Compounds active at neurotensin receptors (NTS1 and NTS2) exert analgesic effects on different types of nociceptive modalities, including thermal, mechanical, and chemical stimuli. The NTS2 preferring peptide JMV-431 (2) and the NTS2 selective nonpeptide compound levocabastine (6) have been shown to be effective in relieving the pain associated with peripheral neuropathies. With the aim of identifying novel nonpeptide compounds selective for NTS2, we examined analogues of SR48692 (5a) using a FLIPR calcium assay in CHO cells stably expressing rat NTS2. This led to the discovery of the NTS2 selective nonpeptide compound 1-({[1-(4-fluorophenyl)-5-(2-methoxyphenyl)-1H-pyrazol-3-yl]carbonyl}amino)cyclohexane carboxylic acid (NTRC-739, 7b) starting from the nonselective compound 5a.
Identification of 1-({[1-(4-fluorophenyl)-5-(2-methoxyphenyl)-1H-pyrazol-3-yl]carbonyl}amino)cyclohexane carboxylic acid as a selective nonpeptide neurotensin receptor type 2 compound.
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作者:Thomas James B, Giddings Angela M, Wiethe Robert W, Olepu Srinivas, Warner Keith R, Sarret Philippe, Gendron Louis, Longpre Jean-Michel, Zhang Yanan, Runyon Scott P, Gilmour Brian P
| 期刊: | Journal of Medicinal Chemistry | 影响因子: | 6.800 |
| 时间: | 2014 | 起止号: | 2014 Jun 26; 57(12):5318-32 |
| doi: | 10.1021/jm5003843 | ||
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