N-Acetyl-L-glutamic Acid丨CAS 1188-37-0

N-Acetyl-L-glutamic Acid丨CAS 1188-37-0
Product Introduction:
CAS No.: 1188-37-0
Product Name: N-Acetyl-L-glutamic acid
Grade: AJI92
Molecular Formula: C7H11NO5
Molecular Weight: 189.17
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Technical Parameters
Description

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N-Acetyl-L-Glutamic Acid is an N-acetylated derivative of L-glutamic acid, an amino acid involved in numerous biochemical processes. Its molecular structure combines an acetylated amino group with a dicarboxylic acid framework, making it relevant to biochemical research, amino acid metabolism studies, and specialty chemical synthesis. This compound is particularly associated with research into nitrogen metabolism and the biochemical pathways in which N-acetylglutamate plays a regulatory role.

 

Chemical Identifiers

 

InChI InChI=1S/C7H11NO5/c1-4(9)8-5(7(12)13)2-3-6(10)11/h5H,2-3H2,1H3,(H,8,9)(H,10,11)(H,12,13)/t5-/m0/s1
InChI Key RFMMMVDNIPUKGG-YFKPBYRVSA-N
Smiles CC(=O)N[C@@H](CCC(=O)O)C(=O)O
EC No. 214-708-4
MDL No. MFCD00002802
PubChem CID 70914

 

 

 

Applications

 

Pharmaceutical Research and Drug Discovery

N-acetylated amino acid derivatives are investigated in a range of biochemical and biomedical research settings. N-Acetyl-L-Glutamic Acid may serve as a research reagent for studying metabolic pathways, enzyme regulation, and related biochemical processes. Its use in a specific pharmaceutical or biomedical application should be guided by experimental evidence and the requirements of the research protocol.

Biochemical and Amino Acid Research

N-Acetyl-L-Glutamic Acid is of interest in studies of amino acid metabolism and nitrogen regulation. N-acetylglutamate is an essential allosteric activator of carbamoyl phosphate synthetase I in mammals, an enzyme involved in the urea cycle. The compound can therefore support biochemical investigations into metabolic regulation and related enzymatic pathways, with experimental use depending on the specific research design.

Organic Synthesis and Chemical Research

As a structurally modified amino acid derivative, N-Acetyl-L-Glutamic Acid may be used in suitable synthetic research involving functionalized amino acids and related organic compounds. Its carboxylic acid groups provide potential sites for further chemical transformations, depending on the intended product, reaction conditions, and compatibility of the functional groups.

Enzyme Activity and Mechanistic Studies

Researchers studying metabolic enzymes may use N-acetylglutamate-related compounds to investigate enzyme activation, substrate interactions, and biochemical reaction mechanisms. N-Acetyl-L-Glutamic Acid can be relevant to research examining the relationship between molecular structure and biological function, including studies involving the urea cycle and nitrogen metabolism.

 

 

 

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