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Antiviral macrocyclic compounds containing a cyclic amine moiety

机译:含有环胺部分的抗病毒大环化合物

摘要

A macrocyclic compound or the acid addition salts and metal complexes thereof has the formula (V): V'-CR1R2-Ar2 or of formula (1a) V"-CR1R2-Ar1-CR3R4-N(R5)-(CR6R7)x-R8 wherein: V' is a cyclic polyamine moiety having a total of 9 to 24 members and from 3 to 6 optionally substituted amine nitrogens spaced by two or more optionally substituted carbon atoms from each together and which may optionally comprise a fused aromatic or heteroaromatic ring; V" is a cyclic polyamine moiety having a total of 9 to 24 members and 2 optionally substituted amine nitrogens spaced by two or more optionally substituted carbon atoms from each together and which may optionally comprise a fused aromatic or heteroaromatic ring;R1 to R7 are independently hydrogen, alkyl or cycloalkyl; Ar1 is an optionally substituted aromatic or heterocyclic group; Ar2 is an optionally substituted aromatic or heterocyclic group or is 4- phenylpiperazinyl or purin-1-ylmethyl; R8 is a heterocyclic group, an optionally substituted aromatic or heteroaromatic group or is mercaptan and x is 1 or 2. The compounds are useful in treating conditions mediated by the CXCR4 or CCR5 receptors.
机译:大环化合物或其酸加成盐和金属配合物具有式(V):V'-CR1R2-Ar2或式(1a)V” -CR1R2-Ar1-CR3R4-N(R5)-(CR6R7)x- R8,其中:V'是环状多胺部分,其具有总共9至24个成员和3至6个任选取代的胺氮,其彼此隔开两个或更多个任选取代的碳原子,并且可以任选地包含稠合的芳族或杂芳族环;“ V”为环状多胺部分,其具有总共9至24个成员和2个任选地取代的胺氮,其彼此隔开两个或更多个任选地取代的碳原子,并且可以任选地包含稠合的芳族或杂芳族环; R 1至R 7为独立地为氢,烷基或环烷基; Ar 1是任选取代的芳族或杂环基; Ar 2是任选取代的芳族或杂环基,或为4-苯基哌嗪基或嘌呤-1-基甲基; R 8为杂环基,任选取代的芳族或杂芳族基团或为硫醇且x为1或2。该化合物可用于治疗由CXCR4或CCR5受体介导的病症。

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