摘要:
Disclosed are 4-sulfide/sulfoxide/sulfonyl-1H-pyrazolyl derivative compounds of formulas (I) or (II): wherein the variables n, R, R1, R2, R3, R3′, R4, R4′, R5 and R6 are as defined in the specification. The compounds are useful for the treatment or prevention of diseases and/or behaviors involving the 5-HT2C receptor.
摘要:
Disclosed are pyrazolyl derivative compounds or purified stereoisomers or stereoisomer mixtures of said compounds and their salts or prodrug forms thereof which have structural formula (I) or (II): wherein the variables R, R1, R2, R5 and R6 are as defined in the specification. The compounds are useful for the treatment or prevention of diseases and/or behaviors involving the 5-HT2C receptor.
摘要翻译:公开了具有结构式(I)或(II)的所述化合物及其盐或前药形式的吡唑基衍生物化合物或纯化的立体异构体或立体异构体混合物:其中变量R 1,R 1, SUB 2,R 5和R 6如说明书中所定义。 该化合物可用于治疗或预防涉及5-HT 2C受体的疾病和/或行为。
摘要:
This invention relates to novel 2,6-substituted chroman derivatives which are useful in the treatment of beta-3 adrenoreceptor-mediated conditions.
摘要:
The present invention relates to compounds of formula (I), pharmaceutical compositions which contain them and methods for treating cancer using compounds of formula (I).
摘要:
The present invention relates to compounds of formula (I), pharmaceutical compositions which contain them and methods for treating cancer using compounds of formula (I).
摘要:
The present invention relates to compounds of formula (I), pharmaceutical compositions which contain them and methods for treating cancer using compounds of formula (I).
摘要:
This invention relates to a compound of Formula I wherein Y is CH or N; Ar1 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each selected independently from (C1-C3)alkoxy, halo, OH, CF3, CN, NO2 and (C1-C3)alkyl, said alkyl being optionally substituted with CF3; Ar2 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each independently selected from halo, OH, CN, NO2, CF3, (C1-C6)alkoxy, NR1R1, S(O)2R2, C(O)R3, and (C1-C6)alkyl optionally substituted with R4, and its use in treating hyper-proliferative disorder.
摘要翻译:本发明涉及式I化合物,其中Y是CH或N; Ar1是各自任选被1或2个独立地选自(C 1 -C 3)烷氧基,卤素,OH,CF 3,CN,NO 2和(C 1 -C 3)烷基)的取代基取代的苯基或吡啶基,所述烷基任选被CF 3取代; Ar 2是苯基或吡啶基,其各自任选被1或2个独立地选自卤素,OH,CN,NO 2,CF 3,(C 1 -C 6)烷氧基,NR 1 R 1,S(O)2 R 2,C(O) 任选被R 4取代的C 1 -C 6)烷基,及其用于治疗高增殖性疾病。
摘要:
This invention relates to a compound of Formula (I) wherein Y is CH or N; Ar1 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each selected independently from (C1-C3)alkoxy halo, OH, CF3, CN, NO2 and (C1-C3)alkyl, said alkyl being optionally substituted with CF3; Ar2 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each independently selected from halo, OH, CN, NO2, CF3, (C1-C6)alkoxy, NR1R1, S(O)2R2, C(O)R3, and (C1-C6)alkyl optionally substituted with R4, and its use in treating hyper-proliferative disorders.