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Z-β-Ala-Phe-Pro-OH is a synthetic peptide composed of four amino acids: β-alanine (β-Ala), phenylalanine (Phe), proline (Pro), and a hydroxyl group (OH) at the end. The "Z" prefix indicates the presence of a carbobenzoxy (Cbz) protecting group, which is commonly used in peptide synthesis to protect the amino group of the first amino acid. This peptide is of interest in the field of medicinal chemistry and drug design, as it can serve as a building block for larger peptide structures or as a precursor for the development of new therapeutic agents. The specific sequence and protective group can influence the peptide's stability, solubility, and biological activity, making it a valuable tool for researchers in the pharmaceutical industry.

82938-84-9

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82938-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82938-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,3 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82938-84:
(7*8)+(6*2)+(5*9)+(4*3)+(3*8)+(2*8)+(1*4)=169
169 % 10 = 9
So 82938-84-9 is a valid CAS Registry Number.

82938-84-9Relevant academic research and scientific papers

Cyclol Formation from Tripeptides containing β-Alanine

Pinnen, Francesco,Zanotti, Giancarlo,Lucente, Gino

, p. 1311 - 1316 (2007/10/02)

Attempts to synthesize stable tetrahedral intermediates (cyclols) from β-alanine containing precursors are described.Cyclization of N-(N-benzyloxycarbonyl-β-alanyl)-Phe-Pro-ONp gave N-(N-benzyloxycarbonyl-β-alanyl)-cyclo-(Phe-D-Pro).Cyclization of N-(N-benzyloxycarbonyl-Ala)-βAla-Pro-ONp and of N--Pro-ONp afforded the corresponding anhydrocyclols.The first example of an oxa-cyclol related to a ten membered cyclodepsitripeptide was synthesized by acylating cyclo-(βAla-Pro) with α-benzyloxypropionyl chloride followed by hydrogenolytic removal of the O-benzyl protecting group.

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