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2-O-hexadecanoyl-3-O-(2,4S,6S-trimethyl-2E-docosenoyl)-6-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-2'-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosa
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Cat. No.: X26-02-ZQ4865

2-O-hexadecanoyl-3-O-(2,4S,6S-trimethyl-2E-docosenoyl)-6-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-2'-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosa

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Synonym: PAT16(22:1(2E)(2Me,4Me[S],6Me[S])/24:0(2Me[R],3OH[R],4Me[S],6Me[S])/24:0(2Me[R],3OH[R],4Me[S],6Me[S])/24:1(2E)(2Me,4Me[S],6Me[S]))

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Product Size
1 mg; 10 mg; 25 mg; 100 mg
Price
Datasheet
Datasheet
MSDS
MSDS
Properties
Description
This di-hydroxylated variant includes a C24 phthienoic acid at the 4'-position to examine how multiple polar sites affect lipid microdomain organization. It is utilized in structural biology to characterize receptor binding pockets.
Molecular Weight
2151.4
Molecular Formula
C134H252O18
Source
Chemical synthesis
Form
Solid or liquid
Purity
≥90%
Identity
Confirmed by NMR/HPLC/MS.
Applications
2-O-hexadecanoyl-3-O-(2,4S,6S-trimethyl-2E-docosenoyl)-6-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-2'-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-4'-O-(2,4S,6S-trimethyl-2E-tetracosenoyl)-α,α-trehalose can be used to investigate the lateral organización of glycolipids with symmetric hydroxylated chains and a single docosenoyl terminal.
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