O-Acetyl-L-carnitine hydrochloride - ≥99% , CAS No.5080-50-2

CAS: 5080-50-2 Cat. No.: A129120 Peso molecular: 239.7 Beilstein Registry Number: 4340103 Número EC: 690-015-4

GRADE & PURITY ≥99%

Synonyms

ACETYL-L-CARNITINE CHLORIDE | AKOS005138019 | acetyl l-carnitine hydrochloride | Oristar ach | 1-Propanaminium, 2-(acetyloxy)-3-carboxy-N,N,N-trimethyl-, chloride, (R)- | AKOS015963427 | ACETYLCARNITINE HYDROCHLORIDE [MI] | Acetylcarnitine L-form hydrochl

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Descripción general

Endogenous mitochondrial metabolite that transports acetyl groups across the mitochondrial membrane. Exogenous acetylcarnitine enhances mitochondrial function in aged rats. As an acetate donor to coenzyme A, it increases the central and peripheral acetylcholine synthesis and function. Acetylcarnitine has antinociceptive activity that may be mediated by enhanced activity of muscarinic cholinergic receptors or mGlu2 glutamate receptors.
A cholinergic agonist that stimulates neuronal response to serotonin and acetylcholine.

Specifications

Sinónimos

ACETYL-L-CARNITINE CHLORIDE | AKOS005138019 | acetyl l-carnitine hydrochloride | Oristar ach | 1-Propanaminium, 2-(acetyloxy)-3-carboxy-N, N, N-trimethyl-, chloride, (R)- | AKOS015963427 | ACETYLCARNITINE HYDROCHLORIDE [MI] | Acetylcarnitine L-form hydrochl

Especificaciones y pureza

≥99%

Mecanismos bioquímicos y fisiológicos

Enables CoA function. Lowers oxidative stress marker levels. Improves mitochondrial function. Blood-brain barrier permeable. Exhibits antidepressant, neuroprotective, analgesic and antinociceptive activities in vivo .

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

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

≥99%

Nombres e identificadores

• Sonrisas canónicas: CC(=O)OC(CC(=O)O)C[N+](C)(C)C.[Cl-]
• IUPAC Name: [(2R)-2-acetyloxy-3-carboxypropyl]-trimethylazanium;chloride
• InChIKey: JATPLOXBFFRHDN-DDWIOCJRSA-N
• INCHI: 1S/C9H17NO4.ClH/c1-7(11)14-8(5-9(12)13)6-10(2,3)4;/h8H,5-6H2,1-4H3;1H/t8-;/m1./s1
• Isómeros SMILES: CC(=O)O[C@H](CC(=O)O)C[N+](C)(C)C.[Cl-]
• WGK Alemania: 3
• Peso molecular: 239.7
• Beilstein: 4340103
• Reaxy-Rn: 4166183
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4166183&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Fatty acid esters

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Fatty acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Acyl carnitines
• Alternative Parents: Dicarboxylic acids and derivatives Tetraalkylammonium salts Carboxylic acid esters Carboxylic acids Organopnictogen compounds Organic oxides Organic chloride salts Hydrocarbon derivatives Carbonyl compounds Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acyl-carnitine - Dicarboxylic acid or derivatives - Tetraalkylammonium salt - Quaternary ammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Carboxylic acid - Organic nitrogen compound - Organic salt - Organic chloride salt - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as acyl carnitines. These are organic compounds containing a fatty acid with the carboxylic acid attached to carnitine through an ester bond.
• 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)

ampC Beta-lactamase AmpC (62480 Activities)

Discover Target: ampC

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water (100 mg/ml), alcohol, and ethanol (10%). Insoluble in ether.
• Sensibilidad: Hygroscopic
• Rotación específica [α]: -28° (C=1,H2O)
• Punto de fusión (°C): 194℃
• Peso molecular: 239.690 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 6
• Exact Mass: 239.092 Da
• Monoisotopic Mass: 239.092 Da
• Topological Polar Surface Area: 63.600 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 219.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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

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