MA23967A1 - Nouveaux derives de piperidine, leur fabrication et leur utilisation comme medicaments - Google Patents
Nouveaux derives de piperidine, leur fabrication et leur utilisation comme medicamentsInfo
- Publication number
- MA23967A1 MA23967A1 MA24347A MA24347A MA23967A1 MA 23967 A1 MA23967 A1 MA 23967A1 MA 24347 A MA24347 A MA 24347A MA 24347 A MA24347 A MA 24347A MA 23967 A1 MA23967 A1 MA 23967A1
- Authority
- MA
- Morocco
- Prior art keywords
- manufacture
- piperidine derivatives
- medicines
- novel piperidine
- novel
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/42—Oxygen atoms attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH254895 | 1995-09-07 | ||
CH187696 | 1996-07-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA23967A1 true MA23967A1 (fr) | 1997-04-01 |
Family
ID=25688898
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA24347A MA23967A1 (fr) | 1995-09-07 | 1996-09-06 | Nouveaux derives de piperidine, leur fabrication et leur utilisation comme medicaments |
Country Status (27)
Country | Link |
---|---|
US (2) | US6051712A (fr) |
EP (1) | EP0863875B1 (fr) |
JP (1) | JP3648251B2 (fr) |
KR (1) | KR100384979B1 (fr) |
CN (1) | CN1256326C (fr) |
AT (1) | ATE242213T1 (fr) |
BR (1) | BR9610385A (fr) |
CA (1) | CA2230931C (fr) |
CY (1) | CY2488B1 (fr) |
CZ (1) | CZ292327B6 (fr) |
DE (1) | DE59610509D1 (fr) |
DK (1) | DK0863875T3 (fr) |
ES (1) | ES2201192T3 (fr) |
HK (1) | HK1016177A1 (fr) |
HU (1) | HUP9900926A3 (fr) |
IL (1) | IL123293A (fr) |
MA (1) | MA23967A1 (fr) |
MY (1) | MY121967A (fr) |
NO (1) | NO310069B1 (fr) |
NZ (1) | NZ315677A (fr) |
PL (1) | PL193686B1 (fr) |
PT (1) | PT863875E (fr) |
RU (1) | RU2167865C2 (fr) |
SA (1) | SA96170317B1 (fr) |
TR (1) | TR199800409T1 (fr) |
TW (1) | TW474932B (fr) |
WO (1) | WO1997009311A1 (fr) |
Families Citing this family (91)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HU221921B1 (hu) | 1996-07-08 | 2003-02-28 | Richter Gedeon Vegyészeti Gyár Rt. | N-benzil-piperidin- és tetrahidropiridinszármazékok és eljárás azok előállítására |
EP0981515B1 (fr) * | 1997-05-14 | 2003-08-27 | Neurosearch A/S | Derives de la piperidine utilises comme inhibiteurs du recaptage des neurotransmetteurs |
WO1998053824A1 (fr) | 1997-05-29 | 1998-12-03 | Smithkline Beecham Corporation | Nouveau procede |
AU9740998A (en) * | 1997-09-08 | 1999-03-29 | F. Hoffmann-La Roche Ag | Piperidine derivatives against malaria |
WO1999052895A1 (fr) | 1998-04-10 | 1999-10-21 | Japan Tobacco Inc. | Composes d'amidine |
US6274735B1 (en) | 1998-08-10 | 2001-08-14 | Hoffmann-La Roche Inc. | Process and intermediates for preparation of substituted piperidines |
US6268499B1 (en) | 1998-08-10 | 2001-07-31 | Hoffman-La Roche Inc. | Process and intermediates for preparation of substituted piperidine-epoxides |
WO2000063173A1 (fr) * | 1999-04-14 | 2000-10-26 | F. Hoffmann-La Roche Ag | Procede de preparation de piperidines substituees |
US6197959B1 (en) * | 1999-04-27 | 2001-03-06 | Hoffmann-La Roche Inc. | Piperidine derivatives |
US6376672B1 (en) * | 1999-04-27 | 2002-04-23 | Hoffmann-La Roche Inc. | Naphthalenylmethoxypiperidines as renin inhibitors |
IT1313702B1 (it) * | 1999-08-02 | 2002-09-09 | Chemi Spa | Processo per la preparazione di derivati 3-sostituiti di 4-fenil-piperidine. |
EP1214303A1 (fr) * | 1999-08-31 | 2002-06-19 | Merck & Co., Inc. | Composes heterocycliques et procedes d'utilisation de ceux-ci |
EP1224175B1 (fr) | 1999-10-15 | 2004-03-17 | F. Hoffmann-La Roche Ag | Derives de benzodiazepines |
JP2004503542A (ja) * | 2000-06-13 | 2004-02-05 | ビーエーエスエフ アクチェンゲゼルシャフト | 殺真菌性5−フェニル置換2−(シアノアミノ)ピリミジン誘導体 |
US20060079533A1 (en) * | 2001-03-23 | 2006-04-13 | Nieman James A | Methods of treating alzheimer's disease |
MXPA04004772A (es) | 2001-11-19 | 2005-06-06 | Elan Pharm Inc | Piperidinas y piperazinas 3,4-disustituidas, 3,5-disustituidas y 3,4,5-sustituidas. |
EP1501830B1 (fr) | 2002-04-29 | 2011-10-05 | Actelion Pharmaceuticals Ltd. | Derives de 7-aryl-3,9-diazabicyclo[3.3.1]non-6-ene et leur utilisation en tant qu'inhibiteurs de renine dans le traitement de l'hypertension, de maladies cardiovasculaires ou renales |
US20060009497A1 (en) * | 2002-06-27 | 2006-01-12 | Actelion Pharmaceuticals, Ltd. | Novel tetrahydropyridine derivatives as renin inhibitors |
WO2004071458A2 (fr) | 2003-02-13 | 2004-08-26 | Albert Einstein College Of Medicine Of Yeshiva University | Regulation de la prise alimentaire et de la production de glucose par modulation des niveaux d'acyl-coa gras de chaine longue dans l'hypothalamus |
US20040204455A1 (en) * | 2003-04-10 | 2004-10-14 | Cody Wayne Livingston | Piperidine derivative rennin inhibitors |
US20040214832A1 (en) * | 2003-04-10 | 2004-10-28 | Cuiman Cai | Piperazine derivative renin inhibitors |
WO2004096804A1 (fr) * | 2003-04-28 | 2004-11-11 | Actelion Pharmaceuticals Ltd | Derives de diazabicyclononene et de tetrahydropyridine utilises comme inhibiteurs de la renine |
RU2005136986A (ru) * | 2003-04-29 | 2006-05-27 | Актелион Фармасьютикалз Лтд. (Ch) | Новые 3,4-дизамещенные производные 1,2,3,6-тетрагидропиридина |
BRPI0409878A (pt) * | 2003-04-30 | 2006-05-23 | Actelion Pharmaceuticals Ltd | compostos, composições farmacêuticas, método para o tratamento ou profilaxia de doenças, e, usos de compostos e de um ou mais compostos em combinação com outros compostos farmacologicamente ativos |
KR20060008937A (ko) * | 2003-04-30 | 2006-01-27 | 액테리온 파마슈티칼 리미티드 | 레닌 억제제로서 3-위치에 헤테로원자를 갖는9-아자비사이클로[3.3.1]논-6-엔 유도체 |
BRPI0409818A (pt) * | 2003-04-30 | 2006-05-09 | Actelion Pharmaceuticals Ltd | compostos, composições farmacêuticas, método para o tratamento ou profilaxia de doenças, e, usos de compostos e de um ou mais compostos em combinação com outros compostos farmacologicamente ativos |
JP2006525259A (ja) * | 2003-05-02 | 2006-11-09 | アクテリオン ファマシューティカルズ リミテッド | 新規ジアザビシクロノネン誘導体 |
AU2004259358B2 (en) * | 2003-07-24 | 2008-03-20 | Euro-Celtique S.A. | Heteroaryl-tetrahydropiperidyl compounds useful for treating or preventing pain |
