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Indolo2,1-b quinazole-6,12-dione antimalarial compounds and methods of treating malaria therewith

机译:吲哚并[2,1-b]喹唑-6,12-二酮抗疟化合物及其治疗疟疾的方法

摘要

Compounds, compositions and methods are provided for treating malaria parasites in vitro and in vivo by administering indolo [2,1-b]quinazoline-6,12-dione compounds of Formula I.; embedded image wherein A, B, C, D, B, F, G and H are independently selected from carbon and nitrogen, or A and B or C and D can be taken together to be nitrogen or sulfur, with the proviso that not more than three of A, B, C, D, E, F, G and H are other than carbon; wherein R1 through R8 are independently selected from the group consisting of, but not limited to H, the halogens (F, Cl, Br, and I), alkyl groups, trifluoromethyl groups, methoxyl groups, the carboxy methyl or carboxy ethyl group (COOCH3 or COOCH2CH3), nitro, aryl, heteroaryl, cyano, amino, dialkylaminoalkyl, 1-(4-alkylpiperazinyl), and the pharmaceutically acceptable salts thereof; and wherein X is independently selected from the group consisting of any atom especially oxygen, or any side chain necessary to make the indolo[2,1-b]quinazoline-6,12-dione compound a “prodrug” as the term is understood by one of ordinary skill in the art of medicinal chemistry. In other words, a side chain having a structure where a carbon-nitrogen double bond bears substituents that make the prodrug more water soluble and bioavailable.
机译:提供了通过施用式I的吲哚[2,1-b]喹唑啉-6,12-二酮化合物在体外和体内治疗疟原虫的化合物,组合物和方法。 “嵌入式图像” 其中A,B,C,D,B,F,G和H独立地选自碳和氮,或者A和B或C和D可以一起为氮或硫,条件是不超过三个A,B,C,D,E,F,G和H中的碳原子除外其中R 1 至R 8 独立地选自但不限于H,卤素(F,Cl,Br和I),烷基,三氟甲基,甲氧基,羧甲基或羧乙基(COOCH 3 或COOCH 2 CH 3 ),硝基,芳基,杂芳基,氰基,氨基,二烷基氨基烷基,1-(4-烷基哌嗪基)及其药学上可接受的盐;其中X独立地选自任何原子,尤其是氧,或使吲哚并[2,1-b]喹唑啉-6,12-二酮化合物成为“前药”所必需的任何侧链,药物化学领域的普通技术之一。换句话说,具有碳氮双键带有取代基的结构的侧链,这些取代基使前药具有更高的水溶性和生物利用度。

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