850174P

06:0 PI(3,5)P2

Avanti Research^™ - A Croda Brand

• Synonym(e): PIP2[3′,5′](6:0/6:0)
• Empirische Formel (Hill-System): C₂₁H₅₀N₃O₁₉P₃
• CAS-Nummer: 799268-61-4
• Molekulargewicht: 741.55
• MDL-Nummer: MFCD22416817
• UNSPSC-Code: 51191904
• NACRES: NA.25

Eigenschaften

• Beschreibung: 1,2-dihexanoyl-sn-glycero-3-phospho-(1′-myo-inositol-3′,5′-bisphosphate) (ammonium salt)
• Assay: >99% (TLC)
• Form: powder
• Verpackung: pkg of 1 × 100 μg (with stopper and crimp cap (850174P-100ug)); pkg of 1 × 500 μg (with stopper and crimp cap (850174P-500ug))
• Hersteller/Markenname: Avanti Research^™ - A Croda Brand
• Lipid-Typ: phospholipids; cardiolipins
• Versandbedingung: dry ice
• Lagertemp.: −20°C
• SMILES String: [H][C@@](COP([O-])(O[C@H]1[C@H](O)[C@@H](OP(O)([O-])=O)[C@H](O)[C@@H](OP([O-])(O)=O)[C@H]1O)=O)(OC(CCCCC)=O)COC(CCCCC)=O.[NH4+].[NH4+].[NH4+]

Beschreibung

Allgemeine Beschreibung

Inositol phospholipid species are membrane-bound signaling molecules that have been implicated in almost all aspects of cellular physiology, including cellular growth, metabolism, proliferation, and survival.

Phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2) is an inositol phospholipid,[1] which accounts for approximately 0.05-0.1% of total cellular phosphatidylinositol (PI).[2] In fungi and higher eukaryotes, this less abundant phosphoinositide is present in the endosomal and lysosomal membranes.[1]

Biochem./physiol. Wirkung

Phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2) is capable of activating ion channels on endosomes and lysosomes. It also activates mammalian target of rapamycin complex 1 (mTORC1) in yeast and in some mammalian cell types.[2]

Verpackung

2 mL Amber Serum Vial with Stopper and Crimp Cap (850174P-100ug)

2 mL Amber Serum Vial with Stopper and Crimp Cap (850174P-500ug)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids