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Z-Phe-Leu-Phe-Phe-OBzl is a peptide compound consisting of five amino acids: phenylalanine (Phe), leucine (Leu), and two additional phenylalanine residues, with a benzyloxycarbonyl (OBzl) group attached to the N-terminus. This specific sequence is often used in the synthesis of larger peptides and proteins, as it serves as a building block for more complex structures. The OBzl group is a protecting group that prevents unwanted side reactions during peptide synthesis, and it is removed at a later stage to expose the free amino group. This particular peptide sequence is of interest in the field of medicinal chemistry and drug design, as it may mimic certain natural peptide sequences or serve as a precursor to bioactive molecules.

80174-70-5

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80174-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80174-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,7 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80174-70:
(7*8)+(6*0)+(5*1)+(4*7)+(3*4)+(2*7)+(1*0)=115
115 % 10 = 5
So 80174-70-5 is a valid CAS Registry Number.

80174-70-5Downstream Products

80174-70-5Relevant academic research and scientific papers

ENZYMIC SYNTHESIS OF OLIGOPETIDE - VI. THE MECHANISTIC FEATURES OF PEPSIN-CATALYSED PEPTIDE SYNTHESIS

Tseng, Min-Jen,Wu, Shih-Hsiung,Wang, Kung-Tsung

, p. 61 - 66 (2007/10/02)

The dipeptide Z-Phe-Phe-OBzl and tripeptide Z-Phe-Phe-Phe-OBzl were synthesized by pepsin catalysis from the incubation of Z-Phe and Phe-OBzl in the reaction solution.The yield ratio of two peptides in relation to reaction time was investigated by HPLC.Another example: The tripeptide Z-Phe-Leu-Phe-OBzl and tetrapeptide Z-Phe-Leu-Phe-Phe-OBzl were also synthesized concurrently from Z-Phe-Leu and Phe-OBzl by pepsin catalysis.These results may have important implication for the transpeptidation of pepsin.But, according to the report of Pellegrini and Luisi, the dipeptide, Z-Ph-Phe-OBzl, synthesized by pepsin catalysis was not contaminated with the tripeptide,Z-Phe-Phe-Phe-OBzl, and the yield was high.In order to investigate the discrepancies between our observation and those reported by Pellegrini and Luisi, a mechanism by which pepsin synthesizes the dipeptide, Z-Phe-Phe-OBzl, and tripeptide, Z-Phe-Phe-Phe-OBzl, is proposed and supporting data demonstrated by HPLC analysis.

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