首页> 外国专利> DERIVATIVES OF PHENANTHRIDINE, METHODS OF THEIR SYNTHESIS AND MEDICINAL AGENTS CONTAINING PHENANTHRIDINE DERIVATIVES

DERIVATIVES OF PHENANTHRIDINE, METHODS OF THEIR SYNTHESIS AND MEDICINAL AGENTS CONTAINING PHENANTHRIDINE DERIVATIVES

机译:菲应的衍生物,其合成方法和含有菲应的药物制剂

摘要

FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to novel derivatives of phenanthridine of the general formula (I) and (II) and their salts where R1 means aromatic carbocyclic residue originating from benzene or naphthalene or it means heterocyclic residue originating from furan, thiophene or pyridine. R1 can involve one or some substituents which are taken among monoamino-, alkylamino-, dialkylamino-, alkyl-, alkoxy-, alkyleneoxy- group and halogen atom; R2 and R3 can be similar or different and mean hydrogen atom, alkoxyl-group, alkyleneoxyl-group, halogen atom or nitro-group. Invention relates to also methods of synthesis of indicated compounds and medicinal agent eliciting antitumor, antibacterial, antifungal, antiviral and anti-inflammatory activity and containing these compounds. Invention can be used in medicine as a medicinal preparation. EFFECT: new compounds indicated above, improved method of synthesis, valuable medicinal properties. 11 cl, 9 dwg, 3 tbl, 6 ex
机译:领域:有机化学,药学。物质:发明涉及通式(I)的菲啶的新衍生物。和(II )<图像文件=“ 00000005.GIF” he =“ 43” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 47” />及其盐,其中R 1 表示源自芳族碳环残基衍生自苯或萘的杂环残基,或指源自呋喃,噻吩或吡啶的杂环残基。 R 1 可涉及一个或一些取代基,其选自单氨基,烷基氨基,二烷基氨基,烷基,烷氧基,亚烷基氧基和卤素原子; R 2 和R 3 可以相同或不同,表示氢原子,烷氧基,亚烷基氧基,卤素原子或硝基。本发明还涉及引起抗肿瘤,抗菌,抗真菌,抗病毒和抗炎活性并含有这些化合物的所示化合物和药物的合成方法。本发明可以在医学上用作药物制剂。效果:以上指出的新化合物,改进的合成方法,有价值的药用特性。 11 cl,9 dwg,3 tbl,6 ex

著录项

  • 公开/公告号RU2180333C2

    专利类型

  • 公开/公告日2002-03-10

    原文格式PDF

  • 申请/专利权人 KLEMENT BERND (DE);

    申请/专利号RU19980108615

  • 发明设计人 KLEMENT BERND (DE);VAJDE MATTIAS (DE);

    申请日1996-10-11

  • 分类号C07D221/18;A61K31/473;A61P35/00;A61P31/00;A61P29/00;

  • 国家 RU

  • 入库时间 2022-08-22 00:28:17

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