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Cited 22 time in webofscience Cited 23 time in scopus
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Discovery of dual-acting opioid ligand and TRPV1 antagonists as novel therapeutic agents for pain

Authors
Lee, H.[Lee, H.]Ahn, S.[Ahn, S.]Ann, J.[Ann, J.]Ha, H.[Ha, H.]Yoo, Y.D.[Yoo, Y.D.]Kim, Y.H.[Kim, Y.H.]Hwang, J.-Y.[Hwang, J.-Y.]Hur, K.-H.[Hur, K.-H.]Jang, C.-G.[Jang, C.-G.]Pearce, L.V.[Pearce, L.V.]Esch, T.E.[Esch, T.E.]Lewin, N.E.[Lewin, N.E.]Blumberg, P.M.[Blumberg, P.M.]Lee, J.[Lee, J.]
Issue Date
15-Nov-2019
Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
Keywords
Analgesic; Dual-acting mechanism; Mu-opioid receptor; TRPV1
Citation
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v.182
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume
182
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/8104
DOI
10.1016/j.ejmech.2019.111634
ISSN
0223-5234
Abstract
In order to discover a novel type of analgesic, we investigated dual activity ligands with TRPV1 antagonism and mu-opioid receptor affinity with the goal of eliciting synergistic analgesia while avoiding the side effects associated with single targeting. Based on a combination approach, a series of 4-benzyl-4-(dimethylamino)piperidinyl analogues were designed, synthesized and evaluated for their receptor activities. Among them, compound 49 exhibited the most promising dual-acting activity toward TRPV1 and the mu-opioid receptor in vitro. In vivo, 49 displayed potent, dose-dependent antinociceptive activity in both the 1st and 2nd phases in the formalin assay. Consistent with its postulated mechanism, we confirmed that in vivo, as in vitro, compound 49 both antagonized TRPV1 and functioned as a mu-opioid agonist. This result indicates that dual-acting TRPV1 antagonist/mu-opioid ligands can be made and represent a new and promising class of analgesic. (C) 2019 Elsevier Masson SAS. All rights reserved.
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