ID28276A - Heterolingkar nitrogen bisiklik - Google Patents
Heterolingkar nitrogen bisiklikInfo
- Publication number
- ID28276A ID28276A IDW20010903A ID20010903A ID28276A ID 28276 A ID28276 A ID 28276A ID W20010903 A IDW20010903 A ID W20010903A ID 20010903 A ID20010903 A ID 20010903A ID 28276 A ID28276 A ID 28276A
- Authority
- ID
- Indonesia
- Prior art keywords
- lower alkyl
- heteroaryl
- aryl
- cycloalkyl
- alkyl
- Prior art date
Links
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title 2
- 229910052757 nitrogen Inorganic materials 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 12
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 238000011282 treatment Methods 0.000 abstract 2
- -1 Amino-substituted dihydropyrimido[4,5-d]pyrimidinones Chemical class 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 208000002249 Diabetes Complications Diseases 0.000 abstract 1
- 206010012655 Diabetic complications Diseases 0.000 abstract 1
- 206010052779 Transplant rejections Diseases 0.000 abstract 1
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 230000001900 immune effect Effects 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 230000000771 oncological effect Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 239000003909 protein kinase inhibitor Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000001356 surgical procedure Methods 0.000 abstract 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- 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
- 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
- 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
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Obesity (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Inorganic Insulating Materials (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9823277.0A GB9823277D0 (en) | 1998-10-23 | 1998-10-23 | Bicycle nitrogen heterocycles |
| GBGB9920044.6A GB9920044D0 (en) | 1998-10-23 | 1999-08-24 | Biciclic nitrogen heterocycles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ID28276A true ID28276A (id) | 2001-05-10 |
Family
ID=26314565
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IDW20010903A ID28276A (id) | 1998-10-23 | 1999-10-13 | Heterolingkar nitrogen bisiklik |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US6150373A (id) |
| EP (1) | EP1123295B1 (id) |
| JP (1) | JP3593035B2 (id) |
| CN (1) | CN1150195C (id) |
| AT (1) | ATE277931T1 (id) |
| AU (1) | AU769989B2 (id) |
| BR (1) | BR9914677A (id) |
| CA (1) | CA2347474C (id) |
| CZ (1) | CZ20011394A3 (id) |
| DE (1) | DE69920732T2 (id) |
| ES (1) | ES2228123T3 (id) |
| HK (1) | HK1041483B (id) |
| HR (1) | HRP20010274A2 (id) |
| HU (1) | HUP0104199A3 (id) |
| ID (1) | ID28276A (id) |
| MA (1) | MA27678A1 (id) |
| MY (1) | MY126478A (id) |
| NO (1) | NO318802B1 (id) |
| NZ (1) | NZ510760A (id) |
| PL (1) | PL347432A1 (id) |
| PT (1) | PT1123295E (id) |
| RU (1) | RU2256662C2 (id) |
| TR (1) | TR200101102T2 (id) |
| TW (1) | TWI227235B (id) |
| WO (1) | WO2000024744A1 (id) |
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW517055B (en) * | 1997-07-02 | 2003-01-11 | Smithkline Beecham Corp | Novel substituted imidazole compounds |
| AU1924699A (en) | 1997-12-19 | 1999-07-12 | Smithkline Beecham Corporation | Compounds of heteroaryl substituted imidazole, their pharmaceutical compositionsand uses |
| US6858617B2 (en) | 1998-05-26 | 2005-02-22 | Smithkline Beecham Corporation | Substituted imidazole compounds |
| US20040044012A1 (en) * | 1998-05-26 | 2004-03-04 | Dobrusin Ellen Myra | Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation |
| YU73300A (sh) | 1998-05-26 | 2003-08-29 | Warner-Lambert Company | Biciklični pirimidini i biciklični 3,4-dihidropirimidini kao inhibitori ćelijske proliferacije |
| WO2000010563A1 (en) | 1998-08-20 | 2000-03-02 | Smithkline Beecham Corporation | Novel substituted triazole compounds |
| AU1909200A (en) | 1998-11-04 | 2000-05-22 | Smithkline Beecham Corporation | Pyridin-4-yl or pyrimidin-4-yl substituted pyrazines |
| TR200201058T2 (tr) | 1999-10-21 | 2002-07-22 | F.Hoffmann-La Roche Ag | P38 protein kinaz inhibitörleri olarak, alkilaminoyla ornatılmış bisiklik, azotlu heterosikller |
| RU2265606C2 (ru) | 1999-10-21 | 2005-12-10 | Ф.Хоффманн-Ля Рош Аг | ГЕТЕРОАЛКИЛАМИНОЗАМЕЩЕННЫЕ БИЦИКЛИЧЕСКИЕ АЗОТСОДЕРЖАЩИЕ ГЕТЕРОЦИКЛЫ В КАЧЕСТВЕ ИНГИБИТОРОВ ПРОТЕИНКИНАЗЫ р38 |
| EP1233951B1 (en) | 1999-11-23 | 2005-06-01 | SmithKline Beecham Corporation | 3,4-dihydro-(1h)quinazolin-2-one compounds as csbp/p38 kinase inhibitors |
| EP1235814B1 (en) | 1999-11-23 | 2004-11-03 | Smithkline Beecham Corporation | 3,4-DIHYDRO-(1H)QUINAZOLIN-2-ONE COMPOUNDS AS CSBP/p38 KINASE INHIBITORS |
| DE60023025T2 (de) | 1999-11-23 | 2006-07-13 | Smithkline Beecham Corp. | 3,4-dihydro-(1h)chinazolin-2-on-verbindungen als csbp/p39-kinase-inhibitoren |
| US6759410B1 (en) | 1999-11-23 | 2004-07-06 | Smithline Beecham Corporation | 3,4-dihydro-(1H)-quinazolin-2-ones and their use as CSBP/p38 kinase inhibitors |
| US7101869B2 (en) | 1999-11-30 | 2006-09-05 | Pfizer Inc. | 2,4-diaminopyrimidine compounds useful as immunosuppressants |
| AR030053A1 (es) * | 2000-03-02 | 2003-08-13 | Smithkline Beecham Corp | 1h-pirimido [4,5-d] pirimidin-2-onas y sales, composiciones farmaceuticas, uso para la fabricacion de un medicamento y procedimiento para producirlas |
| US7235551B2 (en) * | 2000-03-02 | 2007-06-26 | Smithkline Beecham Corporation | 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases |
| CN100525768C (zh) | 2000-10-23 | 2009-08-12 | 史密丝克莱恩比彻姆公司 | 新化合物 |
| CA2441177A1 (en) | 2001-03-12 | 2002-09-19 | Avanir Pharmaceuticals | Benzimidazole compounds for modulating ige and inhibiting cellular proliferation |
| US7119111B2 (en) | 2002-05-29 | 2006-10-10 | Amgen, Inc. | 2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use |
| PA8577501A1 (es) * | 2002-07-25 | 2004-02-07 | Warner Lambert Co | Inhibidores de quinasas |
| DE10235312A1 (de) * | 2002-08-01 | 2004-02-12 | Basf Ag | Verfahren zur Herstellung von Aminoalkoxybenzylaminen und Aminoalkoxybenzonitrilen als Zwischenprodukte |
| US7084270B2 (en) * | 2002-08-14 | 2006-08-01 | Hoffman-La Roche Inc. | Pyrimido compounds having antiproliferative activity |
| AU2003270426A1 (en) | 2002-09-12 | 2004-04-30 | Avanir Pharmaceuticals | PHENYL-INDOLE COMPOUNDS FOR MODULATING IgE AND INHIBITING CELLULAR PROLIFERATION |
| TW200413381A (en) | 2002-11-04 | 2004-08-01 | Hoffmann La Roche | Novel amino-substituted dihydropyrimido [4,5-d]pyrimidinone derivatives, their manufacture and use as pharmaceutical agents |
| US7112676B2 (en) * | 2002-11-04 | 2006-09-26 | Hoffmann-La Roche Inc. | Pyrimido compounds having antiproliferative activity |
| US7098332B2 (en) | 2002-12-20 | 2006-08-29 | Hoffmann-La Roche Inc. | 5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones |
| WO2004089955A1 (en) * | 2003-04-10 | 2004-10-21 | F.Hoffmann-La Roche Ag | Pyrimido compounds |
| DK1619180T3 (da) * | 2003-04-23 | 2010-03-29 | Japan Tobacco Inc | CaSR-antagonist |
| CA2533774A1 (en) | 2003-07-29 | 2005-02-10 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
| EP1768662A2 (en) | 2004-06-24 | 2007-04-04 | Novartis Vaccines and Diagnostics, Inc. | Small molecule immunopotentiators and assays for their detection |
| CN1980933B (zh) * | 2004-08-31 | 2010-07-14 | 霍夫曼-拉罗奇有限公司 | 3-苯基-二氢嘧啶并[4,5-d]嘧啶酮的酰胺衍生物,它们的制备和用作药剂的用途 |
| RU2007111758A (ru) * | 2004-08-31 | 2008-10-10 | Ф.Хоффманн-Ля Рош Аг (Ch) | Аминопроизводные 7- амино-3-фенилдигидропиримидо [4,5-d] пиримидинонов, их получение и применение в качестве ингибиторов протеинкиназ |
| UY29440A1 (es) | 2005-03-25 | 2006-10-02 | Glaxo Group Ltd | Nuevos compuestos |
| CN101374840B (zh) | 2006-01-31 | 2011-09-28 | 霍夫曼-拉罗奇有限公司 | 7h-吡啶并[3,4-d]嘧啶-8-酮、它们的制备及作为蛋白激酶抑制剂的应用 |
| US7897762B2 (en) * | 2006-09-14 | 2011-03-01 | Deciphera Pharmaceuticals, Llc | Kinase inhibitors useful for the treatment of proliferative diseases |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| CN102816162B (zh) * | 2011-06-10 | 2016-04-27 | 中国科学院广州生物医药与健康研究院 | 嘧啶并嘧啶酮类化合物及其药用组合物和应用 |
| GB201204384D0 (en) | 2012-03-13 | 2012-04-25 | Univ Dundee | Anti-flammatory agents |
| HRP20170430T1 (hr) | 2012-06-13 | 2017-06-16 | Incyte Holdings Corporation | Supstituirani triciklični spojevi kao inhibitori fgfr |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| AR095464A1 (es) | 2013-03-15 | 2015-10-21 | Celgene Avilomics Res Inc | Compuestos de heteroarilo y usos de los mismos |
| CA2907243C (en) | 2013-03-15 | 2021-12-28 | Celgene Avilomics Research, Inc. | Substituted dihydropyrimidopyrimidinone compounds and pharmaceutical compositions thereof use fgfr4 inhibitor |
| WO2014144737A1 (en) | 2013-03-15 | 2014-09-18 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| PL2986610T4 (pl) | 2013-04-19 | 2019-06-28 | Incyte Holdings Corporation | Bicykliczne heterocykle jako inhibitory FGFR |
| DK3172213T3 (da) | 2014-07-21 | 2021-12-13 | Dana Farber Cancer Inst Inc | Makrocykliske kinasehæmmere og anvendelser deraf |
| AU2015292818B2 (en) | 2014-07-21 | 2020-01-16 | Dana-Farber Cancer Institute, Inc. | Imidazolyl kinase inhibitors and uses thereof |
| AU2015300782B2 (en) | 2014-08-08 | 2020-04-16 | Dana-Farber Cancer Institute, Inc. | Uses of salt-inducible kinase (SIK) inhibitors |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| MY197720A (en) | 2015-02-20 | 2023-07-10 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| WO2017031116A1 (en) * | 2015-08-18 | 2017-02-23 | The Arizona Board Of Regents On Behalf Of The University Of Arizona | Small molecule inhibitors of ku70/80 and uses thereof |
| WO2018009544A1 (en) * | 2016-07-05 | 2018-01-11 | The Broad Institute, Inc. | Bicyclic urea kinase inhibitors and uses thereof |
| US11241435B2 (en) | 2016-09-16 | 2022-02-08 | The General Hospital Corporation | Uses of salt-inducible kinase (SIK) inhibitors for treating osteoporosis |
| KR20190120331A (ko) | 2017-02-28 | 2019-10-23 | 더 제너럴 하스피탈 코포레이션 | Sik 억제제로서의 피리미도피리미디논의 용도 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| CA3087784A1 (en) | 2018-01-19 | 2019-07-25 | Idorsia Pharmaceuticals Ltd | C5a receptor modulators |
| US11739070B2 (en) | 2018-01-19 | 2023-08-29 | Idorsia Pharmaceuticals Ltd. | C5A receptor modulators |
| BR112020022392A2 (pt) | 2018-05-04 | 2021-02-02 | Incyte Corporation | formas sólidas de um inibidor de fgfr e processos para preparação das mesmas |
| JP7568512B2 (ja) | 2018-05-04 | 2024-10-16 | インサイト・コーポレイション | Fgfr阻害剤の塩 |
| EA202191800A1 (ru) * | 2018-12-27 | 2021-09-13 | Ле Лаборатуар Сервье Сас | Азагетеробициклические ингибиторы мат2а и способы их применения для нацеливания на рак |
| US20230065740A1 (en) | 2018-12-28 | 2023-03-02 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
| WO2020140055A1 (en) * | 2018-12-28 | 2020-07-02 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021011778A1 (en) * | 2019-07-16 | 2021-01-21 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Small molecule inhibitors of ku70/80 and uses thereof |
| US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| JP7675711B2 (ja) | 2019-10-14 | 2025-05-13 | インサイト・コーポレイション | Fgfr阻害剤としての二環式複素環 |
| WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| GB201915828D0 (en) * | 2019-10-31 | 2019-12-18 | Cancer Research Tech Ltd | Compounds, compositions and therapeutic uses thereof |
| CA3163875A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| PE20221504A1 (es) | 2019-12-04 | 2022-09-30 | Incyte Corp | Derivados de un inhibidor de fgfr |
| WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021219731A2 (en) * | 2020-04-28 | 2021-11-04 | Iomx Therapeutics Ag | Bicyclic kinase inhibitors and uses thereof |
| WO2022221170A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| AR126102A1 (es) | 2021-06-09 | 2023-09-13 | Incyte Corp | Heterociclos tricíclicos como inhibidores de fgfr |
| EP4352060A1 (en) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1990010631A1 (en) * | 1989-02-27 | 1990-09-20 | Biocryst | 9-substituted-8-unsubstituted-9-deazaguanines |
| US5654307A (en) * | 1994-01-25 | 1997-08-05 | Warner-Lambert Company | Bicyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family |
| IL117923A (en) * | 1995-05-03 | 2000-06-01 | Warner Lambert Co | Anti-cancer pharmaceutical compositions containing polysubstituted pyrido¬2,3-d¾pyrimidine derivatives and certain such novel compounds |
| GB9619284D0 (en) * | 1996-09-16 | 1996-10-30 | Celltech Therapeutics Ltd | Chemical compounds |
| US6057329A (en) * | 1996-12-23 | 2000-05-02 | Celltech Therapeutics Limited | Fused polycyclic 2-aminopyrimidine derivatives |
| YU73300A (sh) * | 1998-05-26 | 2003-08-29 | Warner-Lambert Company | Biciklični pirimidini i biciklični 3,4-dihidropirimidini kao inhibitori ćelijske proliferacije |
-
1999
- 1999-10-13 NZ NZ510760A patent/NZ510760A/en unknown
- 1999-10-13 TR TR2001/01102T patent/TR200101102T2/xx unknown
- 1999-10-13 HU HU0104199A patent/HUP0104199A3/hu unknown
- 1999-10-13 DE DE69920732T patent/DE69920732T2/de not_active Expired - Fee Related
- 1999-10-13 CZ CZ20011394A patent/CZ20011394A3/cs unknown
- 1999-10-13 AT AT99953796T patent/ATE277931T1/de not_active IP Right Cessation
- 1999-10-13 ES ES99953796T patent/ES2228123T3/es not_active Expired - Lifetime
- 1999-10-13 BR BR9914677-0A patent/BR9914677A/pt not_active IP Right Cessation
- 1999-10-13 PT PT99953796T patent/PT1123295E/pt unknown
- 1999-10-13 CN CNB998124702A patent/CN1150195C/zh not_active Expired - Fee Related
- 1999-10-13 CA CA002347474A patent/CA2347474C/en not_active Expired - Fee Related
- 1999-10-13 HK HK02103084.9A patent/HK1041483B/zh not_active IP Right Cessation
- 1999-10-13 PL PL99347432A patent/PL347432A1/xx not_active Application Discontinuation
- 1999-10-13 HR HR20010274A patent/HRP20010274A2/hr not_active Application Discontinuation
- 1999-10-13 WO PCT/EP1999/007675 patent/WO2000024744A1/en not_active Ceased
- 1999-10-13 EP EP99953796A patent/EP1123295B1/en not_active Expired - Lifetime
- 1999-10-13 JP JP2000578314A patent/JP3593035B2/ja not_active Expired - Fee Related
