H-ARG-ARG-TRP-CYS-TYR-ARG-LYS-CYS-TYR-LYS-GLY-TYR-CYS-TYR-ARG-LYS-CYS-ARG-NH2

Base Information

• Chemical Name: H-ARG-ARG-TRP-CYS-TYR-ARG-LYS-CYS-TYR-LYS-GLY-TYR-CYS-TYR-ARG-LYS-CYS-ARG-NH2
• CAS No.: 147658-54-6
• Molecular Formula: C₁₀₉H₁₆₄N₃₈O₂₂S₄
• Molecular Weight: 2487.01
• Mol file: 147658-54-6.mol

Synonyms:TachyplesinI,1-(N2-L-arginyl-L-arginine)-4-L-tyrosine-6-L-lysine-9-L-lysine-11-L-tyrosine-15-L-lysine-;15,16,46,47-Tetrathia-2,5,8,11,19,22,25,28,31,34,37,40,43-tridecaazabicyclo[28.14.4]octatetracontane,cyclic peptide deriv.; 1: PN: WO2009046834 PAGE: 99 claimed protein; T 22; T 22(peptide)

Chemical Property of H-ARG-ARG-TRP-CYS-TYR-ARG-LYS-CYS-TYR-LYS-GLY-TYR-CYS-TYR-ARG-LYS-CYS-ARG-NH2

Chemical Property:

• Storage Temp.: -15°C

Purity/Quality:

98.5% ^*data from raw suppliers

T22 > 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of H-ARG-ARG-TRP-CYS-TYR-ARG-LYS-CYS-TYR-LYS-GLY-TYR-CYS-TYR-ARG-LYS-CYS-ARG-NH2

There total 2 articles about H-ARG-ARG-TRP-CYS-TYR-ARG-LYS-CYS-TYR-LYS-GLY-TYR-CYS-TYR-ARG-LYS-CYS-ARG-NH2 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C145H204N42O26S4 → C109H164N38O22S4 (147658-54-6,142960-16-5)

Guidance literature:

With immobilized Penicillin G acylase; at 37 ℃; Enzymatic reaction;

DOI:10.1002/chem.201201370

Reference yield:

C127H184N40O24S4 → C109H164N38O22S4 (147658-54-6,142960-16-5)

Guidance literature:

With immobilized Penicillin G acylase; at 37 ℃; Enzymatic reaction;

DOI:10.1002/chem.201201370

Refernces