DE60019577D1 - 4, 5, 6, 7-tetrahydroindazolderivate als antitumormittel - Google Patents
4, 5, 6, 7-tetrahydroindazolderivate als antitumormittelInfo
- Publication number
- DE60019577D1 DE60019577D1 DE60019577T DE60019577T DE60019577D1 DE 60019577 D1 DE60019577 D1 DE 60019577D1 DE 60019577 T DE60019577 T DE 60019577T DE 60019577 T DE60019577 T DE 60019577T DE 60019577 D1 DE60019577 D1 DE 60019577D1
- Authority
- DE
- Germany
- Prior art keywords
- antitum
- agent
- tetrahydroindazole derivatives
- tetrahydroindazole
- derivatives
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- GDSQTWDUCDSZEY-UHFFFAOYSA-N 4,5,6,7-tetrahydro-1h-indazole Chemical class C1CCCC2=C1C=NN2 GDSQTWDUCDSZEY-UHFFFAOYSA-N 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
- A61P9/10—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
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Dermatology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9911053.8A GB9911053D0 (en) | 1999-05-12 | 1999-05-12 | 4,5,6,7-tetrahydroindazole derivatives process for their preparation and their use as antitumour agents |
| GB9911053 | 1999-05-12 | ||
| PCT/EP2000/004208 WO2000069846A1 (en) | 1999-05-12 | 2000-05-04 | 4,5,6,7-tetrahydroindazole derivatives as antitumor agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60019577D1 true DE60019577D1 (de) | 2005-05-25 |
| DE60019577T2 DE60019577T2 (de) | 2006-03-09 |
Family
ID=10853343
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60019577T Expired - Fee Related DE60019577T2 (de) | 1999-05-12 | 2000-05-04 | 4, 5, 6, 7-tetrahydroindazolderivate als antitumormittel |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US6716856B1 (de) |
| EP (1) | EP1177185B1 (de) |
| JP (1) | JP2002544271A (de) |
| KR (1) | KR20010113926A (de) |
| CN (1) | CN1350528A (de) |
| AR (1) | AR023971A1 (de) |
| AT (1) | ATE293618T1 (de) |
| AU (1) | AU4564500A (de) |
| BR (1) | BR0010476A (de) |
| CA (1) | CA2372429A1 (de) |
| CZ (1) | CZ20013970A3 (de) |
| DE (1) | DE60019577T2 (de) |
| EA (1) | EA200101194A1 (de) |
| ES (1) | ES2239595T3 (de) |
| GB (1) | GB9911053D0 (de) |
| HK (1) | HK1045687A1 (de) |
| HU (1) | HUP0201225A3 (de) |
| IL (1) | IL146100A0 (de) |
| MX (1) | MXPA01011441A (de) |
| NO (1) | NO20015477L (de) |
| NZ (1) | NZ514873A (de) |
| PL (1) | PL351611A1 (de) |
| PT (1) | PT1177185E (de) |
| SK (1) | SK15712001A3 (de) |
| WO (1) | WO2000069846A1 (de) |
| ZA (1) | ZA200108530B (de) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2236217T3 (es) | 2000-04-25 | 2005-07-16 | Bristol-Myers Squibb Company | Uso de 5.tio.,sulfinil- y sulfonilpirazolo 3,4-b)-piridinas como inhibidores de la quinasa dependiente de la ciclina. |
| JP2004517840A (ja) * | 2000-11-27 | 2004-06-17 | フアルマシア・イタリア・エツセ・ピー・アー | フェニルアセトアミド−ピラゾール誘導体およびそれの抗腫瘍薬としての使用 |
| DE10148617A1 (de) * | 2001-09-25 | 2003-04-24 | Schering Ag | Substituierte N-(1,4,5,6-Tetrahydro-cyclopentapyrazol-3-yl)-Derivate, deren Herstellung und Verwendung als Arzneimittel |
| DE10148618B4 (de) * | 2001-09-25 | 2007-05-03 | Schering Ag | Substituierte N-(1,4,5,6-Tetrahydro-cyclopentapyrazol-3-yl)-Derivate, deren Herstellung und Verwendung als Arzneimittel |
