Glutamic acid (data page)

Last updated
The complete data for Glutamic acid ()
L-glutamic-acid-skeletal.png L-glutamic-acid-3D-sticks.png General information
Chemical formula : C 5 H 9 N O 4 
Molar mass : 147.13 g·mol−1
Systematic name :
(2S)-2-aminopentanedioic acid
Abbreviations : E, Glu
Synonyms :
2-amino-glutaric acid
Glutacid
Glutaminic acid
Database data
SMILES : OC(=O)CCC(N)C(=O)O
InChI =1/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m0/s1/f/h7,9H - (L)
  ATC : N/A  CAS : [56-86-0]  DrugBank : N/A  EINECS : 200-293-7  PubChem : 23327 (D) a , 33032 (L) a
Physical properties
Structure
Crystal data
Spectral data
UV-Vis
IR
NMR
MS
- Masses of main fragments:
GMD MS Spectrum
Phase behavior
Solid properties
ρsolid : 1.538 g.cm−3
Tm : 247-249 °C
Liquid properties
Gas properties
Hazard properties
MSDS
N/A
Main hazards :
- N/A
NFPA 704 Flash point
- N/A
RTECS number:
N/A
Chemical properties
XLogP : -3.386 pI : 3.22 pKa : 2.16, 4.15, 9.58 Tautomers : 0 Hydrogen bond : donor - 3; acceptor - 5
Pharmacological properties


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Monosodium glutamate (MSG), also known as sodium glutamate, is the sodium salt of glutamic acid. MSG is found naturally in some foods including tomatoes and cheese in this glutamic acid form. MSG is used in cooking as a flavor enhancer with an umami taste that intensifies the meaty, savory flavor of food, as naturally occurring glutamate does in foods such as stews and meat soups.

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PubChem is a database of chemical molecules and their activities against biological assays. The system is maintained by the National Center for Biotechnology Information (NCBI), a component of the National Library of Medicine, which is part of the United States National Institutes of Health (NIH). PubChem can be accessed for free through a web user interface. Millions of compound structures and descriptive datasets can be freely downloaded via FTP. PubChem contains multiple substance descriptions and small molecules with fewer than 100 atoms and 1,000 bonds. More than 80 database vendors contribute to the growing PubChem database.

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N-Acetylglutamic acid (also referred to as N-acetylglutamate, abbreviated NAG, chemical formula C7H11NO5) is biosynthesized from glutamate and acetylornithine by ornithine acetyltransferase, and from glutamic acid and acetyl-CoA by the enzyme N-acetylglutamate synthase. The reverse reaction, hydrolysis of the acetyl group, is catalyzed by a specific hydrolase. It is the first intermediate involved in the biosynthesis of arginine in prokaryotes and simple eukaryotes and a regulator in the process known as the urea cycle that converts toxic ammonia to urea for excretion from the body in vertebrates.

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Ghk.

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References

  1. ^a CID 23327 from PubChem (D-glutamic acid)
  2. ^a CID 33032 from PubChem (L-glutamic acid)