Catalog Number: MDP0177 (20 mg)
Benzyloxycarbonyl-L-phenylalanyl-L-tyrosyl-L-leucine is a high quality Benzyloxycarbonyl-L-phenylalanyl-L-tyrosyl-L-leucine. 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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SKU: MDP0177 Categories: , Tag:


Catalog number: MDP0177
CAS Number: 149697-16-5
Sequence: Benzyloxycarbonyl-L-phenylalanyl-L-tyrosyl-L-leucine
Amount: 20 mg
Molecular Weight: 575.6 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: Woo JT, Yamaguchi K, Hayama T, Kobori T, Sigeizumi S, Sugimoto K, Kondo K, Tsuji T, Ohba Y, Tagami K, Sumitani K. Suppressive effect of N-(benzyloxycarbonyl)-L-phenylalanyl-L-tyrosinal on bone resorption in vitro and in vivo Eur J Pharmacol. 1996 Apr 4;300(1-2):131-5.
2: Mazzarella L, Schön I, Sica F, Zagari A. N-benzyloxycarbonyl-L-aminosuccinyl-L-phenylalaninamide (Z-L-Asu-L-Phe-NH2) Acta Crystallogr C. 1988 May 15;44 ( Pt 5):880-2.
3: Isobe K. Enzymes responsible for metabolism of Nα-benzyloxycarbonyl-L-lysine in microorganisms N Biotechnol. 2010 Dec 31;27(6):751-4.
4: Isobe K, Fukuda N, Nagasawa S. Analysis of selective production of Nalpha-benzyloxycarbonyl-L-aminoadipate-delta-semialdehyde and Nalpha-benzyloxycarbonyl-L-aminoadipic acid by Rhodococcus sp. AIU Z-35-1 J Biosci Bioeng. 2008 Feb;105(2):152-6.
5: Rodríguez-Hernández J, Gatti M, Klok HA. Highly branched poly(L-lysine) Biomacromolecules. 2003 Mar-Apr;4(2):249-58.
6: Gessmann R, Brückner H, Petratos K. The peptide Z-Aib-Aib-Aib-L-Ala-OtBu Acta Crystallogr C Struct Chem. 2014 Apr;70(Pt 4):405-7.
7: Shang Z, Qi S, Tao X, Zhang G. Methyl 2-(2-{[(benz-yloxy)carbon-yl]amino}-propan-2-yl)-5-hy-droxy-6-meth-oxy-pyrimidine-4-carboxyl-ate Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 1;67(Pt 6):o1335.
8: Wharton CW. The structure and mechanism of stem bromelain. Evaluation of the homogeneity of purified stem bromelain, determination of the molecular weight and kinetic analysis of the bromelain-catalysed hydrolysis of N-benzyloxycarbonyl-L-phenylalanyl-L-serine methyl ester Biochem J. 1974 Dec;143(3):575-86.
9: Isobe K, Ishikura K, Shimizu S. Identification and characterization of enzyme catalyzing conversion of N(alpha)-benzyloxycarbonyl-L-aminoadipic-delta-semialdehyde to N(alpha)-benzyloxycarbonyl-L-aminoadipic acid in Aspergillus niger AKU 3302 J Biosci Bioeng. 2008 Oct;106(4):409-11.
10: Nakanishi K, Matsuno R. Kinetics of enzymatic synthesis of peptides in aqueous/organic biphasic systems. Thermolysin-catalyzed synthesis of N-(benzyloxycarbonyl)-L-phenylalanyl-L-phenylalanine methyl ester Eur J Biochem. 1986 Dec 15;161(3):533-40.

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