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nya benso / b / tiofener, benso / b / furaner, tiokromaner och kromaner med antimikrob aktivitet

机译:新型苯并// b /噻吩,具有抗菌活性的苯并/呋喃,硫代色满和色满

摘要

Compounds whose formula is I, IMAGE where n is 0 or a whole number 1-4; p is 0 or 1; q is 0, 1 or 2, R1 and R2 are independently of each other hydrogen or halogen atoms or lower alkyl, lower halogenalkyl, nitro or NR2R3 groups, where R2 and R3 are independently of each other hydrogen atoms or lower alkyl groups; or R and R1 in adjacent positions form a fused saturated or unsaturated carbocyclic ring which can contain 5-7 carbon atoms; X is an acid or a sulphur atom, or a sulphinyl or sulphonyl group; Y is an imidazolyl or 1,2,4-triazolyl group, both of which can be substituted with a lower alkyl or aryl group, where said aryl group is a phenyl, halogenphenyl or lower alkylphenyl group; Z is an alkyl, alkenyl, alkynyl, cycloalkyl or heterocyclic aromatic group, in which there can be at least 1 substituent chosen from halogen atoms and from lower alkyl, lower alkoxy, lower alkylidenedioxy, phenyl and N-(N'-lower alkanoylpiperazinyl) groups, provided that, where n is 0, Z is not 1-alkynyl, and where n is 1-4, Z can also be an alkoxy, alkylthio, aryl, aryloxy or arylthio group, or aryl, aryloxy or arylthio group containing substituents chosen from halogen atoms and lower alkyl, lower alkoxy, lower alkylidenedioxy and N- (N'-lower alkanoylpiperazinyl) groups, where the designation "lower" refers to groups with 1-6 carbon atoms; and the broken line refers to a single bond or a double bond, provided that it is a double bond only when p is 0 and X is a sulphur atom; and the acid addition salts thereof have an antimicrobial, particularly antifungal, antibacterial and antiprotozoal activity. The invention also relates to mixtures, particularly pharmaceutical mixtures which contain these compounds, as well as the method for production thereof.
机译:分子式为I,的化合物,其中n为0或整数1-4; p为0或1; q为0、1或2,R 1和R 2彼此独立地为氢或卤素原子或低级烷基,低级卤代烷基,硝基或NR 2 R 3基团,其中R 2和R 3彼此独立地为氢原子或低级烷基;或R和R1在相邻位置形成稠合的饱和或不饱和碳环,可含有5-7个碳原子; X是酸或硫原子,或亚磺酰基或磺酰基; Y为咪唑基或1,2,4-三唑基,两者均可被低级烷基或芳基取代,其中所述芳基为苯基,卤代苯基或低级烷基苯基; Z为烷基,烯基,炔基,环烷基或杂环芳族基团,其中可以存在至少1个选自卤素原子和选自低级烷基,低级烷氧基,低级亚烷基二氧基,苯基和N-(N'-低级烷酰基哌嗪基)的取代基(n为0时,Z不是1-炔基,n为1-4时,Z也可以是烷氧基,烷硫基,芳基,芳氧基或芳硫基,或含芳基,芳氧基或芳硫基的取代基)选自卤素原子和低级烷基,低级烷氧基,低级亚烷基二氧基和N-(N'-低级烷酰基哌嗪基)基团,其中“低级”是指具有1-6个碳原子的基团;虚线是指单键或双键,只要仅在p为0且X为硫原子时为双键即可。及其酸加成盐具有抗菌作用,特别是抗真菌,抗菌和抗原生动物活性。本发明还涉及混合物,特别是包含这些化合物的药物混合物,以及其制备方法。

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