ZM1290A1 - N-(3-hydroxy-4-piperidinyl)(dihydrobenzofuran,dihyn-(3-hydroxy-4-piperidinyl(dihydrobenzofuran,dihyddro-2h-benzopyran or dihydrobenzodioxin)carboxamidro-2h-benzopyran or dihydrobenzodioxin)carboxamide derivatives e derivatives - Google Patents
N-(3-hydroxy-4-piperidinyl)(dihydrobenzofuran,dihyn-(3-hydroxy-4-piperidinyl(dihydrobenzofuran,dihyddro-2h-benzopyran or dihydrobenzodioxin)carboxamidro-2h-benzopyran or dihydrobenzodioxin)carboxamide derivatives e derivativesInfo
- Publication number
- ZM1290A1 ZM1290A1 ZM12/90A ZM1290A ZM1290A1 ZM 1290 A1 ZM1290 A1 ZM 1290A1 ZM 12/90 A ZM12/90 A ZM 12/90A ZM 1290 A ZM1290 A ZM 1290A ZM 1290 A1 ZM1290 A1 ZM 1290A1
- Authority
- ZM
- Zambia
- Prior art keywords
- dihydrobenzodioxin
- dihydrobenzofuran
- benzopyran
- piperidinyl
- hydroxy
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/10—Laxatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nutrition Science (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US32694189A | 1989-03-22 | 1989-03-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZM1290A1 true ZM1290A1 (en) | 1992-07-31 |
Family
ID=23274437
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZM12/90A ZM1290A1 (en) | 1989-03-22 | 1990-03-21 | N-(3-hydroxy-4-piperidinyl)(dihydrobenzofuran,dihyn-(3-hydroxy-4-piperidinyl(dihydrobenzofuran,dihyddro-2h-benzopyran or dihydrobenzodioxin)carboxamidro-2h-benzopyran or dihydrobenzodioxin)carboxamide derivatives e derivatives |
Country Status (30)
Country | Link |
---|---|
US (12) | US5374637A (fr) |
EP (1) | EP0389037B1 (fr) |
JP (1) | JP2845341B2 (fr) |
KR (1) | KR0163587B1 (fr) |
CN (1) | CN1034502C (fr) |
AT (1) | ATE128132T1 (fr) |
AU (1) | AU616838B2 (fr) |
CA (1) | CA2012432C (fr) |
CY (1) | CY1921A (fr) |
DE (1) | DE69022453T2 (fr) |
DK (1) | DK0389037T3 (fr) |
DZ (1) | DZ1405A1 (fr) |
ES (1) | ES2081340T3 (fr) |
FI (1) | FI101624B (fr) |
GR (1) | GR3017992T3 (fr) |
HK (1) | HK131596A (fr) |
HU (2) | HU221621B1 (fr) |
IE (1) | IE67184B1 (fr) |
IL (1) | IL93817A (fr) |
JO (1) | JO1613B1 (fr) |
MA (1) | MA21778A1 (fr) |
MY (2) | MY106407A (fr) |
NO (1) | NO176101C (fr) |
NZ (1) | NZ232964A (fr) |
PT (1) | PT93531B (fr) |
RU (2) | RU2037492C1 (fr) |
TN (1) | TNSN90032A1 (fr) |
ZA (1) | ZA902188B (fr) |
ZM (1) | ZM1290A1 (fr) |
ZW (1) | ZW3390A1 (fr) |
Families Citing this family (69)
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CA2009542C (fr) * | 1989-02-10 | 2000-03-14 | Albert A. Carr | Guanidines cycliques comme antagonistes du calcium |
GB9005014D0 (en) * | 1990-03-06 | 1990-05-02 | Janssen Pharmaceutica Nv | N.(4.piperidinyl)(dihydrobenzofuran or dihydro.2h.benzopyran)carboxamide derivatives |
FR2674849B1 (fr) * | 1991-04-02 | 1994-12-23 | Logeais Labor Jacques | Nouveaux derives de n-cyclohexyl benzamides ou thiobenzamides, leurs preparations et leurs applications en therapeutique. |
ES2135414T3 (es) * | 1991-09-12 | 1999-11-01 | Smithkline Beecham Plc | Antagonistas del receptor 5-ht4. |
