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Synthesis and characterization of 5,6,7,8-tetrahydroquinoline C5a receptor antagonists
Journal article   Peer reviewed

Synthesis and characterization of 5,6,7,8-tetrahydroquinoline C5a receptor antagonists

J. Kent Barbay, Yong Gong, Mieke Buntinx, Jian Li, Concha Claes, Pamela J. Hornby, Guy Van Lommen, Jean Van Wauwe and Wei He
Bioorganic & medicinal chemistry letters, v 18(8), pp 2544-2548
15 Apr 2008
PMID: 18378452
url
https://doi.org/10.7270/q2jm2bhdView
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Abstract

C5a C5a receptor antagonist C5aR Complement Tetrahydroquinoline
Synthesis and structure–activity relationships of a series of substituted 5,6,7,8-tetrahydroquinoline C5a receptor antagonists are reported. A novel series of substituted 2-aryl-5-amino-5,6,7,8-tetrahydroquinoline C5a receptor antagonists is reported. Synthetic routes were developed that allow the substituents on the tetrahydroquinoline core to be efficiently varied, facilitating determination of structure–activity relationships. Members of the series display high binding affinity for the C5a receptor and are potent functional antagonists.

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Collaboration types
International collaboration
Web of Science research areas
Chemistry, Medicinal
Chemistry, Organic
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