TW200900399A (en) | 2003-10-01 | 2009-01-01 | Speedel Experimenta Ag | Organic compounds |
AR045950A1 (es) * | 2003-10-09 | 2005-11-16 | Speedel Experimenta Ag | Compuestos derivados de piperazina, composiciones farmaceuticas que los contienen y su uso en la fabricacion de medicamentos. |
EP1680427A1 (fr) * | 2003-10-23 | 2006-07-19 | Actelion Pharmaceuticals Ltd. | Derives de diazabicyclononene et de tetrahydropyridine utilises comme inhibiteurs de la renine |
EP1689712B1 (fr) | 2003-11-26 | 2009-08-19 | Novartis AG | Derives de 4-phenylpiperidine utilises en tant qu'inhibiteurs de la renine |
NZ586285A (en) | 2004-03-17 | 2011-12-22 | Novartis Ag | Use of aliskiren in monotherapy for treating diabetes and metabolic disorder (syndrome X) |
JP2007223901A (ja) * | 2004-03-24 | 2007-09-06 | Takeda Chem Ind Ltd | 複素環化合物およびその用途 |
TW200613274A (en) * | 2004-07-09 | 2006-05-01 | Speedel Experimenta Ag | Organic compounds |
ATE462703T1 (de) | 2004-08-25 | 2010-04-15 | Actelion Pharmaceuticals Ltd | Bicyclononen-derivate als renin-inhibitoren |
GB0428526D0 (en) | 2004-12-30 | 2005-02-09 | Novartis Ag | Organic compounds |
GB0500784D0 (en) * | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
MX2007009004A (es) * | 2005-01-28 | 2007-09-14 | Actelion Pharmaceuticals Ltd | Ciclopropil-(2,3-dimetilbencidamida del acido 7-{4-[2-(2,6-dicloro-4-metilfenoxi) etoxi] fenil}-3,9-diazabiciclo [3.3.31]non-6-en-s-carboxilico como inhbidores de renina para el tratamiento de hipertension. |
CA2601108A1 (fr) * | 2005-03-31 | 2006-10-05 | Speedel Experimenta Ag | Piperidine a substitution 3,4,5 utiles en tant qu'inhibiteurs de la renine |
AR055756A1 (es) | 2005-03-31 | 2007-09-05 | Speedel Experimenta Ag | Piperidinas sustituidas; procesos de preparacion y su uso como medicamentos |
TW200722424A (en) | 2005-03-31 | 2007-06-16 | Speedel Experimenta Ag | Substituted piperidines |
ES2352564T3 (es) * | 2005-03-31 | 2011-02-21 | Novartis Ag | Piperidinas sustituidas. |
EP1707202A1 (fr) * | 2005-03-31 | 2006-10-04 | Speedel Experimenta AG | Composes organiques |
EP1897879A3 (fr) | 2005-03-31 | 2008-06-11 | Speedel Experimenta AG | Pipéridines 2,4,5-substituées comme inhibiteurs de la rénine |
GB0508992D0 (en) * | 2005-05-03 | 2005-06-08 | Novartis Ag | Organic compounds |
GB0510810D0 (en) * | 2005-05-26 | 2005-06-29 | Novartis Ag | Organic compounds |
US7799805B2 (en) | 2005-05-27 | 2010-09-21 | Actelion Pharmaceuticals Ltd. | Piperidine carboxylic acid amide derivatives |
WO2006131884A2 (fr) * | 2005-06-07 | 2006-12-14 | Actelion Pharmaceuticals Ltd | Nouveaux derives de thiazole |
GB0514203D0 (en) | 2005-07-11 | 2005-08-17 | Novartis Ag | Organic compounds |
WO2007014851A2 (fr) | 2005-07-29 | 2007-02-08 | F. Hoffmann-La Roche Ag | Derives de indol-3-yl-carbonyl-piperidine et piperazine |
US20070142389A1 (en) * | 2005-12-20 | 2007-06-21 | Pfizer Inc. | Piperidine derivatives |
EP1968940B1 (fr) | 2005-12-30 | 2014-04-02 | Novartis AG | Dérivés de pipéridine 3,5-substitués en tant qu'inhibiteurs de rénine |
