850188P

18:0-20:4 PI(3,4)P2

powder

• Sinónimos: 1-stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1′-myo-inositol-3′,4′-bisphosphate) (ammonium salt)
• Fórmula empírica (notación de Hill): C₄₇H₉₄N₃O₁₉P₃
• Número de CAS: 2315262-41-8
• Peso molecular: 1098.18
• Código UNSPSC: 51191904
• NACRES: NA.25

Propiedades

• Ensayo: 99% (TLC)
• Formulario: powder
• envase: package of 1 × 100 μg (850188P-100UG); package of 1 × 500 μg (850188P-500UG)
• fabricante / nombre comercial: Avanti Research^™ - A Croda Brand
• tipo de lípido: phospholipids
• Condiciones de envío: dry ice
• temp. de almacenamiento: −20°C
• cadena SMILES: [H][C@@](COP([O-])(O[C@H]1[C@H](O)[C@@H](O)[C@H](OP([O-])(O)=O)[C@@H](OP(O)([O-])=O)[C@H]1O)=O)(OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)COC(CCCCCCCCCCCCCCCCC)=O.[NH4+].[NH4+].[NH4+]

Descripción

Descripción general

PI(3,4)P₂ is a lipid secondary messenger.[1] It is obtained from the dephosphorylation of PI(3,4,5)P₃ by 5-phosphatase.[2]

Acciones bioquímicas o fisiológicas

PI(3,4)P₂ plays a role in protein kinase B (PKB) phosphorylation on Ser473 in mast cells.[1] It also binds to certain effectors such as serine/threonine-specific protein kinase (AKT) and dual adaptor of phosphotyrosine and 3-phosphoinositides 1 (DAPP1). It also regulates the activity of actin mesh which is associated with endocytic structures.[2]

Envase

2 mL Amber Serum Vial with Stopper and Crimp Cap (850188P-100UG)
2 mL Amber Serum Vial with Stopper and Crimp Cap (850188P-500UG)

Información legal

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable