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Merck

L7260

Sigma-Aldrich

Oleoyl-L-α-lysophosphatidische Säure Natriumsalz

≥98%, solid

Synonym(e):

1-Oleoyl-sn.-glycerin-3-phosphat Natriumsalz

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About This Item

Empirische Formel (Hill-System):
C21H41O7P · xNa+
CAS-Nummer:
Molekulargewicht:
436.52 (free acid basis)
MDL-Nummer:
UNSPSC-Code:
12352211
PubChem Substanz-ID:
NACRES:
NA.77

Qualitätsniveau

Assay

≥98%

Form

solid

Farbe

white

Lipid-Typ

phosphoglycerides

Lagertemp.

−20°C

SMILES String

O[C@](COP([O-])(O)=O)([H])COC(CCCCCCC/C=C\CCCCCCCC)=O.[Na+]

InChI

1S/C21H41O7P.Na.H/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(23)27-18-20(22)19-28-29(24,25)26;;/h9-10,20,22H,2-8,11-19H2,1H3,(H2,24,25,26);;/b10-9+;;

InChIKey

CHJOEWDRTPWOCY-TTWKNDKESA-N

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Allgemeine Beschreibung

Lysophosphatidic acid (LPA) is an essential metabolite for membrane biosynthesis. LPA interacts with the G protein-coupled receptors (GPCRs), called the LPA receptor and mediates signaling. Oleoyl-L-α-lysophosphatidic acid activates the receptor LPA4. In keratinocytes, oleoyl-L-α-lysophosphatidic acid promotes growth to some extent.

Anwendung

Oleoyl-L-α-lysophosphatidic acid sodium salt has been used:
  • for the activation of Ras homolog gene family, member A (RhoA) and expression of claudin-1 in human breast cancer epithelial cell line
  • in RH7777 cells for cyclic adenosine monophosphate (cAMP) accumulation assay and calcium mobilisation assay
  • in vitro luciferase assay and live-cell imaging

Biochem./physiol. Wirkung

Endogenous agonist for LPA1 and LPA2 receptors. LPA does not induce angiogenesis, but has effects on endothelial cell physiology that are similar to those of sphingosine 1-phosphate. Induces cell migration of cancer and non-cancer cells.

Leistungsmerkmale und Vorteile

This compound is featured on the Lysophospholipid Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Vorsicht

Hygroscopic, photosensitive

Angaben zur Herstellung

Prepared by the action of phospholipase A on L-α-phosphatidic acid, dioleoyl.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Biological roles of lysophosphatidic acid signaling through its production by autotaxin
Okudaira S, et al.
Biochimie, 92(6), 698-706 (2010)
A LATS biosensor screen identifies VEGFR as a regulator of the Hippo pathway in angiogenesis
Azad T, et al.
Nature Communications, 9(1), 1061-1061 (2018)
TRPM7 controls mesenchymal features of breast cancer cells by tensional regulation of SOX4
Kuipers AJ, et al.
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 1864(7), 2409-2419 (2018)
F N van Leeuwen et al.
Biochemical Society transactions, 31(Pt 6), 1209-1212 (2003-12-04)
LPA (lysophosphatidic acid), the simplest of al glycerophospholipids, is a potent inducer of cell proliferation, migration and survival. It does so by activating its cognate G-protein-coupled receptors, four of which have been identified. LPA receptors couple to at least three
Phosphatidic acid has a potential to promote hair growth in vitro and in vivo, and activates mitogen-activated protein kinase/extracellular signal-regulated kinase kinase in hair epithelial cells
Takahashi T, et al.
The Journal of Investigative Dermatology, 121(3), 448-456 (2003)

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