DE69633245D1 - Spiro verbindungen als inhibitoren der fibrinogen-abhängigen blutplättchen aggregation - Google Patents
Spiro verbindungen als inhibitoren der fibrinogen-abhängigen blutplättchen aggregationInfo
- Publication number
- DE69633245D1 DE69633245D1 DE69633245T DE69633245T DE69633245D1 DE 69633245 D1 DE69633245 D1 DE 69633245D1 DE 69633245 T DE69633245 T DE 69633245T DE 69633245 T DE69633245 T DE 69633245T DE 69633245 D1 DE69633245 D1 DE 69633245D1
- Authority
- DE
- Germany
- Prior art keywords
- fibrinogen
- inhibitors
- spiro compounds
- blood plate
- dependent blood
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/20—Spiro-condensed ring systems
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
-
- 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
- C07D471/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Diabetes (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US455795P | 1995-09-29 | 1995-09-29 | |
US4557P | 1995-09-29 | ||
PCT/US1996/015703 WO1997011940A1 (en) | 1995-09-29 | 1996-09-27 | Spiro compounds as inhibitors of fibrinogen-dependent platelet aggregation |
Publications (2)
Publication Number | Publication Date |
---|---|
DE69633245D1 true DE69633245D1 (de) | 2004-09-30 |
DE69633245T2 DE69633245T2 (de) | 2005-09-08 |
Family
ID=21711385
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69633245T Expired - Fee Related DE69633245T2 (de) | 1995-09-29 | 1996-09-27 | Spiroverbindungen als Inhibitoren der Fibrinogen-abhängigen Blutplättchenaggregation |
Country Status (10)
Country | Link |
---|---|
US (3) | US6291469B1 (de) |
EP (1) | EP0854869B1 (de) |
JP (1) | JPH11512723A (de) |
AT (1) | ATE274499T1 (de) |
AU (1) | AU713235B2 (de) |
CA (1) | CA2233204A1 (de) |
DE (1) | DE69633245T2 (de) |
ES (1) | ES2227612T3 (de) |
NZ (1) | NZ320963A (de) |
WO (1) | WO1997011940A1 (de) |
Families Citing this family (73)
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EP1087770A4 (de) | 1998-06-15 | 2001-11-14 | Merck & Co Inc | Inhibitoren der prenyl-protein transferase |
US6455734B1 (en) | 2000-08-09 | 2002-09-24 | Magnesium Diagnostics, Inc. | Antagonists of the magnesium binding defect as therapeutic agents and methods for treatment of abnormal physiological states |
AU1244001A (en) * | 1999-10-27 | 2001-05-08 | Cor Therapeutics, Inc. | Pyridyl-containing spirocyclic compounds as inhibitors of fibrinogen-dependent platelet aggregation |
CN1246321C (zh) * | 1999-12-03 | 2006-03-22 | 小野药品工业株式会社 | 三氮杂螺[5,5]十一烷衍生物和含其作为活性成分的药物组合物 |
EP1263729B1 (de) | 2000-03-06 | 2006-12-20 | Acadia Pharmaceuticals Inc. | Azacyclische verbindungen zur verwendung in der behandlung von mit serotonin verwandten krankheiten |
US6482829B2 (en) * | 2000-06-08 | 2002-11-19 | Hoffmann-La Roche Inc. | Substituted heterocyclic siprodecane compound active as an antagonist of neurokinin 1 receptor |
MXPA03008529A (es) | 2001-03-19 | 2004-06-30 | Ono Pharmaceutical Co | Derivado de triazaspiro [5.5]undecano y composicion farmaceutica que comprende el mismo como ingrediente activo. |
EP1378509A4 (de) * | 2001-03-19 | 2009-03-25 | Ono Pharmaceutical Co | ARZNEIMITTEL MIT TRIAZASPIRO ç5.5]UNDECANDERIVATEN ALS WIRKSTOFF |
EP1390372B1 (de) | 2001-05-14 | 2008-07-16 | F. Hoffmann-La Roche Ag | 1-OXA-3,9-DIAZASPIROç5.5]UNDECAN-2-ONDERIVATE UND DEREN VERWENDUNG ALS ANTAGONISTEN DES NEUROKININREZEPTORS |
DE10130020A1 (de) * | 2001-06-25 | 2003-12-04 | Gruenenthal Gmbh | Substituierte 1-Oxa-2,8-diaza-spiro[4.5]dec-2-en-derivate |
US6911452B2 (en) | 2001-12-28 | 2005-06-28 | Acadia Pharmaceuticals Inc. | Spiroazacyclic compounds as monoamine receptor modulators |
US7538222B2 (en) | 2002-06-24 | 2009-05-26 | Acadia Pharmaceuticals, Inc. | N-substituted piperidine derivatives as serotonin receptor agents |
US7253186B2 (en) | 2002-06-24 | 2007-08-07 | Carl-Magnus Andersson | N-substituted piperidine derivatives as serotonin receptor agents |
MXPA04012893A (es) | 2002-06-24 | 2005-03-31 | Acadia Pharm Inc | Derivados de piperidina n-substituidos como agentes receptores de serotonina. |
JP2006505585A (ja) * | 2002-10-18 | 2006-02-16 | モリケム メディシンズ, インコーポレイテッド | ランチビオティクスで眼乾燥症を処置する方法 |
KR101095939B1 (ko) | 2003-01-16 | 2011-12-19 | 아카디아 파마슈티칼스 인코포레이티드 | 신경퇴행성 질환에 대한 치료제로서 선택적 세로토닌2a/2c 리셉터 역작용제 |
EP1619193A4 (de) * | 2003-04-18 | 2010-08-11 | Ono Pharmaceutical Co | Spiropiperidinverbindung und deren medizinische verwendung |
WO2005044978A2 (en) * | 2003-07-15 | 2005-05-19 | Washington University | Methods of treating, preventing and inhibiting cancer metastasis and tumor formation |
EP1776362A1 (de) * | 2003-07-18 | 2007-04-25 | Virochem Pharma Inc. | Spiroverbindungen und verfahren zur modulation der aktivität des chemokinrezeptors |
EP1786816A4 (de) | 2003-09-10 | 2009-11-04 | Virochem Pharma Inc | Spirohydantoinverbindungen und -verfahren zur modulation von chemokin-rezeptoraktivität |
WO2005047286A1 (ja) * | 2003-11-13 | 2005-05-26 | Ono Pharmaceutical Co., Ltd. | スピロ複素環化合物 |
BRPI0507586A (pt) | 2004-02-10 | 2007-07-03 | Hoffmann La Roche | moduladores de receptor de quimiocina ccr5 |
CA2565457A1 (en) * | 2004-05-06 | 2005-11-17 | Molichem Medicines, Inc. | Treatment of membrane-associated diseases and disorders using lantibiotic containing compositions |
EP1753445A4 (de) * | 2004-05-06 | 2009-05-20 | Molichem Medicines Inc | Behandlung von augenerkrankungen und augenleiden mit lantibiotischen zusammensetzungen |
US20050261278A1 (en) | 2004-05-21 | 2005-11-24 | Weiner David M | Selective serotonin receptor inverse agonists as therapeutics for disease |
US7820695B2 (en) | 2004-05-21 | 2010-10-26 | Acadia Pharmaceuticals, Inc. | Selective serotonin receptor inverse agonists as therapeutics for disease |
WO2006002361A2 (en) | 2004-06-24 | 2006-01-05 | Incyte Corporation | 2-methylpropanamides and their use as pharmaceuticals |
NZ551603A (en) | 2004-06-24 | 2010-11-26 | Incyte Corp | N-substituted piperidines and their use as pharmaceuticals |
US7709642B2 (en) | 2004-06-25 | 2010-05-04 | Virochem Pharma, Inc. | Spirohydantoin compounds and methods for the modulation of chemokine receptor activity |
WO2006006490A1 (ja) * | 2004-07-08 | 2006-01-19 | Ono Pharmaceutical Co., Ltd. | スピロ化合物 |
WO2006022454A1 (ja) * | 2004-08-27 | 2006-03-02 | Ono Pharmaceutical Co., Ltd | 塩基性基を含有する化合物およびその用途 |
