Acetylcholine iodide - 10mM in DMSO , CAS No.2260-50-6

CAS: 2260-50-6 Cat. No.: A422713 Peso molecular: 273.11 Beilstein Registry Number: 3571339 Número EC: 218-862-3 PubChem CID: 75271

GRADE & PURITY 10mM in DMSO

Synonyms

ACh | [2-(acetyloxy)ethyl]trimethylazanium iodide | EINECS 218-862-3 | Acetylholine iodide | Choline acetate (ester), iodide | 1-[3-[2-(Methylsulfonyl)phenothiazin-10-yl]propyl]isonipecotamide | HMS3885B20 | HY-101086 | AS-57315 | NSC-63844 | Ethanaminium

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Sinónimos

ACh | [2-(acetyloxy)ethyl]trimethylazanium iodide | EINECS 218-862-3 | Acetylholine iodide | Choline acetate (ester), iodide | 1-[3-[2-(Methylsulfonyl)phenothiazin-10-yl]propyl]isonipecotamide | HMS3885B20 | HY-101086 | AS-57315 | NSC-63844 | Ethanaminium

Especificaciones y pureza

10mM in DMSO

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

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Nombres e identificadores

• Sonrisas canónicas: CC(=O)OCC[N+](C)(C)C.[I-]
• IUPAC Name: 2-acetyloxyethyl(trimethyl)azanium;iodide
• InChIKey: SMBBQHHYSLHDHF-UHFFFAOYSA-M
• INCHI: 1S/C7H16NO2.HI/c1-7(9)10-6-5-8(2,3)4;/h5-6H2,1-4H3;1H/q+1;/p-1
• Isómeros SMILES: CC(=O)OCC[N+](C)(C)C.[I-]
• WGK Alemania: 3
• RTECS: KH3300000
• PubChem CID: 75271
• Peso molecular: 273.11
• Beilstein: 3571339
• Reaxy-Rn: 3571339

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Quaternary ammonium salts
        • Level5 Cholines
          • Level6 Acyl cholines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Cholines
• Direct Parent: Acyl cholines
• Alternative Parents: Tetraalkylammonium salts Carboxylic acid esters Monocarboxylic acids and derivatives Organopnictogen compounds Organic oxides Organic iodide salts Hydrocarbon derivatives Carbonyl compounds Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acyl choline - Tetraalkylammonium salt - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic iodide salt - Organic salt - Organooxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as acyl cholines. These are acylated derivatives of choline. Choline or 2-Hydroxy-N,N,N-trimethylethanaminium is a quaternary ammonium salt with the chemical formula (CH3)3N+(CH2)2OH.
• 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

Objetivos asociados (no humanos)

Cavia porcellus (23802 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Light Sensitive & Hygroscopic
• Punto de fusión (°C): 162°C
• Peso molecular: 273.110 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 273.023 Da
• Monoisotopic Mass: 273.023 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 115.000
• 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: 2

XLogP3

Referencias

1. Wenli Shi, Wenxin Han, Yijing Liao, Jiaqi Wen, Guowen Zhang.  (2023)  Inhibition mechanism of fisetin on acetylcholinesterase and its synergistic effect with galantamine.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:37769468] [10.1016/j.saa.2023.123452]

2. Wenli Shi, Guowen Zhang, Yijing Liao, Xiaoyun Fei, Deming Gong, Xing Hu.  (2023)  Anti-acetylcholinesterase mechanism of kaempferol and its synergistic effect with galanthamine hydrobromide.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2023.103174]

3. Peng Wenping, Wang Nan, Wang Shunmin, Wang Junzhen, Bian Zixiu.  (2022)  Effects of microwave and exogenous l-phenylalanine treatment on phenolic constituents, antioxidant capacity and enzyme inhibitory activity of Tartary buckwheat sprouts.  FOOD SCIENCE AND BIOTECHNOLOGY,  32  (1): (11-19).  [PMID:36606090] [10.1007/s10068-022-01172-2]

4. Lisiqi Xie, Xiao Huang, Bin Su.  (2017)  Portable Sensor for the Detection of Choline and Its Derivatives Based on Silica Isoporous Membrane and Gellified Nanointerfaces.  ACS Sensors,      [PMID:28723110] [10.1021/acssensors.7b00166]

5. Sihua Qian, Hengwei Lin.  (2015)  Colorimetric Sensor Array for Detection and Identification of Organophosphorus and Carbamate Pesticides.  ANALYTICAL CHEMISTRY,      [PMID:25913282] [10.1021/acs.analchem.5b00738]