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"Z-Lys(Z)-Trp(Mtb)-Gly-OBzl" is a synthetic peptide consisting of four amino acids: Z-protected lysine (Lys), Z-protected tryptophan (Trp) with a methyltyrosine (Mtb) substitution, glycine (Gly), and benzyl-protected (OBzl). This peptide is characterized by the presence of protecting groups, which are essential for preventing unwanted side reactions during synthesis. The Z group is a commonly used protecting group for the amino group of lysine, while the OBzl group protects the hydroxyl group of the side chain in serine or threonine. The Mtb substitution in tryptophan introduces a methyl group to the tyrosine residue, which can alter the peptide's properties and interactions. This specific sequence and structure of "Z-Lys(Z)-Trp(Mtb)-Gly-OBzl" make it a unique peptide with potential applications in various fields, such as drug development, chemical biology, and materials science.

82154-96-9

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82154-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82154-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,5 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82154-96:
(7*8)+(6*2)+(5*1)+(4*5)+(3*4)+(2*9)+(1*6)=129
129 % 10 = 9
So 82154-96-9 is a valid CAS Registry Number.

82154-96-9Downstream Products

82154-96-9Relevant academic research and scientific papers

New Protecting Groups for the Indole Ring of Tryptophan in Peptide Synthesis: 2,4,6-Trimethoxybenzenesulfonyl and 4-Methoxy-2,3,6-trimethylbenzenesulfonyl Groups

Fukuda, Tsunehiko,Wakimasu, Mitsuhiro,Kobayashi, Shigeru,Fujino, Masahiko

, p. 2825 - 2835 (2007/10/02)

Five substituted benzenesulfonyl groups, p-toluenesulfonyl, p-methoxybenzenesulfonyl, 2,4-dimethoxybenzenesulfonyl, 2,4,6-trimethoxybenzenesulfonyl, and 4-methoxy-2,3,6-trimethylbenzenesulfonyl, were introduced at Nin of tryptophan and their protecting group properties were investigated.Among them, 2,4,6-trimethoxybenzenesulfonyl and 4-methoxy-2,3,6-trimethylbenzenesulfonyl are stable to trifluoroacetic acid, but can be readily removed by hydrogen fluoride or methanesulfonic acid, and suppress decomposition and modification of the tryptophan residue during peptide synthesis.These protecting groups were successfully used in syntheses of bombesin, a potent analog of luteinizing hormone-releasing hormone by the solution method and dynorphin by the solid-phase method.Keywords-peptide synthesis; tryptophan; protecting group; 2,4,6-trimethoxybenzenesulfonyl group; 4-methoxy-2,3,6-trimethylbenzenesulfonyl group

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