This di-hydroxylated PAT variant features two hydroxyphthioceranic acid branches to maximize polar interactions in the mycobacterial cell wall. It is utilized to study the role of hydrogen bonding in stabilizing the tuberculosis pathogen surface.
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-(2,4S,6S-trimethyl-2E-tetracosenoyl)-2'-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-4'-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-α,α-trehalose can be used to evaluate the biophysical stability of trehalose lipids with multiple hydroxylated branched chains and 6-tetracosenoyl branching.
Publications
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Publications
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