NO984418L - Arylaminokondenserte pyridiner og pyrimidiner - Google Patents
Arylaminokondenserte pyridiner og pyrimidinerInfo
- Publication number
- NO984418L NO984418L NO984418A NO984418A NO984418L NO 984418 L NO984418 L NO 984418L NO 984418 A NO984418 A NO 984418A NO 984418 A NO984418 A NO 984418A NO 984418 L NO984418 L NO 984418L
- Authority
- NO
- Norway
- Prior art keywords
- arylamino
- pyrimidines
- condensed pyridines
- pyridines
- condensed
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Immunology (AREA)
- Addiction (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Transplantation (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Luminescent Compositions (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1415796P | 1996-03-27 | 1996-03-27 | |
US64661296A | 1996-05-08 | 1996-05-08 | |
US3053696P | 1996-10-31 | 1996-10-31 | |
US3912497P | 1997-02-25 | 1997-02-25 | |
PCT/US1997/004852 WO1997035539A2 (fr) | 1996-03-27 | 1997-03-25 | Pyridines et pyrimidines a fusion arylamino |
Publications (2)
Publication Number | Publication Date |
---|---|
NO984418D0 NO984418D0 (no) | 1998-09-22 |
NO984418L true NO984418L (no) | 1998-11-03 |
Family
ID=27486365
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO984418A NO984418L (no) | 1996-03-27 | 1998-09-22 | Arylaminokondenserte pyridiner og pyrimidiner |
Country Status (21)
Country | Link |
---|---|
US (2) | US6107300A (fr) |
EP (1) | EP0935601A4 (fr) |
JP (1) | JP2002515032A (fr) |
KR (1) | KR20000005037A (fr) |
CN (1) | CN1230184A (fr) |
AU (1) | AU2545897A (fr) |
BR (1) | BR9708261A (fr) |
CA (1) | CA2250241A1 (fr) |
CZ (1) | CZ304098A3 (fr) |
EA (1) | EA199800868A1 (fr) |
EE (1) | EE9800329A (fr) |
HR (1) | HRP970173A2 (fr) |
HU (1) | HUP9902340A3 (fr) |
IL (1) | IL126316A0 (fr) |
LV (1) | LV12262B (fr) |
NO (1) | NO984418L (fr) |
NZ (1) | NZ331874A (fr) |
PL (1) | PL335258A1 (fr) |
SI (1) | SI9720026A (fr) |
SK (1) | SK131798A3 (fr) |
WO (1) | WO1997035539A2 (fr) |
Families Citing this family (65)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2196181T3 (es) | 1995-11-01 | 2003-12-16 | Novartis Ag | Derivados de purina y proceso para su preparacion. |
NZ337164A (en) * | 1997-03-21 | 2001-05-25 | Du Pont Pharm Co | Method of preparing 4-arylamino-1-alkyl-[1,2,3]-triazolo][4,5-c]pyridine derivatives |
EP0994860A1 (fr) * | 1997-07-03 | 2000-04-26 | Du Pont Pharmaceuticals Company | Heterocycles aryl- et arylamino-substitues utilises comme antagonistes de l'hormone corticotrope |
AU2881199A (en) * | 1998-02-26 | 1999-09-15 | Neurogen Corporation | Substituted 1,4-dihydro-4-oxonicotinic carboxamides: gaba brain receptor ligands |
US6531475B1 (en) | 1998-11-12 | 2003-03-11 | Neurocrine Biosciences, Inc. | CRF receptor antagonists and methods relating thereto |
EP1129091B1 (fr) | 1998-11-12 | 2002-10-02 | Neurocrine Biosciences, Inc. | Antagonistes de recepteurs du crf et methodes associees |
DK1129096T3 (da) | 1998-11-12 | 2003-09-15 | Neurocrine Biosciences Inc | CRF-receptorantagonister og fremgangsmåder, der er relateret dertil |