US5240943A (en) * | 1991-12-19 | 1993-08-31 | G. D. Searle & Co. | Benzopyran class iii antiarrhythmic agents |
AU667874B2 (en) * | 1992-02-06 | 1996-04-18 | Smithkline Beecham Plc | Benzopyran, benzothiopyran and benzofuran derivatives as 5-HT4 antagonists |
GB9219163D0 (en) * | 1992-09-10 | 1992-10-28 | Smithkline Beecham Plc | Pharmaceuticals |
TW294595B (fr) * | 1992-11-20 | 1997-01-01 | Janssen Pharmaceutica Nv | |
GB9301660D0 (en) * | 1993-01-28 | 1993-03-17 | Smithkline Beecham Plc | Pharmaceuticals |
US6127379A (en) * | 1993-02-01 | 2000-10-03 | Smithkline Beecham P.L.C. | Benzopyran, benzothiopyran and benzofuran derivatives as 5-HT4 antagonists |
GB9312348D0 (en) * | 1993-06-16 | 1993-07-28 | Smithkline Beecham Plc | Pharmaceuticals |
JPH0820586A (ja) * | 1994-07-05 | 1996-01-23 | Sanwa Kagaku Kenkyusho Co Ltd | 1−アザビシクロ[3.3.0]オクタン誘導体、その塩及び製法並びに用途 |
JPH0873463A (ja) | 1994-07-05 | 1996-03-19 | Sanwa Kagaku Kenkyusho Co Ltd | ベンゾピランカルボキサミド誘導体、その塩及び製法並びに用途 |
CA2200579C (fr) * | 1994-09-27 | 2006-07-04 | Georges Henri Paul Van Daele (Deceased) | Derives benzoates bicycliques de phenyl-oxo-alkyl-(4-piperidinyle) |
BR9509036A (pt) * | 1994-09-27 | 1997-10-14 | Janssen Pharmaceutica Nv | Derivados biciclicos de benzoato de peperidinila n-substituída |
TW490465B (en) * | 1994-11-24 | 2002-06-11 | Janssen Pharmaceutica Nv | Enterokinetic benzamide, the preparation process and the pharmaceutical compositions thereof |
TW360653B (en) * | 1995-03-01 | 1999-06-11 | Janssen Pharmaceutica Nv | A oxadiazole compound having colon motility stimulating properties, its preparation process and its pharmaceutical composition |
JP2000500742A (ja) | 1995-10-30 | 2000-01-25 | スミスクライン・ビーチャム・コーポレイション | プロテアーゼ阻害剤 |
US6586466B2 (en) | 1995-10-30 | 2003-07-01 | Smithkline Beecham Corporation | Carbohydrazide-protease inhibitors |
US6096761A (en) * | 1996-02-15 | 2000-08-01 | Janssen Pharmaceutica N.V. | Esters of 3-hydroxy-piperidinemethanol derivatives |
NZ330263A (en) * | 1996-02-15 | 1999-06-29 | Janssen Pharmaceutica Nv | Esters of 3-hydroxy-piperidinemethanol derivatives to improve gastric emptying |
DZ2285A1 (fr) * | 1996-08-08 | 2002-12-25 | Smithkline Beecham Corp | Inhibiteurs de protéase de la cystéine. |
US20020128476A1 (en) * | 1996-08-08 | 2002-09-12 | Smithkline Beecham Corporation | Inhibitors of cysteine protease |
US6037354A (en) * | 1997-06-18 | 2000-03-14 | Merck & Co., Inc. | Alpha 1a adrenergic receptor antagonists |
WO1998057641A1 (fr) * | 1997-06-18 | 1998-12-23 | Merck & Co., Inc. | ANTAGONISTES DU RECEPTEUR ADRENERGIQUE ALPHA 1a |
TW548103B (en) * | 1997-07-11 | 2003-08-21 | Janssen Pharmaceutica Nv | Bicyclic benzamides of 3- or 4-substituted 4-(aminomethyl)-piperidine derivatives |
BRPI9913542B8 (pt) | 1998-09-10 | 2021-05-25 | Hoffmann La Roche | derivados de dihidrobenzodioxina carboxamida e dihidrobenzodioxina cetona como antagonistas do receptor 5-ht4 bem como composição farmacêutica, processo para a preparação dos referidos derivados e uso dos mesmos |
