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Z-Ala-Phe-Leu-Ala-NH2 is a synthetic peptide consisting of five amino acids: Alanine (Ala), Phenylalanine (Phe), Leucine (Leu), Alanine (Ala), and an amide group (NH2). The "Z" prefix indicates the presence of a carbobenzyloxy (Cbz) protecting group, which is commonly used in peptide synthesis to prevent unwanted side reactions. This peptide is of interest in the field of biochemistry and pharmaceuticals, as it can serve as a building block for larger proteins or as a model for studying peptide-protein interactions. The sequence of amino acids in Z-Ala-Phe-Leu-Ala-NH2 can influence its stability, solubility, and biological activity, making it a valuable tool for researchers in drug design and protein engineering.

87831-92-3

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87831-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87831-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,3 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87831-92:
(7*8)+(6*7)+(5*8)+(4*3)+(3*1)+(2*9)+(1*2)=173
173 % 10 = 3
So 87831-92-3 is a valid CAS Registry Number.

87831-92-3Downstream Products

87831-92-3Relevant academic research and scientific papers

Protease-catalyzed (2+2)-Segment Condensation in an Aqueous-Organic Two-phase System

Kuhl, P.,Doering, G.,Jakubke, H.-D.

, p. 371 - 372 (2007/10/02)

Tetrapeptides Z-Ala-Phe-X-Ala-NH2 can be prepared in good yields by α-chymotrypsin-catalyzed reactions of Z-Ala-Phe-OMe and X-Ala-NH2 in an aqueous-organic two-phase system using CCl4 as solvent.This method is also advantageous for the synthesis of Boc-Al

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