Synthesis and binding properties of cyclopentane analogues of myo-inositol 1,4,5-tris(phosphate)

被引:2
|
作者
Moris, MA
Caron, AZ
Guillemette, G
Schlewer, G
机构
[1] Fac Pharm, UMR 7081 CNRS, Lab Pharmacohim Commun Cellulaire, F-67401 Illkirch Graffenstaden, France
[2] Univ Sherbrooke, Fac Med, Dept Pharmacol, Sherbrooke, PQ J1H 5N4, Canada
关键词
myo-inositol 1,4,5-tris(phosphate); cyclopentane tris(phosphate); IP3; analogues; binding; P-31; NMR;
D O I
10.1016/j.bmc.2004.06.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cyclopentanic analogues of myo-inositol 1,4,5-tris(phosphate) were synthesised starting from cyclopentadiene. The affinities of the trisphosphorylated derivatives for the Ins(1,4,5)P-3 receptors were equipotent to that of compound 4, showing that the relative orientation of the functional groups, particularly of the hydroxyl, is not of prime importance in this series. The P-31 NMR titration curves show that the tris(phosphate) 5 behaves as the superimposition of an independent phosphate and a vicinal bis(phosphate). (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3995 / 4001
页数:7
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