Abstract
The discovery, synthesis and structure-activity relationships of a series of novel benzofuro[3,2-b]pyridines as non-selective endothelin ET(A)/ET(B) as well as selective ET(B) receptor antagonists are described. The most potent non-selective inhibitor 7s displayed an IC50 of 21 nM and 41 nM for ET(A) and ET(B) receptors, respectively, whereas 7ee merely showed affinity for the ET(B) receptor (IC50 = 3.6 nM).
MeSH terms
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Animals
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Endothelin Receptor Antagonists*
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Endothelin-1 / metabolism
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Endothelium, Vascular / drug effects
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Endothelium, Vascular / metabolism
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In Vitro Techniques
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Kidney / drug effects
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Kidney / metabolism
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Pyridines / chemistry
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Pyridines / pharmacology*
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Rabbits
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Rats
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Receptor, Endothelin A
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Receptor, Endothelin B
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Structure-Activity Relationship
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Swine
Substances
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Endothelin Receptor Antagonists
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Endothelin-1
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Pyridines
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Receptor, Endothelin A
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Receptor, Endothelin B