摘要:
The invention relates to thiazolidinones of general formula ( I ), wherein Q, A, B, X, R1 and R2 have the meaning cited in the description, and the general formula (IA) wherein Q, A, B, X, R1 and R2a have the meaning cited in the description, to the production and use thereof as inhibitors of the Polo Like Kinase (PLK) for the treatment of different diseases. The invention also relates to intermediate products for the production of thiazolidinones.
摘要:
The invention relates to selected anthranylamide pyridones that inhibit VEGFR-2 and VEGFR-3 and to their use as medicaments for treating diseases that are triggered by persistent angiogenesis.
摘要:
New 17α-fluoralkyl steroids have general formula (I), in which R1 stands for a methyl or ethyl group; R2 for a radical of formula C¿n?FmHo, in which n equals 2, 3, 4, 5 or 6, m⊃1 and m+o = 2n+1; R?3¿ stands for a free, etherified or esterified hydroxy group; R?4 and R5¿ stand each for a hydrogen atom, or together for an additional bond or a methylene group; St stands for a steroidal ABC ring system of partial formulas (A), (B) or (C), in which R6 stands for a hydrogen atom, a straight chain C¿1?-C4- or branched chain C3-C4-alkyl group or a halogen atom; R?7¿ stands for a hydrogen atom, a straight chain C¿1?-C4- or branched chain C3-C4-alkyl group or, when St stands for a steroidal ABC ring system of formulas (A) or (B), R?6 and R7¿ can form together an additional bond; X stands for an oxygen atom, an hydroxyimino group =N∩OH or two hydrogen atoms; R8 stands for a radical Y or for an aryl radical optionally substituted several times with a group Y, in which Y stands for a hydrogen atom, a halogen atom, an -OH, -NO¿2?, -N3, -CN, -NR?9aR9b¿, -NHSO¿2?R?9, -CO¿2R9, C1-C10-alkyl, C1-C10-alkoxy, C1-C10-alcanoyloxy, benzoyloxy, C1-C10-alkanoyl, C1-C10-hydroxyalkyl or benzoyl group, and R?9a and R9b¿ are the same or different and like R9 represent a hydrogen atom or a C¿1?-C10-alkyl group. Also disclosed are the physiologically admissible salts of these steroids with acids, when they contain the radicals NR?9aR9b¿, and their physiologically admissible salts with bases, when they contain the radicals -CO¿2R?9, in which R9 stands for hydrogen. These new compounds display an extraordinarily strong antigestagenic activity and are suitable for preparing pharmaceutical compositions.
摘要翻译:新的17α-氟烷基甾族化合物具有通式(I),其中R 1代表甲基或乙基; R2代表式C≡nFmHo的基团,其中n等于2,3,4,5或6,m⊃1和m + o = 2n + 1; R 3'代表游离的醚化或酯化的羟基; R 4和R 5分别代表氢原子或一起代表另外的键或亚甲基; St表示部分式(A),(B)或(C)的甾族ABC环系,其中R 6代表氢原子,直链C 1 -C 4或支链C 3 -C 4烷基 基团或卤素原子; R 7代表氢原子,直链C 1 -C 4 - 或支链C 3 -C 4 - 烷基,或当St代表式(A)或(B)的甾体ABC环系时, R 6和R 7可以一起形成另外的键; X代表氧原子,羟基亚氨基=N∩OH或两个氢原子; R 8代表基团Y或任选用基团Y取代若干次的芳基,其中Y代表氢原子,卤素原子,-OH,-NO 2,-N 3,-CN, - -NR 9 R 9,-CO 2 R 9,C 1 -C 10烷基,C 1 -C 10烷氧基,C 1 -C 10烷酰氧基,苯甲酰氧基,C 1 -C 10烷酰基,C 1 -C 10羟基烷基 或苯甲酰基,而R 9a和R 9b可以相同或不同,和R 9一样代表氢原子或C 1 -C 10烷基。 还公开了当这些甾族化合物含有基团-NR9aR9b'时,这些甾族化合物与酸的生理上可接受的盐,以及当它们含有基团-CO2R9,其中R9代表氢时,它们与碱的生理上可接受的盐。 这些新化合物表现出非常强的抗孕激素活性并且适用于制备药物组合物。
摘要:
A method of inhibiting the occurrence of advanced endometrium maturation in a female mammal undergoing fertility treatment is disclosed. The method comprises the administration at least one 17α-fluoralkylated progesterone receptor antagonist to the female mammal.
