The present invention concerns a spiroisoxazoline compound of general formula (I):
in which m and n are 0 or 1, R1 represents, inter alia, an optionally substituted alkyl chain, in particular substituted with fluorine or with a cyclic group, and R2 is chosen from phenyl and optionally substituted benzyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the heterocycles having 5 or 6 vertices comprising at least one atom chosen from S, N and O. The present invention also concerns the use of this compound as a drug, in particular in the treatment of bacterial and mycobacterial infections such as tuberculosis in combination with an antibiotic that is active against bacteria and/or mycobacteria, said compound potentiating the activity of said antibiotic.
本发明涉及一种通式(I)的螺环异氧唑啉化合物:其中m和n为0或1,R1代表,包括但不限于,一个可选择取代的烷基链,特别是取代有
氟或环状基团的烷基链,R2选自苯基和可选择取代的苄基、环丙基、
环丁基、环戊基、环己基,以及含有至少一种来自S、N和O的原子的5个或6个顶点的杂环。本发明还涉及将该化合物用作药物的用途,特别是在与对细菌和/或分枝杆菌活性的抗生素结合治疗细菌和分枝杆菌感染,该化合物增强了该抗生素的活性。