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A0878
Ala-Gly
≥99% (TLC)
Synonym(e):
L-Alanyl-glycin
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About This Item
Lineare Formel:
CH3CH(NH2)CONHCH2COOH
CAS-Nummer:
Molekulargewicht:
146.14
Beilstein:
1723438
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352209
PubChem Substanz-ID:
NACRES:
NA.26
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Produktbezeichnung
Ala-Gly,
Assay
≥99% (TLC)
Qualitätsniveau
Form
powder
Farbe
white
Lagertemp.
−20°C
SMILES String
C[C@H](N)C(=O)NCC(O)=O
InChI
1S/C5H10N2O3/c1-3(6)5(10)7-2-4(8)9/h3H,2,6H2,1H3,(H,7,10)(H,8,9)/t3-/m0/s1
InChIKey
CXISPYVYMQWFLE-VKHMYHEASA-N
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Biochem./physiol. Wirkung
Alanyl dipeptides such as ala-leu, ala-lys, ala-gly, ala-pro, ala-tyr and ala-phe may be used in physicochemical studies or to evaluate dipeptide separation technologies. Alanyl dipeptides may also be used for studying cell uptake mechanisms, dipeptide metabolism or cell growth supplementation benefits.
L-alanylglycine is a simple nutritional dipeptide also used for physical chemistry studies such as hydrogen bonding and heavy metal complexation.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Analysis of vibrational spectra of L-alanylglycine based on density functional theory calculations.
Padmaja L, Ravikumar C, James C, et al.
Spectrochimica Acta Part A: Molecular Spectroscopy, 71, 252-262 (2008)
Masatoshi Watabe et al.
Journal of inorganic biochemistry, 100(10), 1653-1659 (2006-07-22)
We prepared platinum(IV) complexes containing dipeptide and diimine or diamine, the [PtCl(dipeptide-N,N,O)(diimine or diamine)]Cl complex, where -N,N,O means dipeptide coordinated as a tridentate chelate, dipeptide=glycylglycine (NH(2)CH(2)CON(-)CH(2)COO(-), digly, where two protons of dipeptide are detached when the dipeptide coordinates to metal
Aurélien Bornet et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 206(1), 154-156 (2010-07-10)
The transverse relaxation rate R(2) of single quantum coherences, the relaxation rate R(LLC) of long-lived coherences (LLC), and the ratio R(2)/R(LLC) have been studied by experiment, simulation and theory in the two-spin system formed by the Glycine aliphatic protons of
Gregory A Barding et al.
Journal of proteome research, 11(1), 320-330 (2011-10-25)
Although the genetic mechanism of submergence survival for rice varieties containing the SUB1A gene has been elucidated, the downstream metabolic effects have not yet been evaluated. In this study, the metabolomes of Oryza sativa ssp. japonica cv. M202 and cv.
L Padmaja et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(1), 252-262 (2008-02-05)
FT Raman and IR spectra of the crystallized biologically active molecule, L-alanylglycine (L-Ala-Gly) have been recorded and analyzed. The equilibrium geometry, bonding features and harmonic vibrational frequencies of L-Ala-Gly have been investigated with the help of B3LYP density functional theory
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