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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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- 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)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pain & Pain Management (AREA)
- Neurology (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Quinoline Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Indole Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Pyridine Compounds (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 |
| WO2001070743A1 (en) * | 2000-03-20 | 2001-09-27 | Axys Pharmaceuticals, Inc. | Non-amidine containing protease inhibitors |
| JP2003533506A (ja) * | 2000-05-15 | 2003-11-11 | ノバルティス アクチエンゲゼルシャフト | N−置換ペプチジルニトリル |
| GB0108770D0 (en) | 2001-04-06 | 2001-05-30 | Eisai London Res Lab Ltd | Inhibitors |
| EP1446114A4 (de) * | 2001-11-08 | 2005-05-25 | Merck & Co Inc | Zusammensetzungen und verfahren zur behandlung von osteoporose |
| AU2002349621A1 (en) | 2001-11-30 | 2003-06-10 | Santen Pharmaceutical Co., Ltd. | Angiogenesis inhibitor |
| MXPA04005263A (es) | 2001-12-04 | 2004-10-11 | Hoffmann La Roche | 2-amino-cicloalcanocarboxamidas substituidas y su uso como inhibidores de cisteina proteasa. |
| US6759428B2 (en) | 2001-12-04 | 2004-07-06 | Roche Palo Alto Llc | Indole nitriles |
| US7291630B2 (en) | 2002-03-28 | 2007-11-06 | Eisai Co., Ltd. | Azaindoles as inhibitors of c-Jun N-terminal kinases |
| KR20040111445A (ko) | 2002-03-28 | 2004-12-31 | 에자이 가부시키가이샤 | 신경퇴행성 질환 치료용 c─Jun N─말단 키나아제억제제로서의 7─아자인돌 |
| AU2003216591A1 (en) * | 2002-04-10 | 2003-10-20 | Orichid Chemicals And Pharmaceuticals Limited | Amino substituted pyrimidinone derivatives useful in the treatment of inflammation and immunological |
| GB0220187D0 (en) * | 2002-08-30 | 2002-10-09 | Novartis Ag | Organic compounds |
| US7279478B2 (en) | 2002-09-04 | 2007-10-09 | Merck Frosst Canada & Co. | Cathepsin cysteine protease inhibitors |
| 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 |
| TW200608976A (en) | 2004-05-08 | 2006-03-16 | Neurogen Corp | 4,5-disubstituted-2-aryl pyrimidines |
| UA87854C2 (en) | 2004-06-07 | 2009-08-25 | Мерк Энд Ко., Инк. | N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators |
| AU2005302707A1 (en) * | 2004-10-27 | 2006-05-11 | Janssen Pharmaceutica N.V. | Pyridine imidazoles and aza-indoles as progesterone receptor modulators |
| JP5154944B2 (ja) | 2004-12-02 | 2013-02-27 | ビロベイ,インコーポレイティド | システインプロテアーゼインヒビターとしてのスルホンアミド含有化合物 |
| US7709508B2 (en) | 2004-12-09 | 2010-05-04 | Merck Sharp & Dohme | Estrogen receptor modulators |
| EP1827421B1 (de) | 2004-12-09 | 2017-09-27 | Merck Sharp & Dohme Corp. | Östrogenrezeptormodulatoren |
| CN101137412B (zh) | 2005-01-13 | 2012-11-07 | 布里斯托尔-迈尔斯·斯奎布公司 | 用作凝血因子XIa抑制剂的取代的二芳基化合物 |
| 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 |
| DK1865940T3 (da) | 2005-03-21 | 2013-03-04 | Virobay Inc | Alfaketoamidforbindelser som cysteinproteasehæmmere |
| CA2602112A1 (en) * | 2005-03-22 | 2006-09-28 | Celera Genomics | Sulfonyl containing compounds as cysteine protease inhibitors |
