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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- C07—ORGANIC CHEMISTRY
- 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)
- Immunology (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)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Indole 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 |
| WO2001087828A1 (en) * | 2000-05-15 | 2001-11-22 | Novartis Ag | N-substituted peptidyl nitriles as cysteine cathepsin inhibitors |
| GB0108770D0 (en) | 2001-04-06 | 2001-05-30 | Eisai London Res Lab Ltd | Inhibitors |
| CA2465499A1 (en) * | 2001-11-08 | 2003-05-15 | Merck & Co., Inc. | Compositions and methods for treating osteoporosis |
| AU2002349621A1 (en) | 2001-11-30 | 2003-06-10 | Santen Pharmaceutical Co., Ltd. | Angiogenesis inhibitor |
| KR20050044660A (ko) | 2001-12-04 | 2005-05-12 | 에프. 호프만-라 로슈 아게 | 치환된 2-아미노-사이클로알칸카복스아마이드 및 시스테인프로테아제 저해제로서의 이의 용도 |
| US6759428B2 (en) | 2001-12-04 | 2004-07-06 | Roche Palo Alto Llc | Indole nitriles |
| KR20040111445A (ko) | 2002-03-28 | 2004-12-31 | 에자이 가부시키가이샤 | 신경퇴행성 질환 치료용 c─Jun N─말단 키나아제억제제로서의 7─아자인돌 |
| KR20050013534A (ko) | 2002-03-28 | 2005-02-04 | 에자이 가부시키가이샤 | c─Jun N─말단 키나아제 억제용 아자인돌 |
| WO2003084936A2 (en) * | 2002-04-10 | 2003-10-16 | Orchid Chemicals & 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 |
| CA2495939A1 (en) | 2002-09-04 | 2004-03-18 | Merck Frosst Canada & Co./Merck Frosst Canada & Cie | Cathepsin cysteine protease inhibitors |
| SE0203712D0 (sv) | 2002-12-13 | 2002-12-13 | Astrazeneca Ab | Novel compounds |
| EP1599475A2 (de) * | 2003-03-06 | 2005-11-30 | Eisai Co., Ltd. | Jnk-hemmer |
| GB0305142D0 (en) | 2003-03-06 | 2003-04-09 | Eisai London Res Lab Ltd | Synthesis |
| WO2004101565A2 (en) | 2003-05-16 | 2004-11-25 | Eisai Co., Ltd. | Jnk inhibitors |
| BRPI0410979A (pt) | 2003-09-18 | 2006-07-04 | Axys Pharm Inc | composto, composição farmacêutica, e, métodos para tratar uma doença em um animal mediada pela catepsina s e para tratar um paciente submetido a uma terapia |
| EP1745033A4 (de) | 2004-05-08 | 2009-08-26 | Neurogen Corp | 4,5-disubstituierte 2-aryl-pyrimidine |
| UA87854C2 (en) | 2004-06-07 | 2009-08-25 | Мерк Энд Ко., Инк. | N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators |
| US7348432B2 (en) | 2004-10-27 | 2008-03-25 | Janssen Phamaceutica N.V. | Pyridine imidazoles and aza-indoles as progesterone receptor modulators |
| WO2006060810A1 (en) | 2004-12-02 | 2006-06-08 | Schering Aktiengesellschaft | Sulfonamide compounds as cysteine protease inhibitors |
| KR20070085874A (ko) * | 2004-12-09 | 2007-08-27 | 머크 앤드 캄파니 인코포레이티드 | 에스트로겐 수용체 조절제 |
| US7709508B2 (en) | 2004-12-09 | 2010-05-04 | Merck Sharp & Dohme | Estrogen receptor modulators |
| JP5236293B2 (ja) | 2005-01-13 | 2013-07-17 | ブリストル−マイヤーズ スクイブ カンパニー | Xia因子阻害剤としての置換ビアリール化合物 |
| US20090005323A1 (en) * | 2005-01-19 | 2009-01-01 | Michael David Percival | Cathepsin K Inhibitors and Obesity |
