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M6877

Sigma-Aldrich

α-Methyl-DL-serine

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About This Item

Fórmula empírica (notación de Hill):
C4H9NO3
Número de CAS:
5424-29-3
Peso molecular:
119.12
EC Number:
226-565-5
MDL number:
MFCD00021680
UNSPSC Code:
12352200
PubChem Substance ID:
24897122
NACRES:
NA.26

assay

≥98% (TLC)

form

powder

color

white

SMILES string

CC(N)(CO)C(O)=O

InChI

1S/C4H9NO3/c1-4(5,2-6)3(7)8/h6H,2,5H2,1H3,(H,7,8)

InChI key

CDUUKBXTEOFITR-UHFFFAOYSA-N

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Biochem/physiol Actions

α-Methyl-DL-serine is an amino acid derivative.

Storage Class

13 - Non 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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I S Mendelson
Journal of mental deficiency research, 26 (Pt 2), 107-110 (1982-06-01)
An inherited defect in the glycine cleavage enzyme results in the condition of neonatal glycine encephalopathy which has not responded to the current innovative methods of therapy. A re-examination of the enzyme structure and metabolic pathways, leads us to recommend
H Mickos et al.
Acta chemica Scandinavica (Copenhagen, Denmark : 1989), 46(10), 989-993 (1992-10-01)
The three-dimensional structure of the RGD-adhesion sequence has been studied previously by means of linear and cyclic peptides. These peptides show widely differing affinities to integrins, ascribed to a strong dependence on steric factors in the receptor recognition. Insertion of
Francisco Corzana et al.
Chemical communications (Cambridge, England), 47(18), 5319-5321 (2011-04-01)
A novel Tn antigen mimic, in which the natural underlying amino acid has been replaced by the non-natural α-methylserine analogue, is reported. This derivative exhibits a similar affinity for a natural lectin as for the natural Tn and retains the
Ewa Zabłotna et al.
Biochemical and biophysical research communications, 340(3), 823-828 (2005-12-29)
In many complexes formed by serine proteinases and their inhibitors, the hydroxyl group provided by water molecule or by the inhibitor Ser residue is located close to the inhibitor P1-P1' reactive site. In order to investigate the role of this
E Altmann et al.
International journal of peptide and protein research, 32(5), 344-351 (1988-11-01)
The conformational behaviour of host-guest peptides of the type Ac-Ala-Xxx-Ala-Ala-Xxx-Ala-Ala-Xxx-Ala-Ala-NH-PEGM (Xxx = alpha-aminoisobutyric acid (Aib), (S)-2-ethylalanine ((S)-Iva), (S)-2-methylserine ((S)-alpha-MeSer)) has been studied by CD spectroscopy in CF3CH2OH, CH3OH, and water and by i.r. spectroscopy in CHCl3 and in the solid
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