1-[[4-Phenyl-piperidinyl (or
tetrahydropyridinyl)]alkyl]-2,6-piperidinedione and analogs
    52.
    发明授权
    1-[[4-Phenyl-piperidinyl (or tetrahydropyridinyl)]alkyl]-2,6-piperidinedione and analogs 失效
    1- {8 {8-苯基 - 哌啶基(或四氢吡啶基){9烷基{9-2,6-哌啶二酮及其类似物

    公开(公告)号:US4012374A

    公开(公告)日:1977-03-15

    申请号:US617473

    申请日:1975-09-29

    IPC分类号: C07D211/88 C07D401/06

    CPC分类号: C07D211/88

    摘要: Compounds having the formula ##STR1## wherein A is a straight or branched chain alkylene group; R.sub.1 is hydrogen, halogen, alkyl, alkoxy, alkylthio, trifluoromethyl, nitro, amino, or cyano; and n is 0, 1, or 2; are useful central nervous system depressants.

    摘要翻译: 具有式“IMAGE”的化合物,其中A是直链或支链亚烷基; R 1是氢,卤素,烷基,烷氧基,烷硫基,三氟甲基,硝基,氨基或氰基; 并且n为0,1或2; 是有用的中枢神经系统抑制剂。

    Use of 2-(hydroxyalkyl)-1H-benz[de]isoquinoline-1,3(2H)-diones as
anti-allergy agents
    53.
    发明授权
    Use of 2-(hydroxyalkyl)-1H-benz[de]isoquinoline-1,3(2H)-diones as anti-allergy agents 失效
    使用2-(羟基烷基)-1H-苯并[{[{{{[{(异喹啉-1,3(2H) - 二酮)作为抗过敏剂

    公开(公告)号:US4006238A

    公开(公告)日:1977-02-01

    申请号:US608433

    申请日:1975-08-28

    申请人: Peter C. Wade

    发明人: Peter C. Wade

    IPC分类号: A61K31/47

    CPC分类号: A61K31/47

    摘要: Method of treating allergies with a pharmaceutical composition containing as the active ingredient a compound or mixture of compounds of the formula ##STR1## wherein R.sup.1 and R.sup.2 are independently selected from hydrogen, halogen, trifluoromethyl, lower alkyl, lower alkoxy, lower alkylthio, nitro, amino, or cyano; and A is a straight or branched chain alkylene of 1 to 8 carbons.

    摘要翻译: 用含有作为活性成分的药物组合物治疗过敏症的方法,其中R1和R2独立地选自氢,卤素,三氟甲基,低级烷基,低级烷氧基,低级烷硫基,硝基, 氨基或氰基; 并且A是1至8个碳的直链或支链亚烷基。

    3[Substituted-2-(methyl
amino)phenyl]4-[2-oxo-2-(heterocyclic)ethyl]-5-substituted-1,2,4-triazole
s
    54.
    发明授权
    3[Substituted-2-(methyl amino)phenyl]4-[2-oxo-2-(heterocyclic)ethyl]-5-substituted-1,2,4-triazole s 失效
    3 {8取代的-2-(甲基氨基)苯基{9 4- {8 2-氧代-2-(杂环)乙基{9,5-取代-1,2,4-三唑

    公开(公告)号:US3969366A

    公开(公告)日:1976-07-13

    申请号:US582549

    申请日:1975-05-30

    摘要: Compounds of the following formula and their pharmaceutically acceptable salts ##SPC1##Wherein R.sub.1 and R.sub.4 are the same or different and are each a five or six membered N containing heterocycle attached at an available N atom; R.sub.2 is hydrogen, alkyl, trifluoromethyl, phenyl, benzyl, --(CH.sub.2).sub.n --R.sub.4 or --(CH.sub.2).sub.n --N(alkyl).sub.2 ; R.sub.3 is hydrogen, halogen, nitro, trifluoromethyl, alkyl, alkoxy, or alkylthio; and n is an integer from 1 to 4; are disclosed. These compounds are useful as anti-inflammatory agents.

    摘要翻译: 下式的化合物及其药学上可接受的盐,其中R 1和R 4相同或不同,并且各自为在可用的N原子上连接的五或六元N的杂环; R 2是氢,烷基,三氟甲基,苯基,苄基, - (CH 2)n -R 4或 - (CH 2)n -N(烷基)2; R3是氢,卤素,硝基,三氟甲基,烷基,烷氧基或烷硫基; n为1〜4的整数。 被披露。 这些化合物可用作抗炎剂。

    Triazolo[4,3-D][1,4]benzodiazepine-3,6-diones
    55.
    发明授权
    Triazolo[4,3-D][1,4]benzodiazepine-3,6-diones 失效
    三唑并[8,4,3-D {9 {8,1,4]

    公开(公告)号:US3969343A

    公开(公告)日:1976-07-13

    申请号:US544470

    申请日:1975-01-27

    IPC分类号: C07D487/04

    CPC分类号: C07D487/04

    摘要: Triazolo[4,3-d][1,4]benzodiazepine-3,6-diones having in the 2-position an alkyl, phenyl or arylalkyl substituent are useful anti-inflammatory agents.

    摘要翻译: 具有2-位烷基,苯基或芳基烷基取代基的三唑并[4,3-d] [1,4]苯并二氮杂-3,6-二酮是有用的抗炎剂。

    2-[(Dihydroisoquinolinyl or
dihydroisoindol-2-yl)alkyl]-1H-benz[de]isoquinoline-1,3(2H)-diones
    56.
    发明授权
    2-[(Dihydroisoquinolinyl or dihydroisoindol-2-yl)alkyl]-1H-benz[de]isoquinoline-1,3(2H)-diones 失效
    2- {8(二氢异喹啉基或二氢异吲哚-2-基)烷基{9-1H-苯并[{[{{{{{异喹啉-1,3(2H)

    公开(公告)号:US3947452A

    公开(公告)日:1976-03-30

    申请号:US538976

    申请日:1975-01-06

    CPC分类号: C07D221/14

    摘要: Compounds of the following formula and their acid addition salts ##SPC1##Wherein R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are independently selected from hydrogen, halogen, lower alkyl, lower alkoxy, lower alkylthio, nitro, cyano, amino and trifluoromethyl; A is a straight or branched chain alkylene of 1 to 8 carbons; and m is 1 or 2 are disclosed. These compounds exhibit antidepressant and anti-anxiety activity. In addition these compounds are useful as antiinflammatory agents.

    摘要翻译: 下式的化合物及其酸加成盐,其中R 1,R 2,R 3和R 4独立地选自氢,卤素,低级烷基,低级烷氧基,低级烷硫基,硝基,氰基,氨基和三氟甲基; A是1至8个碳的直链或支链亚烷基; 并且公开了m为1或2。 这些化合物显示抗抑郁和抗焦虑活性。 此外,这些化合物可用作抗炎剂。

    2-[[4-(Azine or diazine or
triazine)-1-piperazinyl]alkyl]-1H-benz[de]isoquinoline-1,3(2H)-diones
    57.
    发明授权
    2-[[4-(Azine or diazine or triazine)-1-piperazinyl]alkyl]-1H-benz[de]isoquinoline-1,3(2H)-diones 失效
    2- {8 4-(氮杂或二嗪或三嗪)-1-哌嗪基{9烷基{9-1H-苯并[{de {9异喹啉-1,3(2H) - 二酮

    公开(公告)号:US3940398A

    公开(公告)日:1976-02-24

    申请号:US543558

    申请日:1975-01-23

    CPC分类号: C07D221/14

    摘要: Compounds of the following formula and their acid addition salts ##SPC1##Wherein R.sup.1 and R.sup.2 are independently selected from hydrogen, halogen, lower alkyl, lower alkoxy, lower alkylthio, nitro, cyano, amino and trifluoromethyl; A is a straight or branched chain alkylene of 1 to 8 carbons; and R is a 6-membered unsaturated substituted or unsubstituted heterocyclic ring selected from pyridine, diazine and triazine are disclosed. These compounds exhibit antidepressant activity. In addition these compounds are also useful as antiinflammatory agents.

    摘要翻译: 下式的化合物及其酸加成盐,其中R1和R2独立地选自氢,卤素,低级烷基,低级烷氧基,低级烷硫基,硝基,氰基,氨基和三氟甲基; A是1至8个碳的直链或支链亚烷基; 并且R是选自吡啶,二嗪和三嗪的6元不饱和取代或未取代的杂环。 这些化合物显示抗抑郁活性。 此外,这些化合物也可用作抗炎剂。

    2-[(Substituted-piperazinyl)alkyl]-1H-benz[de]isoquinoline-1,3(2H)-diones
    58.
    发明授权
    2-[(Substituted-piperazinyl)alkyl]-1H-benz[de]isoquinoline-1,3(2H)-diones 失效
    2- {8(取代的哌嗪基)烷基{9-1H-苯并[{[{{{{(异喹啉-1,3(2H) - 二酮

    公开(公告)号:US3940397A

    公开(公告)日:1976-02-24

    申请号:US523293

    申请日:1974-11-13

    IPC分类号: C07D221/14 C07D401/06

    CPC分类号: C07D221/14

    摘要: Compounds of the following formula and their acid addition salts ##SPC1##Wherein R.sup.1 and R.sup.2 are independently selected from hydrogen, halogen, lower alkyl, lower alkoxy, lower alkylthio, nitro, cyano, amino and trifluoromethyl; A is a straight or branched chain alkylene of 1 to 8 carbons; and Z is ##SPC2##Wherein R.sup.3 is selected from phenyl, phenyl-lower alkyl, and substituted phenyl and phenyl-lower alkyl are disclosed. These compounds exhibit antidepressant activity. In addition these compounds are useful as antiinflammatory agents.

    摘要翻译: 下式的化合物及其酸加成盐,其中R1和R2独立地选自氢,卤素,低级烷基,低级烷氧基,低级烷硫基,硝基,氰基,氨基和三氟甲基; A是1至8个碳的直链或支链亚烷基; 并且Z是R 3选自苯基,苯基 - 低级烷基和取代的苯基和苯基 - 低级烷基。 这些化合物显示抗抑郁活性。 此外,这些化合物可用作抗炎剂。