US7790899B2 (en) | 2004-09-27 | 2010-09-07 | Acadia Pharmaceuticals, Inc. | Synthesis of N-(4-fluorobenzyl)-N-(1-methylpiperidin-4-yl)-N′-(4-(2-methylpropyloxy)phenylmethyl)carbamide and its tartrate salt and crystalline forms |
AU2005289635A1 (en) | 2004-09-27 | 2006-04-06 | Acadia Pharmaceuticals Inc. | Salts of N-(4-fluorobenzyl)-N-(1-methylpiperidin-4-yl)-N'-(4-(2-methylpropyloxy)phenylmethyl) carbamide and their preparation |
US20070021612A1 (en) * | 2004-11-04 | 2007-01-25 | University Of Notre Dame Du Lac | Processes and compounds for preparing histone deacetylase inhibitors and intermediates thereof |
US7235688B1 (en) | 2004-11-04 | 2007-06-26 | University Of Notre Dame Du Lac | Process for preparing histone deacetylase inhibitors and intermediates thereof |
GEP20125565B (en) * | 2004-11-10 | 2012-07-10 | Incyte Corp | Lactam compounds and their pharmaceutical use |
US8110581B2 (en) | 2004-11-10 | 2012-02-07 | Incyte Corporation | Lactam compounds and their use as pharmaceuticals |
DE102005044813A1 (de) | 2005-05-19 | 2007-10-04 | Grünenthal GmbH | Substituierte Spiro-Verbindungen und deren Verwendung zur Herstellung von Arzneimitteln |
WO2006129679A1 (ja) | 2005-05-31 | 2006-12-07 | Ono Pharmaceutical Co., Ltd. | スピロピペリジン化合物およびその医薬用途 |
ES2407115T3 (es) | 2005-11-18 | 2013-06-11 | Ono Pharmaceutical Co., Ltd. | Compuesto que contiene un grupo básico y uso del mismo |
WO2007065256A1 (en) * | 2005-12-06 | 2007-06-14 | Virochem Pharma Inc. | Novel spiropiperidine compounds and methods for the modulation of chemokine receptor activity |
US20080247964A1 (en) * | 2006-05-08 | 2008-10-09 | Yuelian Xu | Substituted azaspiro derivatives |
EP2042503B1 (de) * | 2006-05-16 | 2013-01-30 | Ono Pharmaceutical Co., Ltd. | Verbindung mit gegebenenfalls geschützter acider gruppe und anwendung davon |
JP2010517966A (ja) * | 2007-02-01 | 2010-05-27 | グラクソ グループ リミテッド | 摂食障害の処置のための1−オキサ−3−アザスピロ(4.5)デカン−2−オンおよび1−オキサ−3,8−ジアザスピロ(4.5)デカン−2−オン誘導体 |
TW200900060A (en) * | 2007-02-01 | 2009-01-01 | Glaxo Group Ltd | Chemical compounds |
CN101255161B (zh) * | 2007-02-28 | 2011-07-20 | 上海药明康德新药开发有限公司 | 9-pg-3,9-二氮杂-2,4-二氧代-螺[5.5]十一烷的合成方法 |
CN101677971A (zh) | 2007-03-19 | 2010-03-24 | 阿卡蒂亚药品公司 | 5-ht2a反向激动剂和拮抗剂与抗精神病药物的组合 |
AU2008233930A1 (en) | 2007-03-29 | 2008-10-09 | F. Hoffmann-La Roche Ag | Heterocyclic antiviral compounds |
CL2008001839A1 (es) | 2007-06-21 | 2009-01-16 | Incyte Holdings Corp | Compuestos derivados de 2,7-diazaespirociclos, inhibidores de 11-beta hidroxil esteroide deshidrogenasa tipo 1; composicion farmaceutica que comprende a dichos compuestos; utiles para tratar la obesidad, diabetes, intolerancia a la glucosa, diabetes tipo ii, entre otras enfermedades. |
WO2009039431A2 (en) * | 2007-09-21 | 2009-03-26 | Neurogen Corporation | Substituted aryl-fused spirocyclic amines |
WO2009097405A2 (en) * | 2008-01-30 | 2009-08-06 | Neurogen Corporation | Compounds and methods for preparing diazaspiro derivatives |
WO2011140425A1 (en) | 2010-05-06 | 2011-11-10 | Vertex Pharmaceuticals Incorporated | Heterocyclic chromene-spirocyclic piperidine amides as modulators of ion channels |
WO2012064642A1 (en) * | 2010-11-08 | 2012-05-18 | Glaxosmithkline Llc | Fatty acid synthase inhibitors |
PT2670752E (pt) | 2011-02-02 | 2016-06-14 | Vertex Pharma | Piperidinamidas pirrolopirazina-espirocíclicas como moduladores de canais iónicos |
WO2012112743A1 (en) | 2011-02-18 | 2012-08-23 | Vertex Pharmaceuticals Incorporated | Chroman - spirocyclic piperidine amides as modulators of ion channels |
MX347982B (es) * | 2011-03-14 | 2017-05-22 | Vertex Pharma | Morfolina-piperidina espirociclica-amidas como moduladores de canales ionicos. |
JP5964426B2 (ja) * | 2011-08-19 | 2016-08-03 | グラクソスミスクライン、インテレクチュアル、プロパティー、ナンバー2、リミテッドGlaxosmithkline Intellectual Property No.2 Limited | 脂肪酸シンターゼ阻害剤 |
WO2013052716A1 (en) * | 2011-10-07 | 2013-04-11 | Glaxosmithkline Llc | Fatty acid synthase inhibitors |
MX2014008591A (es) * | 2012-01-16 | 2014-08-22 | Vertex Pharma | Piperidinamidas piranoespirociclicas como moduladores de canales de iones. |
WO2014008223A2 (en) * | 2012-07-03 | 2014-01-09 | Glaxosmithkline Llc | Fatty acid synthase inhibitors |
FR3000064A1 (fr) * | 2012-12-21 | 2014-06-27 | Univ Lille Ii Droit & Sante | Composes de type spiroisoxazoline ayant une activite potentialisatrice de l'activite d'un antibiotique-composition et produit pharmaceutiques comprenant de tels composes |
US9751881B2 (en) | 2013-07-31 | 2017-09-05 | Merck Sharp & Dohme Corp. | Inhibitors of the renal outer medullary potassium channel |
US9951052B2 (en) | 2013-10-31 | 2018-04-24 | Merck Sharp & Dohme Corp. | Inhibitors of the renal outer medullary potassium channel |
WO2015096035A1 (en) * | 2013-12-24 | 2015-07-02 | Merck Sharp & Dohme Corp. | Inhibitors of renal outer medullary potassium channel |
EP3134408B1 (de) | 2014-04-22 | 2020-08-12 | Merck Sharp & Dohme Corp. | Faktor-xia-hemmer |
CN104530080B (zh) * | 2014-12-10 | 2017-01-11 | 广东东阳光药业有限公司 | 噁唑烷酮类化合物及其在药物中的应用 |
SI3325444T1 (sl) | 2015-07-20 | 2021-11-30 | Acadia Pharmaceuticals Inc. | Postopki za pripravo N-(4-fluorobenzil)-N-(1-metilpiperidin-4-il)-N'- (4-(2-metilpropiloksi)fenilmetil)karbamida in njegove tartratne soli in polimorfne oblike C |
US10953000B2 (en) | 2016-03-25 | 2021-03-23 | Acadia Pharmaceuticals Inc. | Combination of pimavanserin and cytochrome P450 modulators |
WO2017165635A1 (en) | 2016-03-25 | 2017-09-28 | Acadia Pharmaceuticals Inc. | Combination of pimavanserin and cytochrome p450 modulators |
WO2018118626A1 (en) | 2016-12-20 | 2018-06-28 | Acadia Pharmaceuticals Inc. | Pimavanserin alone or in combination for use in the treatment of alzheimer's disease psychosis |
US11135211B2 (en) | 2017-04-28 | 2021-10-05 | Acadia Pharmaceuticals Inc. | Pimavanserin for treating impulse control disorder |
EP3675827A1 (de) | 2017-08-30 | 2020-07-08 | Acadia Pharmaceuticals Inc. | Formulierungen von pimavanserin |
CN111533739B (zh) * | 2020-05-08 | 2023-05-05 | 上海皓鸿生物医药科技有限公司 | 3-烷基-3,9-二氮杂螺[5,5]十一烷的制备方法 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5534520A (en) | 1990-04-10 | 1996-07-09 | Fisher; Abraham | Spiro compounds containing five-membered rings |
