发明名称 IMIDAZONAPHTHYRIDINES, PHARMACEUTICAL COMPOSITION BASED ON THEREOF, METHOD FOR STIMULATING BIOSYNTHESIS OF CYTOKINE AND INTERMEDIATE COMPOUNDS
摘要 FIELD: organic chemistry, biochemistry, pharmacy. SUBSTANCE: invention relates to new imidazonaphthyridines of formulas (I) and (II) wherein A represents =N-CR=CR-CR=, =CR-N= CR-CR= , = CR-CR= N-CR or =CR-CR=CR-N=; B represents NR -C(R)2-C(R)2-C(R)2, C(R)2-NR-C(R)2-C(R)2, -C(R)2-C(R)2-NR-C(R)2 or C(R)2-C(R)2-C(R)2-NR wherein R is hydrogen atom; R14 is unsubstituted or substituted C1-20-alkyl; C1-20-alkylene-NR3-Q-X-R4 wherein Q represents CO or -SO2-; X is a simple bond, -O- or -NR3; R4 is aryl, heteroaryl, heterocyclyl or C1-20-alkyl or C2-20-alkenyl. Other values of radicals are given in the invention claim. Compounds of formulas (I) and (II) stimulate synthesis of cytokines, such as interferon and tumor necrosis factor and can be used in medicine. Invention relates also to pharmaceutical compositions and intermediate compounds. EFFECT: valuable biological and medicinal properties of compounds. 20 cl, 5 tbl, 213 ex
申请公布号 RU2221798(C2) 申请公布日期 2004.01.20
申请号 RU20000114496 申请日期 1998.12.11
申请人 发明人 LINGSTROM KAJL DZH.;GERSTER DZHON F.
分类号 A61K31/4375;A61K31/4439;A61K31/444;A61K31/4745;A61K31/522;A61P7/00;A61P17/00;A61P29/00;A61P31/12;A61P33/00;A61P35/00;A61P37/02;A61P43/00;C07D213/00;C07D233/00;C07D257/00;C07D401/04;C07D471/04;C07D471/14;C07D471/22;C07D519/00 主分类号 A61K31/4375
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