| UA81790C2 (uk) | 2002-12-19 | 2008-02-11 | Фармация Италия С.П.А. | Заміщені піролопіразольні похідні як інгібітори кінази |
| AU2004240772B2 (en) | 2003-05-22 | 2011-04-28 | Nerviano Medical Sciences S.R.L. | Pyrazolo-quinazoline derivatives,process for their preparation and their use as kinase inhibitors |
| US7141568B2 (en) | 2003-07-09 | 2006-11-28 | Pfizer Italia S.R.L. | Pyrrolo[3,4-c]pyrazole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them |
| TW200526204A (en) | 2004-02-03 | 2005-08-16 | Pharmacia Italia Spa | 1h-thieno[2,3-c]pyrazole derivatives useful as kinase inhibitors |
| CN101027301B (zh) * | 2004-03-09 | 2011-06-29 | 科塞普特治疗公司 | 稠环氮杂十氢化萘糖皮质激素受体调节剂 |
| ES2527770T3 (es) * | 2005-02-25 | 2015-01-29 | Serenex, Inc. | Derivados de tetrahidroindolona y tetrahidroindazolona |
| WO2006133634A1 (en) * | 2005-06-14 | 2006-12-21 | Beijing Gylongly Biodemtech Co., Ltd | Tetrahydroindole derivatives and tetrahydroindazole derivatives, and use thereof |
| WO2007009898A1 (en) | 2005-07-19 | 2007-01-25 | Nerviano Medical Sciences S.R.L. | 1h-thieno[2,3-c]pyrazole compounds useful as kinase inhibitors |
| AU2006292429A1 (en) * | 2005-09-16 | 2007-03-29 | Serenex, Inc. | Carbazole derivatives |
| US7618982B2 (en) | 2005-12-19 | 2009-11-17 | Nerviano Medical Sciences S.R.L. | Heteroarylpyrrolopyridinones active as kinase inhibitors |
| GB0602178D0 (en) * | 2006-02-03 | 2006-03-15 | Merck Sharp & Dohme | Therapeutic treatment |
| US20070207984A1 (en) * | 2006-02-27 | 2007-09-06 | Huang Kenneth H | Cyclohexylamino Benzene, Pyridine, and Pyridazine Derivatives |
| EP1999131B1 (de) | 2006-03-03 | 2013-10-23 | Nerviano Medical Sciences S.r.l. | Als kinaseinhibitoren wirksame bicyclopyrazole |
| US20080119457A1 (en) * | 2006-08-24 | 2008-05-22 | Serenex, Inc. | Benzene, Pyridine, and Pyridazine Derivatives |
| US20080070930A1 (en) * | 2006-08-24 | 2008-03-20 | Huang Kenneth H | Pyrimidine and Pyrazine Derivatives |
| US20080070933A1 (en) * | 2006-08-24 | 2008-03-20 | Huang Kenneth H | Purine, Pyrimidine, and Azaindole Derivatives |
| WO2008024970A2 (en) * | 2006-08-24 | 2008-02-28 | Serenex, Inc. | Tetrahydroindolone and tetrahydroindazolone derivatives |
| WO2008024980A2 (en) * | 2006-08-24 | 2008-02-28 | Serenex, Inc. | Pyrrole, thiophene, furan, imidazole, oxazole, and thiazole derivatives |
| DE102006060598A1 (de) * | 2006-12-21 | 2008-06-26 | Merck Patent Gmbh | Tetrahydrobenzoisoxazole |
| EP2120933B1 (de) | 2007-02-27 | 2015-07-08 | Nerviano Medical Sciences S.r.l. | Isochinolinopyrrolopyridinone als wirksame kinase-hemmer |
| EP2003129B1 (de) | 2007-06-11 | 2017-08-09 | Nerviano Medical Sciences S.r.l. | 1H-Pyrido[3,4-B]indol-1-on und 2,3,4,9-Tetrahydro-1H-Beta-Carbolin-1-on-Derivate |
| WO2010009985A2 (en) | 2008-07-24 | 2010-01-28 | Nerviano Medical Sciences S.R.L. | Therapeutic combination comprising an aurora kinase inhibitor and antiproliferative agents |
| US7741350B1 (en) | 2009-01-28 | 2010-06-22 | Cara Therapeutics, Inc. | Bicyclic pyrazolo-heterocycles |
| WO2010088050A2 (en) | 2009-01-28 | 2010-08-05 | Cara Therapeutics, Inc. | Bicyclic pyrazolo-heterocycles |
| CN102311389A (zh) * | 2010-06-29 | 2012-01-11 | 王小龙 | 一种氮芳香取代吡唑衍生物、及其合成和抗癌应用 |
