EE9800329A - Arüülaminorühmaga liidetud püridiinid ja pürimidiinid - Google Patents
Arüülaminorühmaga liidetud püridiinid ja pürimidiinidInfo
- Publication number
- EE9800329A EE9800329A EE9800329A EE9800329A EE9800329A EE 9800329 A EE9800329 A EE 9800329A EE 9800329 A EE9800329 A EE 9800329A EE 9800329 A EE9800329 A EE 9800329A EE 9800329 A EE9800329 A EE 9800329A
- Authority
- EE
- Estonia
- Prior art keywords
- pyridines
- pyrimidines
- attached
- arylamino group
- arylamino
- Prior art date
Links
- 125000001769 aryl amino group Chemical group 0.000 title 1
- 150000003222 pyridines Chemical class 0.000 title 1
- 150000003230 pyrimidines Chemical class 0.000 title 1
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)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Reproductive Health (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Luminescent Compositions (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 (en) | 1996-03-27 | 1997-03-25 | Arylamino fused pyridines and pyrimidines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EE9800329A true EE9800329A (et) | 1999-06-15 |
Family
ID=27486365
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EE9800329A EE9800329A (et) | 1996-03-27 | 1997-03-25 | Arüülaminorühmaga liidetud püridiinid ja pürimidiinid |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US6107300A (cs) |
| EP (1) | EP0935601A4 (cs) |
| JP (1) | JP2002515032A (cs) |
| KR (1) | KR20000005037A (cs) |
| CN (1) | CN1230184A (cs) |
| AU (1) | AU2545897A (cs) |
| BR (1) | BR9708261A (cs) |
| CA (1) | CA2250241A1 (cs) |
| CZ (1) | CZ304098A3 (cs) |
| EA (1) | EA199800868A1 (cs) |
| EE (1) | EE9800329A (cs) |
| HR (1) | HRP970173A2 (cs) |
| HU (1) | HUP9902340A3 (cs) |
| IL (1) | IL126316A0 (cs) |
| LV (1) | LV12262B (cs) |
| NO (1) | NO984418L (cs) |
| NZ (1) | NZ331874A (cs) |
| PL (1) | PL335258A1 (cs) |
| SI (1) | SI9720026A (cs) |
| SK (1) | SK131798A3 (cs) |
| WO (1) | WO1997035539A2 (cs) |
Families Citing this family (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1066147C (zh) | 1995-11-01 | 2001-05-23 | 诺瓦提斯公司 | 嘌呤衍生物及其制备方法 |
| SK128799A3 (en) * | 1997-03-21 | 2000-05-16 | Du Pont Pharm Co | Method of making arylamino triazolopyridines |
| JP2002510322A (ja) * | 1997-07-03 | 2002-04-02 | デュポン ファーマシューティカルズ カンパニー | 副腎皮質刺激ホルモン放出ホルモン拮抗剤としてのアリールおよびアリールアミノ置換複素環 |
| US6156898A (en) * | 1998-02-26 | 2000-12-05 | 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 |
| NZ510955A (en) | 1998-11-12 | 2003-01-31 | Neurocrine Biosciences Inc | Tricyclic nitrogen containing ring system useful as CRF receptor antagonists |
| DE69908173T2 (de) | 1998-11-12 | 2004-08-19 | Neurocrine Biosciences, Inc., San Diego | Crf rezeptor-antagonisten und darauf bezogene methoden |
| GB9903762D0 (en) | 1999-02-18 | 1999-04-14 | Novartis Ag | Organic compounds |
| CN1377356A (zh) | 1999-09-30 | 2002-10-30 | 纽罗杰有限公司 | 亚烷基二胺取代的杂环 |
| US20020132819A1 (en) * | 1999-12-17 | 2002-09-19 | Metcalf Chester A. | Novel purinse |
| US7115589B2 (en) * | 1999-12-17 | 2006-10-03 | Ariad Pharmaceuticals, Inc. | Purine derivatives |
| KR20030016222A (ko) * | 2000-02-14 | 2003-02-26 | 니뽄 다바코 산교 가부시키가이샤 | 수술후 스트레스 예방ㆍ치료제 |
| US6589952B2 (en) | 2000-07-14 | 2003-07-08 | Bristol-Myers Squibb Pharma Company | Imidazo[1,2-a]pyrazines for the treatment of neurological disorders |
| EP1361880B1 (en) | 2001-02-12 | 2005-09-28 | F. Hoffmann-La Roche Ag | 6-substituted pyrido-pyrimidines |
| CZ20032481A3 (cs) | 2001-03-13 | 2007-12-27 | 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-triazin, jeho enantiomery a farmaceuticky prijatelné soli jakoligandy receptoru faktoru uvolnujícího kortikotropin |
| CN1527710A (zh) | 2001-05-14 | 2004-09-08 | ����˹�ж�-����˹˹����ҩƷ��˾ | 作为促肾上腺皮质激素释放因子配体的取代的吡嗪酮、吡啶和嘧啶 |
| 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 (en) | 2001-07-13 | 2003-01-23 | Bristol-Myers Squibb Pharma Company | Substituted thiazoles and oxazoles as corticotropin releasing hormone ligands |
| 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 |
| WO2003051881A1 (en) * | 2001-12-17 | 2003-06-26 | 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 |
| WO2005026126A1 (ja) * | 2003-09-09 | 2005-03-24 | Ono Pharmaceutical Co., Ltd. | Crf拮抗剤および二環式複素環化合物 |
| EP2210607B1 (en) | 2003-09-26 | 2011-08-17 | Exelixis Inc. | N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide for the treatment of cancer |
| US20070197559A1 (en) * | 2004-03-02 | 2007-08-23 | Rajagopal Bakthavatchalam | Aryl substituted purine analogues |
| EP1598354A1 (en) * | 2004-05-18 | 2005-11-23 | Vasopharm Biotech GmbH | Compounds containing a N-heteroaryl moiety linked to fused ring moieties for the inhibition of NAD(P)H oxidases and platelet activation |
| AU2005270068B2 (en) * | 2004-07-02 | 2012-04-19 | Exelixis, Inc. | C-Met modulators and method of use |
| US7572805B2 (en) | 2004-07-14 | 2009-08-11 | Bristol-Myers Squibb Company | Pyrrolo(oxo)isoquinolines as 5HT ligands |
| CA2573538C (en) * | 2004-07-30 | 2014-11-25 | Methylgene Inc. | Inhibitors of vegf receptor and hgf receptor signaling |
| US7238702B2 (en) * | 2005-02-10 | 2007-07-03 | Bristol-Myers Squibb Company | Dihydroquinazolinones as 5HT modulators |
| EP1703668A1 (en) * | 2005-03-18 | 2006-09-20 | Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO | System for processing quality-of-service parameters in a communication network |
| DK1904504T3 (da) * | 2005-05-20 | 2014-06-23 | Methylgene Inc | Inhibitorer af vegf-receptor- og hgf-receptorsignalering |
| AU2006343808B2 (en) * | 2005-05-20 | 2012-03-29 | Mirati Therapeutics, Inc. | Inhibitors of VEGF receptor and HGF receptor signaling |
| ES2441873T3 (es) | 2005-05-26 | 2014-02-06 | Aldexa Therapeutics, Inc. | Derivados de quinolina para el tratamiento de enfermedades retinianas |
| CA2617102A1 (en) * | 2005-07-28 | 2007-02-08 | Bristol-Myers Squibb Company | Substituted tetrahydro-1h-pyrido[4,3,b]indoles as serotonin receptor agonists and antagonists |
| US7795436B2 (en) * | 2005-08-24 | 2010-09-14 | Bristol-Myers Squibb Company | Substituted tricyclic heterocycles as serotonin receptor agonists and antagonists |
| CA2628936A1 (en) * | 2005-11-08 | 2007-05-18 | F. Hoffmann-La Roche Ag | Thiazolo [4 , 5-c] pyridine derivatives as mglu5 receptor antagonists |
| PE20080145A1 (es) * | 2006-03-21 | 2008-02-11 | Janssen Pharmaceutica Nv | Tetrahidro-pirimidoazepinas como moduladores de trpv1 |
| WO2007107005A1 (en) * | 2006-03-22 | 2007-09-27 | Methylgene, Inc. | Inhibitors of protein tyrosine kinase activity |
| EP2044086A2 (en) * | 2006-06-30 | 2009-04-08 | Janssen Pharmaceutica N.V. | Thiazolopyrimidine modulators of trpv1 |
| WO2008054796A2 (en) | 2006-10-31 | 2008-05-08 | Janssen Pharmaceutica, N.V. | Triazolopyrimidine derivatives as adp p2y12 receptor antagonists |
| WO2008054795A2 (en) * | 2006-10-31 | 2008-05-08 | Janssen Pharmaceutica, N.V. | Triazolopyrimidine derivatives as adp p2y12 receptor antagonists |
| KR20090101370A (ko) * | 2007-01-10 | 2009-09-25 | 알바니 몰레큘라 리써치, 인크. | 5-피리디논 치환된 인다졸 |
| EP2176251B1 (en) * | 2007-07-21 | 2012-02-08 | Albany Molecular Research, Inc. | 5-pyridinone substituted indazoles and pharmaceutical compositions thereof |
| WO2009078999A1 (en) | 2007-12-17 | 2009-06-25 | Janssen Pharmaceutica N.V. | Imidazolo-, oxazolo-, and thiazolopyrimidine modulators of trpv1 |
| AU2009221583B2 (en) * | 2008-03-05 | 2013-06-20 | Methylgene Inc. | Inhibitors of protein tyrosine kinase activity |
| US8273900B2 (en) | 2008-08-07 | 2012-09-25 | Novartis Ag | Organic compounds |
| AU2010204619B2 (en) | 2009-01-16 | 2016-08-11 | Exelixis, Inc. | Malate salt of N-(4-{ [ 6, 7-bis (methyloxy)-quinolin-4-yl] oxy}phenyl)-N'-(4-fluorophenyl) cyclopropane-1,1-dicarboxamide, and crystalline forms thereof for the treatment of cancer |
| UA108618C2 (uk) | 2009-08-07 | 2015-05-25 | Застосування c-met-модуляторів в комбінації з темозоломідом та/або променевою терапією для лікування раку | |
| WO2011072141A1 (en) | 2009-12-11 | 2011-06-16 | Neuron Systems, Inc. | Compositions and methods for the treatment of macular degeneration |
| JP6440625B2 (ja) | 2012-11-14 | 2018-12-19 | ザ・ジョンズ・ホプキンス・ユニバーシティー | 精神分裂病を処置するための方法および組成物 |
| HK1217439A1 (zh) | 2013-01-23 | 2017-01-13 | Aldeyra Therapeutics, Inc. | 与毒性醛相关的疾病和治疗 |
| EP3134405B1 (en) | 2014-04-25 | 2019-08-28 | Pfizer Inc | Heteroaromatic compounds and their use as dopamine d1 ligands |
| CN107709326B (zh) * | 2015-02-18 | 2021-12-17 | 巴克老龄问题研究所 | 降低应激诱导的p-tau的三唑并吡啶和三唑并嘧啶 |
| CA2996183A1 (en) | 2015-08-21 | 2017-03-02 | Aldeyra Therapeutics, Inc. | Deuterated compounds and uses thereof |
| US11370793B2 (en) | 2015-08-27 | 2022-06-28 | Nantneuro, Llc | Triazolopyridines and triazolopyrimidines that lower stress-induced p-tau |
| AU2018348174A1 (en) | 2017-10-10 | 2020-04-23 | Aldeyra Therapeutics, Inc. | Treatment of inflammatory disorders |
| US20210130352A1 (en) * | 2018-06-21 | 2021-05-06 | Janssen Pharmaceutica Nv | Oga inhibitor compounds |
| WO2020033344A1 (en) * | 2018-08-06 | 2020-02-13 | Aldeyra Therapeutics, Inc. | Polymorphic compounds and uses thereof |
| EP3962894A4 (en) | 2019-05-02 | 2023-01-11 | Aldeyra Therapeutics, Inc. | POLYMORPHIC COMPOUNDS AND USES THEREOF |
