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About This Item
Linear Formula:
CH3CH(NH2)CONHCH2COOH
CAS Number:
Molecular Weight:
146.14
Beilstein:
1723438
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
Recommended Products
product name
Ala-Gly,
Assay
≥99% (TLC)
form
powder
color
white
storage temp.
−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
InChI key
CXISPYVYMQWFLE-VKHMYHEASA-N
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Biochem/physiol Actions
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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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
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)
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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