首页> 外国专利> Compound process to produce the same pharmaceutical compositions to antagonize the tachykinin receptor to antagonize a neurokinin receptor a to prevent or treat urination disorders asthma disorders rheumatoid arthritis osteoarthritis migraine pain cough irritable bowel syndrome or emesis processes to antagonize tachykinin receptor in mammals to prevent or treat urination disorders in mammals to prevent or treat asthma disorders migraine irritable bowel syndrome pain cough and emesis in mammals and use of the compound

Compound process to produce the same pharmaceutical compositions to antagonize the tachykinin receptor to antagonize a neurokinin receptor a to prevent or treat urination disorders asthma disorders rheumatoid arthritis osteoarthritis migraine pain cough irritable bowel syndrome or emesis processes to antagonize tachykinin receptor in mammals to prevent or treat urination disorders in mammals to prevent or treat asthma disorders migraine irritable bowel syndrome pain cough and emesis in mammals and use of the compound

机译:制备相同药物组合物以拮抗速激肽受体以拮抗神经激肽受体a以预防或治疗排尿障碍的哮喘病的类风湿性关节炎类风湿性关节炎骨关节炎偏头痛疼痛咳嗽肠易激综合征或呕吐过程以拮抗哺乳动物速激肽受体以预防或治疗排尿预防或治疗哮喘疾病的哺乳动物疾病,偏头痛,肠易激综合征,哺乳动物的咳嗽和呕吐以及该化合物的用途

摘要

Novel compounds of the following general formula or salts thereof. CHEM wherein Ring M is a heterocyclic ring having -N=C, -CO-N or -CS-N as the partial structure -X @ Y; Ra and Rb are bonded to each other to form Ring A, or they are the same or different and represent, independently, a hydrogen atom or a substituent on the Ring M; Ring A and Ring B represent, independently, an optionally substituted homocyclic or heterocyclic ring, and at least one of them is optionally substituted heterocyclic ring; Ring C is optionally substituted homocyclic or heterocyclic ring; Rng Z is an optionally substituted ring; and n represents an integer of from 1 to 6, or a salt thereof, which has an excellent tachykinin receptor antagonistic effect, and their production, and pharmaceutical compositions.
机译:以下通式的新型化合物或其盐。 <CHEM>其中,环M为具有-N = C <,-CO-N <或-CS-N <作为部分结构的-X @ Y <的杂环。 R a和R b彼此键合形成环A,或者它们相同或不同,并且独立地表示环M上的氢原子或取代基;环A和环B独立地表示任选取代的同环或杂环,并且它们中的至少一个是任选取代的杂环;环C为任选取代的同环或杂环; Rng Z是任选取代的环; n为1〜6的整数或其盐,具有极好的速激肽受体拮抗作用,其制法和药物组合物。

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