Exploring a pocket for polycycloaliphatic groups in the CXCR3 receptor with the aid of a modular synthetic strategy
Bioorganic & Medicinal Chemistry Letters(2009)
摘要
The strategic use of specific polycycloaliphatic groups in obtaining small antagonists for the CXCR3 receptor was investigated. 2-Adamantyl- and (iso)bornyl groups proved beneficial.
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关键词
CXCR3,Reductive amination,GPCR,Polycycloaliphatic
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