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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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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
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
Puneet Ahuja et al.
Journal of the American Chemical Society, 131(22), 7498-7499 (2009-05-16)
We report the first observation of long-lived states (LLS) having lifetimes T(LLS) that exceed the corresponding spin-lattice relaxation times T(1) by more than a factor 6 in a protein. Slow diffusion coefficients characteristic of large biomolecules can be determined by
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
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