GB9903762D0 (en) | 1999-02-18 | 1999-04-14 | Novartis Ag | Organic compounds |
DE60026155T2 (de) | 1999-09-30 | 2006-08-10 | Neurogen Corp., Branford | Einige alkylendiamin-substituierte heterocyclen |
AU2583901A (en) * | 1999-12-17 | 2001-06-25 | Ariad Pharmaceuticals, Inc. | Proton pump inhibitors |
US7115589B2 (en) * | 1999-12-17 | 2006-10-03 | Ariad Pharmaceuticals, Inc. | Purine derivatives |
CA2398956A1 (fr) * | 2000-02-14 | 2001-08-16 | Japan Tobacco Inc. | Composition pharmaceutique pour la prophylaxie ou le traitement du stress post-operatoire |
CA2419626A1 (fr) * | 2000-07-14 | 2002-01-24 | Rajagopal Bakthavatachalam | Imidazo¬1,2-a|pyrazines destinees au traitement d'affections neurologiques |
JP4064818B2 (ja) | 2001-02-12 | 2008-03-19 | エフ.ホフマン−ラ ロシュ アーゲー | 6−置換ピリド−ピリミジン類 |
WO2002072202A1 (fr) | 2001-03-13 | 2002-09-19 | Bristol-Myers Squibb Pharma Company | 4-(2-butylamino)-2,7-dimethyl-8-(2-methyl-6-methoxypyrid-3-yl) pyrazolo-[1,5-a]-1,3,5-triazine, ses enantiomeres et sels pharmaceutiquement acceptables en tant que ligands du recepteur de la corticoliberine |
RU2003135424A (ru) | 2001-05-14 | 2005-05-20 | Бристол-Маерс Сквибб Фарма Компани (Us) | Замещенные пиразиноны, пиридины и пиримидины в качестве лигандов кортикотропин высвобождающего фактора |
PE20030008A1 (es) | 2001-06-19 | 2003-01-22 | Bristol Myers Squibb Co | Inhibidores duales de pde 7 y pde 4 |
US6894045B2 (en) | 2001-07-12 | 2005-05-17 | Bristol-Myers Squibb Pharma Company | Tetrahydropurinones and derivatives thereof as corticotropin releasing factor receptor ligands |
WO2003006015A1 (fr) | 2001-07-13 | 2003-01-23 | Bristol-Myers Squibb Pharma Company | Thiazoles et oxazoles substitutes utilises comme ligands hormonaux de liberation de la corticotrophine |
GB0117525D0 (en) | 2001-07-19 | 2001-09-12 | Procter & Gamble | Solvent welding process |
GB0117522D0 (en) | 2001-07-19 | 2001-09-12 | Procter & Gamble | Solvent welding process |
US20030119831A1 (en) | 2001-11-20 | 2003-06-26 | Hartz Richard A. | 3,7-dihydro-purine-2,6-dione derivatives as CRF receptor ligands |
US9967633B1 (en) | 2001-12-14 | 2018-05-08 | At&T Intellectual Property I, L.P. | System and method for utilizing television viewing patterns |
AU2002359732A1 (en) * | 2001-12-17 | 2003-06-30 | Ribapharm Inc. | Substituted purine nucleoside libraries and compounds by solid-phase combinatorial strategies |
GB0219746D0 (en) | 2002-08-23 | 2002-10-02 | Inst Of Ex Botany Ascr | Azapurine derivatives |
SE0301373D0 (sv) * | 2003-05-09 | 2003-05-09 | Astrazeneca Ab | Novel compounds |
US20050065171A1 (en) * | 2003-06-25 | 2005-03-24 | Shakespeare William C. | Substituted purine derivatives |
EP1666468A4 (fr) * | 2003-09-09 | 2007-03-21 | Ono Pharmaceutical Co | Antagonistes crf et composes heterobicycliques |
ATE517091T1 (de) | 2003-09-26 | 2011-08-15 | Exelixis Inc | C-met-modulatoren und verwendungsverfahren |
JP2007526339A (ja) * | 2004-03-02 | 2007-09-13 | ニューロジェン・コーポレーション | アリール置換プリン類縁体 |
