SYNTHESIS OF D-MYO-INOSITOL 3,4,5,6-TETRAKISPHOSPHATE AND 1,4,5,6-TETRAKISPHOSPHATE ANALOGS AND THEIR MEMBRANE-PERMEANT DERIVATIVES

Authors
ROEMER S RUDOLF MT STADLER C SCHULTZ C
Citation
S. Roemer et al., SYNTHESIS OF D-MYO-INOSITOL 3,4,5,6-TETRAKISPHOSPHATE AND 1,4,5,6-TETRAKISPHOSPHATE ANALOGS AND THEIR MEMBRANE-PERMEANT DERIVATIVES, Journal of the Chemical Society, Chemical Communications, (4), 1995, pp. 411-412
Citations number
12
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
4
Year of publication
1995
Pages
411 - 412
Database
ISI
SICI code
0022-4936(1995):4<411:SOD3A1>2.0.ZU;2-7
Abstract
A set of D-myo-inositol 3,4,5,6- and 1,4,5,6-tetrakisphosphates [D-Ins (3,4,5,6)P-4 and D-Ins(1,4,5,6)P-4, respectively] analogues with modif ications of the hydroxy groups is synthesized and subsequently convert ed to the corresponding uncharged, bioactivatable acetoxymethyl esters .