Oleoyl-L-α-lysophosphatidic acid sodium salt - ≥95% , CAS No.22556-62-3

CAS: 22556-62-3 Cat. No.: O299187 Peso molecular: 436.52 (free acid basis) PubChem CID: 23688917

GRADE & PURITY ≥95%

Synonyms

o-LPA | 1-Oleoyl-sn-glycero-3-phosphate sodium salt | sodium;[2-hydroxy-3-[(Z)-octadec-9-enoyl]oxypropyl] hydrogen phosphate | AKOS040744898 | Oleoyl-L-alpha-lysophosphatidic acid sodium salt | Oleoyl-lysophosphatidic acid | Sodium(Z)-2-hydroxy-3-(oleoylo

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

o-LPA | 1-Oleoyl-sn-glycero-3-phosphate sodium salt | sodium;[2-hydroxy-3-[(Z)-octadec-9-enoyl]oxypropyl] hydrogen phosphate | AKOS040744898 | Oleoyl-L-alpha-lysophosphatidic acid sodium salt | Oleoyl-lysophosphatidic acid | Sodium(Z)-2-hydroxy-3-(oleoylo

Especificaciones y pureza

≥95%

Mecanismos bioquímicos y fisiológicos

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.Endogenous agonist

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥95%

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCCC=CCCCCCCCC(=O)OCC(COP(=O)(O)[O-])O.[Na+]
• IUPAC Name: sodium;[2-hydroxy-3-[(Z)-octadec-9-enoyl]oxypropyl] hydrogen phosphate
• InChIKey: XGRLSUFHELJJAB-KVVVOXFISA-M
• INCHI: 1S/C21H41O7P.Na/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);/q;+1/p-1/b10-9-
• Isómeros SMILES: CCCCCCCC/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)[O-])O.[Na+]
• CAS alternativo: 325465-93-8；22556-62-3，22002-87-5
• PubChem CID: 23688917
• Peso molecular: 436.52 (free acid basis)

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Glycerophospholipids
      • Subclass Glycerophosphates
        • Level5 Monoacylglycerophosphates
          • Level6 Lysophosphatidic acids
            • Level7 1-acylglycerol-3-phosphates

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Glycerophospholipids
• Subclass: Glycerophosphates
• Intermediate Tree Nodes: Monoacylglycerophosphates - Lysophosphatidic acids
• Direct Parent: 1-acylglycerol-3-phosphates
• Alternative Parents: Fatty acid esters Alkyl phosphates Secondary alcohols Carboxylic acid esters Monocarboxylic acids and derivatives Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: 1-acylglycerol-3-phosphate - Fatty acid ester - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Secondary alcohol - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic alkali metal salt - Organic salt - Alcohol - Organooxygen compound - Organic oxygen compound - Organic oxide - Carbonyl group - Organic sodium salt - Hydrocarbon derivative - Organic cation - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 1-acylglycerol-3-phosphates. These are lysophosphatidic acids where the glycerol is esterified with a fatty acid at O-1 position.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: Soluble in water, with sonication (5 mg/ml).
• Sensibilidad: Moisture & air & heat & light sensitive
• Peso molecular: 458.500 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 21
• Exact Mass: 458.241 Da
• Monoisotopic Mass: 458.241 Da
• Topological Polar Surface Area: 116.000 Ų
• Heavy Atom Count: 30
• Formal Charge: 0
• Complexity: 474.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 2

XLogP3