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ChemicalBook--->CAS DataBase List--->899827-36-2

899827-36-2

899827-36-2 Structure

899827-36-2 Structure
IdentificationBack Directory
[Name]

PtdIns-(1,2-dioctanoyl) (sodium salt)
[CAS]

899827-36-2
[Synonyms]

VNDIWCAFXLOVPN-RGISUMIPSA-M
PtdIns-(1,2-dioctanoyl) (sodium salt)
[Molecular Formula]

C25H48NaO13P
[MOL File]

899827-36-2.mol
[Molecular Weight]

610.61
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

A lyophilized powder
Hazard InformationBack Directory
[Description]

The phosphatidylinositol (PtdIns) phosphates represent a small percentage of total membrane phospholipids. However, they play a critical role in the generation and transmission of cellular signals.1,2 PtdIns-(1,2-dioctanoyl) is a synthetic analog of natural phosphatidylinositol (PtdIns) containing C8:0 fatty acids at the sn-1 and sn-2 positions. The compound features the same inositol and diacyl glycerol (DAG) stereochemistry as that of the natural compound. The short fatty acid chains of this analog, compared to naturally-occurring PtdIns, gives it different physical properties including high solubility in aqueous media. PtdIns are phosphorylated to mono- (PtdIns-P; PIP), di- (PtdIns-P2; PIP2), and triphosphates (PtdIns-P3; PIP3). Hydrolysis of PtdIns-(4,5)-P2 by phosphoinositide (PI)-specific phospholipase C generates inositol triphosphate (IP3) and DAG which are key second messengers in an intricate biochemical signal transduction cascade.
[References]

1. Exton, J.H. Regulation of phosphoinositide phospholipases by hormones, neurotransmitters, and other agonists linked to G proteins Annu. Rev. Pharmacol. Toxicol. 36,481-509(1996).
2. Majerus, P.W. Inositol phosphate biochemistry Annu. Rev. Biochem. 61,225-250(1992).
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