EP1598354A1 (fr) * | 2004-05-18 | 2005-11-23 | Vasopharm Biotech GmbH | Composes contenant un groupement n-heteroaryle lie a un cycle condense et leur utilisation comme inhibiteurs du nad(p)h oxidases et de l'activation plaquettaire |
EP1773826A4 (fr) | 2004-07-02 | 2009-06-03 | Exelixis Inc | Modulateurs de c-met et leur methode d'utilisation |
US7572805B2 (en) | 2004-07-14 | 2009-08-11 | Bristol-Myers Squibb Company | Pyrrolo(oxo)isoquinolines as 5HT ligands |
MX2007001216A (es) * | 2004-07-30 | 2007-03-23 | Methylgene Inc | Inhibidores de la senalizacion del receptor del factor de crecimiento endotelial vascular y del receptor del factor de crecimiento del hepatocito. |
EP1846410B1 (fr) * | 2005-02-10 | 2009-01-21 | Bristol-Myers Squibb Company | Dihydroquinazolinones utilisees comme modulateurs de la 5ht |
EP1703668A1 (fr) * | 2005-03-18 | 2006-09-20 | Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO | Système pour traiter des paramètres "qualité de service" (qos) dans un réseau de communications |
CA2611370C (fr) | 2005-05-20 | 2014-11-25 | Oscar Mario Saavedra | Inhibiteurs du recepteur de vegf et signalisation du recepteur de hgf |
CN101248080B (zh) * | 2005-05-20 | 2012-09-05 | 梅特希尔基因公司 | Vegf受体和hgf受体信号的抑制剂 |
EP2336117A1 (fr) | 2005-05-26 | 2011-06-22 | Neuron Systems, Inc | Composés hétérocycliques pour le traitement des maladies rétiniennes |
BRPI0614485A2 (pt) * | 2005-07-28 | 2011-03-29 | Bristol-Myers Squibb Company | tetrahidro-1h-pirido [4, 3, b] indóis substituìdos como agonistas e antagonistas receptores de serotonina |
US7795436B2 (en) * | 2005-08-24 | 2010-09-14 | Bristol-Myers Squibb Company | Substituted tricyclic heterocycles as serotonin receptor agonists and antagonists |
ATE553108T1 (de) * | 2005-11-08 | 2012-04-15 | Hoffmann La Roche | Thiazoloä4,5-cüpyridinderivative als antagonisten des mglu5-rezeptors |
PE20080145A1 (es) | 2006-03-21 | 2008-02-11 | Janssen Pharmaceutica Nv | Tetrahidro-pirimidoazepinas como moduladores de trpv1 |
WO2007107005A1 (fr) * | 2006-03-22 | 2007-09-27 | Methylgene, Inc. | Inhibiteurs de l'activité protéine tyrosine kinase |
US20080004253A1 (en) * | 2006-06-30 | 2008-01-03 | Bryan James Branstetter | Thiazolopyrimidine modulators of TRPV1 |
EP2081434A2 (fr) | 2006-10-31 | 2009-07-29 | Janssen Pharmaceutica N.V. | Dérivés de triazolopyrimidine convenant comme antagonistes du récepteur p2y12 de l'adp |
JP2010508350A (ja) * | 2006-10-31 | 2010-03-18 | ヤンセン ファーマシューティカ エヌ.ベー. | Adpp2y12レセプターアンタゴニストとしてのトリアゾロピリミジン誘導体 |
MX2009007337A (es) * | 2007-01-10 | 2009-07-15 | Albany Molecular Res Inc | Indazoles sustituidos con 5-piridinona. |
AU2008279321B2 (en) * | 2007-07-21 | 2013-08-01 | Albany Molecular Research, Inc. | 5-pyridinone substituted indazoles |
US8288397B2 (en) | 2007-12-17 | 2012-10-16 | Janssen Pharmaceutica Nv | Imidazolo-, oxazolo-, and thiazolopyrimidine modulators of TRPV1 |
EP2332536A1 (fr) * | 2008-03-05 | 2011-06-15 | MethylGene Inc. | Inhibiteurs d'activité de kinase de tyrosine de protéine |
US8273900B2 (en) | 2008-08-07 | 2012-09-25 | Novartis Ag | Organic compounds |
