MA27196A1 - Pyrimidines substituees par aryle et leur utilisation - Google Patents
Pyrimidines substituees par aryle et leur utilisationInfo
- Publication number
- MA27196A1 MA27196A1 MA27905A MA27905A MA27196A1 MA 27196 A1 MA27196 A1 MA 27196A1 MA 27905 A MA27905 A MA 27905A MA 27905 A MA27905 A MA 27905A MA 27196 A1 MA27196 A1 MA 27196A1
- Authority
- MA
- Morocco
- Prior art keywords
- treatment
- prevention
- formula
- aryl substituted
- substituted pyrimidines
- Prior art date
Links
- 150000003230 pyrimidines Chemical class 0.000 title abstract 2
- 230000002265 prevention Effects 0.000 abstract 3
- 208000002193 Pain Diseases 0.000 abstract 2
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 abstract 2
- 208000000094 Chronic Pain Diseases 0.000 abstract 1
- 208000032131 Diabetic Neuropathies Diseases 0.000 abstract 1
- 108010052164 Sodium Channels Proteins 0.000 abstract 1
- 102000018674 Sodium Channels Human genes 0.000 abstract 1
- 208000009205 Tinnitus Diseases 0.000 abstract 1
- 230000001154 acute effect Effects 0.000 abstract 1
- 208000005298 acute pain Diseases 0.000 abstract 1
- 230000003288 anthiarrhythmic effect Effects 0.000 abstract 1
- 230000001773 anti-convulsant effect Effects 0.000 abstract 1
- 230000003561 anti-manic effect Effects 0.000 abstract 1
- 239000003416 antiarrhythmic agent Substances 0.000 abstract 1
- 229940125681 anticonvulsant agent Drugs 0.000 abstract 1
- 239000001961 anticonvulsive agent Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 208000028867 ischemia Diseases 0.000 abstract 1
- 239000003589 local anesthetic agent Substances 0.000 abstract 1
- 229960005015 local anesthetics Drugs 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 230000000626 neurodegenerative effect Effects 0.000 abstract 1
- 230000003961 neuronal insult Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- -1 substituted aryl pyrimidine compounds Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
- A61P23/02—Local anaesthetics
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
-
- 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
- A61P9/06—Antiarrhythmics
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Anesthesiology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Pyrimidines Substituées par Aryle Et Leur Utilisation Cette invention a trait à une méthode pour traiter des désordres sensibles à l'obstruction des canaux d'ion sodium en utilisant les nouveaux composés aryles substitués de pyrimidine de la formule I: ou un sel pharmaceutiquement acceptable, ou son solvate, oé A, R1, R2, R3 et R4 sont définis dans la description. L'invention est également dirigée vers l'utilisation des composés de la formule I pour le traitement des dommages neuronaux à la suite d'une ischémie globale et focale, pour le traitement ou la prévention des conditions neurodégénératives telles que la sclérose latérale amyotrophique (SLA), et pour le traitement, l'empêchement ou l'amélioration de la douleur aigue ou chronique, comme agents anti-acouphène, comme anti-convulsivants, et comme dépresseurs antimaniques, comme anesthésiques locaux, comme antiarythmiques et pour le traitement ou la prévention de la neuropathie diabétique.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36354402P | 2002-03-13 | 2002-03-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA27196A1 true MA27196A1 (fr) | 2005-01-03 |
Family
ID=27805282
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA27905A MA27196A1 (fr) | 2002-03-13 | 2004-10-11 | Pyrimidines substituees par aryle et leur utilisation |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US7229993B2 (fr) |
| EP (1) | EP1483247B1 (fr) |
| JP (1) | JP4473583B2 (fr) |
| KR (1) | KR20040099324A (fr) |
| CN (1) | CN1646500A (fr) |
| AP (1) | AP2004003152A0 (fr) |
| AT (1) | ATE434610T1 (fr) |
| AU (1) | AU2003223049A1 (fr) |
| BR (1) | BR0308451A (fr) |
| CA (1) | CA2479036A1 (fr) |
| CO (1) | CO5611139A2 (fr) |
| CR (1) | CR7526A (fr) |
| CY (1) | CY1109355T1 (fr) |
| DE (1) | DE60328087D1 (fr) |
| DK (1) | DK1483247T3 (fr) |
| EA (1) | EA200401120A1 (fr) |
| EC (1) | ECSP045360A (fr) |
| ES (1) | ES2328471T3 (fr) |
| IL (1) | IL163940A0 (fr) |
| IS (1) | IS7468A (fr) |
| MA (1) | MA27196A1 (fr) |
| MX (1) | MXPA04008901A (fr) |
| NO (1) | NO20044311L (fr) |
| PT (1) | PT1483247E (fr) |
| SI (1) | SI1483247T1 (fr) |
| TN (1) | TNSN04174A1 (fr) |
| WO (1) | WO2003076414A2 (fr) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL159765A0 (en) * | 2001-07-16 | 2004-06-20 | Euro Celtique Sa | Aryl substituted thiazolidinone derivatives and pharmaceutical compositions containing the same |
| AR037233A1 (es) | 2001-09-07 | 2004-11-03 | Euro Celtique Sa | Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento |
| JP2006504660A (ja) * | 2002-07-31 | 2006-02-09 | ユーロ−セルティーク エス.エイ. | アリール置換ベンゾイミダゾール類およびナトリウムチャネルブロッカーとしてのそれらの使用 |
| US20050227974A9 (en) * | 2002-08-01 | 2005-10-13 | Euro-Celtique S.A. | Aminoalkyl-substituted aryl compounds and their use as sodium channel blockers |
| US20040152696A1 (en) * | 2002-08-01 | 2004-08-05 | Euro-Celtique S.A. | 2-substituted bicyclic benzoheterocyclic compounds and their use as sodium channel blockers |
| US20040242568A1 (en) | 2003-03-25 | 2004-12-02 | Syrrx, Inc. | Dipeptidyl peptidase inhibitors |
| MXPA06001601A (es) | 2003-08-13 | 2006-08-25 | Takeda Pharmaceutical | Derivados de 4-pirimidona y su uso como inhibidores de dipeptidilpeptidasa. |
| WO2005026148A1 (fr) * | 2003-09-08 | 2005-03-24 | Takeda San Diego, Inc. | Inhibiteurs de la dipeptidylpeptidase |
| JP4790703B2 (ja) * | 2004-04-07 | 2011-10-12 | 武田薬品工業株式会社 | 環式化合物 |
| CN101184493A (zh) * | 2005-03-04 | 2008-05-21 | 阿尔斯根公司 | 用乙胺嘧啶及类似物治疗肌萎缩性侧索硬化 |
| US20070135437A1 (en) * | 2005-03-04 | 2007-06-14 | Alsgen, Inc. | Modulation of neurodegenerative diseases |
| NZ566799A (en) | 2005-09-14 | 2011-04-29 | Takeda Pharmaceutical | Dipeptidyl peptidase inhibitors for treating diabetes |
| WO2007035629A2 (fr) | 2005-09-16 | 2007-03-29 | Takeda Pharmaceutical Company Limited | Inhibiteurs de dipeptidylpeptidase |
| TW200838536A (en) | 2006-11-29 | 2008-10-01 | Takeda Pharmaceutical | Polymorphs of succinate salt of 2-[6-(3-amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethy]-4-fluor-benzonitrile and methods of use therefor |
| JP2013531687A (ja) | 2010-07-16 | 2013-08-08 | パーデュー、ファーマ、リミテッド、パートナーシップ | ナトリウムチャネル遮断剤としてのピリジン化合物 |
| EP2616441B1 (fr) | 2010-09-17 | 2019-08-07 | Purdue Pharma L.P. | Composés de pyridine et ses utilisations |
| KR20130095772A (ko) | 2010-10-05 | 2013-08-28 | 퍼듀 퍼머 엘피 | 나트륨 채널 차단제로서 퀴나졸린 화합물 |
| US9656959B2 (en) | 2010-12-22 | 2017-05-23 | Purdue Pharma L.P. | Substituted pyridines as sodium channel blockers |
| US9163008B2 (en) | 2011-09-02 | 2015-10-20 | Purdue Pharma, L.P. | Pyrimidines as sodium channel blockers |
| AU2012321111A1 (en) | 2011-10-31 | 2013-05-16 | Purdue Pharma L.P. | Quaternized amines as sodium channel blockers |
| WO2013064883A1 (fr) | 2011-10-31 | 2013-05-10 | Purdue Pharma L.P. | Composés hétéroaryliques comme agents de blocage des canaux sodiques |
| WO2013072758A1 (fr) | 2011-11-15 | 2013-05-23 | Purdue Pharma L.P. | Pyrimidine diol amides comme bloqueurs des canaux sodiques |
| WO2013136170A1 (fr) | 2012-03-16 | 2013-09-19 | Purdue Pharma L.P. | Pyridines substituées en tant que bloqueurs des canaux sodiques |
| EP2935257B1 (fr) | 2012-12-20 | 2018-02-07 | Purdue Pharma LP | Sulfonamides cycliques en tant que bloquants des canaux sodiques |
| JP6110516B2 (ja) | 2013-03-04 | 2017-04-05 | パーデュー、ファーマ、リミテッド、パートナーシップ | ナトリウムチャネル遮断剤としてのピリミジンカルボキサミド |
| US9120786B2 (en) | 2013-03-04 | 2015-09-01 | Purdue Pharma, L.P. | Triazine carboxamides as sodium channel blockers |
| EP3666274A1 (fr) | 2013-03-15 | 2020-06-17 | Purdue Pharma LP | Dérivés de carboxamide et leur utilisation |
| WO2015031036A1 (fr) | 2013-08-26 | 2015-03-05 | Purdue Pharma L.P. | Dérivés d'azaspiro[4.5] décane et leur utilisation |
| US9359330B2 (en) | 2013-08-26 | 2016-06-07 | Purdue Pharma L.P. | Substituted piperidines as sodium channel blockers |
| US9828348B2 (en) | 2013-11-08 | 2017-11-28 | Purdue Pharma L.P. | Benzimidazole derivatives and use thereof |
| US9340504B2 (en) | 2013-11-21 | 2016-05-17 | Purdue Pharma L.P. | Pyridine and piperidine derivatives as novel sodium channel blockers |
| WO2015094443A1 (fr) * | 2013-12-20 | 2015-06-25 | Purdue Pharma L.P. | Pyrimidines et leur utilisation |
| CA2934473C (fr) | 2013-12-23 | 2019-08-20 | Purdue Pharma L.P. | Indazoles et leur utilisation |
| US9695144B2 (en) | 2013-12-23 | 2017-07-04 | Purdue Pharma L.P. | Dibenzazepine derivatives and use thereof |
| WO2015102682A1 (fr) | 2013-12-30 | 2015-07-09 | Purdue Pharma L.P. | Analogues de morphinane pyridone-sulfones utilisés comme ligands de récepteurs opioïdes |
| US10047075B2 (en) | 2014-01-24 | 2018-08-14 | Purdue Pharma L.P. | Pyridines and pyrimidines and use thereof |
| US10738026B2 (en) | 2014-02-12 | 2020-08-11 | Purdue Pharma L.P. | Isoquinoline derivatives and use thereof |
| US10730866B2 (en) | 2014-04-07 | 2020-08-04 | Purdue Pharma L.P. | Indole derivatives and use thereof |
| CA2948144A1 (fr) | 2014-05-06 | 2015-11-12 | Purdue Pharma L.P. | Analogues du benzomorphane et leur utilisation |
| CA2951697A1 (fr) | 2014-06-13 | 2015-12-17 | Purdue Pharma L.P. | Derives d'azamophinan et leur utilisation |
| EP3154971A4 (fr) | 2014-06-13 | 2017-11-01 | Purdue Pharma L.P. | Dérivés hétérocycliques de morphinan et leur utilisation |
| AU2016219879A1 (en) | 2015-02-19 | 2017-08-24 | Purdue Pharma L.P. | Methods and compositions for decreasing gastric emptying |
| US10745402B2 (en) | 2017-01-02 | 2020-08-18 | Purdue Pharma L.P. | Morphinan derivatives and use thereof |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1122533B (de) * | 1959-04-18 | 1962-01-25 | Knoll Ag Chemischer Fabriken | Verfahren zur Herstellung basisch substituierter 4-Amino-6-hydroxypyrimidine |
| MA18829A1 (fr) | 1979-05-18 | 1980-12-31 | Ciba Geigy Ag | Derives de la pyrimidine,procedes pour leur preparation,compositions pharmaceutiques contenant ces composes et leur utilisation therapeutique |
| US4492792A (en) * | 1982-02-04 | 1985-01-08 | Ube Industries, Ltd. | Process for preparing 4-amino-5-dialkoxy-methylpyrimidine derivatives |
| GB8909560D0 (en) | 1989-04-26 | 1989-06-14 | Smith Kline French Lab | Chemical compounds |
