摘要:
The invention provides an indazole derivative of formula (1), or a pharmaceutically acceptable salt or N-oxide thereof, wherein R1, R2, R3 and R4 are as defined herein. The indazole derivatives are capable of blockading voltage dependent sodium channels and they are useful in the treatment or prevention of normal tension glaucoma, multiple sclerosis, a motorneurone disease, stroke, spinal cord injury, Alzheimer's disease, Parkinson's disease or pain.
摘要:
The present invention relates to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein Z is OR1 or NR1R2 wherein each of R1 and R2 is independently H, or a hydrocarbyl group; X is an alkylene, alkenylene, or alkynylene group, each of which may be optionally substituted by one or more substituents selected from alkyl, COOH, CO2-alkyl, alkenyl, CN, NH2, hydroxy, halo, alkoxy, CF3 and nitro; Y is a polar functional group selected from OH, NO2, CN, COR3, COOR3, NR3R4, CONR3R4, SO3H, SO2—R3, SO2NR3R4 and CF3, where each of R3 and R4 is independently H or a hydrocarbyl group; A is an aryl or heteroaryl group, each of which may be optionally substituted; and B is (CH2)n where n is 0, 1, 2, 3, 4 or 5; with the proviso that: (i) when A is phenyl, n is 0, and Z is OH, X—Y is other than meta-C≡—C—(CH2)2CO2H, meta-C≡—C—(CH2)2OH, meta-C≡C—(CH2)2CO2Me, meta-(CH2)4CO2H, ortho-CH2CO2H, ortho-(CH2)2CO2H and ortho-(CH2)4CO2H; and (ii) when A is phenyl, n is 0, and Z is OMe, X—Y is other than meta-C≡C—(CH2)4OH. Further aspects of the invention relate to the use of such compounds in the preparation of a medicament for the treatment of a muscular disorder, a gastrointestinal disorder, or for controlling spasticity or tremors.
摘要翻译:本发明涉及式(I)化合物或其药学上可接受的盐,其中Z为OR 1或NR 1 R 2,其中R 1和R 2各自独立地为H或烃基; X是亚烷基,亚烯基或亚炔基,其各自可以任选地被一个或多个选自烷基,COOH,CO 2 - 烷基,烯基,CN,NH 2,羟基,卤素,烷氧基,CF 3和硝基的取代基取代; Y是选自OH,NO2,CN,COR3,COOR3,NR3R4,CONR3R4,SO3H,SO2-R3,SO2NR3R4和CF3的极性官能团,其中R3和R4各自独立地为H或烃基; A是芳基或杂芳基,其各自可以任选被取代; 和B是(CH 2)n,其中n是0,1,2,3,4或5; 条件是:(i)当A是苯基时,n是0,Z是OH,X-Y不是间位-C≡-C-(CH 2)2 CO 2 H,间-C≡C-(CH 2) (CH 2)2 CO 2 Me,间 - (CH 2)4 CO 2 H,邻-CH 2 CO 2 H,邻 - (CH 2)2 CO 2 H和邻 - (CH 2)4 CO 2 H; 和(ii)当A是苯基时,n是0,Z是OMe,X-Y不是间位-C≡C-(CH 2)4 OH。 本发明的其它方面涉及这样的化合物在制备用于治疗肌肉疾病,胃肠道疾病或用于控制痉挛或震颤的药物中的用途。
摘要:
The present invention relates to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein Z is OR1 or NR1R2 wherein each of R1 and R2 is independently H, or a hydrocarbyl group; X is an alkylene, alkenylene, or alkynylene group, each of which may be optionally substituted by one or more substituents selected from alkyl, COOH, CO2-alkyl, alkenyl, CN, NH2, hydroxy, halo, alkoxy, CF3 and nitro; Y is a polar functional group selected from OH, NO2, CN, COR3, COOR3, NR3R4, CONR3R4, SO3H, SO2—R3, SO2NR3R4 and CF3, where each of R3 and R4 is independently H or a hydrocarbyl group; A is an aryl or heteroaryl group, each of which may be optionally substituted; and B is (CH2)n where n is 0, 1, 2, 3, 4 or 5; with the proviso that: (i) when A is phenyl, n is 0, and Z is OH, X—Y is other than meta-C≡—C—(CH2)2CO2H, meta-C≡—C—(CH2)2OH, meta-C≡C—(CH2)2CO2Me, meta-(CH2)4CO2H, ortho-CH2CO2H, ortho-(CH2)2CO2H and ortho-(CH2)4CO2H; and (ii) when A is phenyl, n is 0, and Z is OMe, X—Y is other than meta-C≡C—(CH2)4OH. Further aspects of the invention relate to the use of such compounds in the preparation of a medicament for the treatment of a muscular disorder, a gastrointestinal disorder, or for controlling spasticity or tremors.
摘要:
The present invention relates to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein Z is OR1 or NR1R2 wherein each of R1 and R2 is independently H, or a hydrocarbyl group; X is an alkylene, alkenylene, or alkynylene group, each of which may be optionally substituted by one or more substituents selected from alkyl, COOH, CO2-alkyl, alkenyl, CN, NH2, hydroxy, halo, alkoxy, CF3 and nitro; Y is a polar functional group selected from OH, NO2, CN, COR3, COOR3, NR3R4, CONR3R4, SO3H, SO2—R3, SO2NR3R4 and CF3, where each of R3 and R4 is independently H or a hydrocarbyl group; A is an aryl or heteroaryl group, each of which may be optionally substituted; and B is (CH2)n where n is 0, 1, 2, 3, 4 or 5; with the proviso that: (i) when A is phenyl, n is 0, and Z is OH, X—Y is other than meta-C≡—C—(CH2)2CO2H, meta-C≡—C—(CH2)2OH, meta-C≡C—(CH2)2CO2Me, meta-(CH2)4CO2H, ortho-CH2CO2H, ortho-(CH2)2CO2H and ortho-(CH2)4CO2H; and (ii) when A is phenyl, n is 0, and Z is OMe, X—Y is other than meta-C≡C—(CH2)4OH. Further aspects of the invention relate to the use of such compounds in the preparation of a medicament for the treatment of a muscular disorder, a gastrointestinal disorder, or for controlling spasticity or tremors.
摘要翻译:本发明涉及式(I)化合物或其药学上可接受的盐,其中Z为OR 1或NR 1 R 2,其中R 1和R 2各自独立地为H或烃基; X是亚烷基,亚烯基或亚炔基,其各自可以任选地被一个或多个选自烷基,COOH,CO 2 - 烷基,烯基,CN,NH 2,羟基,卤素,烷氧基,CF 3和硝基的取代基取代; Y是选自OH,NO2,CN,COR3,COOR3,NR3R4,CONR3R4,SO3H,SO2-R3,SO2NR3R4和CF3的极性官能团,其中R3和R4各自独立地为H或烃基; A是芳基或杂芳基,其各自可以任选被取代; 和B是(CH 2)n,其中n是0,1,2,3,4或5; 条件是:(i)当A是苯基时,n是0,Z是OH,X-Y不是间位-C≡-C-(CH 2)2 CO 2 H,间-C≡C-(CH 2) (CH 2)2 CO 2 Me,间 - (CH 2)4 CO 2 H,邻-CH 2 CO 2 H,邻 - (CH 2)2 CO 2 H和邻 - (CH 2)4 CO 2 H; 和(ii)当A是苯基时,n是0,Z是OMe,X-Y不是间位-C≡C-(CH 2)4 OH。 本发明的其它方面涉及这样的化合物在制备用于治疗肌肉疾病,胃肠道疾病或用于控制痉挛或震颤的药物中的用途。
摘要:
The present invention relates to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein Z is OR1 or NR1R2 wherein each of R1 and R2 is independently H, or a hydrocarbyl group; X is an alkylene, alkenylene, or alkynylene group, each of which may be optionally substituted by one or more substituents selected from alkyl, COOH, CO2-alkyl, alkenyl, CN, NH2, hydroxy, halo, alkoxy, CF3 and nitro; Y is a polar functional group selected from OH, NO2, CN, COR3, COOR3, NR3R4, CONR3R4, SO3H, SO2—R3, SO2NR3R4 and CF3, where each of R3 and R4 is independently H or a hydrocarbyl group; A is an aryl or heteroaryl group, each of which may be optionally substituted; and B is (CH2)n where n is 0, 1, 2, 3, 4 or 5; with the proviso that: (i) when A is phenyl, n is 0, and Z is OH, X—Y is other than meta-C≡—C—(CH2)2CO2H, meta-C≡—C—(CH2)2OH, meta-C≡C—(CH2)2CO2Me, meta-(CH2)4CO2H, ortho-CH2CO2H, ortho-(CH2)2CO2H and ortho-(CH2)4CO2H; and (ii) when A is phenyl, n is 0, and Z is OMe, X—Y is other than meta-C≡C—(CH2)4OH. Further aspects of the invention relate to the use of such compounds in the preparation of a medicament for the treatment of a muscular disorder, a gastrointestinal disorder, or for controlling spasticity or tremors.
摘要翻译:本发明涉及式(I)化合物或其药学上可接受的盐,其中Z为OR 1或NR 1 R 2,其中R 1和R 2各自独立地为H或烃基; X是亚烷基,亚烯基或亚炔基,其各自可以任选地被一个或多个选自烷基,COOH,CO 2 - 烷基,烯基,CN,NH 2,羟基,卤素,烷氧基,CF 3和硝基的取代基取代; Y是选自OH,NO2,CN,COR3,COOR3,NR3R4,CONR3R4,SO3H,SO2-R3,SO2NR3R4和CF3的极性官能团,其中R3和R4各自独立地为H或烃基; A是芳基或杂芳基,其各自可以任选被取代; 和B是(CH 2)n,其中n是0,1,2,3,4或5; 条件是:(i)当A是苯基时,n是0,Z是OH,X-Y不是间位-C≡-C-(CH 2)2 CO 2 H,间-C≡C-(CH 2) (CH 2)2 CO 2 Me,间 - (CH 2)4 CO 2 H,邻-CH 2 CO 2 H,邻 - (CH 2)2 CO 2 H和邻 - (CH 2)4 CO 2 H; 和(ii)当A是苯基时,n是0,Z是OMe,X-Y不是间位-C≡C-(CH 2)4 OH。 本发明的其它方面涉及这样的化合物在制备用于治疗肌肉疾病,胃肠道疾病或用于控制痉挛或震颤的药物中的用途。
摘要:
The present invention relates to a compound of formula I, or a pharmaceutically acceptable salt thereof. Formula (I), wherein R1 and R2 are each independently H or alkyl; Y is an alkyl group. CONR3R4, COOR5SO2NR16R17, NHSO2R18 or CN; X is an aryl or heteroaryl group, each of which may be optionally substituted with one or more substituents selected from (CH2)mZ where Z is halogen, OH, CN, alkyl, alkoxy, NO2, CF3, CONR6R7, CN, NR8R9, COOR10 or NHCOR11 and m is 0 to 3; R3 to R11 are each independently H, alkyl or aryl, wherein said alkyl and aryl groups are optionally substituted by one or more substituents selected from halogen, OH, CN, alkyl, alkoxy, NO2, CF3, CONR12R13, CN, NH2, COOR14, NHCOR15, and CN; R12 to R18 are each independently H or alkyl, more preferably H or Me; n is 1 to 6; wherein the compound is other than 3′,5′-dimethyl-4-(1,1-dimethylheptyl)-1,1′-biphenyl-2-ol. Further aspects of the invention related to the use of such compounds in the preparation of a medicament for the treatment of a muscular disorder, a gastrointestinal disorder, or for controlling spasticity or tremors.
摘要:
The invention relates to a polypeptide or part thereof which inhibits the apoptotic activity of the tumor suppressor protein p53, and includes screening methods to identify agents which interfere with the activity of the polypeptide.
摘要:
Compounds of Formula I and pharmaceutically acceptable salts thereof, are capable of blockading voltage-dependent sodium channels and are useful in particular, in treating glaucoma and multiple sclerosis.