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About This Item
Empirical Formula (Hill Notation):
C19H44NO6P
CAS Number:
Molecular Weight:
413.53
UNSPSC Code:
51191904
NACRES:
NA.25
Product Name
C16 LPA, 1-O-hexadecyl-2-hydroxy-sn-glycero-3-phosphate (ammonium salt), powder
assay
>99% (LPA; may contain up to 10% of the 2-LPA isomer, TLC)
form
powder
packaging
pkg of 1 × 1 mg (857223P-1mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 857223P
lipid type
cardiolipins
phospholipids
shipped in
dry ice
storage temp.
−20°C
SMILES string
O[C@](COP([O-])(O)=O)([H])COCCCCCCCCCCCCCCCC.[NH4+]
InChI
1S/C19H41O6P.H3N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-24-17-19(20)18-25-26(21,22)23;/h19-20H,2-18H2,1H3,(H2,21,22,23);1H3/t19-;/m1./s1
InChI key
CZAOPXJWCUFSOL-FSRHSHDFSA-N
General description
Lysophosphatidic acid (LPA) is a lysophospholipid (LPL), that is made up of glycerol 3-phosphate (G3P), fatty acids, and phosphates. It is mainly produced in plants.
Biochem/physiol Actions
Lysophosphatidic acid (LPA) participates in the synthesis of phosphatidic acid (PA).
Packaging
5 mL Amber Glass Screw Cap Vial (857223P-1mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class
11 - Combustible Solids
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Bioactive lipids in gintonin-enriched fraction from ginseng
Cho HJ, et al.
Journal of ginseng research (2017)
Jesica R Williams et al.
The Journal of biological chemistry, 284(25), 17304-17319 (2009-04-16)
Lysophosphatidic acid (LPA) is a ligand for LPA(1-3) of the endothelial differentiation gene family G-protein-coupled receptors, and LPA(4-8) is related to the purinergic family G-protein-coupled receptor. Because the structure-activity relationship (SAR) of GPR92/LPA(5) is limited and whether LPA is its
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 857223P-1MG | 04061835232086 |