Benzyloxycarbonylglycyl-L-phenylalanine amide

<strong>Benzyloxycarbonylglycyl-L-phenylalanine amide</strong> <strong>Catalog number:</strong> MDP0035 <strong>CAS Number: </strong>73167-84-7 <strong>Sequence: </strong>Benzyloxycarbonylglycyl-L-phenylalanine amide <strong>Amount:</strong> 100 mg <strong>Molecular Weight:</strong> 355.2 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: Rzeszotarska B, Karolak-Wojciechowska J, Broda MA, Gałdecki Z, Trzeźwińska B, Kozioł AE. Conformational investigation of alpha, beta-dehydropeptides. Part VI. Molecular and crystal structure of benzyloxycarbonylglycyl-(Z)-dehydrophenylalanine Int J Pept Protein Res. 1994 Oct;44(4):313-9. 2: Whitaker JR. Kinetics of the carboxypeptidase A-catalyzed hydrolysis of benzyloxycarbonylglycyl-L-phenylalanine Biochem Biophys Res Commun. 1966 Jan 4;22(1):6-12. 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: Inouye Y, Kawaguchi Y, Nakamura S. Affinity chromatography of neutral metalloendopeptidase produced by Streptomyces mauvecolor on N-benzyloxycarbonylglycyl-D-leucylaminohexyl-Sepharose Chem Pharm Bull (Tokyo). 1985 Apr;33(4):1544-51. 5: Voigt B, Wagner G. [Synthesis of N alpha-(benzoylglycyl)- and N alpha-(benzyloxycarbonylglycyl)-4-amidinophenylalanine amides as thrombin inhibitors] Pharmazie. 1985 Aug;40(8):527-9. 6: Wolf DH, Ehmann C. Carboxypeptidase S- and carboxypeptidase Y-deficient mutants of Saccharomyces cerevisiae J Bacteriol. 1981 Aug;147(2):418-26. 7: Friedman TC, Orlowski M, Wilk S. Prolyl endopeptidase: inhibition in vivo by N-benzyloxycarbonyl-prolyl-prolinal J Neurochem. 1984 Jan;42(1):237-41. 8: 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. 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/7228497">10: 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. </a> <br><strong>Products Related to Benzyloxycarbonylglycyl-L-phenylalanine amide can be found at</strong> <a href="https://moleculardepot.com/product-category/Peptides/"> Peptides</a>