| AU8405991A (en) * | 1990-08-31 | 1992-03-30 | Nippon Shinyaku Co. Ltd. | Pyrimidine derivative and medicine |
| DE4124942A1 (de) * | 1991-07-27 | 1993-01-28 | Thomae Gmbh Dr K | 5-gliedrige heterocyclen, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
| JPH0558997A (ja) | 1991-09-04 | 1993-03-09 | Mitsubishi Kasei Corp | チオカルバモイルアセトニトリル誘導体 |
| US5232945A (en) * | 1992-07-20 | 1993-08-03 | Pfizer Inc. | 3-aryl-2-hydroxypropionic acid derivatives and analogs as antihypertensives |
| WO1994007867A1 (fr) * | 1992-09-28 | 1994-04-14 | Pfizer Inc. | Pyrimidines substituees pour le controle des complications diabetiques |
| EP0665224A1 (fr) | 1992-10-16 | 1995-08-02 | Nippon Soda Co., Ltd. | Derive de pyrimidine |
| WO1994026721A1 (fr) | 1993-05-13 | 1994-11-24 | Nkk Corporation | Derive de pyrimidine et composition pharmaceutique |
| GB2281295A (en) * | 1993-08-26 | 1995-03-01 | Zeneca Ltd | (2-Fluoroethyl) thio-substituted pyrimidines as nematicides |
| US5569655A (en) * | 1993-09-14 | 1996-10-29 | Sterling Winthrop Inc. | Substituted heterocyclylisoquinolinium salts and compositions and method of use thereof |
| US5602156A (en) * | 1993-09-17 | 1997-02-11 | The United States Of America As Represented By The Department Of Health And Human Services | Method for inhibiting metalloproteinase expression |
| US5744492A (en) * | 1993-09-17 | 1998-04-28 | United States Of America | Method for inhibiting angiogenesis |
| EP0724573A1 (fr) | 1993-10-20 | 1996-08-07 | PHARMACIA & UPJOHN COMPANY | Pyrimidinones utilisees comme antiarthritiques et anti-inflammatoires |
| US5795905A (en) * | 1995-06-06 | 1998-08-18 | Neurocrine Biosciences, Inc. | CRF receptor antagonists and methods relating thereto |
| US5874440A (en) * | 1995-06-07 | 1999-02-23 | Cell Pathways, Inc. | Method of treating a patient having precancerous lesions with phenyl pyrimidinone derivatives |
| GB9525296D0 (en) * | 1995-12-11 | 1996-02-07 | Merck Sharp & Dohme | Therapeutic agents |
| HUP0103836A3 (en) | 1998-06-02 | 2003-05-28 | Osi Pharmaceuticals Inc Uniond | Pyrrolo[2,3d]pyrimidine compositions and their use |
| IL145508A0 (en) * | 1999-03-26 | 2002-06-30 | Euro Celtique Sa | Aryl substituted pyrazole, imidazole, oxazole, thiazole and pyrrole derivatives and pharmaceutical compositions containing the same |
| CO5210940A1 (es) | 1999-05-04 | 2002-10-30 | Novartis Ag | Compuestos plaguicidas derivados de pirimidina y composiciones que los contienen |
| WO2001010842A2 (fr) | 1999-08-04 | 2001-02-15 | Millennium Pharmaceuticals, Inc. | Composes fixant les recepteurs de melanocortine-4 et procedes d'utilisation de ces composes |
| DE19948434A1 (de) | 1999-10-08 | 2001-06-07 | Gruenenthal Gmbh | Substanzbibliothek enthaltend bicyclische Imidazo-5-amine und/oder bicyclische Imidazo-3-amine |
| ES2269217T3 (es) | 1999-12-02 | 2007-04-01 | Osi Pharmaceuticals, Inc. | Compuestos especificos para los receptores a1, a2a y a3 de adenosina y sus usos. |
| AR029489A1 (es) * | 2000-03-10 | 2003-07-02 | Euro Celtique Sa | Piridinas, pirimidinas, pirazinas, triazinas sustituidas por arilo, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento |
| EP1292577B1 (fr) * | 2000-03-24 | 2012-10-24 | Euro-Celtique S.A. | Pyrazoles, triazoles et tetrazoles a substitution aryle et leur utilisation |
| JP2003529589A (ja) * | 2000-03-31 | 2003-10-07 | ユーロ−セルティック エス. ア. | アミノピリジンならびにこれらの鎮痙薬およびナトリウムチャンネル遮断薬としての使用 |