摘要:
New 17 alpha -fluoralkyl steroids have general formula (I), in which R stands for a methyl or ethyl group; R for a radical of formula CnFmHo, in which n equals 2, 3, 4, 5 or 6, m>1 and m+o = 2n+1; R stands for a free, etherified or esterified hydroxy group; R and R stand each for a hydrogen atom, or together for an additional bond or a methylene group; St stands for a steroidal ABC ring system of partial formulas (A), (B) or (C), in which R stands for a hydrogen atom, a straight chain C1-C4- or branched chain C3-C4-alkyl group or a halogen atom; R stands for a hydrogen atom, a straight chain C1-C4- or branched chain C3-C4-alkyl group or, when St stands for a steroidal ABC ring system of formulas (A) or (B), R and R can form together an additional bond; X stands for an oxygen atom, an hydroxyimino group =N SIMILAR OH or two hydrogen atoms; R stands for a radical Y or for an aryl radical optionally substituted several times with a group Y, in which Y stands for a hydrogen atom, a halogen atom, an -OH, -NO2, -N3, -CN, -NR R , -NHSO2R , -CO2R , C1-C10-alkyl, C1-C10-alkoxy, C1-C10-alcanoyloxy, benzoyloxy, C1-C10-alkanoyl, C1-C10-hydroxyalkyl or benzoyl group, and R and R are the same or different and like R represent a hydrogen atom or a C1-C10-alkyl group. Also disclosed are the physiologically admissible salts of these steroids with acids, when they contain the radicals NR R , and their physiologically admissible salts with bases, when they contain the radicals -CO2R , in which R stands for hydrogen. These new compounds display an extraordinarily strong antigestagenic activity and are suitable for preparing pharmaceutical compositions.
摘要翻译:新的17α-氟烷基甾族化合物具有通式(I),其中R 1代表甲基或乙基; R 2代表式C n F m H o的基团,其中n等于2,3,4,5或6,m> 1且m + o = 2n + 1; R3表示游离的,醚化或酯化的羟基; R 4和R 5分别代表氢原子或一起代表另外的键或亚甲基; St代表部分式(A),(B)或(C)的甾族ABC环系,其中R 6代表氢原子,直链C 1 -C 4或支链C 3 -C 4烷基 基团或卤素原子; R 7代表氢原子,直链C 1 -C 4或支链C 3 -C 4烷基,或者当St代表式(A)或(B)的甾体ABC环系统时,R 6 和R 7可以一起形成另外的键; X代表氧原子,羟基亚氨基= N-X OH或两个氢原子; R 8代表基团Y或任选用基团Y取代若干次的芳基,其中Y代表氢原子,卤素原子,-OH,-NO 2,-N 3,-CN, - NR 9 R 9b,-NHSO 2 R 9,-CO 2 R 9,C 1 -C 10烷基,C 1 -C 10烷氧基,C 1 -C 10烷酰氧基,苯甲酰氧基,C 1 -C 10烷酰基,C 1 -C 10 羟基烷基或苯甲酰基,并且R 9a和R 9b相同或不同,并且如R 9代表氢原子或C 1 -C 10烷基。 还公开了这些类固醇与酸的生理上可接受的盐,当它们含有基团NR 9 R 9b时,以及它们与碱的生理上可接受的盐,当它们含有基团-CO 2 R 9时, 9>代表氢。 这些新化合物表现出非常强的抗孕激素活性并且适用于制备药物组合物。