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A METHOD OF INDUCING CHOLECYSTOKININ AGONIST ACTIVITY USING 1,4-BENZODIAZEPINE COMPOUNDS

机译:1,4-苯二氮杂P类化合物诱导胆囊收缩素激动剂活性的方法

摘要

PCT No. PCT/EP95/01335 Sec. 371 Date Oct. 11, 1996 Sec. 102(e) Date Oct. 11, 1996 PCT Filed Apr. 13, 1995 PCT Pub. No. WO95/28399 PCT Pub. Date Oct. 26, 1995A method of inducing a Cholescystokinin-A receptor agonist response in a mammal by administering a compound of formula (I), IMAGE (I) where R1 is C1-C6alkyl, C3-6cycloalkyl, phenyl, or substituted phenyl; R2 is C3-6alkyl, C3-6cycloalkyl, C3-6alkenyl, benzyl, phenylC1-3alkyl or substituted phenyl; or NR1R2 together form 1,2,3,4-tetrahydroquinoline or benzazepine mono-, di-, or trisubstituted independently with C1-6alkyl, C1-6alkoxy or halogen substituents; n is an integer selected from the grouping consisting of 0,1,2 or 3; p is the integer 0 or 1; q is the integer 0 or 1; r is the integer 0 or 1, provided that when q is 0 then r is 0; R3, R4, R5 and R8 are selected from a variety of substituents; X is nitrogen, nitroso or R8; m is an integer selected from the group consisting of 0, 1, 2 or 3; Y and Z are hydrogen or halogen, novel intermediates, a pharmaceutical composition for treating obesity, gall bladder stasis, disorders of pancreatic secretion, methods for such treatment and processes for preparing compounds of formula (I).
机译:PCT号PCT / EP95 / 01335秒371日期1996年10月11日102(e)日期1996年10月11日PCT 1995年4月13日提交PCT Pub。 WO95 / 28399 PCT公开号日期1995年10月26日一种在哺乳动物中诱导胆囊收缩素A受体激动剂应答的方法,该方法是通过给予式(I),(I)化合物,其中R1为C1-C6烷基,C3-6环烷基,苯基或取代基苯基R2是C3-6烷基,C3-6环烷基,C3-6链烯基,苄基,苯基C1-3烷基或取代的苯基;或NR 1 R 2一起形成分别被C 1-6烷基,C 1-6烷氧基或卤素取代基取代的1,2,3,4-四氢喹啉或苯并ze庚因单,二或三取代; n是选自0、1、2或3的整数; p是整数0或1; q是整数0或1; r是整数0或1,前提是当q为0时r为0; R3,R4,R5和R8选自多种取代基; X是氮,亚硝基或R 8; m是选自0、1、2或3的整数; Y和Z是氢或卤素,新型中间体,用于治疗肥胖症,胆囊淤滞,胰腺分泌失调的药物组合物,这种治疗方法和制备式(I)化合物的方法。

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