| IL159765A0 (en) * | 2001-07-16 | 2004-06-20 | Euro Celtique Sa | Aryl substituted thiazolidinone derivatives and pharmaceutical compositions containing the same |
| AR037233A1 (es) * | 2001-09-07 | 2004-11-03 | Euro Celtique Sa | Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento |
| AR036873A1 (es) * | 2001-09-07 | 2004-10-13 | Euro Celtique Sa | Piridinas aril sustituidas a, composiciones farmaceuticas y el uso de las mismas para la preparacion de un medicamento |
-
2003
- 2003-03-13 CA CA002479036A patent/CA2479036A1/fr not_active Abandoned
- 2003-03-13 PT PT03719019T patent/PT1483247E/pt unknown
- 2003-03-13 SI SI200331664T patent/SI1483247T1/sl unknown
- 2003-03-13 MX MXPA04008901A patent/MXPA04008901A/es unknown
- 2003-03-13 US US10/386,483 patent/US7229993B2/en not_active Expired - Lifetime
- 2003-03-13 IL IL16394003A patent/IL163940A0/xx unknown
- 2003-03-13 KR KR10-2004-7014305A patent/KR20040099324A/ko not_active Withdrawn
- 2003-03-13 AP APAP/P/2004/003152A patent/AP2004003152A0/en unknown
- 2003-03-13 CN CNA038083833A patent/CN1646500A/zh active Pending
- 2003-03-13 DK DK03719019T patent/DK1483247T3/da active
- 2003-03-13 WO PCT/IB2003/001837 patent/WO2003076414A2/fr not_active Ceased
- 2003-03-13 ES ES03719019T patent/ES2328471T3/es not_active Expired - Lifetime
- 2003-03-13 BR BR0308451-5A patent/BR0308451A/pt not_active Application Discontinuation
- 2003-03-13 EA EA200401120A patent/EA200401120A1/ru unknown
- 2003-03-13 DE DE60328087T patent/DE60328087D1/de not_active Expired - Lifetime
- 2003-03-13 AT AT03719019T patent/ATE434610T1/de active
- 2003-03-13 EP EP03719019A patent/EP1483247B1/fr not_active Expired - Lifetime
- 2003-03-13 AU AU2003223049A patent/AU2003223049A1/en not_active Abandoned
- 2003-03-13 JP JP2003574634A patent/JP4473583B2/ja not_active Expired - Fee Related
-
2004
- 2004-09-10 TN TNP2004000174A patent/TNSN04174A1/en unknown
- 2004-09-24 IS IS7468A patent/IS7468A/is unknown
- 2004-10-11 MA MA27905A patent/MA27196A1/fr unknown
- 2004-10-12 NO NO20044311A patent/NO20044311L/no unknown
- 2004-10-12 EC EC2004005360A patent/ECSP045360A/es unknown
- 2004-10-12 CO CO04101907A patent/CO5611139A2/es not_active Application Discontinuation
- 2004-10-13 CR CR7526A patent/CR7526A/es not_active Application Discontinuation
-
2009
- 2009-09-10 CY CY20091100941T patent/CY1109355T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AP2004003152A0 (en) | 2004-12-31 |
| EA200401120A1 (ru) | 2005-02-24 |
| CY1109355T1 (el) | 2014-07-02 |
| US7229993B2 (en) | 2007-06-12 |
| IS7468A (is) | 2004-09-24 |
| PT1483247E (pt) | 2009-08-18 |
| CO5611139A2 (es) | 2006-02-28 |
| CR7526A (es) | 2008-08-12 |
| JP4473583B2 (ja) | 2010-06-02 |
| DE60328087D1 (de) | 2009-08-06 |
| BR0308451A (pt) | 2005-01-11 |
| ECSP045360A (es) | 2005-01-03 |
| EP1483247A2 (fr) | 2004-12-08 |
| KR20040099324A (ko) | 2004-11-26 |
| AU2003223049A1 (en) | 2003-09-22 |
| IL163940A0 (en) | 2005-12-18 |
| US20030236273A1 (en) | 2003-12-25 |
| EP1483247B1 (fr) | 2009-06-24 |
| JP2005526069A (ja) | 2005-09-02 |
| ES2328471T3 (es) | 2009-11-13 |
| CA2479036A1 (fr) | 2003-09-18 |
| WO2003076414A3 (fr) | 2003-12-24 |
| CN1646500A (zh) | 2005-07-27 |
| TNSN04174A1 (en) | 2007-03-12 |
| NO20044311L (no) | 2004-12-10 |
| ATE434610T1 (de) | 2009-07-15 |
| SI1483247T1 (sl) | 2009-12-31 |
| DK1483247T3 (da) | 2009-08-17 |
| WO2003076414A2 (fr) | 2003-09-18 |
| MXPA04008901A (es) | 2004-11-26 |
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