Discovery of 10466-61-2

When you point to this article, it is believed that you are also very interested in this compound(10466-61-2)HPLC of Formula: 10466-61-2 and due to space limitations, I can only present the most important information.

The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《The specificity of leucine aminopeptidase》. Authors are Smith, Emil L.; Slonim, N. Balfour.The article about the compound:H-Leu-NH2.HClcas:10466-61-2,SMILESS:N[C@@H](CC(C)C)C(N)=O.[H]Cl).HPLC of Formula: 10466-61-2. Through the article, more information about this compound (cas:10466-61-2) is conveyed.

A highly purified preparation of leucine aminopeptidase (I) from hog intestinal mucosa, activated by Mn++ or Mg++, was found to hydrolyze only a single peptide bond of glycyl-L-leucinamide. The purification procedure of Smith and Bergmann (C.A. 38, 4965.7) was supplemented by precipitation with 33% acetone at room temperature followed by dialysis and removal of precipitate Since glycyl-L-leucine is not hydrolyzed by I, hydrolysis is thought to occur at the terminal peptide bond. I is devoid of endopeptidase activity. Compounds with free NH2 groups, such as L-leucyl-L-glutamic acid and L-glutamyl-L-leucinamide, are readily hydrolyzed, the latter compound only at one peptide bond. L-Leucylglycylglycine and L-leucylglycine are hydrolyzed most rapidly, whereas L-leucyl-L-glutamic acid is acted upon more slowly. Glycylglycyl-DL-leucylglycine is hydrolyzed very slowly. It is pointed out that in view of these findings the concept of the aminoexopeptidase must be amended to the extent that the free NH2 group need not be present on the amino acid residue which possesses the sensitive peptide bond. The synthesis of a number of aminopeptidase substrates is described. A simple synthesis for L-leucinamide-HCl by amidation of L-leucine methyl ester-HCl is reported. Glycyl-L-leucinamide-HCl ([α]26D = -19.0° (5% solution in water)) was synthesized from carbobenzoxyglycyl-L-leucine methyl ester. Syntheses for L-glutamyl-L-leucinamide ([α]27D = +6.7° (2.1% in water)) from carbobenzoxy-L-glutamyl anhydride and L-leucine methyl ester and for L-leucyl-L-glutamic acid ([α]24D = +10.5° (2% in M HCl)) from carbobenzoxy-L-leucine hydrazide are reported.

When you point to this article, it is believed that you are also very interested in this compound(10466-61-2)HPLC of Formula: 10466-61-2 and due to space limitations, I can only present the most important information.

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare