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A0878

Sigma-Aldrich

Ala-Gly

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Synonym(s):
L-Alanyl-glycine
Linear Formula:
CH3CH(NH2)CONHCH2COOH
CAS Number:
Molecular Weight:
146.14
Beilstein:
1723438
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.26

Assay

≥99% (TLC)

Quality Level

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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1 of 4

This Item
G3882C6154A9502
Ala-Gly

Sigma-Aldrich

A0878

Ala-Gly

Gly-Gly-Gly-Gly

Sigma-Aldrich

G3882

Gly-Gly-Gly-Gly

Z-Gln-Gly γ-glutamyl donor substrate

Sigma-Aldrich

C6154

Z-Gln-Gly

Ala-Ala

Sigma-Aldrich

A9502

Ala-Ala

form

powder

form

powder

form

powder

form

powder

color

white

color

white to off-white

color

-

color

white

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

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


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Gly-Gly ≥99% (titration)

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Cys-Gly ≥85% (TLC)

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D-Ala-D-Ala

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D-Ala-D-Ala

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
E K Patterson
The Journal of biological chemistry, 264(14), 8004-8011 (1989-05-15)
Bestatin, [(2S,3R)-3-amino-2-hydroxy-4-phenyl-butanoyl]-L-leucine, a known inhibitor of aminopeptidases, is shown to be a potent linear competitive inhibitor (KI,2.7 nM) of a dipeptidase purified from Ehrlich-Lettré hyperdiploid mouse ascites tumor cells. This inhibition can be classified as "slow binding" but not as
W M Zuk et al.
Biopolymers, 28(11), 2025-2044 (1989-11-01)
The CH-stretching vibrational CD (VCD) spectra of glycyl-L-alanine, L-alanylglycine, and L-alanyl-L-alanine have been studied at neutral, high, and low pH in D2O solution. The intense positive VCD band attributed to the C alpha H stretch of the alanyl residue in
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.

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