- 1999-10-13 RU RU2001113444/04A patent/RU2256662C2/ru not_active IP Right Cessation
- 1999-10-13 AU AU10363/00A patent/AU769989B2/en not_active Ceased
- 1999-10-13 ID IDW20010903A patent/ID28276A/id unknown
- 1999-10-21 US US09/422,451 patent/US6150373A/en not_active Expired - Fee Related
- 1999-10-21 MY MYPI99004545A patent/MY126478A/en unknown
- 1999-11-03 TW TW088119157A patent/TWI227235B/zh active
-
2001
- 2001-04-19 NO NO20011929A patent/NO318802B1/no unknown
- 2001-04-20 MA MA26172A patent/MA27678A1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TR200101102T2 (tr) | 2002-01-21 |
| BR9914677A (pt) | 2001-07-17 |
| EP1123295A1 (en) | 2001-08-16 |
| JP2002528455A (ja) | 2002-09-03 |
| NO20011929L (no) | 2001-04-19 |
| ATE277931T1 (de) | 2004-10-15 |
| TWI227235B (en) | 2005-02-01 |
| HUP0104199A2 (hu) | 2002-04-29 |
| EP1123295B1 (en) | 2004-09-29 |
| JP3593035B2 (ja) | 2004-11-24 |
| MY126478A (en) | 2006-10-31 |
| AU769989B2 (en) | 2004-02-12 |
| ES2228123T3 (es) | 2005-04-01 |
| PT1123295E (pt) | 2005-01-31 |
| DE69920732D1 (de) | 2004-11-04 |
| WO2000024744A1 (en) | 2000-05-04 |
| CN1324360A (zh) | 2001-11-28 |
| CZ20011394A3 (cs) | 2001-12-12 |
| NZ510760A (en) | 2003-08-29 |
| HUP0104199A3 (en) | 2002-12-28 |
| PL347432A1 (en) | 2002-04-08 |
| US6150373A (en) | 2000-11-21 |
| MA27678A1 (fr) | 2006-01-02 |
| NO318802B1 (no) | 2005-05-09 |
| RU2256662C2 (ru) | 2005-07-20 |
| NO20011929D0 (no) | 2001-04-19 |
| CA2347474A1 (en) | 2000-05-04 |
| DE69920732T2 (de) | 2006-02-23 |
| HK1041483A1 (en) | 2002-07-12 |
| CN1150195C (zh) | 2004-05-19 |
| HRP20010274A2 (en) | 2002-06-30 |
| CA2347474C (en) | 2008-08-26 |
| AU1036300A (en) | 2000-05-15 |
| HK1041483B (zh) | 2004-12-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ID28276A (id) | Heterolingkar nitrogen bisiklik | |
| EA200300248A1 (ru) | Бициклопиразолы, активные в качестве ингибиторов киназы, способ их получения и включающие их фармацевтические композиции | |
| NO20025601L (no) | Arylmetylaminderivater for anvendelse som tryptaseinhibitorer | |
| WO2001019829A3 (en) | Pyrazolopyrimidines as therapeutic agents | |
| BRPI0418112A (pt) | inibidores de p-38 quinase bicìclico heterocìclicos | |
| NO20014303L (no) | JAK-3-inhibitorer for behandling av allergiske lidelser | |
| NO944643L (no) | Protein-kinase-C-hemmere | |
| NO995006L (no) | Nye forbindelser | |
| NO20045677L (no) | Inhibitorer av JAK- og CDK2-proteinkinaser | |
| MY143466A (en) | Inhibitors of tyrosine kinases | |
| CA2309551A1 (en) | Aminothiazole inhibitors of cyclin dependent kinases | |
| WO2002090332A3 (en) | Novel aeylheteroalkylaminε derivatives | |
| SE9701304D0 (sv) | Compounds | |
| NO20005400L (no) | Kinoloner anvendt som MRS-inhibitorer og baktericider | |
| WO2000040583A3 (de) | Imidazo[4,5-c]-pyridin-4-on-derivate | |
| SE9803518D0 (sv) | Novel compounds | |
| NO20016201L (no) | Tienopyrimidiner som fosfodiesteraseinhibitorer | |
| ATE389655T1 (de) | Pyrimidinderivate | |
| WO1999012933A3 (en) | Pyrrolopyrrolone derivatives as inhibitors of neutrophil elastase | |
| WO2002083622A3 (en) | Novel aminophenyl ketone derivatives | |
| DE69619259D1 (de) | Amidin- und isothioharnstoffderivate als inhibitoren der stickstoffoxid-synthase | |
| YU29301A (sh) | Biciklična azotna heterociklična jedinjenja | |
| AU2001234314A1 (en) | Novel phenylheteroalkylamine derivatives | |
| ATE324368T1 (de) | Heteroarylheteroalkylamin derivate und deren verwendung als inhibitoren der stickoxidsynthase | |
| SE0102639D0 (sv) | Novel compounds |