Benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucine 4-methylcoumaryl-7-amide

Product Description

Benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucine 4-methylcoumaryl-7-amide
Catalog number: MDP0225
CAS Number: N/A
Sequence: Benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucine 4-methylcoumaryl-7-amide
Amount: 1 mg
Molecular Weight: 648.4 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.

References:
1: Lu C, Li X, Xia W, Lu S, Luo H, Ye D, Zhang Y, Liu D. Poly(ε-benzyloxycarbonyl-L-lysine)-grafted branched polyethylenimine as efficient nanocarriers for indomethacin with enhanced oral bioavailability and anti-inflammatory efficacy Acta Biomater. 2017 Feb;49:434-443.
2: 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.
3: Németh K, Bugovics G, Székely JI. Antiapoptotic effect of benzyloxycarbonyl-aspartyl-(beta-tertier-butyl ester)-bromomethylketone (Z-D(OtBu)-Bmk), an intermediate of interleukin-1 beta converting enzyme inhibitors Int J Immunopharmacol. 1997 Apr;19(4):215-25.
4: Mason RW, Bartholomew LT, Hardwick BS. The use of benzyloxycarbonyl[125I]iodotyrosylalanyldiazomethane as a probe for active cysteine proteinases in human tissues Biochem J. 1989 Nov 1;263(3):945-9.
5: 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.
6: 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.
7: Rodríguez-Hernández J, Gatti M, Klok HA. Highly branched poly(L-lysine) Biomacromolecules. 2003 Mar-Apr;4(2):249-58.
8: Mitić D, Milenković M, Milosavljević S, Godevac D, Miodragović Z, Andelković K, Miodragović D. Synthesis, characterization and antimicrobial activity of Co(II), Zn(II) and Cd(II) complexes with N-benzyloxycarbonyl-S-phenylalanine Eur J Med Chem. 2009 Apr;44(4):1537-44.
9: Mackenzie NE, Malthouse JP, Scott AI. Chemical synthesis and papain-catalysed hydrolysis of N-alpha-benzyloxycarbonyl-L-lysine p-nitroanilide Biochem J. 1985 Mar 1;226(2):601-6.
10: Yanagisawa T, Hino N, Iraha F, Mukai T, Sakamoto K, Yokoyama S. Wide-range protein photo-crosslinking achieved by a genetically encoded N(ε)-(benzyloxycarbonyl)lysine derivative with a diazirinyl moiety Mol Biosyst. 2012 Apr;8(4):1131-5.

Products Related to Benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucine 4-methylcoumaryl-7-amide can be found at Peptides