| DE102005007694A1 (de) * | 2005-02-18 | 2006-09-21 | Henkel Kgaa | Mittel zum Färben von keratinhaltigen Fasern |
| WO2006102243A2 (en) | 2005-03-21 | 2006-09-28 | Applera Corporation | Alpha ketoamide compounds as cysteine protease inhibitors |
| EP1866277B1 (de) | 2005-03-22 | 2014-06-25 | Virobay, Inc. | Sulfonylhaltige verbindungen als cysteinproteaseinhibitoren |
| AU2006265735B2 (en) | 2005-07-06 | 2011-08-04 | Merck Canada Inc. | Cathepsin cysteine protease inhibitors |
| GB0516156D0 (en) | 2005-08-05 | 2005-09-14 | Eisai London Res Lab Ltd | JNK inhibitors |
| ZA200902477B (en) | 2006-10-04 | 2010-08-25 | Virobay Inc | Di-fluoro containing compounds as cysteine protease inhibitors |
| US7893112B2 (en) | 2006-10-04 | 2011-02-22 | Virobay, Inc. | Di-fluoro containing compounds as cysteine protease inhibitors |
| KR20100023948A (ko) | 2007-06-08 | 2010-03-04 | 닛뽕 케미파 가부시키가이샤 | 뇌동맥류의 치료 또는 예방약 |
| WO2009001127A1 (en) * | 2007-06-26 | 2008-12-31 | Astrazeneca Ab | Cyanocyclopropylcarboxamides as cathepsin inhibitors |
| EP2170879B1 (de) * | 2007-06-26 | 2013-01-16 | AstraZeneca AB | 1-cyanocyclopropylderivate als cathepsin-k-inhibitoren |
| WO2009054454A1 (ja) | 2007-10-24 | 2009-04-30 | National University Corporation Tokyo Medical And Dental University | 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 |
| JP5539221B2 (ja) | 2007-12-21 | 2014-07-02 | リガンド・ファーマシューティカルズ・インコーポレイテッド | 選択的アンドロゲン受容体モジュレーター(sarm)およびその使用 |
| WO2009087379A2 (en) | 2008-01-09 | 2009-07-16 | Amura Therapeutics Limited | Tetrahydrofuro (3, 2 -b) pyrrol- 3 -one derivatives as inhibitors of cysteine proteinases |
| EP2245022A4 (de) * | 2008-02-25 | 2012-02-22 | Panmira Pharmaceuticals Llc | Antagonisten von prostaglandin-d2-rezeptoren |
| PE20091888A1 (es) * | 2008-04-18 | 2010-01-17 | Glaxo Group Ltd | Inhibidores de catepsina c |
| 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 |
| US8680152B2 (en) | 2011-05-02 | 2014-03-25 | Virobay, Inc. | Cathepsin inhibitors for the treatment of bone cancer and bone cancer pain |
| SG11201405328SA (en) | 2012-03-16 | 2014-11-27 | Vitae Pharmaceuticals Inc | Liver x receptor modulators |
| SMT201700009T1 (it) | 2012-03-16 | 2017-03-08 | Vitae Pharmaceuticals Inc | Modulatori del recettore x del fegato |
| EP2650682A1 (de) | 2012-04-09 | 2013-10-16 | Fundació Privada Institut de Recerca Biomèdica | Asymmetrische Ester von als Schmiermittel geeigneten Fettsäuren |
| BR112014030750A2 (pt) | 2012-06-06 | 2017-08-22 | Inst Catalana Recerca Estudis Avancats | Método para diagnóstico, prognóstico e tratamento da metástase do câncer pulmonar |
| ES2906586T3 (es) | 2012-10-12 | 2022-04-19 | Inbiomotion Sl | Método para el diagnóstico, pronóstico y tratamiento de metástasis de cáncer de próstata |
| US10119171B2 (en) | 2012-10-12 | 2018-11-06 | Inbiomotion S.L. | Method for the diagnosis, prognosis and treatment of prostate cancer metastasis |
| KR20150122731A (ko) | 2013-03-15 | 2015-11-02 | 펀다시오 인스티튜트 드 르세르카 바이오메디카 (아이알비 바르셀로나) | 암 전이의 예후 및 치료 방법 |
