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A4625

Sigma-Aldrich

N-Acetyl-L-alanine

~99%

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About This Item

Formule empirique (notation de Hill):
C5H9NO3
Numéro CAS:
97-69-8
Poids moléculaire :
131.13
Numéro CE :
202-602-0
Numéro MDL:
MFCD00063132
Code UNSPSC :
12352209
eCl@ss :
32160406
ID de substance PubChem :
24890887
Nomenclature NACRES :
NA.26

product name

N-Acetyl-L-alanine, ~99%

Pureté

~99%

Forme

powder

Couleur

white to off-white

Application(s)

cell analysis

Température de stockage

2-8°C

Chaîne SMILES 

C[C@H](NC(C)=O)C(O)=O

InChI

1S/C5H9NO3/c1-3(5(8)9)6-4(2)7/h3H,1-2H3,(H,6,7)(H,8,9)/t3-/m0/s1

Clé InChI

KTHDTJVBEPMMGL-VKHMYHEASA-N

Application

N-Acetyl-L-alanine has been used to study its effect on cytosolic and mitochondrial reduction-oxidation sensitive green fluorescent protein (roGFP).

Actions biochimiques/physiologiques

N-Acetyl-L-alanine may be used with other L-aminoacylated amino acids as a substrate for the identification, differentiation and characterization of aminoacylase(s)/amidohydrolase(s).

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

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Abnormalities in the white matter of the brain may occur in individuals with schizophrenia as well as with normal aging. Therefore, elderly schizophrenic patients may suffer further cognitive decline as they age. This study determined whether elderly schizophrenia participants, especially
Bram Boeckx et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 86, 366-374 (2011-11-18)
The conformational landscape of N-acetylalanine has been investigated by a theoretical and matrix-isolation FT-IR study. Optimizations of N-acetylalanine structures has been conducted at successive higher levels of theory HF/3-21G, DFT(B3LYP)/6-31++G** and MP2/6-31++G**. This resulted in three stable conformations. Among these
Eiko Suzuki et al.
European journal of drug metabolism and pharmacokinetics, 42(6), 965-972 (2017-04-28)
Human in vitro and dog in vitro/in vivo researches indicate that the drug-drug interaction (DDI) of decreased plasma valproic acid (VPA) concentration by co-administration of carbapenem antibiotics is caused by inhibition of acylpeptide hydrolase (APEH)-mediated VPA acylglucuronide (VPA-G) hydrolysis by
S Mori et al.
Journal of biomolecular NMR, 7(1), 77-82 (1996-01-01)
A technique for separating intramolecular NOE and solvent-proton exchange peaks in exchange spectroscopy is demonstrated. This method utilizes the large differences in relaxation and coupling properties of water and macromolecules to separate the two effects. The spin-echo filter consists of
Improved sensitivity of HSQC spectra of exchanging protons at short interscan delays using a new fast HSQC (FHSQC) detection scheme that avoids water saturation.
S Mori et al.
Journal of magnetic resonance. Series B, 108(1), 94-98 (1995-07-01)
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