Benzyloxycarbonyl-L-phenylalanyl-L-tyrosine

<strong>Benzyloxycarbonyl-L-phenylalanyl-L-tyrosine</strong> <strong>Catalog number:</strong> MDP0061 <strong>CAS Number: </strong>113866-00-5 <strong>Sequence: </strong>Benzyloxycarbonyl-L-phenylalanyl-L-tyrosine <strong>Amount:</strong> 100 mg <strong>Molecular Weight:</strong> 462.4 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: 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. 2: Isobe K. Enzymes responsible for metabolism of Nα-benzyloxycarbonyl-L-lysine in microorganisms N Biotechnol. 2010 Dec 31;27(6):751-4. 3: 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. 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: 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. 6: Rodríguez-Hernández J, Gatti M, Klok HA. Highly branched poly(L-lysine) Biomacromolecules. 2003 Mar-Apr;4(2):249-58. 7: 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. 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: 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. <a href="https://pubmed.ncbi.nlm.nih.gov/17964487">10: Isobe K, Nagasawa S. Characterization of Nalpha-benzyloxycarbonyl-L-lysine oxidizing enzyme from Rhodococcus sp. AIU Z-35-1 J Biosci Bioeng. 2007 Sep;104(3):218-23. </a> <br><strong>Products Related to Benzyloxycarbonyl-L-phenylalanyl-L-tyrosine can be found at</strong> <a href="https://moleculardepot.com/product-category/Peptides/"> Peptides</a>