Synthesis and biological characterization of [3H] (2-amino-4,5,6,7-tetrahydrobenzo[b]thiophen-3-yl)(4-chlorophenyl)-methanone, the first radiolabelled adenosine A1 allosteric enhancer

被引:11
作者
Baraldi, PG [1 ]
Pavani, MG
Leung, E
Moorman, AR
Varani, K
Vincenzi, F
Borea, PA
Romagnoli, R
机构
[1] Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
[2] King Pharmaceut Res & Dev Inc, Cary, NC 27513 USA
[3] Univ Ferrara, Dipartimento Med Clin & Sperimentale, Sez Farmacol, I-44100 Ferrara, Italy
关键词
allosteric enhancer; adenosine A(1) receptor; radiolabelled compound;
D O I
10.1016/j.bmcl.2005.11.037
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Among the adenosine A(1) allosteric enhancers reported so far, compound (2-amino-4,5,6,7-tetrahydrobenzo[b]thiophen-3-yl)-(4-chlorophenyl)-methanone 1 (named T-62) has shown biological properties similar to those of PD 81,723, the reference A(1) allosteric enhancer and it has been more fully pharmacologically investigated. The preparation of the radiolabelled form of compound 1 and its characterization by saturation binding experiments are reported. These studies allowed us to demonstrate for the first time the existence of a specific, allosteric site on the A(1) receptor. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1402 / 1404
页数:3
相关论文
共 17 条
[1]   Synthesis and biological effects of a new series of 2-amino-3-benzoylthiophenes as allosteric enhancers of A1-adenosine receptor [J].
Baraldi, PG ;
Zaid, AN ;
Lampronti, I ;
Fruttarolo, F ;
Pavani, MG ;
Tabrizi, MA ;
Shryock, JC ;
Leung, E ;
Romagnoli, R .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (17) :1953-1957
[2]   Synthesis and biological effects of novel 2-amino-3-naphthoylthiophenes as allosteric enhancers of the A1 adenosine receptor [J].
Baraldi, PG ;
Romagnoli, R ;
Pavani, MG ;
Nuñez, MD ;
Tabrizi, MA ;
Shryock, JC ;
Leung, E ;
Moorman, AR ;
Uluoglu, C ;
Iannotta, V ;
Merighi, S ;
Borea, PA .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (05) :794-809
[3]  
BARALDI PG, 1997, Patent No. 5939432
[4]  
BORROWS ET, 1949, J CHEM SOC, V42, P185
[5]  
BRUNS RF, 1990, MOL PHARMACOL, V38, P950
[6]  
BRUNS RF, 1990, MOL PHARMACOL, V38, P939
[7]   Allosteric modulation of adenosine A1 receptor coupling to G-proteins in brain [J].
Childers, SR ;
Li, XH ;
Xiao, RY ;
Eisenach, JC .
JOURNAL OF NEUROCHEMISTRY, 2005, 93 (03) :715-723
[8]   Allosteric binding sites on cell-surface receptors: Novel targets for drug discovery [J].
Christopoulos, A .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (03) :198-210
[9]   2-AMINO-THIOPHENE AUS METHYLENAKTIVEN NITRILEN CARBONYLVERBINDUNGEN UND SCHWEFEL [J].
GEWALD, K ;
SCHINKE, E ;
BOTTCHER, H .
CHEMISCHE BERICHTE-RECUEIL, 1966, 99 (01) :94-&
[10]  
Lee YW, 1996, J PHARMACOL EXP THER, V277, P1642