首页> 外国专利> PYRROLOPYRAZINE DERIVATIVES, PHARMACEUTICAL COMPOSITION, METHOD FOR PREVENTION AND TREATMENT OF DISEASES, APPLICATION AS PHOSPHODIESTERASE IV AND/OR TUMOR NECROSIS FACTOR PRODUCTION INHIBITOR

PYRROLOPYRAZINE DERIVATIVES, PHARMACEUTICAL COMPOSITION, METHOD FOR PREVENTION AND TREATMENT OF DISEASES, APPLICATION AS PHOSPHODIESTERASE IV AND/OR TUMOR NECROSIS FACTOR PRODUCTION INHIBITOR

机译:焦磷酸吡嗪衍生物,药物成分,疾病的预防和治疗方法,用作磷酸酯酶IV和/或肿瘤坏死因子的生产抑制剂

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to the novel inhibitor of phosphodiesterase (PDE) IV and/or to the tumor necrosis factor (TNF) production inhibitor, which corresponds to the compound with formula (I), where R1 is: (1) mono- or di(inferior)alkylamino, (2) phenyl, (3) saturated or unsaturated 5-or 6-membered heteromonocyclic group, selected from a group which includes pyrrolidinyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, furanyl, thienyl and piridinyl, or (4) inferior alkyl not necessarily substituted with (i) inferior alkoxi or (ii) saturated 5- or 6-membered heteromonocyclic group, selected from the group, consisting of piperazinyl and morpholinyl, where the inferior alkoxi is not necessarily substituted with cyclo(inferior)alkyl or piridinyl, R2 corresponds to R7 or - A2R7 , where A2 is -(CH2)n- or -(CH=CH)m- [where n is an even number within 2 to 6, and m is an even number 1 or 2], and R7 is a hydrogen, inferior alkylsulfonyl, carboxy, etherificated carboxy or piridinyl; R3 is: (1) phenyl, not necessarily substituted with inferior alkyl, cyclo(inferior)alkyl, inferior alkoxi, halogen, cyano or carbamoyl; or (2) quinolinyl; or piridinyl, substituted with inferior alkyl, cyclo(inferior)alkyl, inferior alkoxi, carbamoyl or halogen, and R4 corresponds to the inferior alkyl, or its pharmaceutically acceptable salt. The application of the compound with formula is invented, for producing the therapeutic agent with the PDE IV and/or TNF production inhibiting activity and the pharmaceutical composition containing the effective amount of compounds with formula (I) mixed with the pharmaceutically acceptable carriers. The method for prevention and treatment of the diseases where the application of the PDE IV and/or TNF production inhibitor is considered to be reasonable, including the administration of the therapeutically effective amount of the compound with formula (I). The method for prevention and treatment of asthma, chronic obstructive pulmonary disease, fibrous disorders, acute and fulminant hepatitis, hepatic steatosis, chronic hepatitis, cirrhosis, autoimmune hepatitis, autoimmune inflammatory intestine disease, atopic dermatitis, Alzheimer's disease or viral infection, including the administration of the therapeutically or preventively effective amount of the compound with formula (I).;EFFECT: compound with the PDE IV and/or TNF production inhibiting activity.;11 cl, 2 tbl, 672 ex
机译:发明领域本发明涉及磷酸二酯酶(PDE)IV的新型抑制剂和/或涉及肿瘤坏死因子(TNF)产生的抑制剂,其对应于具有式(I)的化合物,其中R Sup 1 为:(1)单或二(下)烷基氨基,(2)苯基,(3)饱和或不饱和的5或6元杂环单环基团,选自吡咯烷基,吡咯基,恶唑基,异恶唑基,噻唑基,呋喃基,噻吩基和吡啶基基团,或(4)不一定被(i)弱烷氧基或(ii)饱和的5元或6元杂环单环基团取代的下级烷基,如果下部烷烃不一定被环(下部)烷基或吡啶啶基取代,则R 2 对应于R 7 或-A 2 R < Sup> 7 ,其中A 2 是-(CH 2 n -或-(CH = CH) m -[其中n是2到6之间的偶数,m是偶数nu 1或2],且R 7 是氢,亚烷基磺酰基,羧基,醚化羧基或吡啶基; R 3 为:(1)未必被亚烷基,环(亚)烷基,亚烷氧基,卤素,氰基或氨基甲酰基取代的苯基;或(2)喹啉基;或或亚吡啶基,被亚烷基,环(亚)烷基,亚烷基,氨基甲酰基或卤素取代,并且R 4对应于亚烷基或其药学上可接受的盐。发明了具有式<图像文件=“ 00000002.GIF” he =“ 35” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 55” />的化合物的用途,用于生产PDE IV的治疗剂和/或抑制TNF产生的活性,以及​​药物组合物,其包含与药学上可接受的载体混合的有效量的式(I)的化合物。认为预防和治疗PDE IV和/或TNF产生抑制剂合理的疾病的方法,包括给予治疗有效量的式(I)化合物。预防和治疗哮喘,慢性阻塞性肺疾病,纤维性疾病,急性和暴发性肝炎,肝脂肪变性,慢性肝炎,肝硬化,自身免疫性肝炎,自身免疫性炎性肠病,特应性皮炎,阿尔茨海默氏病或​​病毒感染的方法,包括给药;疗效:具有PDE IV和/或TNF产生抑制活性的化合物; 11 cl,2 tbl,672 ex

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