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Merck
CN

Nicotinamide N-oxides as CXCR2 antagonists.

Bioorganic & medicinal chemistry letters (2001-07-19)
N S Cutshall, R Ursino, K A Kucera, J Latham, N C Ihle
摘要

A series of nicotinamide N-oxides was synthesized and shown to be novel, potent, and selective antagonists of the CXCR2 receptor. Furthermore, these compounds showed significant functional activity against GRO-alpha-driven human neutrophil chemotaxis. Compounds of this class may be useful for the treatment of inflammatory, auto-immune, and allergic disorders.