摘要:
The invention provides compounds of formula (I): wherein R1, R2, R3, R6, Z, Q, m, n, X1, X2, X3, X4 and T are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them, and their use in therapy, especially for the treatment of chemokine receptor related diseases and conditions.
摘要:
The invention provides compounds of formula (I) wherein R1, R2, R3, R6, Z, Q, m, n, X1, X2, X3, X4 and T are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them, and their use in therapy, especially for the treatment of chemokine receptor related diseases and conditions
摘要:
The invention provides a compound of formula (I): wherein R1, R2, R3, R4, R5, N, X and Y are as defined in the specification, processes, for their preparation, pharmaceutical compositions containing them, and their use in therapy, especially for the treatment of chemokine receptor related diseases and conditions.
摘要翻译:本发明提供式(I)化合物:其中R 1,R 2,R 3,R 4, R 5,N,X和Y如说明书中所定义,其制备方法,含有它们的药物组合物及其在治疗中的用途,特别是用于治疗趋化因子受体相关疾病 和条件。
摘要:
The invention provides compounds of formula (I) wherein: T is C(O) or S(O)2; W is C(O) or S(O)2; X is CH2, O or NH; Y is CR11 or N; n is 0, 1 or 2; m is 1 or, when Y is CR11 m is 0; R1 is optionally substituted aryl or optionally substituted heterocyclyl; R2, R3, R,4, R5, R6, R7 and R8 are, independently, hydrogen or C?1-6#191 alkyl; R9 is hydrogen or C1-C6 alkyl; R10 is alkyl, optionally substituted aryl, optionally substituted aralkyl or optionally substituted heterocyclyl; and R11 is hydrogen or C1-C6 allkyl; that are modulators of chemokine (especially CCR3) activity and are especially useful for treating asthma and/or rhinitis.
摘要翻译:本发明提供式(I)化合物,其中:T为C(O)或S(O)2; W是C(O)或S(O)2。 X是CH 2,O或NH; Y是CR 11或N; n为0,1或2; m为1或Y为CR 11时m为0; R 1是任选取代的芳基或任选取代的杂环基; R 2,R 3,R 3,R 5,R 5,R 6, R 7和R 8分别独立地为氢或C 1-6烷基; R 9是氢或C 1 -C 6烷基; R 9是氢或C 1 -C 6烷基; R 10是烷基,任选取代的芳基,任选取代的芳烷基或任选取代的杂环基; 并且R 11是氢或C 1 -C 6烷基; 它们是趋化因子(特别是CCR3)活性的调节剂,特别适用于治疗哮喘和/或鼻炎。
摘要:
The invention provides a compound of formula (I), wherein: T is C(O) or S(O)2; W is C(O) or S(O)2; X is CH2, O or NH; Y is CR5 or N; R1 is optionally substituted aryl or optionally substituted heterocyclyl; R2 is hydrogen or C1-6alkyl; R3 is hydrogen or optionally substituted C1-6alkyl; and R4 is alkyl, optionally substituted aryl, optionally substituted aralkyl or optionally substituted heterocyclyl; that are modulators of chemokine (especially CCR3) activity and are especially useful for treating asthma and/or rhinitis
摘要翻译:本发明提供式(I)化合物,其中:T是C(O)或S(O)2; W是C(O)或S(O)2。 X是CH 2,O或NH; Y是CR 5或N; R 1是任选取代的芳基或任选取代的杂环基; R 2是氢或C 1-6烷基; R 3是氢或任选取代的C 1-6烷基; 和R 4是烷基,任选取代的芳基,任选取代的芳烷基或任选取代的杂环基; 它们是趋化因子(特别是CCR3)活性的调节剂,特别适用于治疗哮喘和/或鼻炎
摘要:
The invention provides anhydrous and hydrated forms of sodium salt of N-[[4-(3,4-dichlorophenoxy)[1,4′-bipiperidin]-1′-yl]carbonyl]-4-methyl-benzenesulfonamide and crystalline forms of N-[[4-(3,4-dichlorophenoxy)[1,4′-bipiperidin]-1′-yl]carbonyl]-4-methyl-benzenesulfonamide; and such compounds are modulators of chemokine (especially CCR3) activity and are especially useful for treating asthma and/or rhinitis.
摘要:
The present invention provides a compound of a formula (I): wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a chemokine (such as CCR3) or H1 mediated disease state.
摘要:
The present invention relates to compounds of formula (I): The variables recited in formula (I) are defined in the specification. The present invention also relates to processes of preparing compounds of formula (I) and uses of such compounds for treating a chemokine (e.g., CCR3) or H1 mediated disease state.
摘要:
The present invention provides a compound of a formula (I): [Chemical formula should be inserted here. Please see paper copy] wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a chemokine (such as CCR3) mediated disease state.
摘要:
The present invention provides a compound of a formula (I): wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a chemokine (such as CCR3) or H1 mediated disease state.