| EP1902031B1 (de) * | 2005-07-06 | 2012-04-11 | Merck Canada Inc. | Cathepsincysteinproteasehemmer |
| GB0516156D0 (en) | 2005-08-05 | 2005-09-14 | Eisai London Res Lab Ltd | JNK inhibitors |
| DK2079683T3 (en) | 2006-10-04 | 2015-04-27 | Virobay Inc | Difluoro-containing compounds as cysteine protease inhibitors |
| US7893112B2 (en) | 2006-10-04 | 2011-02-22 | Virobay, Inc. | Di-fluoro containing compounds as cysteine protease inhibitors |
| US20110092484A1 (en) | 2007-06-08 | 2011-04-21 | Nippon Chemiphar Co., Ltd. | Therapeutic or prophylactic agent for cerebral aneurysm |
| WO2009001127A1 (en) * | 2007-06-26 | 2008-12-31 | Astrazeneca Ab | Cyanocyclopropylcarboxamides as cathepsin inhibitors |
| AU2008269513B2 (en) | 2007-06-26 | 2011-06-16 | Astrazeneca Ab | 1-cyanocyclopropyl-derivatives as cathepsin K inhibitors |
| JPWO2009054454A1 (ja) | 2007-10-24 | 2011-03-03 | 国立大学法人 東京医科歯科大学 | カテプシン阻害剤を有効成分として含有するToll様受容体のシグナル伝達の調整剤 |
| PT2222636E (pt) | 2007-12-21 | 2013-07-16 | Ligand Pharm Inc | Moduladores seletivos de recetores de andrógeno (sarms) e suas utilizações |
| WO2009087379A2 (en) | 2008-01-09 | 2009-07-16 | Amura Therapeutics Limited | Tetrahydrofuro (3, 2 -b) pyrrol- 3 -one derivatives as inhibitors of cysteine proteinases |
| WO2009108720A2 (en) * | 2008-02-25 | 2009-09-03 | Amira Pharmaceuticals, Inc. | Antagonists of prostaglandin d2 receptors |
| AR071369A1 (es) * | 2008-04-18 | 2010-06-16 | Glaxo Group Ltd | Compuesto de 1- ciano-3-pirrolidinil-n-sustituido-sulfonamida, su uso para preparar un medicamento util para tratar una enfermedad pulmonar obstructiva cronica y composicion farmaceutica que lo comprende |
| 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 |
| DK3091085T3 (da) | 2010-10-06 | 2019-05-06 | Inst Catalana Recerca Estudis Avancats | Fremgangsmåde til at designe en terapi mod brystcancermetastase |
| WO2012151319A1 (en) | 2011-05-02 | 2012-11-08 | Virobay, Inc. | Cathepsin inhibitors for the treatment of bone cancer and bone cancer pain |
| JP6114815B2 (ja) | 2012-03-16 | 2017-04-12 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 肝臓xレセプターモジュレーター |
| EP2825541B1 (de) | 2012-03-16 | 2016-06-22 | Vitae Pharmaceuticals, Inc. | Leber-x-rezeptormodulatoren |
| 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 |
| US10119171B2 (en) | 2012-10-12 | 2018-11-06 | Inbiomotion S.L. | Method for the diagnosis, prognosis and treatment of prostate cancer metastasis |
| JP6074049B2 (ja) | 2012-10-12 | 2017-02-01 | インバイオモーション エセ.エレ. | c−MAFを用いた前立腺がん転移の診断、予後診断および処置のための方法 |
| AU2014229505B2 (en) | 2013-03-15 | 2020-02-27 | Fundacio Institut De Recerca Biomedica (Irb Barcelona) | Method for the prognosis and treatment of cancer metastasis |
| US20160032399A1 (en) | 2013-03-15 | 2016-02-04 | Inbiomotion S.L. | Method for the Prognosis and Treatment of Renal Cell Carcinoma Metastasis |
| JP6550045B2 (ja) | 2013-10-09 | 2019-07-24 | 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) | 乳がんに由来する骨の転移がんの予後診断および処置のための方法 |
| 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 |
| CA2986083A1 (en) | 2015-06-11 | 2016-12-15 | Basilea Pharmaceutica International AG | Efflux-pump inhibitors and therapeutic uses thereof |
| PT3458610T (pt) | 2016-05-25 | 2021-06-29 | Inbiomotion Sl | Tratamento terapêutico de cancro da mama baseado no estado de c-maf |
| WO2019102380A1 (en) | 2017-11-22 | 2019-05-31 | Inbiomotion S.L. | Therapeutic treatment of breast cancer based on 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 |
| MX2021012690A (es) | 2019-04-19 | 2022-01-31 | Ligand Pharm Inc | Formas cristalinas y metodos para producir formas cristalinas de un compuesto. |
| 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 |
| KR20230040386A (ko) * | 2020-06-09 | 2023-03-22 | 파르데스 바이오사이언시스, 인크. | 시스테인 프로테아제의 억제제 및 이의 사용 방법 |
| 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 |
|---|---|---|---|---|
| CA2189036A1 (en) * | 1994-04-29 | 1995-11-09 | Roland E. Dolle | Halomethyl amides as il-1.beta. protease inhibitors |
| US6075055A (en) | 1995-05-31 | 2000-06-13 | Kumiai Chemical Industry Co., Ltd. | Phenylalkane amide derivatives and agricultural or horticultural fungicides |
| AU725852B2 (en) * | 1996-04-02 | 2000-10-19 | Bayer Aktiengesellschaft | Substituted phenylketoenols as pesticides and herbicides |
| WO2000049008A1 (en) | 1999-02-20 | 2000-08-24 | Astrazeneca Ab | Di- and tripeptide nitrile derivatives as inhibitors of cathepsin l and cathepsin s |
| GB9903861D0 (en) * | 1999-02-20 | 1999-04-14 | Zeneca Ltd | Chemical compounds |
| WO2000049007A1 (en) * | 1999-02-20 | 2000-08-24 | Astrazeneca Ab | Acetamido acetonitrile derivatives as inhibitors of cathepsin l and/or cathepsin s |
| EP1161415B1 (de) * | 1999-03-15 | 2005-07-13 | Axys Pharmaceuticals, Inc. | N-cyanomethylamide als protease inhibitoren |
| WO2001019796A1 (en) * | 1999-09-16 | 2001-03-22 | Axys Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions as cathepsin s inhibitors |
-
2001
- 2001-01-05 US US09/754,962 patent/US6525036B2/en not_active Expired - Fee Related
- 2001-01-05 AT AT01900903T patent/ATE387199T1/de not_active IP Right Cessation
- 2001-01-05 AU AU26314/01A patent/AU779855B2/en not_active Ceased
- 2001-01-05 JP JP2001549656A patent/JP2003525874A/ja not_active Withdrawn
- 2001-01-05 CA CA002396257A patent/CA2396257A1/en not_active Abandoned
- 2001-01-05 DE DE60132975T patent/DE60132975T2/de not_active Expired - Fee Related
- 2001-01-05 EP EP01900903A patent/EP1248612B1/de not_active Expired - Lifetime
- 2001-01-05 WO PCT/US2001/000341 patent/WO2001049288A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001049288A1 (en) | 2001-07-12 |
| CA2396257A1 (en) | 2001-07-12 |
| EP1248612A4 (de) | 2005-09-07 |
| DE60132975D1 (de) | 2008-04-10 |
| US6525036B2 (en) | 2003-02-25 |
| AU779855B2 (en) | 2005-02-17 |
| WO2001049288A9 (en) | 2001-10-25 |
| JP2003525874A (ja) | 2003-09-02 |
| AU2631401A (en) | 2001-07-16 |
| DE60132975T2 (de) | 2009-02-26 |
| EP1248612B1 (de) | 2008-02-27 |
| US20020052378A1 (en) | 2002-05-02 |
| EP1248612A1 (de) | 2002-10-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |