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PIPERAZINE DERIVATIVES FOR THE REPLICATION INHIBITION OF HUMAN IMMUNODICITY VIRUS

机译:哌嗪衍生物可抑制人免疫力病毒的复制

摘要

The invention concerns the use of a piperazine derivative of formula (I)wherein: A and B=C=O, C=S or CR7R8 with R7=H, methyl, cyano, cyanomethyl, CO2CH3 or (C=O)CH3 and R8=H or phenyl; R1 to R6=H, OH, or C1-C5 alkoxy; X represents: either C=O, O(C=O), O(C=S), O(SO2), NH(C=O), NH(C=S), NH(SO2), S(C=O) or S(C=S), then Y=NR9R10, CR9R10R11 in which R9, R10 and R11=H, C1-C5 alkyl, C2-C5 alkenyl, or C2-C5 alkynyl or Y=nitrogenous heterocycle comprising 5 to 10 atoms; or X represents O, S, O(C=O)O, NH(C=O)O, or S(C=O)O, then Y=CR9R10R11 with R9, R10, R11 as above; or one of its pharmaceutically acceptable salts for preparing a medicine inhibiting HIV. The invention is useful for treating HIV infection.
机译:本发明涉及式(I)的哌嗪衍生物的用途,其中:A和B = C = O,C = S或CR 7 R 8,其中R 7 = H,甲基,氰基,氰甲基,CO 2 CH 3或(C = O)CH 3和R 8 = H或苯基; R1至R6 = H,OH或C1-C5烷氧基; X表示:C = O,O(C = O),O(C = S),O(SO2),NH(C = O),NH(C = S),NH(SO2),S(C = O)或S(C = S),则Y = NR9R10,CR9R10R11,其中R9,R10和R11 = H,C1-C5烷基,C2-C5烯基或C2-C5炔基或Y =含5至10的氮杂环原子或X代表O,S,O(C = O)O,NH(C = O)O或S(C = O)O,则Y = CR9R10R11,具有如上所述的R9,R10,R11;或其药学上可接受的盐之一,用于制备抑制HIV的药物。本发明可用于治疗HIV感染。

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