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Z-L-Phe-L-His-L-Leu-OMe is a synthetic peptide consisting of four amino acids: phenylalanine (L-Phe), histidine (L-His), leucine (L-Leu), and a methoxy group (OMe) attached to the N-terminus. The "Z" prefix indicates the presence of a benzyloxycarbonyl (Cbz) protecting group, which is commonly used in peptide synthesis to prevent unwanted side reactions. This specific sequence of amino acids is of interest in the field of biochemistry and pharmaceuticals, as it may have potential applications in drug development, particularly in the design of peptide-based therapeutics. The protecting group and the specific arrangement of these amino acids can influence the peptide's stability, solubility, and biological activity, making it a subject of study for researchers aiming to understand and harness its properties for various applications.

26061-21-2

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26061-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26061-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,6 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26061-21:
(7*2)+(6*6)+(5*0)+(4*6)+(3*1)+(2*2)+(1*1)=82
82 % 10 = 2
So 26061-21-2 is a valid CAS Registry Number.

26061-21-2Downstream Products

26061-21-2Relevant academic research and scientific papers

Mechanism of enantioselective ester cleavage by histidine-containing peptides at a micellar interface. 2. Effect of changing peptide chain length

Cleij, Marco C.,Drenth, Wiendelt,Nolte, Roeland J. M.

, p. 459 - 468 (2007/10/02)

Chiral p-nitrophenyl esters derived from the amino acid phenylalanine are cleaved by various histidine-containing tripeptides and higher oligopeptides as catalysts at a micellar interface.It is assumed that the oligopeptides adopt an internally hydrogen-b

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