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Buy Bulk N-Acetyl-L-glutamic acid丨CAS 1188-37-0
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
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.

