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Use of nucleoside and nucleotide analogues to treat Viral Infections and / or paramyxovirus Orthomyxovirus, related compounds and Pharmaceutical compositions containing them

机译:核苷和核苷酸类似物在治疗病毒感染和/或副粘病毒,正粘病毒,相关化合物和含有它们的药物组合物中的用途

摘要

1. Claim 1: number of effective treatments using a formula compound (1),Or a pharmaceutically acceptable salt for the preparation of a drug for the improvement or treatment of a virus infection selected for parasite virus infection or orthopedic virus infection, in which the compound of formula (1) has a structure and B1A is selected from a base group. a. Selective substitution of heterocyclic ring and selective heterocyclic group by protected Amin group; R1a was selected from hydrogen group, alternative acid or formula group (2);Na is 0, 1 or 2; R2A and R3a are independent of hydrogen group, an alternative C1-6 tar and an alternative C1-6 halide substitute; R4A is selected from the group consisting of hydrogen, halogen and a alternative C1-6 tar (= O) R19A; R5a is selected from hydrogen, halogen, C1-6 alternative tar groups, - or20a and - OC (= O) r21a; r6a is selected from hydrogen, halogen, C1-6 alternative tar groups, - Or22a and - OC (= O) r23a; or r5a and r6a are two oxygen atoms and are combined by one carbon group;R7a is selected from the group consisting of hydrogen, halogen, a selective alternative C1-6 tar (= or24a and - OC (= O) r25a); R8a is selected from the group consisting of hydrogen, a selective alternative C1-6 tar and a selective alternative C1-6 halotar; r9a and r12a are either absent or hydrogen; R10a does not exist or is hydrogen; each r11a does not exist or is hydrogen independently; r13a does not exist or is hydrogen; r14a is selected from a group consisting of an alternative arilo, an alternative alien arilo and an alternative heterocycle,R15a is an alternative amino acid linker or an alternative amino acid linker derivative, or r14a is an alternative amino acid linker or an alternative amino acid linker derivative, R15a is an amino acid associated with alternative n or an amino acid derivative associated with alternative n; or r14a is an O -,Hydrogen Xi or un-o-asphalt C1-6 can be replaced optionally, r15a and r5a together are o; r16a is selected from a group consisting of an alternative arilo, an alternative heterosexual and an alternative heterosexual, R17a is an alternative amino acid and n-complex or an alternative amino acid derivative; or r16a is an alternative amino acid and n-complex or an alternative amino acid derivative, R17a is an amino acid that can selectively replace n or an amino acid derivative that can selectively replace n; or r16a is an O -,Hydrogen Xi or un-o-asphalt C1-6 can be replaced, r17a and r5a together are o; r18a, r20a, r22a and r24a are independent hydrogen or C1-6 alternative aspha R19A, r21a, The selection of r23a and r25a is independent of a group consisting of a selectively substituted C1-6 tar and a selectively substituted C3-6 cyclic Gaul tar.
机译:1.权利要求1的方法,其使用式化合物(1)或药学上可接受的盐制备用于改善或治疗选自寄生虫病毒感染或整形外科病毒感染的病毒感染的药物的有效治疗方法,其中式(1)的化合物具有结构并且B1A选自碱基。一种。被保护的Amin基团选择性取代杂环和杂环基团; R1a选自氢基,替代酸或式(2)基; Na为0、1或2; R 2A和R 3a独立于氢基团,可替代的C 1-6焦油和可替代的C 1-6卤化物。 R4A选自氢,卤素和替代的C1-6焦油(= O)R19A; R5a选自氢,卤素,C1-6替代焦油基团-或20a和-OC(= O)r21a; r6a选自氢,卤素,C1-6替代焦油基团,-Or22a和-OC(= O)。或r5a和r6a是两个氧原子并被一个碳原子结合; R7a选自氢,卤素,选择性的C1-6焦油(= or24a和-OC(= O)r25a); R8a选自氢,选择性替代的C1-6焦油和选择性替代的C1-6卤代烃; r9a和r12a不存在或为氢; R10a不存在或为氢;每个r 11a不存在或独立地为氢; r13a不存在或为氢; r14a选自由另一个芳基,另一个外来芳基和另一个杂环组成的组,R15a是另一个氨基酸接头或另一个氨基酸接头衍生物,或r14a是另一个氨基酸接头或另一个氨基酸接头。衍生物,R15a是与替代n相关的氨基酸或与替代n相关的氨基酸衍生物;或r 14a为O-,氢Xi或非-o-沥青C 1-6可以被任意取代,r 15a和r 5a一起为o;或r16a选自由另一芳基,另一异性和另一异性组成的组,R17a为另一氨基酸和n-络合物或另一氨基酸衍生物。或r16a为可替代的氨基酸和n-络合物或可替代的氨基酸衍生物,R17a为可选择性取代n的氨基酸或可选择性替代n的氨基酸衍生物;或r16a是O-,氢or或un-o-沥青C1-6可以被取代,r17a和r5a一起是o; r18a,r20a,r22a和r24a是独立的氢或C1-6替代沥青; R 19A,R 21a,r 23a和r 25a的选择独立于由选择性取代的C 1-6焦油和选择性取代的C 3-6环状高卢焦油组成的组。

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