Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation. [electronic resource]
Producer: 19950518Description: 971-85 p. digitalISSN:- 0968-0896
- Amino Acid Sequence
- Animals
- Camphor -- analogs & derivatives
- Female
- Humans
- Kidney -- metabolism
- Kinetics
- Liver -- metabolism
- Male
- Models, Molecular
- Molecular Conformation
- Molecular Sequence Data
- Oxytocin -- antagonists & inhibitors
- Piperazines -- chemical synthesis
- Rats
- Receptors, Oxytocin -- antagonists & inhibitors
- Receptors, Vasopressin -- drug effects
- Structure-Activity Relationship
- Sulfonamides -- chemical synthesis
- Tritium
- Uterine Contraction -- drug effects
- Uterus -- metabolism
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Publication Type: Comparative Study; Journal Article
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