WO2000030640A1 (fr) * | 1998-11-23 | 2000-06-02 | Janssen Pharmaceutica N.V. | Utilisation de prucalopride dans la production d'un medicament de traitement de la dyspepsie |
TW570920B (en) | 1998-12-22 | 2004-01-11 | Janssen Pharmaceutica Nv | 4-(aminomethyl)-piperidine benzamides for treating gastrointestinal disorders |
US20030144175A1 (en) * | 1998-12-23 | 2003-07-31 | Smithkline Beecham Corporation | Protease inhibitors |
US20030044399A1 (en) * | 1998-12-23 | 2003-03-06 | Smithkline Beecham Corporation | Method of treatment |
TW592709B (en) * | 1999-04-29 | 2004-06-21 | Janssen Pharmaceutica Nv | Prucalopride oral solution |
AU1474801A (en) | 1999-11-10 | 2001-06-06 | Smithkline Beecham Corporation | Protease inhibitors |
US6596715B1 (en) | 1999-11-10 | 2003-07-22 | Smithkline Beecham Corporation | Protease inhibitors |
US6583137B1 (en) | 1999-11-10 | 2003-06-24 | Smithkline Beecham Corporation | Protease inhibitors |
US7071184B2 (en) * | 2000-03-21 | 2006-07-04 | Smithkline Beecham Corporation | Protease inhibitors |
US20040038965A1 (en) * | 2001-10-09 | 2004-02-26 | Marquis, Jr. Robert W. | Protease inhibitors |
KR100471499B1 (ko) * | 2002-01-08 | 2005-03-09 | 학교법인 이화학당 | 크로만 유도체 및 이를 활성성분으로 함유하는 약학적조성물 |
PL214274B1 (pl) * | 2002-01-16 | 2013-07-31 | Movetis N V | N-Tlenek prukaloprydu, sposób jego wytwarzania i zastosowanie oraz zawierająca go kompozycja i sposób jej wytwarzania |
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US7557076B2 (en) * | 2002-06-06 | 2009-07-07 | The Procter & Gamble Company | Organic catalyst with enhanced enzyme compatibility |
TW200409637A (en) * | 2002-06-26 | 2004-06-16 | Glaxo Group Ltd | Compounds |
DE10251394A1 (de) * | 2002-11-05 | 2004-05-13 | Clariant Gmbh | Blaues Farbmittel mit besonders hoher Reinheit und positiver triboelektrischer Steuerwirkung |
EP1593668A4 (fr) * | 2003-02-14 | 2007-07-11 | Wako Pure Chem Ind Ltd | Procede de production de compose hydroxylamine dans lequel un catalyseur au platine fixe sur une resine echangeuse d'ions est utilise |
JO2478B1 (en) * | 2003-06-19 | 2009-01-20 | جانسين فارماسوتيكا ان. في. | (Aminomethyl) -biperidine benzamides as 5 HT4 antagonists |
WO2005003122A1 (fr) * | 2003-06-19 | 2005-01-13 | Janssen Pharmaceutica N.V. | 4-(aminomethyl)-piperidine benzamides antagonistes des recepteurs 5ht4 |
WO2005003124A1 (fr) * | 2003-06-19 | 2005-01-13 | Janssen Pharmaceutica N.V. | 4-(aminomethyl)-piperidine benzamides substitues par des heterocycles, utilises comme antagonistes des recepteurs 5ht4 |
US20050113246A1 (en) * | 2003-11-06 | 2005-05-26 | The Procter & Gamble Company | Process of producing an organic catalyst |
MXPA06005686A (es) * | 2003-11-20 | 2006-08-17 | Janssen Pharmaceutica Nv | 2-quinolinonas y 2-quinoxalinonas 7-fenilaquilo sustituidas como inhibidores de la poli(adp-ribosa)polimerasa. |
EP1687277B1 (fr) | 2003-11-20 | 2018-04-04 | Janssen Pharmaceutica NV | 2-quinolinones et 2-quinoxalinones substituees par 6-alcenyle et 6-phenylalkyle utilisees comme inhibiteurs de la poly(adp-ribose) polymerase (parp) |
