86363-41-9 Usage
Chemical class
Glycolipids A class of lipids that contain a carbohydrate (glycosyl) group attached to a lipid.
Composition
Two hexadecyl (C16) chains These are long-chain fatty acids that contribute to the compound's amphiphilic nature.
Glycerol backbone
The central structure to which the hexadecyl chains and maltose sugar molecule are attached.
Sugar molecule
Maltose A disaccharide composed of two glucose units, which is bound to the glycerol backbone.
Position of sugar attachment
3-O-beta Indicates that the maltose sugar is attached to the third carbon of the glycerol backbone through a beta-glycosidic linkage.
Biological location
Plant membranes Commonly found in the lipid bilayer of plant cell membranes.
Role in thylakoid membranes
Key component Plays a crucial role in maintaining the integrity and stability of the lipid bilayer structure in thylakoid membranes.
Cellular processes
Involved in regulation Contributes to the regulation of various cellular processes within plant cells.
Therapeutic potential
Treatment of diseases Due to its unique structure and biological activities, it has been of interest as a potential therapeutic agent for various diseases.
Amphiphilic nature
Both hydrophilic (water-loving) and hydrophobic (water-avoiding) properties This characteristic allows the compound to interact with both polar and nonpolar molecules, which is essential for its role in cell membranes.
Check Digit Verification of cas no
The CAS Registry Mumber 86363-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,6 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86363-41:
(7*8)+(6*6)+(5*3)+(4*6)+(3*3)+(2*4)+(1*1)=149
149 % 10 = 9
So 86363-41-9 is a valid CAS Registry Number.
InChI:InChI=1/C47H92O13/c1-4-7-9-11-13-15-17-19-21-23-25-27-29-31-34-56-46(53)43(60-44-42(52)41(51)40(50)38(36-48)58-44)39(37-49)59-45(55-33-6-3)47(46,54)57-35-32-30-28-26-24-22-20-18-16-14-12-10-8-5-2/h38-45,48-54H,4-37H2,1-3H3/t38-,39-,40-,41+,42-,43-,44-,45-,46-,47-/m1/s1
86363-41-9Relevant academic research and scientific papers
AN EFFICIENT AND STEREOSELECTIVE SYNTHESIS OF 1,2-O-DIALKYL-3-O-β-D-GLYCOSYL-sn-GLYCEROLS
Six, Lambert,Ruess, Klaus-Peter,Lieflaender, Manfred
, p. 1229 - 1232 (2007/10/02)
Long chain 1,2-O-dialkyl-3-β-D-glucosyl-(maltosyl)sn-glycerols - model-compounds for glycolipids of archaebacteria - were efficiently synthetized in a stereochemically unambigous manner.
