N-palmitoylglycine - ≥98% , CAS No.2441-41-0

CAS: 2441-41-0 Cat. No.: N130777 Molecular Weight: 313.475 EC Number: 627-023-4

GRADE & PURITY ≥98%

Synonyms

HY-W074890 | Q27094364 | N-Palmitoyl glycine | PALGLY | BDBM212439 | hexadecanoylglycine | N-hexadecanoyl-glycine | DTXSID40179163 | SCHEMBL515102 | DTXSID2041624 | N-palmitoyl-Gly | CCRIS 3857 | D76997 | Glycine, N-(1-oxohexadecyl)- | N-(1-oxooctadecyl)-

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Synonyms

HY-W074890 | Q27094364 | N-Palmitoyl glycine | PALGLY | BDBM212439 | hexadecanoylglycine | N-hexadecanoyl-glycine | DTXSID40179163 | SCHEMBL515102 | DTXSID2041624 | N-palmitoyl-Gly | CCRIS 3857 | D76997 | Glycine, N-(1-oxohexadecyl)- | N-(1-oxooctadecyl)-

Specifications & Purity

≥98%

Biochemical and Physiological Mechanisms

PalGly is an endogenous signaling lipid that modulates calcium influx and nitric oxide production. PalGly inhibits heat-evoked firing of wide dynamic range (WDR) neurons, activates calcium influx in DRG cells and stimulates NO production. Preliminary stud

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Action Type

MODULATOR

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488188228
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188228
• Canonical Smiles: CCCCCCCCCCCCCCCC(=O)NCC(=O)O
• IUPAC Name: 2-(hexadecanoylamino)acetic acid
• InChIKey: KVTFEOAKFFQCCX-UHFFFAOYSA-N
• INCHI: 1S/C18H35NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-17(20)19-16-18(21)22/h2-16H2,1H3,(H,19,20)(H,21,22)
• Isomeric SMILES: CCCCCCCCCCCCCCCC(=O)NCC(=O)O
• WGK Germany: 2
• Molecular Weight: 313.475
• Reaxy-Rn: 1798313
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1798313&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 N-acyl-alpha amino acids and derivatives
              • Level8 N-acyl-alpha amino acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives - N-acyl-alpha amino acids and derivatives
• Direct Parent: N-acyl-alpha amino acids
• Alternative Parents: N-acyl amines Secondary carboxylic acid amides Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: N-acyl-alpha-amino acid - Fatty amide - N-acyl-amine - Fatty acyl - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids. These are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom.
• External Descriptors: N-acyl amines

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

Associated Targets(Human)

HaCaT (4069 Activities)

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HeLa (62764 Activities)

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Associated Targets(non-human)

RAW264.7 (28094 Activities)

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RBL-2H3 (1162 Activities)

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Mechanisms of Action

Chemical and Physical Properties

• Solubility: DMSO: >10 mg/mL
• Molecular Weight: 313.500 g/mol
• XLogP3: 6.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 16
• Exact Mass: 313.262 Da
• Monoisotopic Mass: 313.262 Da
• Topological Polar Surface Area: 66.400 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 280.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1