EP1816122A3 (fr) * | 2006-01-19 | 2007-09-19 | Speedel Experimenta AG | Pipéridines substituées 3,4,5 en tant que composants thérapeutiques |
TW200804359A (en) * | 2006-01-19 | 2008-01-16 | Speedel Experimenta Ag | Substituted 4-phenylpiperidines |
NZ570828A (en) | 2006-02-02 | 2011-07-29 | Actelion Pharmaceuticals Ltd | Secondary amines as renin inhibitors |
US8084485B2 (en) | 2006-03-31 | 2011-12-27 | Vitae Pharmaceuticals, Inc. | 6-(aminoalkyl)indazoles |
JP5420398B2 (ja) | 2006-05-19 | 2014-02-19 | アッヴィ・バハマズ・リミテッド | Cns活性縮合ビシクロ複素環置換アザ二環式アルカン誘導体 |
WO2007141318A1 (fr) | 2006-06-08 | 2007-12-13 | Speedel Experimenta Ag | Pipéridines 2,5-disubstituées |
CL2007002689A1 (es) | 2006-09-18 | 2008-04-18 | Vitae Pharmaceuticals Inc | Compuestos derivados de piperidin-1-carboxamida, inhibidores de la renina; compuestos intermediarios; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como hipertension, insuficiencia cardiaca, fibrosis cardiaca, entre otras. |
JP2010510176A (ja) * | 2006-11-17 | 2010-04-02 | メルク フロスト カナダ リミテツド | レニン阻害剤 |
US7638541B2 (en) | 2006-12-28 | 2009-12-29 | Metabolex Inc. | 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine |
EP1987834A3 (fr) | 2007-02-13 | 2008-11-19 | Speedel Experimenta AG | Pipéridines substituées en tant que composants thérapeutiques |
CN101657432B (zh) * | 2007-04-19 | 2013-04-10 | 弗·哈夫曼-拉罗切有限公司 | 二氢-苯并[b][1,4]二氮杂*-2-酮磺酰胺衍生物 |
AU2008243874B2 (en) | 2007-04-27 | 2012-01-19 | Purdue Pharma L.P. | TRPV1 antagonists and uses thereof |
EA016446B1 (ru) | 2007-06-25 | 2012-05-30 | Новартис Аг | Производные n5-(2-этоксиэтил)-n3-(2-пиридинил)-3,5-пиперидиндикарбоксамида, предназначенные для применения в качестве ингибиторов ренина |
US8183381B2 (en) * | 2007-07-19 | 2012-05-22 | Metabolex Inc. | N-linked heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders |
EP2018862A1 (fr) | 2007-07-25 | 2009-01-28 | Speedel Experimenta AG | Pipéridines substituées en tant que composants thérapeutiques |
AR068887A1 (es) | 2007-10-18 | 2009-12-16 | Speedel Experimenta Ag | Piperidinas trisustituidas |
TW200922596A (en) | 2007-10-25 | 2009-06-01 | Speedel Experimenta Ag | 4,4-disubstituted piperidines |
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TW200932241A (en) | 2007-12-05 | 2009-08-01 | Speedel Experimenta Ag | Organic compounds |
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EP2303859A4 (fr) * | 2008-06-20 | 2012-08-22 | Metabolex Inc | Agonistes des récepteurs gpr119 aryles et utilisations associées |
JPWO2010013849A1 (ja) | 2008-08-01 | 2012-01-12 | 日本ケミファ株式会社 | Gpr119作動薬 |
EP2163245A1 (fr) | 2008-09-10 | 2010-03-17 | Novartis Ag | Inhibiteurs de la rénine pour le traitement du psoriasis |
JP2010090110A (ja) * | 2008-09-12 | 2010-04-22 | Sumitomo Chemical Co Ltd | N−置換−トランス−4−アジドピペリジン−3−オールの製造方法 |
WO2010066028A1 (fr) * | 2008-12-10 | 2010-06-17 | Merck Frosst Canada Ltd. | Dérivés de pipéridine à substitution en 3,4 utilisés comme inhibiteurs de rénine |
US20120115907A1 (en) | 2009-04-24 | 2012-05-10 | Cadila Healthcare Limited | Novel compounds as inhibitors of renin |
