A0878
Ala-Gly
≥99% (TLC)
Synonym(s):
L-Alanyl-glycine
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1 G
1 090,00 kr
About This Item
Linear Formula:
CH3CH(NH2)CONHCH2COOH
CAS Number:
Molecular Weight:
146.14
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
211-699-9
MDL number:
Beilstein/REAXYS Number:
1723438
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Product Name
Ala-Gly,
InChI key
CXISPYVYMQWFLE-VKHMYHEASA-N
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
SMILES string
C[C@H](N)C(=O)NCC(O)=O
assay
≥99% (TLC)
form
powder
color
white
storage temp.
−20°C
Quality Level
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Related Categories
1 of 4
This Item | G3882 | P3501 | C6154 |
|---|---|---|---|
| form powder | form powder | form powder | form powder |
| assay ≥99% (TLC) | assay ≥98% (TLC) | assay ≥99% | assay - |
| storage temp. −20°C | storage temp. −20°C | storage temp. −20°C | storage temp. −20°C |
| color white | color white to off-white | color white | color - |
| Quality Level 200 | Quality Level 200 | Quality Level 100 | 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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_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
C J Gray et al.
Biomedical peptides, proteins & nucleic acids : structure, synthesis & biological activity, 2(1), 13-18 (1996-01-01)
The methodology for the incorporation of azaamino-acid residues into peptides synthesised by a solid-phase method has been extended to allow azaalanine peptides to be prepared. In this way, Ac-Leu-Ser-Gly-azaAla-Gly-Phe-Ser-Leu-NH2 H-Ala-Ala-Lys-Glu-Ala-Ala-Glu-Ala -Ala-Glu-Lys-Ala-azaAla-Glu-Leu-Ala-Leu-N2H3, and H-Ala-azaAla-Lys-Glu-Ala-Ala-Glu-Ala-Ala-Glu-Lys-Ala-Ala-Glu-Leu-A la-Leu-N2H3 have been prepared. A new analogue
C L Welch et al.
The Journal of membrane biology, 54(1), 39-50 (1980-01-01)
Isolated renal brush border microvilli vesicles were employed to study the uptake of radiolabel from L-Ala. [3H]Gly and D-Ala.[3H]Gly as well as to determine the presence of dipeptidase activity. Microvilli vesicles were prepared from porcine kidney cortex by differential centrifugation
Gregory A Barding et al.
Journal of proteome research, 12(2), 898-909 (2012-12-05)
Natural disasters such as drought, extreme temperatures, and flooding can severely impact crop production. Understanding the metabolic response of crops threatened with these disasters provides insights into biological response mechanisms that can influence survival. In this study, a comparative analysis
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