KR102187034B1 (ko) | 2009-01-16 | 2020-12-04 | 엑셀리시스, 인코포레이티드 | 암 치료용 n-(4-{〔6,7-비스(메틸옥시)퀴놀린-4-일〕옥시}페닐)-n'-(4-플루오로페닐)사이클로프로판-1,1-디카르복사미드의 말산염 및 그 결정형 |
UA108618C2 (uk) | 2009-08-07 | 2015-05-25 | Застосування c-met-модуляторів в комбінації з темозоломідом та/або променевою терапією для лікування раку | |
CA2782015C (fr) | 2009-12-11 | 2020-08-25 | Neuron Systems, Inc. | Compositions ophthalmiques topiques et methodes de traitement de la degenerescence maculaire |
US10154988B2 (en) | 2012-11-14 | 2018-12-18 | The Johns Hopkins University | Methods and compositions for treating schizophrenia |
EP3134405B1 (fr) | 2014-04-25 | 2019-08-28 | Pfizer Inc | Composes hetero-aromatiques et leur utilisation comme ligands d1 de la dopamine |
EP3259274B1 (fr) * | 2015-02-18 | 2023-06-28 | Buck Institute for Research on Aging | Triazolopyridines et triazolopyrimidines qui abaissent la p-tau provoquée par le stress |
WO2017035528A1 (fr) * | 2015-08-27 | 2017-03-02 | Nantneuro, Llc | Triazolopyridines et triazolopyrimidines qui abaissent la p-tau induite par le stress |
US11040039B2 (en) | 2017-10-10 | 2021-06-22 | Aldeyra Therapeutics, Inc. | Treatment of inflammatory disorders |
JP2021527687A (ja) * | 2018-06-21 | 2021-10-14 | ヤンセン ファーマシューティカ エヌ.ベー. | Oga阻害剤化合物 |
EP3833660A4 (fr) * | 2018-08-06 | 2022-05-11 | Aldeyra Therapeutics, Inc. | Composés polymorphes et leurs utilisations |
JP2022530967A (ja) | 2019-05-02 | 2022-07-05 | アルデイラ セラピューティクス, インコーポレイテッド | 多形化合物およびその使用 |
US12098132B2 (en) | 2019-05-02 | 2024-09-24 | Aldeyra Therapeutics, Inc. | Process for preparation of aldehyde scavenger and intermediates |
JP2023526016A (ja) | 2020-05-13 | 2023-06-20 | アルデイラ セラピューティクス, インコーポレイテッド | 医薬製剤およびその使用 |
Family Cites Families (21)
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---|---|---|---|---|
GB1544419A (en) * | 1975-11-19 | 1979-04-19 | Science Union & Cie | Purines and pyrazolo-pyrimidines a process for their preparation and pharmaceutical compositions containing them |
US4076711A (en) * | 1976-04-05 | 1978-02-28 | Schering Corporation | Triazolo [4,5-d]-pyrimidines |
JPS5962595A (ja) * | 1982-09-30 | 1984-04-10 | Ss Pharmaceut Co Ltd | 3,5,7―トリ置換―トリアゾロピリミジン誘導体 |
EP0155911A1 (fr) * | 1984-03-19 | 1985-09-25 | Ciba-Geigy Ag | Dérivés de la purine pour la régulation de croissance des plantes |
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CA2100863A1 (fr) * | 1991-01-23 | 1992-07-24 | David A. Bullough | Inhibiteurs de l'adenosine-kinase |
US5250679A (en) * | 1991-10-18 | 1993-10-05 | Genentech, Inc. | Nonpeptidyl platelet aggregation inhibitors having specificity for the GPIIb III.sub. receptor |
KR0184911B1 (ko) * | 1991-11-25 | 1999-05-01 | 알렌 제이. 스피겔 | 인돌유도체 |
DK0625158T3 (da) * | 1992-01-06 | 1999-10-11 | Wellcome Found | Terapeutiske nucleosider af 2',3'-dideoxy-3'-fluorpurinrækken |
US5424297A (en) * | 1992-04-27 | 1995-06-13 | University Of Virginia Alumni Patents Foundation | Adenosine dextran conjugates |
TW370529B (en) * | 1992-12-17 | 1999-09-21 | Pfizer | Pyrazolopyrimidines |
KR100263429B1 (ko) * | 1994-06-06 | 2000-08-01 | 디. 제이. 우드 | 코르티코트로핀-방출 인자(crf) 길항 활성을 갖는 치환된 피라졸 |
TW574214B (en) * | 1994-06-08 | 2004-02-01 | Pfizer | Corticotropin releasing factor antagonists |
CZ287613B6 (en) * | 1994-06-16 | 2001-01-17 | Pfizer | Pyrazolo- and pyrrolopyridines and pharmaceutical preparations based thereon |
JPH10506126A (ja) * | 1995-05-12 | 1998-06-16 | ニューロゲン コーポレイション | 新規なデアザプリン誘導体;crf1特異性リガンドの新規なクラス |
EP0778277B1 (fr) * | 1995-12-08 | 2003-06-25 | Pfizer Inc. | Derivés hétérocycliques substitués comme CRF antagonistes |
-
1997
- 1997-03-21 US US08/823,029 patent/US6107300A/en not_active Expired - Lifetime
- 1997-03-25 PL PL97335258A patent/PL335258A1/xx unknown
- 1997-03-25 SI SI9720026A patent/SI9720026A/sl not_active IP Right Cessation
- 1997-03-25 SK SK1317-98A patent/SK131798A3/sk unknown
- 1997-03-25 EP EP97916991A patent/EP0935601A4/fr not_active Withdrawn
- 1997-03-25 IL IL12631697A patent/IL126316A0/xx unknown
- 1997-03-25 EA EA199800868A patent/EA199800868A1/ru unknown
- 1997-03-25 EE EE9800329A patent/EE9800329A/xx unknown
- 1997-03-25 BR BR9708261-9A patent/BR9708261A/pt not_active IP Right Cessation
- 1997-03-25 CZ CZ983040A patent/CZ304098A3/cs unknown
- 1997-03-25 JP JP53457797A patent/JP2002515032A/ja active Pending
- 1997-03-25 CN CN97194897A patent/CN1230184A/zh active Pending
- 1997-03-25 CA CA002250241A patent/CA2250241A1/fr not_active Abandoned
- 1997-03-25 NZ NZ331874A patent/NZ331874A/xx unknown
- 1997-03-25 AU AU25458/97A patent/AU2545897A/en not_active Abandoned
- 1997-03-25 WO PCT/US1997/004852 patent/WO1997035539A2/fr not_active Application Discontinuation
- 1997-03-25 KR KR1019980707661A patent/KR20000005037A/ko not_active Application Discontinuation
- 1997-03-25 HU HU9902340A patent/HUP9902340A3/hu unknown
- 1997-03-26 HR HR60/039,124A patent/HRP970173A2/hr not_active Application Discontinuation
-
1998
- 1998-09-22 NO NO984418A patent/NO984418L/no unknown
- 1998-10-30 LV LVP-98-195A patent/LV12262B/en unknown
-
2000
- 2000-03-14 US US09/525,619 patent/US6448261B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP0935601A2 (fr) | 1999-08-18 |
HUP9902340A2 (hu) | 1999-11-29 |
BR9708261A (pt) | 2001-12-04 |
EA199800868A1 (ru) | 1999-04-29 |
SK131798A3 (en) | 2000-05-16 |
SI9720026A (sl) | 1999-04-30 |
US6448261B1 (en) | 2002-09-10 |
HRP970173A2 (en) | 1999-08-31 |
AU2545897A (en) | 1997-10-17 |
WO1997035539A3 (fr) | 1999-05-14 |
LV12262A (lv) | 1999-04-20 |
NZ331874A (en) | 2000-03-27 |
CA2250241A1 (fr) | 1997-10-02 |
PL335258A1 (en) | 2000-04-10 |
JP2002515032A (ja) | 2002-05-21 |
EP0935601A4 (fr) | 2002-08-07 |
US6107300A (en) | 2000-08-22 |
IL126316A0 (en) | 1999-05-09 |
HUP9902340A3 (en) | 2001-02-28 |
CN1230184A (zh) | 1999-09-29 |
WO1997035539A2 (fr) | 1997-10-02 |
EE9800329A (et) | 1999-06-15 |
CZ304098A3 (cs) | 1999-02-17 |
NO984418D0 (no) | 1998-09-22 |
LV12262B (en) | 1999-10-20 |
KR20000005037A (ko) | 2000-01-25 |
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