| WO2020223717A1 (en) | 2019-05-02 | 2020-11-05 | Aldeyra Therapeutics, Inc. | Process for preparation of aldehyde scavenger and intermediates |
| CN115697336A (zh) | 2020-05-13 | 2023-02-03 | 奥尔德拉医疗公司 | 药物制剂及其用途 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
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| US5424297A (en) * | 1992-04-27 | 1995-06-13 | University Of Virginia Alumni Patents Foundation | Adenosine dextran conjugates |
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| TW530047B (en) * | 1994-06-08 | 2003-05-01 | Pfizer | Corticotropin releasing factor antagonists |
| PL181895B1 (pl) * | 1994-06-16 | 2001-10-31 | Pfizer | Nowe pirazolo-i pirolopirydyny _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ PL PL PL PL |
| DE69603240T2 (de) * | 1995-05-12 | 2000-01-05 | Neurogen Corp., Branford | Neue deazapurinderivate; eine neue klasse von crf1-spezifischen liganden |
| DE69628804T2 (de) * | 1995-12-08 | 2003-12-18 | Pfizer Inc., New York | Substitutierte heterozyclische Derivate als CRF Antagonisten |
-
1997
- 1997-03-21 US US08/823,029 patent/US6107300A/en not_active Expired - Lifetime
- 1997-03-25 BR BR9708261-9A patent/BR9708261A/pt not_active IP Right Cessation
- 1997-03-25 EA EA199800868A patent/EA199800868A1/ru unknown
- 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 JP JP53457797A patent/JP2002515032A/ja active Pending
- 1997-03-25 IL IL12631697A patent/IL126316A0/xx unknown
- 1997-03-25 HU HU9902340A patent/HUP9902340A3/hu unknown
- 1997-03-25 EE EE9800329A patent/EE9800329A/xx unknown
- 1997-03-25 AU AU25458/97A patent/AU2545897A/en not_active Abandoned
- 1997-03-25 KR KR1019980707661A patent/KR20000005037A/ko not_active Withdrawn
- 1997-03-25 CA CA002250241A patent/CA2250241A1/en not_active Abandoned
- 1997-03-25 WO PCT/US1997/004852 patent/WO1997035539A2/en not_active Ceased
- 1997-03-25 SK SK1317-98A patent/SK131798A3/sk unknown
- 1997-03-25 EP EP97916991A patent/EP0935601A4/en not_active Withdrawn
- 1997-03-25 CN CN97194897A patent/CN1230184A/zh active Pending
- 1997-03-25 CZ CZ983040A patent/CZ304098A3/cs unknown
- 1997-03-25 NZ NZ331874A patent/NZ331874A/xx 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 |
|---|---|
| KR20000005037A (ko) | 2000-01-25 |
| CA2250241A1 (en) | 1997-10-02 |
| IL126316A0 (en) | 1999-05-09 |
| NO984418D0 (no) | 1998-09-22 |
| WO1997035539A2 (en) | 1997-10-02 |
| CZ304098A3 (cs) | 1999-02-17 |
| HUP9902340A3 (en) | 2001-02-28 |
| WO1997035539A3 (en) | 1999-05-14 |
| EP0935601A2 (en) | 1999-08-18 |
| LV12262A (lv) | 1999-04-20 |
| HRP970173A2 (en) | 1999-08-31 |
| EA199800868A1 (ru) | 1999-04-29 |
| EP0935601A4 (en) | 2002-08-07 |
| LV12262B (en) | 1999-10-20 |
| US6448261B1 (en) | 2002-09-10 |
| PL335258A1 (en) | 2000-04-10 |
| JP2002515032A (ja) | 2002-05-21 |
| BR9708261A (pt) | 2001-12-04 |
| SK131798A3 (en) | 2000-05-16 |
| NO984418L (no) | 1998-11-03 |
| US6107300A (en) | 2000-08-22 |
| SI9720026A (sl) | 1999-04-30 |
| AU2545897A (en) | 1997-10-17 |
| CN1230184A (zh) | 1999-09-29 |
| HUP9902340A2 (hu) | 1999-11-29 |
| NZ331874A (en) | 2000-03-27 |
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