N-Acetylglutamic acid

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N-Acetylglutamic acid
IUPAC name (2S)-2-Acetamidopentanedioic acid
Other names Acetylglutamic acid, N-Acetylglutamic acid, N-Acetyl-L-glutamic acid, N-Acetyl-Glu, Ac-Glu-OH, NAcGlu
Identifiers
CAS number 1188-37-0
PubChem 70914
SMILES OC(=O)CC[C@H](NC(=O)C)C(=O)O
InChI InChI=1/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)
Properties
Molecular formula C7H11NO5
Molar mass 189.17 g/mol
Density 1 g/cm3
Melting point

191 - 194 °C

Solubility in water 36 g/l
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

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Overview

N-Acetylglutamic acid (abbreviated NAcGlu) is biosynthesized from glutamic acid and acetyl-CoA by the enzyme N-acetylglutamate synthase. Arginine is the activator for this reaction.

The reverse reaction, hydrolysis of the acetyl group, is catalyzed by a specific hydrolase.

NAcGlu activates carbamoyl phosphate synthase in the urea cycle.

See also

External links

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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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