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公开(公告)号:US06090805A
公开(公告)日:2000-07-18
申请号:US095232
申请日:1998-06-10
申请人: Peter D. Williams , Michelle A. Sparks , Ian Bell , Debra S. Perlow , Kenneth Stauffer , Roger M. Freidinger
发明人: Peter D. Williams , Michelle A. Sparks , Ian Bell , Debra S. Perlow , Kenneth Stauffer , Roger M. Freidinger
IPC分类号: C07D413/04 , C07D413/14 , A61K31/535 , A61K31/47 , C07D215/16 , C07D265/12
CPC分类号: C07D413/04 , C07D413/14
摘要: This invention relates to certain novel benzoxazinone compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor in mammals, especially humans. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery.
摘要翻译: 本发明涉及某些新的苯并恶嗪酮化合物及其衍生物,其合成及其作为催产素受体拮抗剂的用途。 这些化合物的一种应用是在哺乳动物,特别是人类中治疗早产。 化合物放松哺乳动物子宫收缩的能力也使它们可用于治疗痛经并在剖宫产分娩前停止劳动。
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公开(公告)号:US5726172A
公开(公告)日:1998-03-10
申请号:US779296
申请日:1997-01-06
IPC分类号: C07D413/04 , C07D413/14 , C07D417/14 , C07D451/06 , C07D265/12 , A61K31/535
CPC分类号: C07D451/06 , C07D413/04 , C07D413/14 , C07D417/14
摘要: This invention relates to certain novel benzoxazinone compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery. A typical compound is as follows: ##STR1##
摘要翻译: 本发明涉及某些新的苯并恶嗪酮化合物及其衍生物,其合成及其作为催产素受体拮抗剂的用途。 这些化合物的一种应用是治疗早产。 化合物放松哺乳动物子宫收缩的能力也使它们可用于治疗痛经并在剖宫产分娩前停止劳动。 典型的化合物如下:
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公开(公告)号:US5968938A
公开(公告)日:1999-10-19
申请号:US86107
申请日:1998-05-29
IPC分类号: C07D211/46 , C07D211/96 , C07D213/74 , C07D235/06 , C07D239/42 , C07D241/20 , C07D295/185 , A61K31/495 , C07D401/12 , C07D403/12
CPC分类号: C07D213/74 , C07D211/46 , C07D211/96 , C07D235/06 , C07D239/42 , C07D241/20 , C07D295/185
摘要: This invention relates to certain novel piperazine compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor in mammals, especially humans. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery.
摘要翻译: 本发明涉及某些新的哌嗪化合物及其衍生物,其合成及其作为催产素受体拮抗剂的用途。 这些化合物的一种应用是在哺乳动物,特别是人类中治疗早产。 化合物放松哺乳动物子宫收缩的能力也使它们可用于治疗痛经并在剖宫产分娩前停止劳动。
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