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An efficient synthesis of optically active D-myo-inositol 1,4,5-triphosphate

✍ Scribed by Yeuk-Chuen Liu; Ching-Shih Chen


Publisher
Elsevier Science
Year
1989
Tongue
French
Weight
261 KB
Volume
30
Category
Article
ISSN
0040-4039

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✦ Synopsis


An effective synthesis of IJ-w-inositol 1,4,5_triphosphate was developed using a chiral inositide precursor which can be prepared via a facile enzymatic or chemical method. Recently, much attention has been focused on the metabolic cascade of membrane phosphoinositides, which regulates intracellular Ca +2 mobilization in response to a variety of extracellular signalsl. This complex information-transducing process is initiated by a receptor-mediated breakdown of phosphatidyl inositol 4,5-bisphosphate with the formation of Q-z-inositol 1,4,5-triphosphate [Ins(1,4,5)P3] (A) and 1,2-diacylglycerol, both of which function as second messengers eliciting specific intracellular responses.


πŸ“œ SIMILAR VOLUMES


Synthesis of D-myo-inositol 1,4,5-tripho
✍ Colin B Reese; John G Ward πŸ“‚ Article πŸ“… 1987 πŸ› Elsevier Science 🌐 French βš– 270 KB

The conversion of myo-inositol into the ammonium salts both of racemic and enantiomerically pure I&myo-inositol 1,4,5\_trisphosphate ( 6) is described. The n.m.r. spectroscopic properties and biological activity of synthetic and naturally-isolated (6) are virtually identical.

Synthesis of enantiomerically pure D-myo
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The. synthesis of enantiomerically pure Dq&nositol 1.5.~bisphosphate fkom myoinositol involving two sequential rcgiosdective pmtections of hydroxyl groups in the intcmwdiate selfresolving rnp-inositol camphor monoacetal has been accomplished Recent investigations of the phosphoinositide signal trans