LM1900

17:0-20:4 PI(3)P

Avanti Research^™ - A Croda Brand

• Synonyme(s) : 1-heptadecanoyl-2-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phospho-(1′-myo-inositol-3′-phosphate) (ammonium salt)
• Formule empirique (notation de Hill): C₄₆H₈₈N₂O₁₆P₂
• Numéro CAS: 1246304-67-5
• Poids moléculaire : 987.14
• Code UNSPSC : 12352211
• Nomenclature NACRES : NA.25

Propriétés

• Forme: powder
• Fabricant/nom de marque: Avanti Research^™ - A Croda Brand
• Conditionnement: 1 ea of 1 × (with stopper and crimp cap (LM1900-1EA))
• Application(s): lipidomics; metabolomics
• Conditions d'expédition: dry ice
• Température de stockage: −20°C
• Chaîne SMILES: [H][C@@](COP([O-])(O[C@H]1[C@H](O)[C@@H](O)[C@H](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(CCCCCCCCCCCCCCCC)=O.[NH4+].[NH4+]
• Clé InChI: IOJKXWHTFCVKEI-DOKNWMIYSA-N

Description

Description générale

17:0-20:4 PI(3)P, phosphatidylinositol 3?phosphate, is the predominant phosphoinositide localized in endosomes and yeast vacuoles.[1] It is synthesized by phosphatidylinositol 3?kinase (PI3K) from phosphatidylinositol.[1][2]

Application

17:0-20:4 PI(3)P has been used as an internal standard for targeted lipidomic analysis.[3]

Actions biochimiques/physiologiques

17:0-20:4 PI(3)P plays a vital role in intracellular membrane trafficking and recruitment of effector proteins, which possess PI(3)P-binding motifs to membranes.[1][2] It also regulates the formation of autophagosomes.[4]

Conditionnement

2 mL Amber Serum Vial with Stopper and Crimp Cap (LM1900-1EA)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids