ATE387199T1 - Neue substanzen und verbindungen als protease- inhibitoren - Google Patents
Neue substanzen und verbindungen als protease- inhibitorenInfo
- Publication number
- ATE387199T1 ATE387199T1 AT01900903T AT01900903T ATE387199T1 AT E387199 T1 ATE387199 T1 AT E387199T1 AT 01900903 T AT01900903 T AT 01900903T AT 01900903 T AT01900903 T AT 01900903T AT E387199 T1 ATE387199 T1 AT E387199T1
- Authority
- AT
- Austria
- Prior art keywords
- protease inhibitors
- compounds
- new substances
- formula
- pharmaceutically acceptable
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 1
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 title 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 title 1
- 239000000126 substance Substances 0.000 title 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 239000002852 cysteine proteinase inhibitor Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
Classifications
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- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Neurology (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Indole Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17497800P | 2000-01-06 | 2000-01-06 | |
| US25679300P | 2000-12-19 | 2000-12-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE387199T1 true ATE387199T1 (de) | 2008-03-15 |
Family
ID=26870749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT01900903T ATE387199T1 (de) | 2000-01-06 | 2001-01-05 | Neue substanzen und verbindungen als protease- inhibitoren |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6525036B2 (de) |
| EP (1) | EP1248612B1 (de) |
| JP (1) | JP2003525874A (de) |
| AT (1) | ATE387199T1 (de) |
| AU (1) | AU779855B2 (de) |
| CA (1) | CA2396257A1 (de) |
| DE (1) | DE60132975T2 (de) |
| WO (1) | WO2001049288A1 (de) |
Families Citing this family (69)
| Publication number | Priority date | Publication date | Assignee | Title |
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| GB9723407D0 (en) * | 1997-11-05 | 1998-01-07 | Ciba Geigy Ag | Organic compounds |
| US20030203900A1 (en) * | 1999-05-18 | 2003-10-30 | Martin Quibell | Cysteine protease inhibitors |
| GB0003111D0 (en) * | 2000-02-10 | 2000-03-29 | Novartis Ag | Organic compounds |
| CA2402516A1 (en) * | 2000-03-20 | 2001-09-27 | Roopa Rai | Non-amidine containing protease inhibitors |
| ATE304526T1 (de) * | 2000-05-15 | 2005-09-15 | Novartis Pharma Gmbh | N-substituierte peptidylnitrile als cystein- cathepsin-inhibitoren |
| GB0108770D0 (en) | 2001-04-06 | 2001-05-30 | Eisai London Res Lab Ltd | Inhibitors |
| US20040235728A1 (en) * | 2001-11-08 | 2004-11-25 | Stoch Selwyn Aubrey | Compositions and methods for treating osteoporosis |
| EP1457205A4 (de) * | 2001-11-30 | 2006-07-05 | Santen Pharmaceutical Co Ltd | Angiogenesehemmer |
| HUP0402344A2 (hu) | 2001-12-04 | 2005-02-28 | F. Hoffmann-La Roche Ag | Helyettesített 2-amino-cikloalkán-karboxamidok, felhasználásuk cisztein-proteáz-inhibitorként, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények |
| US6759428B2 (en) | 2001-12-04 | 2004-07-06 | Roche Palo Alto Llc | Indole nitriles |
| DE60316542T2 (de) | 2002-03-28 | 2008-07-03 | Eisai R&D Management Co., Ltd. | 7-azaindole als inhibitoren c-jun n-terminaler kinasen zur behandlung neurodegenerativer störungen |
