Abstract
Structure-activity studies on the oxytocin antagonist 1 (L-371,257; Ki = 9.3 nM) have led to the identification of a related series of compounds containing an ortho-trifluoroethoxyphenylacetyl core which are orally bioavailable and have significantly improved potency in vitro and in vivo, e.g., compound 8 (L-374,943; Ki = 1.4 nM).
MeSH terms
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Animals
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Benzoxazines
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Cell Line
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Humans
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Inhibitory Concentration 50
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Kinetics
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Oxazines / chemical synthesis*
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Oxazines / pharmacokinetics*
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Oxytocin / antagonists & inhibitors*
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Piperidines / chemical synthesis*
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Piperidines / pharmacokinetics*
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Rats
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Structure-Activity Relationship
Substances
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Benzoxazines
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L 371257
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Oxazines
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Piperidines
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Oxytocin