Synthesis of an analogue of D,L-MYO-inositol-1,2-cyclic phosphate: inhibition of phosphatidylinositol-specific phospholipase C
- 13 May 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (20), 2207-2210
- https://doi.org/10.1016/s0040-4039(00)79682-1
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Synthesis of 6-O-(2-aminoethyl)-D,L-MYO- inositol-1,2-cyclic phosphate: a model of a putative insulin second messengerTetrahedron, 1991
- Recent insights in phosphatidylinositol signalingCell, 1990
- Inositol phosphates and cell signallingNature, 1989
- Cyclic and noncyclic inositol phosphates are formed at different ratios by phospholipase C isozymesBiochemical and Biophysical Research Communications, 1989
- Mechanism and Catalysis of Nucleophilic Substitution in Phosphate EstersPublished by Elsevier ,1989
- Recent developments in the synthesis of myo-inositol phosphatesChemical Society Reviews, 1989
- Syntheses of some fluorine-containing halomethanephosphonate and methylenebisphosphonate estersJournal of Organometallic Chemistry, 1988
- Synthesis of mono- and unsymmetrical bis-orthoesters of scyllo-inositolThe Journal of Organic Chemistry, 1985
- Inositol cyclic phosphates are produced by cleavage of phosphatidylphosphoinositols (polyphosphoinositides) with purified sheep seminal vesicle phospholipase C enzymes.Proceedings of the National Academy of Sciences, 1985
- Cyclic phosphate and phosphite triesters - A P31 N.M.R. studyTetrahedron Letters, 1964