Benzyloxycarbonylglycyl-L-phenylalanine amide


Catalog Number: MDP0035 (100 mg)
Benzyloxycarbonylglycyl-L-phenylalanine amide is a high quality Benzyloxycarbonylglycyl-L-phenylalanine amide. 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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Benzyloxycarbonylglycyl-L-phenylalanine amide
Catalog number: MDP0035
CAS Number: 73167-84-7
Sequence: Benzyloxycarbonylglycyl-L-phenylalanine amide
Amount: 100 mg
Molecular Weight: 355.2 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.

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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.
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.

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Additional information

Weight 48 oz
Dimensions 8 × 8 × 8 in

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