NZ547193A (en) * | 2003-12-05 | 2010-03-26 | Janssen Pharmaceutica Nv | 6-Substituted 2-quinolinones and 2-quinoxalinones as poly(adp-ribose) polymerase inhibitors |
US7803795B2 (en) * | 2004-06-30 | 2010-09-28 | Janssen Pharmaceutica N.V. | Phthalazine derivatives as parp inhibitors |
CN1980913B (zh) | 2004-06-30 | 2011-12-14 | 詹森药业有限公司 | 作为parp抑制剂的喹唑啉二酮衍生物 |
UA86237C2 (uk) * | 2004-06-30 | 2009-04-10 | Янссен Фармацевтика Н.В. | Похідні заміщеного 2-алкілхіназолінону як інгібітори parp |
AR051659A1 (es) * | 2005-06-17 | 2007-01-31 | Procter & Gamble | Una composicion que comprende un catalizador organico con compatibilidada enzimatica mejorada |
GB0525661D0 (en) * | 2005-12-16 | 2006-01-25 | Glaxo Group Ltd | Novel compounds |
EP2134691B1 (fr) * | 2007-03-08 | 2012-01-25 | Janssen Pharmaceutica, N.V. | Dérivés de quinolinone comme inhibiteurs de parp et de tank |
US8404713B2 (en) * | 2007-10-26 | 2013-03-26 | Janssen Pharmaceutica Nv | Quinolinone derivatives as PARP inhibitors |
AU2009228945B2 (en) * | 2008-03-27 | 2013-05-02 | Janssen Pharmaceutica Nv | Quinazolinone derivatives as tubulin polymerization inhibitors |
CN101981013B (zh) | 2008-03-27 | 2013-05-29 | 詹森药业有限公司 | 作为parp和微管蛋白聚合抑制剂的四氢菲啶酮和四氢环戊二烯并喹啉酮 |
CN102295594B (zh) * | 2011-07-12 | 2016-01-20 | 上海医药工业研究院 | 4-n-取代-1-(3-甲氧基丙基)-4-哌啶胺类化合物及制备和应用 |
CN102942542B (zh) * | 2012-11-20 | 2015-08-05 | 南京华威医药科技开发有限公司 | 2,3-二氢苯并呋喃类化合物的制备方法 |
CN103755689B (zh) * | 2013-12-25 | 2016-06-29 | 连云港恒运医药科技有限公司 | 普卡必利降解杂质的制备方法 |
CN103664912B (zh) * | 2013-12-31 | 2015-11-25 | 南京正大天晴制药有限公司 | 一种普卡必利的合成工艺 |
US11053255B2 (en) * | 2015-06-22 | 2021-07-06 | Georgetown University | Synthesis of mahanine and related compounds |
WO2017137910A1 (fr) | 2016-02-11 | 2017-08-17 | Symed Labs Limited | Procédés pour la préparation de succinate de prucalopride très pur et de ses intermédiaires |
JP7416537B2 (ja) | 2018-09-28 | 2024-01-17 | 武田薬品工業株式会社 | 複素環化合物 |
CN110938064B (zh) * | 2019-11-06 | 2022-12-27 | 广东东阳光药业有限公司 | N-取代哌啶酰胺衍生物及其用途 |
CN116082319A (zh) * | 2020-06-04 | 2023-05-09 | 南京恒通医药开发有限公司 | 一种琥珀酸普芦卡必利的连续合成方法 |
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CA1317940C (fr) * | 1987-09-25 | 1993-05-18 | Georges H. P. Van Daele | N-(1-alkyl-3-hydroxy-4-piperidinyl) benzamides a substituant |
US4863921A (en) * | 1988-04-27 | 1989-09-05 | Rorer Pharmaceutical Corporation | Dibenzofurancarboxamides and their pharmaceutical compositions and methods |
TW294595B (fr) * | 1992-11-20 | 1997-01-01 | Janssen Pharmaceutica Nv |
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1990
- 1990-03-06 US US07/489,419 patent/US5374637A/en not_active Expired - Lifetime
- 1990-03-13 DE DE69022453T patent/DE69022453T2/de not_active Expired - Fee Related
- 1990-03-13 AT AT90200589T patent/ATE128132T1/de not_active IP Right Cessation
- 1990-03-13 DK DK90200589.1T patent/DK0389037T3/da active
- 1990-03-13 EP EP90200589A patent/EP0389037B1/fr not_active Expired - Lifetime
- 1990-03-13 ES ES90200589T patent/ES2081340T3/es not_active Expired - Lifetime
