G9003
D-Glutamine
≥98% (HPLC)
Sinonimo/i:
D-2-Aminoglutaramic acid, D-Glutamic acid 5-amide
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About This Item
Formula empirica (notazione di Hill):
C5H10N2O3
Numero CAS:
Peso molecolare:
146.14
Beilstein:
1723796
Numero MDL:
Codice UNSPSC:
12352209
ID PubChem:
NACRES:
NA.32
Prodotti consigliati
product name
D-Glutamine, ≥98% (HPLC)
Saggio
≥98% (HPLC)
Forma fisica
powder
Colore
white
applicazioni
cell analysis
Stringa SMILE
N[C@H](CCC(N)=O)C(O)=O
InChI
1S/C5H10N2O3/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H2,7,8)(H,9,10)/t3-/m1/s1
ZDXPYRJPNDTMRX-GSVOUGTGSA-N
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Descrizione generale
Glutamine is a non-essential and the most abundant free amino acid present in the human body. It is an important component of proteins and is one of the 20 proteinogenic amino acids. It forms 5-6% of bound amino acids.
Applicazioni
D-Glutamine has been used to study its role in conferring protection against acetaldehyde-induced disruption of barrier function in Caco-2 cell monolayer.
Azioni biochim/fisiol
Glutamine forms the central metabolite in amino acid transamination via a-ketoglutarate and glutamic acid. This amino acid is metabolized by different enzymes, such as glutaminase, present in liver, and glutamine synthetase, present in skeletal muscle. It is produced in the cytoplasm from other amino acids, predominantly from branched-chain amino acids and glutamate. It plays an essential role in ammonia metabolism and detoxification. Its skeletal muscle levels are significantly reduced post trauma, operation and inflammatory states. It servers as a prognostic marker in fatal sepsis during which its skeletal muscle levels are decreased by 90%.
Altre note
Unnatural isomer of glutamine
Applicazioni
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
Certificati d'analisi (COA)
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Chromatograms
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