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Merck
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Key Documents

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A0878

Sigma-Aldrich

Ala-Gly

≥99% (TLC)

Sinónimos:

L-Alanyl-glycine

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About This Item

Fórmula lineal:
CH3CH(NH2)CONHCH2COOH
Número de CAS:
687-69-4
Peso molecular:
146.14
Beilstein/REAXYS Number:
1723438
EC Number:
211-699-9
MDL number:
MFCD00065107
UNSPSC Code:
12352209
PubChem Substance ID:
24890462
NACRES:
NA.26

product name

Ala-Gly,

assay

≥99% (TLC)

Quality Level

200

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Phe-Ala

Sigma-Aldrich

P3251

Phe-Ala

Gly-Sar

Sigma-Aldrich

G3127

Gly-Sar

Cys-Gly ≥85% (TLC)

Sigma-Aldrich

C0166

Cys-Gly

D-Ala-D-Ala

Sigma-Aldrich

A0912

D-Ala-D-Ala

2-Pyrrolidone-5-carboxylic acid 99%

Sigma-Aldrich

292915

2-Pyrrolidone-5-carboxylic acid

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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