700168P
Avanti
16:0 stigmasteryl glucose
6-O-palmitoyl-stigmasteryl-β-D-glucose, powder
Synonym(s):
3-O-[(6′-O-palmitoyl)-β-D-glucopyranosyl] stigmasterol
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About This Item
Empirical Formula (Hill Notation):
C51H88O7
CAS Number:
Molecular Weight:
813.24
UNSPSC Code:
12352211
NACRES:
NA.25
Recommended Products
Assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (700168P-1mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 700168P
shipped in
dry ice
storage temp.
−20°C
General description
Stigmasteryl glucoside (SG) comprises the glucose attached to the C3-hydroxyl of the sterol backbone. The acylstigmasteryl glucoside has a fatty acid at the C6 position of glucose. Palmitic acid is the acyl component in 16:0 stigmasteryl glucose and is a predominant acyl group in Arabidopsis seeds.
Biochem/physiol Actions
The levels of the 16:0 (palmitic) and other acyl steryl glycosides (ASG) are depleted when there is a mutation in the DP-glucose:sterol glucosyltransferase (UGT) enzyme.
Packaging
5 mL Amber Glass Screw Cap Vial (700168P-1mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
11 - Combustible Solids
Certificates of Analysis (COA)
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Kathrin Schrick et al.
Lipids, 47(2), 185-193 (2011-08-11)
Establishment of sensitive methods for the detection of cellular sterols and their derivatives is a critical step in developing comprehensive lipidomics technology. We demonstrate that electrospray ionization tandem (triple quadrupole) mass spectrometry (ESI-MS/MS) is an efficient method for monitoring steryl
Daniel F Stucky et al.
Journal of experimental botany, 66(1), 189-201 (2014-10-16)
Steryl glucosides (SG) are abundant steroid conjugates in plant membranes. Beyond structural roles in lipid bilayers, functions in sugar transport, storage, and/or signalling are predicted. UDP-glucose:sterol glucosyltransferase 80A2 (UGT80A2) and UGT80B1, which share similarity to fungal counterparts, are implicated in
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