Abstract
A series of N-(2-hydroxy-3-sulfonamidobenzene)-N'-arylcyanoguanidines was prepared. In general, these compounds proved to be potent antagonists of CXCR2 while the selectivity versus CXCR1 ranged from non-selective to >200-fold.
MeSH terms
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Guanidines / chemistry
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Guanidines / pharmacology*
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Humans
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Receptors, Interleukin-8A / antagonists & inhibitors*
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Receptors, Interleukin-8B / antagonists & inhibitors*
Substances
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Guanidines
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Receptors, Interleukin-8A
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Receptors, Interleukin-8B
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dicyandiamido