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Kluczowe dokumenty
G9003
D-Glutamine
≥98% (HPLC)
Synonim(y):
D-2-Aminoglutaramic acid, D-Glutamic acid 5-amide
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About This Item
Wzór empiryczny (zapis Hilla):
C5H10N2O3
Numer CAS:
Masa cząsteczkowa:
146.14
Beilstein:
1723796
Numer MDL:
Kod UNSPSC:
12352209
Identyfikator substancji w PubChem:
NACRES:
NA.32
Polecane produkty
Nazwa produktu
D-Glutamine, ≥98% (HPLC)
Poziom jakości
Próba
≥98% (HPLC)
Formularz
powder
kolor
white
Zastosowanie
cell analysis
ciąg SMILES
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
Klucz InChI
ZDXPYRJPNDTMRX-GSVOUGTGSA-N
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Opis ogólny
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.
Zastosowanie
D-Glutamine has been used to study its role in conferring protection against acetaldehyde-induced disruption of barrier function in Caco-2 cell monolayer.
Działania biochem./fizjol.
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%.
Inne uwagi
Unnatural isomer of glutamine
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Kod klasy składowania
11 - Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 3
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Środki ochrony indywidualnej
Eyeshields, Gloves, type N95 (US)
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Chromatograms
application for HPLCapplication for HPLCNasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.
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