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G2754

Sigma-Aldrich

Gly-DL-Asp

≥98%, suitable for electrophoresis

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About This Item

Formula empirica (notazione di Hill):
C6H10N2O5
Numero CAS:
79731-35-4
Peso molecolare:
190.15
Numero MDL:
MFCD00066049
Codice UNSPSC:
12352202
ID PubChem:
24895102
NACRES:
NA.26

product name

Gly-DL-Asp,

Saggio

≥98%

Livello qualitativo

200

Forma fisica

powder

tecniche

electrophoresis: suitable

Colore

white

Temperatura di conservazione

−20°C

Stringa SMILE

NCC(=O)NC(CC(O)=O)C(O)=O

InChI

1S/C6H10N2O5/c7-2-4(9)8-3(6(12)13)1-5(10)11/h3H,1-2,7H2,(H,8,9)(H,10,11)(H,12,13)
SCCPDJAQCXWPTF-UHFFFAOYSA-N

Informazioni sul gene

human ... SLC15A1(6564)

Applicazioni

Glycyl dipeptides such as glycyl-L-aspartate are useful as model compounds for the development of chiral separation technologies such as chiral ligand-exchange capillary electrophoresis and capillary electrochromatography (CEC).

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

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E C O'Brien et al.
Journal of inorganic biochemistry, 77(3-4), 135-139 (2000-03-04)
The first solution studies at physiological pH for the formation of metal complexes of taurine, +NH3CH2CH2S03-, one of the most abundant low molecular weight organic compounds in the animal kingdom, are reported. The complexes Cu(Gly-GlyH-1) (1) and [Cu(Gly-AspH-1)] (2) react
R Kaul et al.
Journal of neurochemistry, 56(1), 129-135 (1991-01-01)
Canavan disease, an autosomal recessive disorder, is characterized biochemically by N-acetylaspartic aciduria and aspartoacylase (N-acyl-L-aspartate amidohydrolase; EC 3.5.1.15) deficiency. However, the role of aspartoacylase and N-acetylaspartic acid in brain metabolism is unknown. Aspartoacylase has been purified to apparent homogeneity with
R Chitra et al.
Acta crystallographica. Section C, Crystal structure communications, 63(Pt 1), o11-o13 (2007-01-09)
The title bis(glycyl-L-aspartic acid) oxalate complex {systematic name: bis[2-(2-ammonioacetamido)butanedioic acid] oxalate 0.4-hydrate}, 2C6H11N2O5+.C2O4(2-).4H2O, crystallizes in a triclinic space group with the planar peptide unit in a trans conformation. The asymmetric unit consists of two glycyl-L-aspartic acid molecules with positively charged
D S Eggleston et al.
International journal of peptide and protein research, 19(2), 206-211 (1982-02-01)
The crystal structure of the acidic dipeptide glycyl-L-aspartic acid dihydrate, Gly-L-Asp X 2H2O, C6H10N2O5 X 2H2O, has been determined by means of three-dimensional counter X-ray data. The dipeptide crystallizes in space group P212121 of the orthorhombic system with four formula
Christina Gatschelhofer et al.
Journal of biochemical and biophysical methods, 69(1-2), 67-77 (2006-03-25)
Novel particle-loaded monolithic capillary electrochromatography (CEC) phases for chiral separations were prepared via ring-opening metathesis polymerization (ROMP) within the confines of fused silica columns with 200 microm i.d. using norborn-2-ene (NBE), 1,4,4a,5,8,8a-hexahydro-1,4,5,8,exo,endo-dimethanonaphthalene (DMN-H6) as monomers, 2-propanol and toluene as porogens
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