Catalog Number: MDP0110 (20 mg)
Glycylglycyl-L-histidine is a high quality Glycylglycyl-L-histidine. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Catalog number: MDP0110
CAS Number: 149231-65-2
Sequence: Glycylglycyl-L-histidine
Amount: 20 mg
Molecular Weight: 269.2 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20 °C
WARNING: For in vitro Research Use Only. NOT for use on humans or animals.
Grade: Biotechnology grade. All products are highly pure.

1: Hay RW, Hassan MM, You-Quan C. Kinetic and thermodynamic studies of the copper (II) and nickel(II) complexes of glycylglycyl-L-histidine J Inorg Biochem. 1993 Oct 1;52(1):17-25.
2: Wong LF, Cooper JC, Margerum DW. Kinetics of copper(II)–glycylglycyl-L-histidine reactions. Acid decomposition and proton-assisted nucleophilic displacement by triethylenetetramine J Am Chem Soc. 1976 Nov 10;98(23):7268-74.
3: Inoue S, Kawanishi S. ESR evidence for superoxide, hydroxyl radicals and singlet oxygen produced from hydrogen peroxide and nickel(II) complex of glycylglycyl-L-histidine Biochem Biophys Res Commun. 1989 Mar 15;159(2):445-51.
4: Cutler AC, Brittain T, Boyd PD. A spectroscopic and electrochemical study of the interaction between copper (II) glycylglycyl-L-histidine-N-methylamide and iron (III) tetra-p-sulfophenylporphine J Inorg Biochem. 1985 Jul;24(3):199-209.
5: Cooper JC, Wong LF, Venezky DL, Margerum DW. Letter: Ligand displacement of glycylglycyl-L-histidine from its copper (II) complex. A proton-assisted mechanism initiated at a nonterminal position J Am Chem Soc. 1974 Nov 27;96(24):7560-2.
6: de Meester P, Hodgson DJ. Oxidative decarboxylation of a tripeptide. The reaction of copper(II) hydroxide and glycylglycyl-L-histidine J Am Chem Soc. 1976 Oct 27;98(22):7086-7.
7: Ueda J, Saito N, Ozawa T. Detection of free radicals produced from reactions of lipid hydroperoxide model compounds with Cu(II) complexes by ESR spectroscopy Arch Biochem Biophys. 1996 Jan 1;325(1):65-76.
8: Brown KC, Kodadek T. Protein cross-linking mediated by metal ion complexes Met Ions Biol Syst. 2001;38:351-84.
9: Shi X, Dalal NS, Kasprzak KS. Generation of free radicals from lipid hydroperoxides by Ni2+ in the presence of oligopeptides Arch Biochem Biophys. 1992 Nov 15;299(1):154-62.
10: Guo Y, Stroka JR, Kandemir B, Dickerson CE, Bren KL. Cobalt Metallopeptide Electrocatalyst for the Selective Reduction of Nitrite to Ammonium J Am Chem Soc. 2018 Dec 12;140(49):16888-16892.

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