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Z-Lys(Z)-D-Trp-Gly-OH is a synthetic peptide consisting of four amino acids: Z-protected lysine (Lys), D-tryptophan (Trp), glycine (Gly), and a hydroxyl group (OH) at the end. The Z group is a protecting group used in peptide synthesis to prevent unwanted side reactions. This specific sequence of amino acids is known for its potential biological activity, often studied for its interactions with various receptors in the body. The peptide is of interest in pharmaceutical research due to its possible applications in drug development, particularly in the areas of pain management and other therapeutic areas where the modulation of receptor activity is crucial.

84553-07-1

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84553-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84553-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,5 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84553-07:
(7*8)+(6*4)+(5*5)+(4*5)+(3*3)+(2*0)+(1*7)=141
141 % 10 = 1
So 84553-07-1 is a valid CAS Registry Number.

84553-07-1Downstream Products

84553-07-1Relevant 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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