Benzyloxycarbonylglycyl-L-prolyl-L-leucine

<strong>Benzyloxycarbonylglycyl-L-prolyl-L-leucine</strong> <strong>Catalog number:</strong> MDP0056 <strong>CAS Number: </strong>113865-85-3 <strong>Sequence: </strong>Benzyloxycarbonylglycyl-L-prolyl-L-leucine <strong>Amount:</strong> 10 mg <strong>Molecular Weight:</strong> 419.2 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: Friedman TC, Orlowski M, Wilk S. Prolyl endopeptidase: inhibition in vivo by N-benzyloxycarbonyl-prolyl-prolinal J Neurochem. 1984 Jan;42(1):237-41. 2: Wolf DH, Ehmann C. Carboxypeptidase S- and carboxypeptidase Y-deficient mutants of Saccharomyces cerevisiae J Bacteriol. 1981 Aug;147(2):418-26. 3: Steinauer R, Chen FM, Benoiton NL. Studies on racemization associated with the use of benzotriazol-1-yl-tris (dimethylamino)phosphonium hexafluorophosphate (BOP) Int J Pept Protein Res. 1989 Oct;34(4):295-8. 4: Benoiton NL, Kuroda K. Studies on racemization during couplings using a series of model tripeptides involving activated residues with unfunctionalized side chains Int J Pept Protein Res. 1981 Feb;17(2):197-204. 5: Alecio MR, Dann ML, Lowe G. The specificity of the S1' subsite of papain Biochem J. 1974 Aug;141(2):495-501. 6: Seber JF, Toomey TP, Powell JT, Brew K, Awad WM Jr. Proteolytic enzymes of the K-1 strain of Streptomyces griseus obtained from a commercial preparation (Pronase). Purification and characterization of the carboxypeptidase J Biol Chem. 1976 Jan 10;251(1):204-8. 7: Gray CJ, Barker SA, Dhariwal MS, Sullivan JM. Assay of the high-alkaline proteinase from alkalophilic bacillus PB92 using a chromogenic tripeptide substrate Biotechnol Bioeng. 1985 Dec;27(12):1717-20. 8: Whitaker JR. Kinetics of the carboxypeptidase A-catalyzed hydrolysis of benzyloxycarbonylglycyl-L-phenylalanine Biochem Biophys Res Commun. 1966 Jan 4;22(1):6-12. 9: Leytus SP, Patterson WL, Mangel WF. New class of sensitive and selective fluorogenic substrates for serine proteinases. Amino acid and dipeptide derivatives of rhodamine Biochem J. 1983 Nov 1;215(2):253-60. <a href="https://pubmed.ncbi.nlm.nih.gov/939322">10: Tomatis R, Ferroni R, Guarneri M, Benassi CA. [Use of oximinoiminopyrrazoline esters in the synthesis of solids phase peptides: synthesis of bradykinin] Farmaco Sci. 1976 Jan;31(1):70-9.</a> <br><strong>Products Related to Benzyloxycarbonylglycyl-L-prolyl-L-leucine can be found at</strong> <a href="https://moleculardepot.com/product-category/Peptides/"> Peptides</a>