L-Lysine 4-methylcoumaryl-7-amide

CAT:
952-MDP0179
Size:
1 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
L-Lysine 4-methylcoumaryl-7-amide - image 1

L-Lysine 4-methylcoumaryl-7-amide

  • Description:

    L-Lysine 4-methylcoumaryl-7-amide Catalog number: MDP0179 CAS Number: 156192-32-4 Sequence: L-Lysine 4-methylcoumaryl-7-amide Amount: 1 mg Molecular Weight: 303.2 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. References: 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.
    Products Related to L-Lysine 4-methylcoumaryl-7-amide can be found at Peptides
  • Short Description:

    Catalog Number: MDP0179 (1 mg)
  • Weight:

    0.15
  • Length:

    2
  • Width:

    0.5
  • Height:

    0.5
  • Height :

    0.5