Benzoylglycyl-L-lysine

<strong>Benzoylglycyl-L-lysine</strong> <strong>Catalog number:</strong> MDP0063 <strong>CAS Number: </strong>109358-46-5 <strong>Sequence: </strong>Benzoylglycyl-L-lysine <strong>Amount:</strong> 100 mg <strong>Molecular Weight:</strong> 307.2 g/mol <strong>Supplied as:</strong> Powder <strong>Applications:</strong> molecular tool for various biochemical applications <strong>Storage:</strong> -20 °C <strong>WARNING:</strong> For in vitro Research Use Only. NOT for use on humans or animals. <strong>Grade:</strong> Biotechnology grade. All products are highly pure. <strong>References:</strong> 1: Moore GJ, Benoiton NL. Effect of Nepsilon-alkylation of the substrate on the hydrolysis of benzoylglycyl-L-lysine by carboxypeptidase B1 Can J Biochem. 1975 Nov;53(11):1145-9. 2: Kamgang Nzekoue F, Henle T, Caprioli G, Sagratini G, Hellwig M. Food Protein Sterylation: Chemical Reactions between Reactive Amino Acids and Sterol Oxidation Products under Food Processing Conditions Foods. 2020 Dec 17;9(12):1882. 3: Shimozu Y, Hirano K, Shibata T, Shibata N, Uchida K. 4-Hydroperoxy-2-nonenal is not just an intermediate but a reactive molecule that covalently modifies proteins to generate unique intramolecular oxidation products J Biol Chem. 2011 Aug 19;286(33):29313-29324. 4: Puttaiah S, Zhang Y, Pilch HA, Pfahler C, Oya-Ito T, Sayre LM, Nagaraj RH. Detection of dideoxyosone intermediates of glycation using a monoclonal antibody: characterization of major epitope structures Arch Biochem Biophys. 2006 Feb 15;446(2):186-96. 5: Globisch M, Schindler M, Kreßler J, Henle T. Studies on the reaction of trans-2-heptenal with peanut proteins J Agric Food Chem. 2014 Aug 20;62(33):8500-7. 6: Moore GJ, Benoiton NL. Effect of the basic amino-acid side chain length and the penultimate residue on the hydrolysis of benzoldipeptides by carboxypeptidase B Can J Biochem. 1978 May;56(5):315-8. 7: Itakura K, Uchida K. Reaction of N(alpha)-hippuryllysine with 2-hydroxyheptanal: a model for lysine-directed protein modifications by lipid peroxidation Chem Phys Lipids. 2003 Jul;124(2):81-8. 8: Baudin B, Giboudeau J. Carboxypeptidase A hydrolyses benzoylglycyl-histidyl-leucine but not furylacryloyl-phenylalanyl-glycyl-glycine, two usual substrates for angiotensin I-converting enzyme Enzyme Protein. 1994-1995;48(2):81-9. 9: Ishino K, Shibata T, Ishii T, Liu YT, Toyokuni S, Zhu X, Sayre LM, Uchida K. Protein N-acylation: H2O2-mediated covalent modification of protein by lipid peroxidation-derived saturated aldehydes Chem Res Toxicol. 2008 Jun;21(6):1261-70. <a href="https://pubmed.ncbi.nlm.nih.gov/12675602">10: Tardioli PW, Fernández-Lafuente R, Guisán JM, Giordano RL. Design of new immobilized-stabilized carboxypeptidase a derivative for production of aromatic free hydrolysates of proteins Biotechnol Prog. 2003 Mar-Apr;19(2):565-74. </a> <br><strong>Products Related to Benzoylglycyl-L-lysine can be found at</strong> <a href="https://moleculardepot.com/product-category/Peptides/"> Peptides</a>