This molecule introduces a hydroxylated branch at the 6-position to explore how specific acylation sites modify glycolipid bioactivity. It assists in mapping the biosynthetic regulation and enzymatic pathways of PATs.
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-tetracosenoyl)-6-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-2'-O-(2,4S,6S-trimethyl-2E-docosenoyl)-4'-O-(2,4S,6S-trimethyl-2E-docosenoyl)-α,α-trehalose serves as a synthetic probe to analyze the specificity of carbohydrate-recognition domains in the innate immune system.
Publications
Publications (0)
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Publications
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