| WO2003082869A1 (en) * | 2002-03-28 | 2003-10-09 | Eisai Co., Ltd. | Azaindoles as inhibitors of c-jun n-terminal kinases |
| AU2003216585A1 (en) * | 2002-04-10 | 2003-10-20 | Orchid Chemicals And Pharmaceuticals Limited | Pyrimidinedione derivatives useful for the treatment of inflammation and immunological diseases |
| GB0220187D0 (en) * | 2002-08-30 | 2002-10-09 | Novartis Ag | Organic compounds |
| EP1537074B1 (de) | 2002-09-04 | 2019-02-27 | Merck Canada Inc. | Cathepsin-cystein-protease-inhibitoren |
| SE0203712D0 (sv) | 2002-12-13 | 2002-12-13 | Astrazeneca Ab | Novel compounds |
| EP2295433A3 (de) * | 2003-03-06 | 2011-07-06 | Eisai R&D Management Co., Ltd. | JNK Inhibitoren |
| GB0305142D0 (en) | 2003-03-06 | 2003-04-09 | Eisai London Res Lab Ltd | Synthesis |
| US7612086B2 (en) | 2003-05-16 | 2009-11-03 | Eisai R & D Management Co. Ltd. | JNK inhibitors |
| PT1663958E (pt) | 2003-09-18 | 2015-06-01 | Virobay Inc | Compostos contendo haloalquilo como inibidores de protease de cisteína |
| JP4906715B2 (ja) | 2004-05-08 | 2012-03-28 | ニューロジェン・コーポレーション | 4,5−ジ置換−2−アリールピリミジン類 |
| UA87854C2 (en) | 2004-06-07 | 2009-08-25 | Мерк Энд Ко., Инк. | N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators |
| JP4953457B2 (ja) * | 2004-10-27 | 2012-06-13 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | プロゲステロン受容体モジュレーターとしてのピリジンイミダゾール及びアザ−インドール |
| EP1819667B1 (de) | 2004-12-02 | 2012-10-17 | ViroBay, Inc. | Sulfonamidverbindungen als cysteinprotease-inhibitoren |
| US7709508B2 (en) | 2004-12-09 | 2010-05-04 | Merck Sharp & Dohme | Estrogen receptor modulators |
| WO2006062876A2 (en) * | 2004-12-09 | 2006-06-15 | Merck & Co., Inc. | Estrogen receptor modulators |
| EP1841504B1 (de) | 2005-01-13 | 2014-11-19 | Bristol-Myers Squibb Company | Substituierte biaryl-verbindungen als faktor-xia-hemmer |
| EP1841419A4 (de) * | 2005-01-19 | 2009-02-25 | Merck Frosst Canada Ltd | Cathepsin-k- und adipositas-inhibitoren |
| DE102005007694A1 (de) * | 2005-02-18 | 2006-09-21 | Henkel Kgaa | Mittel zum Färben von keratinhaltigen Fasern |
| US7488848B2 (en) | 2005-03-21 | 2009-02-10 | Virobay, Inc. | Alpha ketoamide compounds as cysteine protease inhibitors |
| US7893093B2 (en) | 2005-03-22 | 2011-02-22 | Virobay, Inc. | Sulfonyl containing compounds as cysteine protease inhibitors |
| CN103172568A (zh) * | 2005-07-06 | 2013-06-26 | 默克弗罗斯特加拿大有限公司 | 组织蛋白酶半胱氨酸蛋白酶抑制剂 |
| GB0516156D0 (en) | 2005-08-05 | 2005-09-14 | Eisai London Res Lab Ltd | JNK inhibitors |
| US7893112B2 (en) | 2006-10-04 | 2011-02-22 | Virobay, Inc. | Di-fluoro containing compounds as cysteine protease inhibitors |
| EP2079683B1 (de) | 2006-10-04 | 2015-01-21 | Virobay, Inc. | Difluorhaltige verbindungen als cysteinproteasehemmer |
| WO2008149971A1 (ja) | 2007-06-08 | 2008-12-11 | Kyoto University | 脳動脈瘤の治療または予防薬 |
| WO2009001127A1 (en) * | 2007-06-26 | 2008-12-31 | Astrazeneca Ab | Cyanocyclopropylcarboxamides as cathepsin inhibitors |
| WO2009001129A1 (en) | 2007-06-26 | 2008-12-31 | Astrazeneca Ab | 1-cyanocyclopropyl-derivatives as cathepsin k inhibitors |
| US20100331545A1 (en) | 2007-10-24 | 2010-12-30 | Nippon Chemiphar Co., Ltd. | Regulator for signaling toll-like receptor, which comprises cathepsin inhibitor as active ingredient |
| EP2222636B1 (de) | 2007-12-21 | 2013-04-10 | Ligand Pharmaceuticals Inc. | Selektive androgenrezeptormodulatoren (sarms) und ihre verwendung |
| EP2240491B1 (de) | 2008-01-09 | 2015-07-15 | Amura Therapeutics Limited | TETRAHYDROFURO(2,3-b)PYRROL-3-ON DERIVATE ALS INHIBITOREN VON CYSTEIN PROTEINASEN |
| JP2011513242A (ja) * | 2008-02-25 | 2011-04-28 | アミラ ファーマシューティカルズ,インク. | プロスタグランジンd2受容体アンタゴニスト |
| WO2009129365A1 (en) * | 2008-04-18 | 2009-10-22 | Glaxo Group Limited | Cathepsin c inhibitors |
| US8324417B2 (en) | 2009-08-19 | 2012-12-04 | Virobay, Inc. | Process for the preparation of (S)-2-amino-5-cyclopropyl-4,4-difluoropentanoic acid and alkyl esters and acid salts thereof |
| WO2011056985A2 (en) * | 2009-11-04 | 2011-05-12 | Gilead Sciences, Inc. | Substituted heterocyclic compounds |
| EP3517630B1 (de) | 2010-10-06 | 2022-01-19 | Institució Catalana de Recerca i Estudis Avançats | Verfahren zur diagnose, prognose und behandlung von brustkrebsmetastasen |
| US8680152B2 (en) | 2011-05-02 | 2014-03-25 | Virobay, Inc. | Cathepsin inhibitors for the treatment of bone cancer and bone cancer pain |
| WO2013138568A1 (en) | 2012-03-16 | 2013-09-19 | Vitae Pharmaceuticals, Inc. | Liver x reception modulators |
| CN104203951B (zh) | 2012-03-16 | 2016-11-02 | 生命医药公司 | 肝x受体调节剂 |
| EP2650682A1 (de) | 2012-04-09 | 2013-10-16 | Fundació Privada Institut de Recerca Biomèdica | Asymmetrische Ester von als Schmiermittel geeigneten Fettsäuren |
| EP3467124A1 (de) | 2012-06-06 | 2019-04-10 | Fundació Institut de Recerca Biomèdica IRB (Barcelona) | Verfahren zur diagnose, prognose und behandlung von lungenkrebsmetastasen |
| KR101872965B1 (ko) | 2012-10-12 | 2018-06-29 | 인바이오모션 에스.엘. | C―maf를 이용하는 전립선암 전이의 진단, 예후 및 치료 방법 |
| US10119171B2 (en) | 2012-10-12 | 2018-11-06 | Inbiomotion S.L. | Method for the diagnosis, prognosis and treatment of prostate cancer metastasis |
| WO2014184679A2 (en) | 2013-03-15 | 2014-11-20 | Inbiomotion S.L. | Method for the prognosis and treatment of renal cell carcinoma metastasis |
| JP6577873B2 (ja) | 2013-03-15 | 2019-09-18 | フンダシオ、インスティトゥト、デ、レセルカ、ビオメディカ(イエレベ、バルセロナ)Fundacio Institut De Recerca Biomedica (Irb Barcelona) | がんの転移の予後診断および処置のための方法 |
| TR201907389T4 (tr) | 2013-10-09 | 2019-06-21 | Fundacio Inst De Recerca Biomedica Irb Barcelona | Meme kanserinden kaynaklanan metastazlı kemik kanserinin prognozu ve tedavisine yönelik yöntem. |
| US10441567B2 (en) | 2014-01-17 | 2019-10-15 | Ligand Pharmaceuticals Incorporated | Methods and compositions for modulating hormone levels |
| ES2864079T3 (es) | 2014-05-30 | 2021-10-13 | Pfizer | Derivados de carbonitrilo como moduladores selectivos del receptor de andrógenos |
| KR20170093182A (ko) | 2014-12-11 | 2017-08-14 | 인바이오모션 에스.엘. | 인간 c-maf에 대한 결합 구성원 |
| CN107709314A (zh) | 2015-06-11 | 2018-02-16 | 巴斯利尔药物国际股份公司 | 外排泵抑制剂及其治疗性用途 |
| AU2017271385B2 (en) | 2016-05-25 | 2023-10-05 | Inbiomotion S.L. | Therapeutic treatment of breast cancer based on c-MAF status |
| MX2020005182A (es) | 2017-11-22 | 2020-08-17 | Inbiomotion Sl | Tratamiento terapeutico del cancer de mama basado en el estado del c-maf. |
| US20210078986A1 (en) * | 2018-01-09 | 2021-03-18 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Inhibitors for the b-catenin/b-cell lymphoma 9 (bcl9) protein-protein interaction |