- 1990-03-16 NZ NZ232964A patent/NZ232964A/en unknown
- 1990-03-16 CA CA002012432A patent/CA2012432C/fr not_active Expired - Fee Related
- 1990-03-19 JO JO19901613A patent/JO1613B1/en active
- 1990-03-20 MY MYPI90000431A patent/MY106407A/en unknown
- 1990-03-20 MY MYPI94003195A patent/MY131911A/en unknown
- 1990-03-20 ZW ZW33/90A patent/ZW3390A1/xx unknown
- 1990-03-20 DZ DZ900052A patent/DZ1405A1/fr active
- 1990-03-20 JP JP2068541A patent/JP2845341B2/ja not_active Expired - Fee Related
- 1990-03-20 IL IL9381790A patent/IL93817A/en unknown
- 1990-03-20 MA MA22042A patent/MA21778A1/fr unknown
- 1990-03-21 ZM ZM12/90A patent/ZM1290A1/xx unknown
- 1990-03-21 NO NO901306A patent/NO176101C/no not_active IP Right Cessation
- 1990-03-21 AU AU52091/90A patent/AU616838B2/en not_active Ceased
- 1990-03-21 PT PT93531A patent/PT93531B/pt not_active IP Right Cessation
- 1990-03-21 FI FI901421A patent/FI101624B/fi not_active IP Right Cessation
- 1990-03-21 CN CN90101524A patent/CN1034502C/zh not_active Expired - Fee Related
- 1990-03-21 ZA ZA902188A patent/ZA902188B/xx unknown
- 1990-03-21 RU SU904743491A patent/RU2037492C1/ru not_active IP Right Cessation
- 1990-03-21 KR KR1019900003782A patent/KR0163587B1/ko not_active IP Right Cessation
- 1990-03-21 IE IE104090A patent/IE67184B1/en not_active IP Right Cessation
- 1990-03-21 HU HU9001627A patent/HU221621B1/hu not_active IP Right Cessation
- 1990-03-22 TN TNTNSN90032A patent/TNSN90032A1/fr unknown
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1993
- 1993-11-02 RU RU93050009A patent/RU2108332C1/ru not_active IP Right Cessation
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1994
- 1994-09-07 US US08/301,825 patent/US5552553A/en not_active Expired - Fee Related
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1995
- 1995-03-31 US US08/414,676 patent/US5521314A/en not_active Expired - Fee Related
- 1995-03-31 US US08/414,673 patent/US5616738A/en not_active Expired - Fee Related
- 1995-04-03 US US08/415,888 patent/US5554772A/en not_active Expired - Fee Related
- 1995-04-03 US US08/415,953 patent/US5565582A/en not_active Expired - Fee Related
- 1995-04-03 US US08/415,885 patent/US5576448A/en not_active Expired - Fee Related
- 1995-04-13 US US08/421,658 patent/US5616583A/en not_active Expired - Fee Related
- 1995-04-13 US US08/421,727 patent/US5602129A/en not_active Expired - Fee Related
- 1995-04-13 US US08/421,826 patent/US5739134A/en not_active Expired - Fee Related
- 1995-04-13 US US08/421,659 patent/US5536733A/en not_active Expired - Fee Related
- 1995-04-13 US US08/421,728 patent/US5610157A/en not_active Expired - Fee Related
- 1995-06-21 HU HU95P/P00311P patent/HU211171A9/hu unknown
- 1995-11-08 GR GR950403101T patent/GR3017992T3/el unknown
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1996
- 1996-07-18 HK HK131596A patent/HK131596A/xx not_active IP Right Cessation
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1997
- 1997-03-07 CY CY192197A patent/CY1921A/xx unknown
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