50170
Gly-Asp
≥99.0%
Sinonimo/i:
Glycyl-L-aspartic acid
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About This Item
Formula condensata:
NH2CH2CONHCH(COOH)CH2COOH
Numero CAS:
Peso molecolare:
190.15
Beilstein:
1727387
Numero CE:
Numero MDL:
Codice UNSPSC:
12352209
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
≥99.0%
Attività ottica
[α]20/D +12.0±2°, c = 5% in H2O
Impiego in reazioni chimiche
reaction type: solution phase peptide synthesis
Punto di fusione
195-210 °C (dec.)
applicazioni
peptide synthesis
Stringa SMILE
NCC(=O)N[C@@H](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)/t3-/m0/s1
SCCPDJAQCXWPTF-VKHMYHEASA-N
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
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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Florian Rohm et al.
Molecular nutrition & food research, 63(5), e1801094-e1801094 (2018-12-07)
Peptide transporter 1 (PEPT1) function is well understood, yet little is known about its contribution toward the absorption of dietary amino acids in the form of di- and tripeptides. In the present human study, changes in plasma concentrations of a
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
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