4-Methyl-2-oxovaleric acid - Moligand™, ≥90%, used for Role in Human Brain Ketometabolism: 4-Methyl-2-oxovaleric acid has been implicated in the temporal patterns of ketometabolism in cerebral microdialysis fluids of patients with traumatic brain injury,

CAS: 816-66-0 Cat. No.: M401024 Fórmula: C₆H₁₀O₃ Peso molecular: 130.14 Beilstein Registry Number: 1701823 Número EC: 212-435-5

GRADE & PURITY Moligand™, ≥90%

Synonyms

2-keto-4-methyl-pentanoate | 2-oxo-4-methylpentanoate | 2-Oxo-4-methylvaleric acid | NCGC00246997-01 | D82408 | Isopropylpyruvic acid | STR07443 | HY-W012722 | UNII-4GUJ8AH400 | a-Ketoisocapronate | 2-Keto-4-methylpentanoic acid | 4-Methyl-2-oxovaleric ac

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Descripción general

4-Methyl-2-oxovaleric acid, also known as α-ketoisocaproic acid (KIC), is a metabolite of leucine. It is commonly used as a building block in the synthesis of leucine and its derivatives, and it plays a role in amination reactions and asymmetric synthesis. Additionally, KIC serves as an intermediate in the formation of Strecker aldehydes.

Specifications

Sinónimos

2-keto-4-methyl-pentanoate | 2-oxo-4-methylpentanoate | 2-Oxo-4-methylvaleric acid | NCGC00246997-01 | D82408 | Isopropylpyruvic acid | STR07443 | HY-W012722 | UNII-4GUJ8AH400 | a-Ketoisocapronate | 2-Keto-4-methylpentanoic acid | 4-Methyl-2-oxovaleric ac

Especificaciones y pureza

Moligand™, ≥90%

Aplicación

Role in Human Brain Ketometabolism: 4-Methyl-2-oxovaleric acid has been implicated in the temporal patterns of ketometabolism in cerebral microdialysis fluids of patients with traumatic brain injury, underscoring its significance in biochemical pathways w

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.

Grado

Moligand™

Pureza

≥90%

Nombres e identificadores

Pubchem Sid

508809649

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508809649

Sonrisas canónicas

CC(C)CC(=O)C(=O)O

IUPAC Name

4-methyl-2-oxopentanoic acid

InChIKey

BKAJNAXTPSGJCU-UHFFFAOYSA-N

INCHI

1S/C6H10O3/c1-4(2)3-5(7)6(8)9/h4H,3H2,1-2H3,(H,8,9)

Isómeros SMILES

CC(C)CC(=O)C(=O)O

WGK Alemania

3

Número ONU

3265

Peso molecular

130.14

Beilstein

1701823

Reaxy-Rn

1701823

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1701823&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Keto acids and derivatives
      • Subclass Short-chain keto acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Keto acids and derivatives
• Subclass: Short-chain keto acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Short-chain keto acids and derivatives
• Alternative Parents: Methyl-branched fatty acids Alpha-keto acids and derivatives Alpha-hydroxy ketones Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Branched fatty acid - Methyl-branched fatty acid - Short-chain keto acid - Alpha-keto acid - Fatty acyl - Alpha-hydroxy ketone - Ketone - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organic oxide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as short-chain keto acids and derivatives. These are keto acids with an alkyl chain the contains less than 6 carbon atoms.
• External Descriptors: 2-oxo monocarboxylic acid

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 (humanos)

SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

Discover Target: SLC16A1

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

SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)

Discover Target: SLC16A3

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

Objetivos asociados (no humanos)

Catharanthus roseus (29 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: Heat sensitive; Moisture sensitive
• Índice de refracción: 1.431
• Punto de inflamación (°C): 83 °C
• Punto de ebullición (°C): 85 °C
• Punto de fusión (°C): 8-10°C
• Peso molecular: 130.139 g/mol
• XLogP3: 0.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 130.063 Da
• Monoisotopic Mass: 130.063 Da
• Topological Polar Surface Area: 54.400 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 126.000
• 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