| CN103298816A (zh) | 2010-12-17 | 2013-09-11 | 内尔维阿诺医学科学有限公司 | 作为激酶抑制剂的取代的吡唑并-喹唑啉衍生物 |
| WO2012094618A1 (en) | 2011-01-07 | 2012-07-12 | Corcept Therapeutics, Inc. | Combination steroid and glucocorticoid receptor antagonist therapy |
| JP2015520143A (ja) * | 2012-05-11 | 2015-07-16 | バイエル ファーマ アクチエンゲゼルシャフト | 癌を治療するためのbub1阻害薬としての置換されているシクロアルケノピラゾール類 |
| US12226412B2 (en) | 2012-05-25 | 2025-02-18 | Corcept Therapeutics, Inc. | Heteroaryl-ketone fused azadecalin glucocorticoid receptor modulators |
| US8859774B2 (en) | 2012-05-25 | 2014-10-14 | Corcept Therapeutics, Inc. | Heteroaryl-ketone fused azadecalin glucocorticoid receptor modulators |
| MY180141A (en) | 2013-11-25 | 2020-11-23 | Corcept Therapeutics Inc | Octahydro fused azadecalin glucocorticoid receptor modulators |
| CA3055076C (en) | 2017-03-31 | 2022-02-22 | Corcept Therapeutics, Inc. | Glucocorticoid receptor modulators to treat cervical cancer |
| US11234971B2 (en) | 2018-12-19 | 2022-02-01 | Corcept Therapeutics Incorporated | Methods of treating cancer comprising administration of a glucocorticoid receptor modulator and a cancer chemotherapy agent |
| WO2020132046A1 (en) | 2018-12-19 | 2020-06-25 | Corcept Therapeutics Incorporated | Methods of treating cancer comprising administration of a glucocorticoid receptor modulator and a cancer chemotherapy agent |
| PT3897589T (pt) | 2018-12-19 | 2026-01-21 | Corcept Therapeutics Incorporated | Formulações farmacêuticas contendo relacorilant, um composto de azadecalina fundido com heteroaril-cetona |
| CN113490496A (zh) | 2019-02-22 | 2021-10-08 | 科赛普特治疗学股份有限公司 | 一种杂芳基-酮稠合氮杂萘烷糖皮质激素受体调节剂瑞拉可兰的治疗用途 |
| KR20220113767A (ko) | 2019-12-11 | 2022-08-16 | 코어셉트 쎄라퓨틱스 인코포레이티드 | 미리코릴란트로 항정신병약-유도 체중 증가를 치료하는 방법 |
| JP2023507138A (ja) | 2019-12-20 | 2023-02-21 | ファイザー・インク | ベンゾイミダゾール誘導体 |
| WO2022134033A1 (en) | 2020-12-25 | 2022-06-30 | Corcept Therapeutics Incorporated | Methods of preparing heteroaryl-ketone fused azadecalin glucocorticoid receptor modulators |
| IL312348A (en) | 2021-10-29 | 2024-06-01 | Arcus Biosciences Inc | HIF-2ALPHA inhibitors and methods of using it |
| JP2025535043A (ja) | 2022-10-06 | 2025-10-22 | コーセプト セラピューティクス, インコーポレイテッド | グルココルチコイド受容体調節因子の製剤 |
| US12433882B2 (en) | 2022-10-28 | 2025-10-07 | Corcept Therapeutics Incorporated | Treatments for amyotrophic lateral sclerosis using dazucorilant |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3657438A (en) * | 1968-09-27 | 1972-04-18 | Ciba Geigy Corp | Compositions and methods for treating inflammation |
| US3657270A (en) * | 1970-01-16 | 1972-04-18 | Parke Davis & Co | 1-phenyl-1h-indazole-4-acetic acids |
| US3691180A (en) * | 1970-07-31 | 1972-09-12 | Ciba Geigy Corp | Cycloalkano (c)pyrazoles |
| JPS60130521A (ja) | 1983-12-19 | 1985-07-12 | Morishita Seiyaku Kk | 抗癌剤 |
| JPS6299361A (ja) | 1985-10-25 | 1987-05-08 | Morishita Seiyaku Kk | インデノ〔1,2−c〕ピラゾ−ル誘導体 |
| KR880009024A (ko) | 1987-01-27 | 1988-09-13 | 게리 디.스트리트 | 기관지 확장제용 디피라졸 |
| GB8828669D0 (en) | 1988-12-08 | 1989-01-11 | Lilly Industries Ltd | Organic compounds |
| GB9718913D0 (en) * | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
