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Key Documents

02676

Sigma-Aldrich

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
Beilstein/REAXYS Number:
1720922
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥98.0% (TLC)

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

color

colorless to white

application(s)

peptide synthesis

SMILES string

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

InChI

1S/C4H9NO2/c1-3(5-2)4(6)7/h3,5H,1-2H3,(H,6,7)/t3-/m0/s1

InChI key

GDFAOVXKHJXLEI-VKHMYHEASA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Zijuan Lai et al.
Nature methods, 15(1), 53-56 (2017-11-28)
Novel metabolites distinct from canonical pathways can be identified through the integration of three cheminformatics tools: BinVestigate, which queries the BinBase gas chromatography-mass spectrometry (GC-MS) metabolome database to match unknowns with biological metadata across over 110,000 samples; MS-DIAL 2.0, a
K Lakshminarayana et al.
Indian journal of experimental biology, 38(4), 373-378 (2001-02-24)
Spontaneous mutants resistant to methionine sulfoximine (Msx), methyl alanine (Mal) and methyl ammonium chloride (Mac) were derived from A. chroococcum strain A103. Msx and Mal-resistant mutants expressed 1.73 to 10.98% of the fully derepressed nitrogenase activity when grown in Burk's
Z Grzonka et al.
Journal of medicinal chemistry, 26(4), 555-559 (1983-04-01)
Eight analogues of oxytocin and arginine-vasopressin were synthesized, in which the proline residue in position 7 was replaced by either sarcosine or N-methylalanine; some of the pharmacological properties of these analogues were evaluated. In peptides containing a beta-mercaptopropionic acid residue
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
C H Tan et al.
Biochemical pharmacology, 39(5), 955-958 (1990-03-01)
Synaptosomes isolated from adult rat cerebral cortices were used for studying the uptake of L-leucine by the Na(+)-dependent route. Three non-metabolizable amino acid analogues, which had been used previously to discriminate the Na(+)-dependent A-type uptake system of animal cells, were

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