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Principaux documents

4071

Sigma-Aldrich

myo-Inositol - CAS 87-89-8 - Calbiochem

Synonyme(s) :

i-Inositol, meso-Inositol

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About This Item

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Essai

98%

Forme

crystalline solid

Couleur

white

Description générale

A growth factor for animals as well as microorganisms.
A growth factor for animals as well as microorganisms. The most abundant form of polyols that serves as a structural element of secondary messengers in eukaryotic cells.

Actions biochimiques/physiologiques

A growth factor for animals as well as microorganisms

Code de la classe de stockage

10-13 - German Storage Class 10 to 13


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J C Ruf et al.
Biochemical medicine and metabolic biology, 48(1), 46-55 (1992-08-01)
Diabetes is known to be associated with an increase in aldose reductase activity, platelet hyperaggregability, lipid peroxidation, and cataract formation. A molecule, D-myo-inositol 1,2,6-trisphosphate (PP-56), derived from phytic acid, could in principle, by supplying myoinositol to tissues and acting as
C P Downes et al.
European journal of biochemistry, 193(1), 1-18 (1990-10-05)
The discovery of the second-messenger functions of inositol 1,4,5-trisphosphate and diacylglycerol, the products of hormone-stimulated inositol phospholipid hydrolysis, marked a turning point in studies of hormone function. This review focuses on the myo-inositol moiety which is involved in an increasingly
B Tesfamariam et al.
The Journal of pharmacology and experimental therapeutics, 263(1), 153-157 (1992-10-01)
A possible relationship between aldose reductase activity and myo-inositol levels and endothelium-dependent relaxations was examined in isolated rabbit aorta incubated with elevated concentrations of glucose (44 mM) for 6 hr to mimic hyperglycemic conditions. Rings of aorta incubated in elevated
B J Holub
Annual review of nutrition, 6, 563-597 (1986-01-01)
Alterations in the level of dietary inositol can significantly influence the concentration of free inositol and inositol-containing phospholipid in the circulation and in selected mammalian tissues and cells. The 1-stearoyl 2-arachidonyl molecular species that commonly predominates in cellular phosphoinositides may

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