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Z-D-Trp-Gly-OBzl is a synthetic peptide consisting of three amino acids: D-tryptophan (D-Trp), glycine (Gly), and a benzyloxycarbonyl (OBzl) group. D-tryptophan is a non-natural amino acid with a D-configuration, meaning its chiral center is opposite to that of the naturally occurring L-tryptophan. Glycine is the simplest amino acid, and OBzl is a protecting group used in peptide synthesis to prevent unwanted side reactions. This specific sequence of amino acids is often used in research and drug development, as it can be a building block for larger peptides or proteins with potential therapeutic applications. The OBzl group is crucial for protecting the peptide's amino terminus during synthesis, ensuring that the peptide maintains its integrity and can be further modified or studied as needed.

84553-05-9

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84553-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84553-05-9 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 84553-05:
(7*8)+(6*4)+(5*5)+(4*5)+(3*3)+(2*0)+(1*5)=139
139 % 10 = 9
So 84553-05-9 is a valid CAS Registry Number.

84553-05-9Downstream Products

84553-05-9Relevant 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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