By placing the hydroxylated branch at the 2' position, this lipid allows researchers to explore the regiospecific impact of hydroxylation on mycobacterial immune signaling. It provides a vital tool for studying the recognition of specialized glycolipids.
Molecular Weight
2105.4
Molecular Formula
C132H246O17
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-(2,4S,6S-trimethyl-2E-tetracosenoyl)-2'-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-4'-O-(2,4S,6S-trimethyl-2E-docosenoyl)-α,α-trehalose can be used to study the positional effects of hydroxylated branched chains on 6-tetracosenoyl branched trehalose lipids.
Publications
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Publications
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