| WO2020148325A1 (en) | 2019-01-15 | 2020-07-23 | Phenex-Fxr Gmbh | Neutral lxr modulators |
| WO2020214834A1 (en) | 2019-04-19 | 2020-10-22 | Ligand Pharmaceuticals Inc. | Crystalline forms and methods of producing crystalline forms of a compound |
| US11124497B1 (en) | 2020-04-17 | 2021-09-21 | Pardes Biosciences, Inc. | Inhibitors of cysteine proteases and methods of use thereof |
| US11174231B1 (en) | 2020-06-09 | 2021-11-16 | Pardes Biosciences, Inc. | Inhibitors of cysteine proteases and methods of use thereof |
| BR112021023814A2 (pt) * | 2020-06-09 | 2022-12-20 | Pardes Biosciences Inc | Inibidores de proteases de cisteína e métodos de uso das mesmas |
| WO2023275715A1 (en) | 2021-06-30 | 2023-01-05 | Pfizer Inc. | Metabolites of selective androgen receptor modulators |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI964342A7 (fi) * | 1994-04-29 | 1996-10-28 | Vertex Pharma | Halogeenimetyyliamideja IL-1beta-proteaasi-inhibiittoreina |
| RU2156235C2 (ru) * | 1995-05-31 | 2000-09-20 | Кумиай Кемикал Индастри Ко., Лтд. | Производные фенилалканамида, способы их получения и сельскохозяйственный или садовый фунгицид |
| BR9708425B1 (pt) * | 1996-04-02 | 2012-02-22 | fenilcetoenóis substituìdos, processo para preparação e uso dos mesmos, bem como pesticidas ou herbicidas e método para controle de pragas e ervas daninhas. | |
| EP1155011A1 (de) | 1999-02-20 | 2001-11-21 | AstraZeneca AB | Di- und tripeptidnitril-derivate als inhibitoren von cathepsin l und cathepsin s |
| JP2002537293A (ja) * | 1999-02-20 | 2002-11-05 | アストラゼネカ アクチボラグ | カテプシンlおよび/またはカテプシンsの阻害剤としてのアセタミドアセトニトリル誘導体 |
| GB9903861D0 (en) * | 1999-02-20 | 1999-04-14 | Zeneca Ltd | Chemical compounds |
| DE60021254T2 (de) * | 1999-03-15 | 2006-04-20 | AXYS Pharmaceuticals, Inc., South San Francisco | N-cyanomethylamide als protease inhibitoren |
| EP1212302A1 (de) * | 1999-09-16 | 2002-06-12 | Axys Pharmaceuticals, Inc. | Verbindungen und pharmazeutische zusammensetzungen als cathepsin-s-hemmer |
-
2001
- 2001-01-05 DE DE60132975T patent/DE60132975T2/de not_active Expired - Fee Related
- 2001-01-05 CA CA002396257A patent/CA2396257A1/en not_active Abandoned
- 2001-01-05 EP EP01900903A patent/EP1248612B1/de not_active Expired - Lifetime
- 2001-01-05 AU AU26314/01A patent/AU779855B2/en not_active Ceased
- 2001-01-05 US US09/754,962 patent/US6525036B2/en not_active Expired - Fee Related
- 2001-01-05 WO PCT/US2001/000341 patent/WO2001049288A1/en not_active Ceased
- 2001-01-05 AT AT01900903T patent/ATE387199T1/de not_active IP Right Cessation
- 2001-01-05 JP JP2001549656A patent/JP2003525874A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001049288A9 (en) | 2001-10-25 |
| DE60132975T2 (de) | 2009-02-26 |
| CA2396257A1 (en) | 2001-07-12 |
| DE60132975D1 (de) | 2008-04-10 |
| AU779855B2 (en) | 2005-02-17 |
| EP1248612A4 (de) | 2005-09-07 |
| US6525036B2 (en) | 2003-02-25 |
| EP1248612A1 (de) | 2002-10-16 |
| JP2003525874A (ja) | 2003-09-02 |
| US20020052378A1 (en) | 2002-05-02 |
| WO2001049288A1 (en) | 2001-07-12 |
| EP1248612B1 (de) | 2008-02-27 |
| AU2631401A (en) | 2001-07-16 |
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| Date | Code | Title | Description |
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| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |