Baumeister, Bodo; Sakai, Naomi; Matile, Stefan published the artcile< p-Octiphenyl β-barrels with ion channel and esterase activity>, Application In Synthesis of 112-63-0, the main research area is octiphenyl beta barrel ion channel esterase activity.
Design, synthesis, and esterase and ion channel activity of a novel barrel-stave supramol. with hydrophobic exterior and histidine-rich interior are reported. Voltage-dependent binding of pyrenyl-8-oxy-1,3,6-trisulfonates by histidines within p-octiphenyl β-barrels (and not monomers) via ionic (and not hydrophobic) interactions (KD, KI, KM < 1 μM) is the basis for superb esterolytic proficiency up to (kcat/KM)/kuncat = 9.6 × 105 in water and bilayer membranes. The conductance of labile ion channels formed in planar bilayer membranes is shown to be reduced by 8-hydroxypyrene-1,3,6-trisulfonate on the single- and multichannel level. Organic Letters published new progress about Electric conductivity. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Application In Synthesis of 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics