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公开(公告)号:PT94954A
公开(公告)日:1991-04-18
申请号:PT9495490
申请日:1990-08-09
Applicant: GLAXO INC.,
Inventor: THOMAS N. WHEELER , JOEL E. SHAFFER , TERRENCE KENAKIN
IPC: A61K31/50 , A61P9/00 , A61P9/04 , C07D237/04
Abstract: Pyridazinones of the following formula (I): where R -R are a variety of substituents and L is a linking group, a pharmaceutical composition for treating congestive heart failure, novel intermediates, methods for such treatment and processes for preparing compounds of formula (I).
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公开(公告)号:AU6310090A
公开(公告)日:1991-03-28
申请号:AU6310090
申请日:1990-09-21
Applicant: GLAXO INC
Inventor: WHEELER THOMAS N , SHAFFER JOEL E , KENAKIN TERRENCE
IPC: A61K31/44 , A61K31/4418 , A61P9/00 , C07D213/85 , A61K31/535
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公开(公告)号:AU6081690A
公开(公告)日:1991-02-14
申请号:AU6081690
申请日:1990-08-09
Applicant: GLAXO INC
Inventor: WHEELER THOMAS N , SHAFFER JOEL E , KENAKIN TERRENCE
IPC: A61K31/50 , A61P9/00 , A61P9/04 , C07D237/04 , A61K31/535
Abstract: Pyridazinones of the following formula (I): where R -R are a variety of substituents and L is a linking group, a pharmaceutical composition for treating congestive heart failure, novel intermediates, methods for such treatment and processes for preparing compounds of formula (I).
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公开(公告)号:ZA9001123B
公开(公告)日:1990-12-28
申请号:ZA9001123
申请日:1990-02-14
Applicant: GLAXO INC
Inventor: FELDMAN PAUL L , PAUL L FELDMAN , JAMES MICHAEL K , MICHAEL K JAMES , BRACKEEN MARCUS F , MARCUS F BRACKEEN , JOHNSON MICHAEL ROSS , MICHAEL ROSS JOHNSON , LEIGHTON HARRY JEFFERSON , HARRY JEFFERSON LEIGHTON
IPC: A61K20060101 , C07D20060101 , C07D211/14 , C07D , A61K
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公开(公告)号:PT93137A
公开(公告)日:1990-08-31
申请号:PT9313790
申请日:1990-02-14
Applicant: GLAXO INC
Inventor: FELDMAN PAUL L , JAMES MICHAEL K , BRACKEEN MARCUS F , JOHNSON MICHAEL ROSS , LEIGHTON HARRY JEFFERSON
IPC: A61K20060101 , A61K31/445 , A61K31/4465 , A61P25/04 , C07B57/00 , C07D20060101 , C07D211/14 , C07D211/58
Abstract: N-Phenyl-N-(4-piperdinyl)amide derivatives are disclosed having the general formula (I). wherein: X is a member selected from the group consisting of: alkoxy-carbonyl-lower alkyl, lower alkyl-carbonyloxy-lower alkyl, alkenyloxy-carbonyl-lower alkyl, and (C1-2)alkoxy-(C1-2)alkoxy-carbonyl-lower alkyl. Ar is a member selected from the group consisting of phenyl, mono-, di- and tri-substituted phenyl, wherein each subtitutuent is independently selected from the group consisting of halo, lower alkyl, lower alkoxy and trifluoromethyl; R is a member selected from the group consisting of lower alkyl, and lower alkoxy-lower alkyl; R is a member selected from the group consisting of hydrogen, lower alkoxy-carbonyl, and methoxymethyl; and R is a member selected from the group consisting of hydrogen and methyl; and the diastereomeric and enantiomeric isomers thereof, and the acid addition salts of said compounds and isomers. The compounds exhibit analgesic activity having relatively short durations of analgesic action. The invention embraces the compounds (I), pharmaceutical compositions of (I) and methods of providing analgesia with (I). Also included are certain novel intermediates for making (I).
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公开(公告)号:CA2010011A1
公开(公告)日:1990-08-15
申请号:CA2010011
申请日:1990-02-14
Applicant: GLAXO INC
Inventor: FELDMAN PAUL L , JAMES MICHAEL K , BRACKEEN MARCUS F , JOHNSON MICHAEL R , LEIGHTON HARRY J
IPC: A61K20060101 , A61K31/445 , A61K31/4465 , A61P25/04 , C07B57/00 , C07D20060101 , C07D211/14 , C07D211/58 , C07D211/66
Abstract: N-Phenyl-N-(4-piperdinyl)amide derivatives are disclosed having the general formula (I). wherein: X is a member selected from the group consisting of: alkoxy-carbonyl-lower alkyl, lower alkyl-carbonyloxy-lower alkyl, alkenyloxy-carbonyl-lower alkyl, and (C1-2)alkoxy-(C1-2)alkoxy-carbonyl-lower alkyl. Ar is a member selected from the group consisting of phenyl, mono-, di- and tri-substituted phenyl, wherein each subtitutuent is independently selected from the group consisting of halo, lower alkyl, lower alkoxy and trifluoromethyl; R is a member selected from the group consisting of lower alkyl, and lower alkoxy-lower alkyl; R is a member selected from the group consisting of hydrogen, lower alkoxy-carbonyl, and methoxymethyl; and R is a member selected from the group consisting of hydrogen and methyl; and the diastereomeric and enantiomeric isomers thereof, and the acid addition salts of said compounds and isomers. The compounds exhibit analgesic activity having relatively short durations of analgesic action. The invention embraces the compounds (I), pharmaceutical compositions of (I) and methods of providing analgesia with (I). Also included are certain novel intermediates for making (I).
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公开(公告)号:DK544888A
公开(公告)日:1990-03-30
申请号:DK544888
申请日:1988-09-29
Applicant: GLAXO INC
Abstract: A device for dispensing an aerosol from an aerosol module A includes a cocking device comprising lever 36 and spring 60 for readying it for release of the pressurized aerosol, a sear 64 for retaining the cocking device in a non-operative position following readying and a vane 79 operable by inhalation on the part of a user to disable the sear to thus release the cocking device to effect expulsion of aerosol from the aerosol module.
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公开(公告)号:ZA8903555B
公开(公告)日:1990-03-28
申请号:ZA8903555
申请日:1989-05-12
Applicant: GLAXO INC
Inventor: FRANZ ROBERT MICHAEL , ROBERT MICHAEL FRANZ
IPC: A61K9/30 , A61K9/28 , A61K9/36 , A61K31/34 , A61K47/14 , A61K47/30 , A61K47/38 , A61P43/00 , A61K
CPC classification number: A61K9/2866 , A61K31/34
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公开(公告)号:NL8901199A
公开(公告)日:1989-12-01
申请号:NL8901199
申请日:1989-05-12
Applicant: GLAXO INC
Abstract: This invention relates to an improved polymeric film coating for a ranitidine Hydrocholride (HCl) tablet in which the plasticizer triacetin had been added to the polymeric film coating medium. A tablet of this invention has been found to have great stability than a tablet coating with a polymeric film which does not contain triacetin.
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公开(公告)号:IE891564L
公开(公告)日:1989-11-13
申请号:IE156489
申请日:1989-05-12
Applicant: GLAXO INC
IPC: A61K9/30 , A61K9/28 , A61K9/36 , A61K31/34 , A61K47/14 , A61K47/30 , A61K47/38 , A61P43/00 , A61K9/00
Abstract: This invention relates to an improved polymeric film coating for a ranitidine Hydrocholride (HCl) tablet in which the plasticizer triacetin had been added to the polymeric film coating medium. A tablet of this invention has been found to have great stability than a tablet coating with a polymeric film which does not contain triacetin.
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