摘要:
The invention encompasses compounds of Formula I, pharmaceutically acceptable salts thereof, compositions, and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV.
摘要:
Indole compounds of Formula I are described. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV. Different forms and compositions comprising the compounds are also described as well as methods of preparing the compounds.
摘要:
This invention describes compounds of Formula (I) which are modulators of potassium channels and are useful for treating conditions affected by abnormal potassium channel activity including erectile dysfunction and irritable bowel syndrome.
摘要:
There is provided novel cinnamide derivatives of Formula I: wherein R is C1-4 alkyl or trifluoromethyl; R1 is selected from the group consisting of pyridinyl, quinolinyl, thienyl, furanyl, 1,4-benzodioxanyl, 1,3-benzodioxolyl, chromanyl, indanyl, biphenylyl, phenyl and substituted phenyl in which said substituted phenyl is substituted with one or two substituents each independently selected-from the group consisting of halogen, C1-4 alkyl, C1-4 alkoxy, trifluoromethyl, trifluoromethoxy and nitro; R2 and R3 are each independently selected from the group consisting of hydrogen, C1-4 alkyl, and halogen; R4 is selected from the group consisting of di(C1-4 alkyl)amino, trifluoromethoxy and optionally substituted morpholin-4-yl, pyridinyl, pyrimidinyl, piperazinyl, and pyrazinyl with one or two substituents in which said substituent is independently selected from the group consisting of C1-4 alkyl, aminomethyl, hydroxymethyl, chloro or fluoro; R5 is hydrogen, chloro or fluoro; or R4 and R5 taken together are —CH═CH—CH═CH— or —X(CH2)mY— in which X and Y are each independently selected from the group consisting of CH2, (CH2)nN(R9)— and O, wherein m is 1 or 2; n is 0 or 1; and R6, R7, and R8 are each independently selected from hydrogen, chloro and fluoro; and R9 is selected from the group consisting of hydrogen, C1-4 alkyl, hydroxyethyl, C1-4 alkoxyethyl, cyclopropylmethyl, —CO2(C1-4alkyl), and —CH2CH2NR10R11 in which R10 and R11 are each independently hydrogen or C1-4 alkyl, which are openers of the KCNQ potassium channels and are useful in the treatment of disorders which are responsive to the opening of the KCNQ potassium channels.
摘要翻译:提供式I的新颖的肉桂酰胺衍生物:其中R是C 1-4烷基或三氟甲基; R 1选自吡啶基,喹啉基,噻吩基,呋喃基,1,4-苯并二恶烷基,1,3-苯并二恶唑基,苯并二氢吡喃基,茚满基,联苯基,苯基和取代的苯基,其中所述取代的苯基被一个 或两个各自独立地选自卤素,C 1-4烷基,C 1-4烷氧基,三氟甲基,三氟甲氧基和硝基的取代基; R 2和R 3各自独立地选自氢,C 1-4烷基和卤素; R 4选自二(C 1-4烷基)氨基,三氟甲氧基和任选取代的吗啉-4-基,吡啶基,嘧啶基,哌嗪基和吡嗪基,其中一个或两个取代基独立地选自所述取代基 由C1-4烷基,氨基甲基,羟甲基,氯或氟组成的基团; R 5是氢,氯或氟; 或R 4和R 5一起为-CH = CH-CH = CH-或-X(CH 2)mY-,其中X和Y各自独立地选自CH 2,(CH 2)n N (R 9) - 和O,其中m为1或2; n为0或1; 和R 6,R 7和R 8各自独立地选自氢,氯和氟; 并且R 9选自氢,C 1-4烷基,羟乙基,C 1-4烷氧基乙基,环丙基甲基,-CO 2(C 1-4烷基)和-CH 2 CH 2 NR 10 R 11, 10>和R 11各自独立地是氢或C 1-4烷基,其是KCNQ钾通道的开放剂,并且可用于治疗对开放KCNQ钾通道有响应的病症。
摘要:
The present invention provides novel [1,2,4]triazole-3-one derivatives having the general formula (I) wherein: Q is and R1, R2, R3, R4, R5 and R6 are as defined herein or a nontoxic pharmaceutically acceptable salt or solvate thereof which are smooth muscle relaxants and useful in treating disorders responsive to relaxation of smooth muscle such as asthma, irritable bowel syndrome, male erectile dysfunction and urinary incontinence.
摘要:
The present invention provides novel oxadiazolone derivatives having the general formula ##STR1## wherein A, B, D and R are as defined herein, or a nontoxic pharmaceutically acceptable salt or solvate thereof and are useful in the treatment of disorders which are responsive to the opening of the large conductance calcium-activated potassium channels.
摘要:
The present invention provides novel 4-aryl-3-aminoquinolin-2-one derivatives having the general formula ##STR1## wherein R, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5 and R.sup.6 are as defined herein, or a non-toxic pharmaceutically acceptable salt thereof which are modulators of the large conductance calcium-activated K.sup.+ channels and are useful in the treatment of disorders which are responsive to the opening of the potassium channels.
摘要:
The present invention provides novel phosphate derivatives having the general formula wherein A, R.sup.1 and R.sup.2 are as defined herein, or a nontoxic pharmaceutically acceptable salt or solvate thereof and are useful in the treatment of disorders which are responsive to the opening of potassium channels.
摘要:
The invention encompasses compounds of formula I as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV.
摘要:
The invention encompasses compounds of formula I as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV.