SYNTHESIS OF SELECTIVE NON-CA2+-MOBILIZING INHIBITORS OF D-MYO-INOSITOL 1,4,5-TRISPHOSPHATE 5-PHOSPHATASE

被引:61
作者
LAMPE, D [1 ]
LIU, CS [1 ]
POTTER, BVL [1 ]
机构
[1] UNIV BATH,SCH PHARM & PHARMACOL,DEPT MED CHEM,BATH BA2 7AY,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1021/jm00033a007
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Syntheses of novel phosphorothioate-based non-Ca2+-releasing inhibitors of myo-inositol 1,4,5-trisphosphate 5-phosphatase are described. 1L-myo-Inositol 1,4,5-trisphosphorothioate, myoinositol 1,3,5-trisphosphorothioate, and 1L-chiro-inositol 1,4,6-trisphosphorothioate have been synthesized from 1L-2,3,6-tri-O-benzyl-1-O-(cis-prop-1-enyl)-myo-inositol, 2,4,6-tris-O-(p-methoxybenzyl)-myo-inositol orthoformate and 1L-2,3,5-tri-O-benzyl-chiro-inositol, respectively. 1L-2,3,5-Tri-O-benzyl-chiro-inositol was also used to prepare 1L-chiro-inositol 1,4,6-trisphosphate. The phosphorothioates did not mobilize intracellular Ca2+ but were highly potent inhibitors of Ins(1,4,5)P(3)5-phosphatase, and myo-inositol 1,3,5-trisphosphorothioate and 1L-chiro-inositol 1,4,6-trisphosphorothioate were selective for this enzyme.
引用
收藏
页码:907 / 912
页数:6
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