2-HYDROXY METHYLCYCLOPRO PYLIDENEMETHYL PURINES AND -PYRIMIDINES AS ANTIVIRAL AGENTS
    26.
    发明公开
    2-HYDROXY METHYLCYCLOPRO PYLIDENEMETHYL PURINES AND -PYRIMIDINES AS ANTIVIRAL AGENTS 有权
    2-羟基甲基环庚基甲基嘌呤和作为抗病毒剂的嘧啶

    公开(公告)号:EP1165560A1

    公开(公告)日:2002-01-02

    申请号:EP00913872.8

    申请日:2000-03-10

    Abstract: Compounds which are active against viruses have Formulas (1, 2, 3 and 4) wherein B is a purine or pyrimidine heterocyclic ring and is preferably selected from the group consisting of 6-aminopurine (adenine), 2,6-diaminopurine, 2-amino-6-azidopurine, 2-amino-6-cyclopropylaminopurine, 6-hydroxypurine (hypoxanthine), 2-amino-6-halo substituted purines, 2-amino-6-alkoxy substituted purines, 2-amino-6-hydroxypurine (guanine), 3-deazapurines, 7-deaza-purines, 8-azapurines, cytosine, 5-halo substituted cytosines, 5-alkyl substituted cytosines, thymine, uracil and 6-azapyrimidines; X is O; and, R1 and R2 are alkyl or aryl groups. The compounds of the present invention also include the R- and S-enantiomers of the above compounds. The R1X and/or R2X can also be amino acid residues with X as NH.

    Abstract translation: 对病毒具有活性的化合物具有式(1,2,3和4),其中B是嘌呤或嘧啶杂环并且优选选自6-氨基嘌呤(腺嘌呤),2,6-二氨基嘌呤,2-氨基嘌呤, 氨基-6-叠氮基嘌呤,2-氨基-6-环丙基氨基嘌呤,6-羟基嘌呤(次黄嘌呤),2-氨基-6-卤代嘌呤,2-氨基-6-烷氧基取代的嘌呤,2-氨基-6-羟基嘌呤(鸟嘌呤 ),3-脱氮嘌呤,7-脱氮嘌呤,8-氮杂嘌呤,胞嘧啶,5-卤代取代的胞嘧啶,5-烷基取代的胞嘧啶,胸腺嘧啶,尿嘧啶和6-氮杂嘧啶; X是O; 并且,R1和R2是烷基或芳基。 本发明的化合物还包括上述化合物的R-和S-对映体。 R1X和/或R2X也可以是X为NH的氨基酸残基。

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