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Synthesis and biological evaluation of 2-(arylethynyl)quinoline derivatives as mGluR5 antagonists for the treatment of neuropathic pain

Authors
Son, Myung-HeeKim, Ji YoungLim, Eun JeongBaek, Du-JongChoi, KihangLee, Jae KyunPae, Ae NimMin, Sun-JoonCho, Yong Seo
Issue Date
Mar-2013
Publisher
Pergamon Press Ltd.
Keywords
Metabotropic glutamate receptor; Antagonist; Quinoline; Sonogashira reaction; Neuropathic pain
Citation
Bioorganic and Medicinal Chemistry Letters, v.23, no.5, pp 1472 - 1476
Pages
5
Indexed
SCI
SCIE
SCOPUS
Journal Title
Bioorganic and Medicinal Chemistry Letters
Volume
23
Number
5
Start Page
1472
End Page
1476
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/28795
DOI
10.1016/j.bmcl.2012.12.056
ISSN
0960-894X
1464-3405
Abstract
We described here the synthesis and biological evaluation of mGluR5 antagonists containing a quinoline ring structure. Using intracellular calcium mobilization assay (FDSS assay), we identified compound 5n, showing high inhibitory activity against mGluR5. In addition, it was found that compound 5n has excellent stability profile. Finally, this compound exhibited favorable analgesic effects in spinal nerve ligation model of neuropathic pain, which is comparable to gabapentin. (c) 2012 Elsevier Ltd. All rights reserved.
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ERICA 공학대학 (ERICA 에너지바이오학과)
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