N-Acetyl-D-glutamine

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N-Acetyl-D-glutamine
Category Others
Catalog number BBF-05690
CAS 161579-61-9
Molecular Weight 188.18
Molecular Formula C7H12N2O4
Purity ≥95% by HPLC

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Description

N-Acetyl-D-glutamine is a pivotal biomedical formulation, serving as a crucial precursor to the vital antioxidant glutathione. It efficaciously aids in the research of hepatic disorders, immune system dysregulation and afflictions pertaining to the gastrointestinal tract.

Specification

Synonyms Ac-D-Gln-OH; N(2)-acetyl-D-glutamine; (R)-2-Acetamido-5-amino-5-oxopentanoic acid; acetyl-D-glutamine; acetyl-D-glutamine
Storage Store at -20°C
IUPAC Name (2R)-2-acetamido-5-amino-5-oxopentanoic acid
Canonical SMILES CC(=O)NC(CCC(=O)N)C(=O)O
InChI InChI=1S/C7H12N2O4/c1-4(10)9-5(7(12)13)2-3-6(8)11/h5H,2-3H2,1H3,(H2,8,11)(H,9,10)(H,12,13)/t5-/m1/s1
InChI Key KSMRODHGGIIXDV-RXMQYKEDSA-N

Properties

Appearance White to Off-white Solid
Boiling Point 604.9±50.0°C at 760 mmHg
Density 1.3±0.1 g/cm3

Reference Reading

1. Enantioseparation of N-acetyl-glutamine enantiomers by LC-MS/MS and its application to a plasma protein binding study
Lei Gao, Yunwen Xue, Zunjian Zhang, Yuan Tian Biomed Chromatogr . 2019 Sep;33(9):e4559. doi: 10.1002/bmc.4559.
A novel chiral method was developed and validated to determine N-acetyl-glutamine (NAG) enantiomers by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Enantioseparation was achieved on a Chiralpak QD-AX column (150 × 4.6 mm i.d., 5 μm) using methanol-water (50 mm ammonium formate, pH 4.3; 70:30, v/v) at a flow rate of 500 μL/min. The detection was operated with an electrospray ionization source interface in positive mode. The ion transition for NAG enantiomers was m/z 189.0 → 130.0. The retention time of N-acetyl-l-glutamine and N-acetyl-d-glutamine were 15.2 and 17.0 min, respectively. Calibration curves were linear over the range of 0.02-20 μg/mL with r > 0.99. The deviation of accuracy and the coefficient of variation of within-run and between-run precision were within 10% for both enantiomers, except for the lower limit of quantification (20 ng/mL), where they deviated 88% and no obvious matrix effect was observed. This method was successfully applied to investigate the plasma protein binding of NAG enantiomers in rats. The results showed that the plasma protein binding of NAG enantiomers was stereoselective. The assay method also exhibited good application prospects for the clinical monitoring of free drugs in plasma.

Bio Calculators

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* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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