Nicotinamide N-oxides as CXCR2 antagonists
- Bioorg Med Chem Lett. 2001 Jul 23;11(14):1951-4. doi: 10.1016/s0960-894x(01)00326-2.
- 1. Department of Chemistry, Celltech R&D, Inc., 1631 220th Street SE, 98021, Bothell, WA, USA. [email protected]
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.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Drug Metabolite; CXCR; Oxidative Phosphorylation; Endogenous Metabolite; Isotope-Labeled CompoundsResearch Areas: Inflammation/Immunology