cell lines.