WO2011030139A1 (fr) | 2009-09-11 | 2011-03-17 | Astrazeneca Ab | Derives de 4-(pyrimidin-2-yl)-piperazine et de 4-(pyrimidin-2-yl)-piperidine utilises en tant que modulateurs du gpr119 |
ES2497566T3 (es) * | 2009-10-01 | 2014-09-23 | Cymabay Therapeutics, Inc. | Sales de tetrazol-1-il-fenoximetil-tiazol-2-il-piperidinil-pirimidina sustituida |
EP2585048B1 (fr) | 2010-06-23 | 2018-04-11 | CymaBay Therapeutics, Inc. | Compositions de 5-éthyl-2-{4-[4-(4-tétrazol-1-yl-phénoxyméthyl)-thiazol-2-yl]-pipéridin-1-yl}-pyrimidine |
US20120184572A1 (en) * | 2011-01-13 | 2012-07-19 | Metabolex, Inc. | Aryl gpr119 agonists and uses thereof |
CN105693712A (zh) | 2011-06-22 | 2016-06-22 | 普渡制药公司 | 包含二羟基取代基的trpv1拮抗剂及其用途 |
WO2013088452A2 (fr) | 2011-11-11 | 2013-06-20 | Sun Pharma Advanced Research Company Ltd. | Dérivés de quinoléine utilisés en tant qu'inhibiteurs de la rénine |
WO2013084241A1 (fr) | 2011-12-09 | 2013-06-13 | Cadila Healthcare Limited | Composés inhibiteurs de rénine |
CN104370813A (zh) * | 2014-10-22 | 2015-02-25 | 上海大学 | 异喹啉-6-甲醛的制备方法 |
KR20190035752A (ko) | 2016-08-03 | 2019-04-03 | 사이머베이 쎄라퓨틱스, 인코퍼레이티드 | 염증성 위장 질환 또는 위장 상태를 치료하기 위한 옥시메틸렌 아릴 화합물 |
CN110041212B (zh) * | 2019-05-21 | 2020-10-02 | 吉林大学 | 一种含氟多胺单体及其制备方法、一种聚酰亚胺及其制备方法和一种聚酰亚胺膜 |
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DE1545792B2 (de) * | 1965-02-27 | 1975-08-07 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von 4-Hydroxyplperidinen |
GB1422263A (en) * | 1973-01-30 | 1976-01-21 | Ferrosan As | 4-phenyl-piperidine compounds |
IE45511B1 (en) * | 1976-09-01 | 1982-09-08 | Ciba Geigy Ag | New derivatives of perhydro-aza-heterocycles and processesfor the production thereof |
DK715988D0 (da) * | 1988-12-22 | 1988-12-22 | Ferrosan As | Etherifikation og dealkylering af piperidin-derivater samt intermediater |
US5272156A (en) * | 1989-09-19 | 1993-12-21 | Allergan, Inc. | Acetylenes disubstituted with a heteroaromatic group and a 2-substituted 1,2,3,4-tetrahydroquinolinyl group having retinoid-like activity |
RU2097378C1 (ru) * | 1991-03-26 | 1997-11-27 | Ф.Хоффманн-Ля Рош Аг | ПРОИЗВОДНЫЕ N-АЦИЛ- α -АМИНОКИСЛОТЫ ИЛИ ИХ ФИЗИОЛОГИЧЕСКИ ПРИЕМЛЕМЫЕ СОЛИ, ПРОСТЫЕ ИЛИ СЛОЖНЫЕ ЭФИРЫ, АМИДЫ ИЛИ ГИДРАТЫ И КОМПОЗИЦИЯ ИНГИБИРУЮЩАЯ СВЯЗЫВАНИЕ АДГЕЗИВНЫХ ПРОТЕИНОВ С ТРОМБОЦИТАМИ И АГРЕГАЦИЮ ТРОМБОЦИТОВ |
US5545658A (en) * | 1991-03-26 | 1996-08-13 | Hoffman-La Roche Inc. | Amino acid derivatives |
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1996
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- 1996-08-29 CZ CZ1998684A patent/CZ292327B6/cs not_active IP Right Cessation
- 1996-08-29 WO PCT/EP1996/003803 patent/WO1997009311A1/fr active IP Right Grant
- 1996-08-29 EP EP96927715A patent/EP0863875B1/fr not_active Expired - Lifetime
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- 1996-09-02 TW TW085110684A patent/TW474932B/zh not_active IP Right Cessation
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1998
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