MEMBRANE-PERMEANT ANALOGS OF THE PUTATIVE 2ND-MESSENGER MYOINOSITOL 3,4,5,6-TETRAKISPHOSPHATE

For future investigations of the binding properties of D-myo-inositol 3,4,5,6- and 1,4,5,6-tetrakisphosphate [D-Ins(3,4,5,6)P-4 and D-Ins(1, 4,5,6)P-4, respectively] to their putative target proteins, a set of a nalogues with modifications of the 1(3)- and/or 2-hydroxy group has be en prepared, The reaction sequences started from D-3,4,5,6-tetra-O-ben zyl-myo-inositol or its D-1,4,5,6-enantiomer, respectively and allowed the introduction of groups with degenerative hydrogen-bonding potenti al like methoxy or chloride, replacing the hydroxy groups. Additionall y, the corresponding DL-scyllo-inositol precursor 24 was prepared by a stereochemically optimized reduction of the 2-inosose derivative 23, Classical protection/deprotection chemistry and subsequent phosphoryla tion employing a common phosphite approach yielded the tetrakisphospha te analogues la-e, 3, These derivatives were converted to the uncharge d, bioactivatable acetoxymethyl esters 2a-e, 4, To avoid cyclization o f phosphates during acetoxymethyl alkylation and to increase lipophili city of the potentially membrane-permeant InsP(4) derivatives hydroxy groups of the monosubstituted tetrakisphosphates were covered by intra cellularly hydrolysable butyrates.