Abstract
Synthesis and structure-activity relationships (SAR) of orally active arginine vasopressin (AVP) receptor antagonists are discussed. Potent and orally active AVP receptor antagonists are produced when ring A of VPA-985 (1) is replaced with a 3-pyridinyl unit (2b).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aminopyridines / chemical synthesis*
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Aminopyridines / pharmacology*
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Aminopyridines / urine
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Animals
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Antidiuretic Hormone Receptor Antagonists*
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Azepines / chemical synthesis*
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Azepines / pharmacology
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Benzamides / chemical synthesis*
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Benzamides / pharmacology
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Benzodiazepines / chemical synthesis*
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Benzodiazepines / pharmacology*
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Benzodiazepines / urine
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Inhibitory Concentration 50
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Kidney / drug effects
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Liver / drug effects
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Pyrroles
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Rats
Substances
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Aminopyridines
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Antidiuretic Hormone Receptor Antagonists
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Azepines
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Benzamides
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Pyrroles
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Benzodiazepines
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lixivaptan
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CL 385004