Results 211 to 220 of about 132,246 (241)
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Inositol treatment raises CSF inositol levels
Brain Research, 1993Inositol is a key precursor for synthesis of phosphatidylinositol in a major second messenger signalling system. It is biologically active in syndromes such as respiratory distress syndrome but has been thought to be excluded from CNS by the blood-brain barrier.
J, Levine +7 more
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Inositol polyphosphate multikinase regulates inositol 1,4,5,6-tetrakisphosphate
Biochemical and Biophysical Research Communications, 2006The human inositol phosphate multikinase (IPMK, 5-kinase) has a preferred 5-kinase activity over 3-kinase and 6-kinase activities and a substrate preference for inositol 1,3,4,6-tetrakisphosphate (Ins(1,3,4,6)P4) over inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) and inositol 1,3,4,5-tetrakisphosphate (Ins(1,3,4,5)P4).
Shao-Chun, Chang, Philip W, Majerus
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Cerebral Lithium, Inositol and Inositol Monophosphates
Pharmacology & Toxicology, 1991Abstract:Cerebral regional inositol, inositol‐1‐phosphate (InslP), and inositol‐4‐phosphate (Ins4P), intermediates in phosphoinositide (PI) cycle, and brain lithium levels were studied in male HamWistar rats 24 hr after an intraperitoneal injection of a single dose (2, 5–1. mEq./kg) of LiCl.
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INOSITOL PHOSPHATE BIOCHEMISTRY
Annual Review of Biochemistry, 1992PERSPECTIVES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 225 C ONVENTIONAL PHOSPHA TIDYLIN OSITOLS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 226 PHOSPHOLIPASE C . . . . . . . . . .
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Configuration of Inositol Phosphate in Liver Phosphatidyl Inositol
Nature, 1960THE hydrolysis of synthetic glycerol 1-(inositol 2-phosphate)1,2 has recently been compared with that of the glycerylphosphoryl inositol isolated from hydrolysates of liver phosphatidyl inositol3. The results suggest that the phosphate group in the original lipid is attached to the 1- or 2-hydroxyl of the myoinositol.
J N, HAWTHORNE, P, KEMP, R B, ELLIS
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1976
Publisher Summary This chapter describes the general metabolism of myo-inositol lipids. Myo-inositol is generally included among the vitamins. It can be synthesized from glucose in various tissues. The major route, in which CDP-diacylglycerol is a key intermediate, is studied.
J N, Hawthorne, D A, White
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Publisher Summary This chapter describes the general metabolism of myo-inositol lipids. Myo-inositol is generally included among the vitamins. It can be synthesized from glucose in various tissues. The major route, in which CDP-diacylglycerol is a key intermediate, is studied.
J N, Hawthorne, D A, White
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Journal of the Chemical Society, Perkin Transactions 1, 1993
Four of the nine isomeric inositols have been prepared by hydrolytic opening of epoxides derived from 3-halogenocyclohexa-3,5-diene-1,2-diol by further oxidation with potassium permanganate or by reduction of chiro-3-inosose (2L-2,3,6/4,5-pentahydroxycyclohexanone).
Martin Mandel, Tomas Hudlicky
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Four of the nine isomeric inositols have been prepared by hydrolytic opening of epoxides derived from 3-halogenocyclohexa-3,5-diene-1,2-diol by further oxidation with potassium permanganate or by reduction of chiro-3-inosose (2L-2,3,6/4,5-pentahydroxycyclohexanone).
Martin Mandel, Tomas Hudlicky
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Detection of Inositol and Inositol Diphosphate on Paper Chromatograms
Nature, 1958A COLOUR reaction, known as Scherer's test, is extensively used as a specific, qualitative test for inositol. It is based on the formation of the coloured alkaline earth metal salt (usually calcium salt) of rhodizonic acid on the oxidation of inositol with concentrated nitric acid1,2.
Y, NAGAI, Y, KIMURA
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Practical synthesis of all inositol stereoisomers from myo-inositol
Bioorganic & Medicinal Chemistry Letters, 1999Synthesis of six inositol stereoisomers was successfully carried out via conduritol intermediates prepared from myo-inositol. Dihydroxylation and epoxidation followed by ring opening of the conduritol B, C and F derivatives gave epi-, allo-, muco-, neo-, DL-chiro- and scyllo-inositol.
Chung, SK, Kwon, YU
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