155741-86-9

Basic information

• Product Name: methyl 2-[[[2-butyl-1-[4-(carboxyphenyl)methyl]-1H-imidazol-5-yl]methyl]amino]benzoate
• Synonyms: methyl 2-[[[2-butyl-1-[4-(carboxyphenyl)methyl]-1H-imidazol-5-yl]methyl]amino]benzoate
• CAS NO: 155741-86-9
• Molecular Weight: 421.496
• Mol File: 155741-86-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-[[[2-butyl-1-[4-(carboxyphenyl)methyl]-1H-imidazol-5-yl]methyl]amino]benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-[[[2-butyl-1-[4-(carboxyphenyl)methyl]-1H-imidazol-5-yl]methyl]amino]benzoate(155741-86-9)
• EPA Substance Registry System: methyl 2-[[[2-butyl-1-[4-(carboxyphenyl)methyl]-1H-imidazol-5-yl]methyl]amino]benzoate(155741-86-9)

Safety Data

• Hazardous Substances Data: 155741-86-9(Hazardous Substances Data)

Upstream product

• 134-20-3 2-carbomethoxyaniline 
• 155740-67-3 methyl 2-[[[2-butyl-1-[[4-(methoxycarbonyl)phenyl]methyl]-1H-imidazol-5-yl]methyl]amino]benzoate 

Downstream Products

• 155763-64-7 methyl 2-[[[2-butyl-1-[(4-((((2-chlorophenyl)sulfonyl)amino)carbonyl)phenyl)methyl]-1H-imidazol-5-yl]methyl]amino]benzoate 
• 155763-78-3 methyl 2-[[[2-butyl-1-[(4-((((2-azidophenyl)sulfonyl)amino)carbonyl)phenyl)methyl]-1H-imidazol-5-yl]methyl]amino]benzoate 

Relevant articles and documents

Specific nonpeptide photoprobes as tools for the structural study of the angiotensin II AT1 receptor

The aim of this work was to obtain photoactivatable nonpeptide antagonists of the angiotensin II AT1 receptor. Based on structure-function relationships, two chemical structures as well as appropriate synthetic schemes were chosen as a frame for the design of radiolabeled azido probes. The feasibility of the strategy was first assessed by the synthesis of two tritiated ligands 21 and 22 possessing a high affinity for the AT1 receptor and a low nonspecific binding to membrane or cell preparations. We then prepared two unlabeled azido derivatives 7 and 14 which retained a fairly high affinity for the AT1 receptor. The latter compound proved to be suitable for receptor irreversible labeling and was prepared in its tritiated form 28. This tritiated azido nonpeptide probe displayed a K(d) value of 11.8 nM and a low nonspecific binding. It was suitable for specific and efficient covalent labeling of the recombinant AT(1A) receptor stably expressed in CHO cells. The electrophoretic pattern of the specifically labeled entity was strictly identical to that of purified receptor photolabeled with a biotinylated peptidic photoactivatable probe. This new tool should be useful for the mapping of the nonpeptide receptor binding site. These potential applications are discussed in light of the current knowledge of molecular mechanisms of G-protein coupled receptor activation and inactivation.