02676
N-Methyl-L-alanine
≥98.0% (TLC)
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About This Item
Empirical Formula (Hill Notation):
C4H9NO2
CAS Number:
Molecular Weight:
103.12
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
1720922
InChI
1S/C4H9NO2/c1-3(5-2)4(6)7/h3,5H,1-2H3,(H,6,7)/t3-/m0/s1
SMILES string
CN[C@@H](C)C(O)=O
InChI key
GDFAOVXKHJXLEI-VKHMYHEASA-N
assay
≥98.0% (TLC)
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
color
colorless to white
application(s)
peptide synthesis
Quality Level
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Y Nishina et al.
Journal of biochemistry, 99(2), 329-337 (1986-02-01)
Resonance Raman (RR) spectra were obtained for the purple complexes of D-amino acid oxidase (DAO) with D-lysine or N-methylalanine. RR spectra of a complex of oxidized DAO with the oxidation product of D-lysine or D-proline were also measured. The isotope
Zarixia Zavala-Ruiz et al.
The Journal of biological chemistry, 278(45), 44904-44912 (2003-09-04)
Crystal structures of the class II major histocompatibilty complex (MHC) protein, HLA-DR1, generally show a tight fit between MHC and bound peptide except in the P6/P7 region of the peptide-binding site. In this region, there is a shallow water-filled pocket
G Yadid et al.
Neuroscience, 55(4), 1147-1152 (1993-08-01)
[3H]Glycine is actively taken up into bovine isolated adrenal medulla chromaffin cells with the subsequent catecholamine release. [3H]Glycine uptake has two interaction sites based on relative Km measurements. These sites are inherently distinct since the effects of strychnine and temperature
D Gazis et al.
International journal of peptide and protein research, 23(1), 78-83 (1984-01-01)
Substituting sarcosine or N-methylalanine for proline in the inhibitory vasopressin analogs dPAVP and d(CH2)5AVP had the following effects: 1) milk ejection and antidiuretic activities were severely depressed, 2) pressor antagonism was maintained but weakened somewhat, and 3) antagonism in the
Z Grzonka et al.
International journal of peptide and protein research, 25(4), 375-381 (1985-04-01)
The 600 MHz proton n.m.r. spectra of (sarcosyl7)-oxytocin and (N-methylalanyl7) oxytocin in 2H2O solution have been recorded and completely assigned. In each case the spectrum indicates the presence of two slowly interconverting conformers, which are the cis-trans isomers about the
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