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SYNTHESIS AND CYTOTOXIC STUDIES OF BARBITURIC ACID DERIVATIVES

机译:巴比酸衍生物的合成及细胞毒性研究

摘要

Novel barbituric acid derivatives of formula (I) wherein "—" represents a bond or no bond; Gr represents a group of formulae selected from wherein R1 and R2 are independently selected from hydrogen, halogen, hydroxy, lower alkyloxy, lower alkyl (C1-C4), substituted or unsubstituted aryloxy, aralkoxy; heteroaryloxy, heteroaralkoxy, cycloalkyloxy, cycloalkoxy; ii) indole benzenesulphonyl derivative of formula wherein R4, R5, R6 and R7 are independently selected from hydrogen, halogen, hydroxyl, cyano, nitro, amino, amido, thio, C2-C5 lower alkyl, lower alkylo"xy, lower alkanoyloxy, lower akanoyl; or its pharmaceutically acceptable salts, solvates, polymorphs, tautomers, optical and geometric isomers thereof, and one or more pharmaceutically acceptable carriers for the treatment of renal cancer.
机译:式(I)的新巴比妥酸衍生物,其中“-”代表一个键或没有键; Gr代表选自下式的一组基团:其中R1和R2独立地选自氢,卤素,羟基,低级烷氧基,低级烷基(C1-C4),取代或未取代的芳氧基,芳烷氧基;杂芳氧基,杂芳烷氧基,环烷氧基,环烷氧基; ii)下式的吲哚苯磺酰基衍生物,其中R 4,R 5,R 6和R 7独立地选自氢,卤素,羟基,氰基,硝基,氨基,酰胺基,硫代,C 2 -C 5低级烷基,低级烷基“ xy”,低级烷酰氧基,低级akanoyl;或其药学上可接受的盐,溶剂化物,多晶型物,互变异构体,光学和几何异构体,以及一种或多种治疗肾癌的药学上可接受的载体。

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