Abstract
Twenty-seven N,N',N"-trisubstituted thiourea derivatives were prepared. Among them, 1-[3-(4'-hydroxy-3'-methoxy-phenyl)-propyl]-1,3-diphenethyl-thiourea (8l, IC(50)=0.32 microM), showed 2-fold higher antagonistic activity than that of capsazepine (3, IC(50)=0.65 microM) against the vanilloid receptor in a (45)Ca(2+)-influx assay.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Calcium / metabolism
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Calcium Isotopes
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Capsaicin / analogs & derivatives
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Inhibitory Concentration 50
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Ion Channels / antagonists & inhibitors
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Neurons / cytology
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Neurons / drug effects
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Neurons / physiology
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Rats
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Receptors, Drug / antagonists & inhibitors*
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Structure-Activity Relationship
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Thiourea / chemical synthesis*
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Thiourea / pharmacology
Substances
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Calcium Isotopes
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Ion Channels
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Receptors, Drug
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Thiourea
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Capsaicin
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Calcium