1-estearoil-2-linoleoil-sn-glicero-3-fosfoetanolamina - ≥99% , CAS No.7266-53-7

CAS: 7266-53-7 Cat. No.: S130474 Peso molecular: 744.034 PubChem CID: 9546749

GRADE & PURITY ≥99%

Synonyms

PE(18:0/18:2(9Z,12Z))|1-stearoyl-2-linoleoyl-sn-glycero-3-phosphoethanolamine|7266-53-7|PE(18:0/18:2)|PE(18:0/18:2n6)|PE(18:0/18:2w6)|18:0-18:2 PE|Estearina, 2-linoleo-1-, 3-fosfato, 2-aminoetil éster, D-(-|1-estearoil-2-linoleoil-GPE|1-octadecanoil-2-(9Z

Storage

Conservar a -20°C

Shipped In

Hielera + almohadillas de hielo

Application

228,229

Descripción general

La fosfatidiletanolamina (PE) es un fosfolípido de membrana cuyos tipos dependen de la combinación de ácidos grasos libres en posición α y β.

la fosfatidiletanolamina (PE) 18:0-18:2 es adecuada para su uso

- en la preparación de monocapas

- en la preparación de glucosa-PE y lactosa-PE como patrones en la monitorización de reacciones múltiples (MRM) y en el análisis por espectrometría de masas (MS/MS)

- como patrones para espectrometría de masas-ionización por electroespray (MS-ESI)

Specifications

Sinónimos

PE(18:0/18:2(9Z, 12Z)) | 1-stearoyl-2-linoleoyl-sn-glycero-3-phosphoethanolamine | 7266-53-7 | PE(18:0/18:2) | PE(18:0/18:2n6) | PE(18:0/18:2w6) | 18:0-18:2 PE | Estearina, 2-linoleo-1-, 3-fosfato, 2-aminoetil éster, D-(- | 1-estearoil-2-linoleoil-GPE | 1-octadecanoil-2-(9Z

Especificaciones y pureza

≥99%

Mecanismos bioquímicos y fisiológicos

La fosfatidiletanolamina (PE) está implicada en numerosas funciones, como la fusión de membranas, el ciclo celular, la autofagia, la apoptosis y la función cognitiva. la fosfatidiletanolamina (PE) 18:0-18:2 es una de las PE no glicadas de la leche en polv

Condiciones de almacenamiento de almacenamiento

Conservar a -20°C

Enviado en

Hielera + almohadillas de hielo

Pureza

≥99%

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCCN)OC(=O)CCCCCCCC=CCC=CCCCCC
• IUPAC Name: [(2R)-3-[2-aminoethoxy(hydroxy)phosphoryl]oxy-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxypropyl] octadecanoate
• InChIKey: YDTWOEYVDRKKCR-KNERPIHHSA-N
• INCHI: 1S/C41H78NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-40(43)47-37-39(38-49-51(45,46)48-36-35-42)50-41(44)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h12,14,18,20,39H,3-11,13,15-17,19,21-38,42H2,1-2H3,(H,45,46)/b14-12-,20-18-/t39-/m1/s1
• Isómeros SMILES: CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN)OC(=O)CCCCCCC/C=C\C/C=C\CCCCC
• PubChem CID: 9546749
• Peso molecular: 744.034

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Glycerophospholipids
      • Subclass Glycerophosphoethanolamines

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Glycerophospholipids
• Subclass: Glycerophosphoethanolamines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phosphatidylethanolamines
• Alternative Parents: Phosphoethanolamines Fatty acid esters Dialkyl phosphates Dicarboxylic acids and derivatives Carboxylic acid esters Amino acids and derivatives Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Diacylglycero-3-phosphoethanolamine - Phosphoethanolamine - Fatty acid ester - Dialkyl phosphate - Dicarboxylic acid or derivatives - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Amino acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Organic nitrogen compound - Primary amine - Carbonyl group - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phosphatidylethanolamines. These are glycerophosphoetahnolamines in which two fatty acids are bonded to the glycerol moiety through ester linkages.
• External Descriptors: Diacylglycerophosphoethanolamines

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

• Peso molecular: 744.000 g/mol
• XLogP3: 10.800
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 41
• Exact Mass: 743.547 Da
• Monoisotopic Mass: 743.547 Da
• Topological Polar Surface Area: 134.000 Ų
• Heavy Atom Count: 51
• Formal Charge: 0
• Complexity: 897.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 2
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 2
• Covalently-Bonded Unit Count: 1

Referencias

1. Fenghua Wang, Zehui Guo, Zixuan Yang, Xueying Li, Xue Zhang, Xiangyang Ma, Zhuoxuan Han, Fuping Lu, Yihan Liu.  (2022)  Utilization of Soybean Oil Waste for a High-Level Production of Ceramide by a Novel Phospholipase C as an Environmentally Friendly Process.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:35229592] [10.1021/acs.jafc.1c08362]

2. Qiao Liu, Ruhui Long, Chaoxiang Lin, Xinping Bi, Zhibin Liang, Yi Zhen Deng.  (2024)  Phosphatidylethanolamines link ferroptosis and autophagy during appressorium formation of rice blast fungus.  MOLECULAR PLANT PATHOLOGY,  25  (7): (e13489).  [PMID:38956897] [10.1111/mpp.13489]