首页> 外国专利> Indolo2,3-b-, Indeno1,2-b- and Indeno2,1-bpyrido2,3-f quinoxaline-3-carboxylic acids and esters, processes for their preparation and their use as antiviral, antibiotic and antitumor agents

Indolo2,3-b-, Indeno1,2-b- and Indeno2,1-bpyrido2,3-f quinoxaline-3-carboxylic acids and esters, processes for their preparation and their use as antiviral, antibiotic and antitumor agents

机译:吲哚并[2,3-b]-,茚并[1,2-b]-和茚并[2,1-b]吡啶并[2,3-f]喹喔啉-3-羧酸和酯的制备方法和它们用作抗病毒药,抗生素和抗肿瘤药

摘要

The present invention relates to novel quinoxaline derivatives represented by regioisomeric structures of quinoxalines of general formulas I and/or II,wherein the COOR1 group independently is an acid, an ester and/or a salt, Y1 and/or Y2 are independently halogen and/or H, in particular Y1 is fluorine, A is oxo (C=O), C(R3)2 and/or N-R2, wherein each R3 and/or R2 independently are H, linear, branched or cyclic unsubstituted or substituted hydrocarbon and X1 is H, halogen, linear, branched or cyclic unsubstituted or substituted hydrocarbon. The present invention relates further to a process for the production of the quinoxalines of formulas I and II, a key precursor as well as their use as pharmaceutical active agents, in particular as agents that are active against cancer, as antibiotic and/or at least one virus.
机译:本发明涉及由通式I和/或II的喹喔啉的区域异构结构表示的新型喹喔啉衍生物, <图像文件=“ IMGA0001.GIF” he =“ 47” imgContent =“ chem” imgFormat =“ GIF” wi =“ 105” /> 其中COOR 1 基团独立地是酸,酯和/或盐,Y 1 和/或Y 2 独立地是卤素和/或H,特别是Y 1 是氟,A是氧代(C = O),C(R 3 2 和/或NR 2 ,其中每个R 3 和/或R 2 独立地为H,直链,支链或环状的未取代或取代的烃,X 1 是氢,卤素,直链,支链或环状未取代或取代的烃。本发明进一步涉及制备式I和II的喹喔啉,关键前体的方法及其作为药物活性剂的用途,特别是作为抗癌活性的剂,抗生素和/或至少一种病毒。

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