1-palmitoyl-2-hydroxy-sn-glycero-3-phosphoethanolamine - ≥99% , CAS No.53862-35-4

CAS: 53862-35-4 Cat. No.: P130501 Peso molecular: 453.55

GRADE & PURITY ≥99%

Synonyms

1-16:0-2-lysophosphatidylethanolamine | CHEBI:73004 | 1-palmitoyl-GPE | 1-hexadecanoyl-sn-glycero-3-phosphoethanolamine zwitterion | BP-29606 | PD088583 | 2-azaniumylethyl [(2R)-3-hexadecanoyloxy-2-hydroxypropyl] phosphate | 16:0 Lyso PE | 16:0 Lyso PE, 1

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Application

Drug Delivery, Surface Modification, PEGylation of Protein, Peptide & Oligo

Specifications

Sinónimos

1-16:0-2-lysophosphatidylethanolamine | CHEBI:73004 | 1-palmitoyl-GPE | 1-hexadecanoyl-sn-glycero-3-phosphoethanolamine zwitterion | BP-29606 | PD088583 | 2-azaniumylethyl [(2R)-3-hexadecanoyloxy-2-hydroxypropyl] phosphate | 16:0 Lyso PE | 16:0 Lyso PE, 1

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

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

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488201908
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488201908
• Sonrisas canónicas: CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[NH3+])O
• IUPAC Name: 2-azaniumylethyl [(2R)-3-hexadecanoyloxy-2-hydroxypropyl] phosphate
• InChIKey: YVYMBNSKXOXSKW-HXUWFJFHSA-N
• INCHI: 1S/C21H44NO7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-21(24)27-18-20(23)19-29-30(25,26)28-17-16-22/h20,23H,2-19,22H2,1H3,(H,25,26)/t20-/m1/s1
• Isómeros SMILES: CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[NH3+])O
• Peso molecular: 453.55
• Reaxy-Rn: 2484858
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2484858&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Glycerophospholipids
      • Subclass Glycerophosphoethanolamines
        • Level5 Lysophosphatidylethanolamines
          • Level6 1-acyl-sn-glycero-3-phosphoethanolamines

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Glycerophospholipids
• Subclass: Glycerophosphoethanolamines
• Intermediate Tree Nodes: Lysophosphatidylethanolamines
• Direct Parent: 1-acyl-sn-glycero-3-phosphoethanolamines
• Alternative Parents: Phosphoethanolamines Fatty acid esters Dialkyl phosphates Secondary alcohols Carboxylic acid esters Amino acids and derivatives Monocarboxylic acids and derivatives Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: 1-monoacyl-sn-glycero-3-phosphoethanolamine - Phosphoethanolamine - Fatty acid ester - Dialkyl phosphate - Organic phosphoric acid derivative - Fatty acyl - Alkyl phosphate - Phosphoric acid ester - Amino acid or derivatives - Carboxylic acid ester - Secondary alcohol - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Primary aliphatic amine - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Amine - Organooxygen compound - Primary amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 1-acyl-sn-glycero-3-phosphoethanolamines. These are glycerophoethanolamines in which the glycerol is esterified with a fatty acid at O-1 position, and linked at position 3 to a phosphoethanolamine.
• External Descriptors: Monoacylglycerophosphoethanolamines

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

Referencias

1. Zhu Huajie, Xu Cuihong, Chen Yicun, Liang Yan.  (2022)  His-Ala-Phe-Lys peptide from Burkholderia arboris possesses antifungal activity.  Frontiers in Microbiology,      [PMID:36560956] [10.3389/fmicb.2022.1071530]