| EP1023063B1 (de) * | 1997-10-06 | 2003-09-10 | Abbott GmbH & Co. KG | INDENO[1,2-c]-,NAPHTHO[1,2-C]-UND BENZO[6,7]CYCLOHEPTA[1,2-c]PYRAZOLDERIVATE |
| US6335342B1 (en) | 2000-06-19 | 2002-01-01 | Pharmacia & Upjohn S.P.A. | Azaindole derivatives, process for their preparation, and their use as antitumor agents |
-
1999
- 1999-05-12 GB GBGB9911053.8A patent/GB9911053D0/en not_active Ceased
-
2000
- 2000-05-04 PL PL00351611A patent/PL351611A1/xx not_active Application Discontinuation
- 2000-05-04 WO PCT/EP2000/004208 patent/WO2000069846A1/en not_active Ceased
- 2000-05-04 JP JP2000618263A patent/JP2002544271A/ja not_active Withdrawn
- 2000-05-04 EP EP00927184A patent/EP1177185B1/de not_active Expired - Lifetime
- 2000-05-04 BR BR0010476-0A patent/BR0010476A/pt not_active Application Discontinuation
- 2000-05-04 CZ CZ20013970A patent/CZ20013970A3/cs unknown
- 2000-05-04 KR KR1020017014383A patent/KR20010113926A/ko not_active Withdrawn
- 2000-05-04 IL IL14610000A patent/IL146100A0/xx unknown
- 2000-05-04 HU HU0201225A patent/HUP0201225A3/hu unknown
- 2000-05-04 CN CN00807465A patent/CN1350528A/zh active Pending
- 2000-05-04 AT AT00927184T patent/ATE293618T1/de not_active IP Right Cessation
- 2000-05-04 SK SK1571-2001A patent/SK15712001A3/sk not_active Application Discontinuation
- 2000-05-04 AU AU45645/00A patent/AU4564500A/en not_active Abandoned
- 2000-05-04 DE DE60019577T patent/DE60019577T2/de not_active Expired - Fee Related
- 2000-05-04 PT PT00927184T patent/PT1177185E/pt unknown
- 2000-05-04 HK HK02107036.9A patent/HK1045687A1/zh unknown
- 2000-05-04 EA EA200101194A patent/EA200101194A1/ru unknown
- 2000-05-04 CA CA002372429A patent/CA2372429A1/en not_active Abandoned
- 2000-05-04 ES ES00927184T patent/ES2239595T3/es not_active Expired - Lifetime
- 2000-05-04 US US09/926,478 patent/US6716856B1/en not_active Expired - Fee Related
- 2000-05-04 MX MXPA01011441A patent/MXPA01011441A/es active IP Right Grant
- 2000-05-04 NZ NZ514873A patent/NZ514873A/xx unknown
- 2000-05-12 AR ARP000102286A patent/AR023971A1/es unknown
-
2001
- 2001-10-17 ZA ZA200108530A patent/ZA200108530B/xx unknown
- 2001-11-08 NO NO20015477A patent/NO20015477L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| CZ20013970A3 (cs) | 2002-04-17 |
| WO2000069846A1 (en) | 2000-11-23 |
| GB9911053D0 (en) | 1999-07-14 |
| ATE293618T1 (de) | 2005-05-15 |
| US6716856B1 (en) | 2004-04-06 |
| NZ514873A (en) | 2004-05-28 |
| AR023971A1 (es) | 2002-09-04 |
| PT1177185E (pt) | 2005-08-31 |
| HUP0201225A2 (en) | 2002-08-28 |
| ZA200108530B (en) | 2003-02-03 |
| KR20010113926A (ko) | 2001-12-28 |
| NO20015477L (no) | 2002-01-11 |
| JP2002544271A (ja) | 2002-12-24 |
| CA2372429A1 (en) | 2000-11-23 |
| HK1045687A1 (zh) | 2002-12-06 |
| PL351611A1 (en) | 2003-05-05 |
| ES2239595T3 (es) | 2005-10-01 |
| NO20015477D0 (no) | 2001-11-08 |
| SK15712001A3 (sk) | 2002-06-04 |
| IL146100A0 (en) | 2002-07-25 |
| MXPA01011441A (es) | 2002-10-21 |
| EP1177185A1 (de) | 2002-02-06 |
| EP1177185B1 (de) | 2005-04-20 |
| DE60019577T2 (de) | 2006-03-09 |
| BR0010476A (pt) | 2003-07-01 |
| HUP0201225A3 (en) | 2003-11-28 |
| CN1350528A (zh) | 2002-05-22 |
| AU4564500A (en) | 2000-12-05 |
| EA200101194A1 (ru) | 2002-06-27 |
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