US5272158A (en) | 1991-10-29 | 1993-12-21 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
WO1993013101A1 (en) | 1991-12-27 | 1993-07-08 | Yoshitomi Pharmaceutical Industries, Ltd. | Pyridonecarboxylate compound, pharmaceutical use thereof, and spiro compound |
WO1994008577A1 (en) | 1992-10-14 | 1994-04-28 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
DE69327536T2 (de) | 1992-10-14 | 2000-07-06 | Merck & Co Inc | Fibrinogenrezeptor-antagonisten |
CA2150550A1 (en) | 1992-12-01 | 1994-06-09 | Melissa S. Egbertson | Fibrinogen receptor antagonists |
NZ262664A (en) | 1993-02-22 | 1997-04-24 | Merck & Co Inc | Heterocyclic substituted derivatives, and medicaments thereof |
US5441952A (en) | 1993-04-05 | 1995-08-15 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
IL110172A (en) * | 1993-07-22 | 2001-10-31 | Lilly Co Eli | Bicycle compounds and pharmaceuticals containing them |
US5817756A (en) * | 1993-09-09 | 1998-10-06 | Scios Inc. | Pseudo- and non-peptide bradykinin receptor antagonists |
CA2134192A1 (en) | 1993-11-12 | 1995-05-13 | Michael L. Denney | 5, 6-bicyclic glycoprotein iib/iiia antagonists |
US5849736A (en) | 1993-11-24 | 1998-12-15 | The Dupont Merck Pharmaceutical Company | Isoxazoline and isoxazole fibrinogen receptor antagonists |
JPH09505590A (ja) | 1993-11-24 | 1997-06-03 | ザ・デュポン・メルク・ファーマシュウティカル・カンパニー | 新規なイソオキサゾリンおよびイソオキサゾールフィブリノーゲン受容体拮抗剤 |
US5451578A (en) | 1994-08-12 | 1995-09-19 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
US5739336A (en) * | 1995-06-23 | 1998-04-14 | Syntex (U.S.A.) Inc. | 1,3,8-triaza- and 3,8-diaza-1-oxaspiro 4,5! decane derivatives |
-
1996
- 1996-09-27 CA CA002233204A patent/CA2233204A1/en not_active Abandoned
- 1996-09-27 JP JP9513756A patent/JPH11512723A/ja active Pending
- 1996-09-27 EP EP96936093A patent/EP0854869B1/de not_active Expired - Lifetime
- 1996-09-27 AT AT96936093T patent/ATE274499T1/de not_active IP Right Cessation
- 1996-09-27 WO PCT/US1996/015703 patent/WO1997011940A1/en active IP Right Grant
- 1996-09-27 DE DE69633245T patent/DE69633245T2/de not_active Expired - Fee Related
- 1996-09-27 AU AU73828/96A patent/AU713235B2/en not_active Ceased
- 1996-09-27 ES ES96936093T patent/ES2227612T3/es not_active Expired - Lifetime
- 1996-09-27 NZ NZ320963A patent/NZ320963A/xx unknown
- 1996-09-27 US US09/043,846 patent/US6291469B1/en not_active Expired - Lifetime
-
2001
- 2001-07-06 US US09/899,886 patent/US6528534B2/en not_active Expired - Fee Related
-
2003
- 2003-01-29 US US10/354,265 patent/US6693109B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP0854869B1 (de) | 2004-08-25 |
JPH11512723A (ja) | 1999-11-02 |
US20020013325A1 (en) | 2002-01-31 |
US6693109B2 (en) | 2004-02-17 |
EP0854869A1 (de) | 1998-07-29 |
US20030171373A1 (en) | 2003-09-11 |
CA2233204A1 (en) | 1997-04-03 |
US6291469B1 (en) | 2001-09-18 |
AU713235B2 (en) | 1999-11-25 |
ES2227612T3 (es) | 2005-04-01 |
US6528534B2 (en) | 2003-03-04 |
ATE274499T1 (de) | 2004-09-15 |
DE69633245T2 (de) | 2005-09-08 |
WO1997011940A1 (en) | 1997-04-03 |
AU7382896A (en) | 1997-04-17 |
NZ320963A (en) | 1999-08-30 |
MX9802379A (es) | 1998-08-30 |
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