| WO2014184679A2 (en) | 2013-03-15 | 2014-11-20 | Inbiomotion S.L. | Method for the prognosis and treatment of renal cell carcinoma metastasis |
| AU2014333513B2 (en) | 2013-10-09 | 2020-11-26 | Fundacio Institut De Recerca Biomedica (Irb Barcelona) | Method for the prognosis and treatment of metastasizing cancer of the bone originating from breast cancer |
| WO2015108988A2 (en) | 2014-01-17 | 2015-07-23 | Ligand Pharmaceuticals, Inc. | 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 |
| EP3229909B1 (de) | 2014-12-11 | 2020-10-14 | Inbiomotion S.L. | Bindeelemente für menschliches c-maf |
| WO2016198691A1 (en) | 2015-06-11 | 2016-12-15 | Basilea Pharmaceutica Ag | Efflux-pump inhibitors and therapeutic uses thereof |
| MX2018014279A (es) | 2016-05-25 | 2019-07-08 | Inbiomotion Sl | Tratamiento terapeutico de cancer de mama con base en estado de c-maf. |
| US11654153B2 (en) | 2017-11-22 | 2023-05-23 | Inbiomotion S.L. | Therapeutic treatment of breast cancer based on c-MAF status |
| 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 |
| KR20220003554A (ko) | 2019-04-19 | 2022-01-10 | 리간드 파마슈티칼스 인코포레이티드 | 화합물의 결정질 형태 및 결정질 형태를 제조하는 방법 |
| US11124497B1 (en) | 2020-04-17 | 2021-09-21 | Pardes Biosciences, Inc. | Inhibitors of cysteine proteases and methods of use thereof |
| AU2021286560A1 (en) * | 2020-06-09 | 2023-02-02 | 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 |
| 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 |
|---|---|---|---|---|
| WO1995029672A1 (en) * | 1994-04-29 | 1995-11-09 | Sanofi Winthrop, Inc. | HALOMETHYL AMIDES AS IL-1β PROTEASE INHIBITORS |
| RU2156235C2 (ru) * | 1995-05-31 | 2000-09-20 | Кумиай Кемикал Индастри Ко., Лтд. | Производные фенилалканамида, способы их получения и сельскохозяйственный или садовый фунгицид |
| CA2250417A1 (en) | 1996-04-02 | 1997-10-09 | Bayer Aktiengesellschaft | Substituted phenyl keto enols as pesticides and herbicides |
| GB9903861D0 (en) * | 1999-02-20 | 1999-04-14 | Zeneca Ltd | Chemical compounds |
| 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 |
| JP2002537294A (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及びカテプシンsの阻害剤としてのジ−及びトリペプチドニトリル誘導体 |
| EA200100972A1 (ru) * | 1999-03-15 | 2002-02-28 | Аксис Фармасьютикалз, Инк. | Новые соединения и композиции как ингибиторы протеаз |
| AU7490900A (en) * | 1999-09-16 | 2001-04-17 | Axys Pharmaceuticals, Inc. | Chemical compounds and compositions and their use as cathepsin s inhibitors |
-
2001
- 2001-01-05 JP JP2001549656A patent/JP2003525874A/ja not_active Withdrawn
- 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 EP EP01900903A patent/EP1248612B1/de not_active Expired - Lifetime
- 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 DE DE60132975T patent/DE60132975T2/de not_active Expired - Fee Related
- 2001-01-05 CA CA002396257A patent/CA2396257A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CA2396257A1 (en) | 2001-07-12 |
| EP1248612A4 (de) | 2005-09-07 |
| JP2003525874A (ja) | 2003-09-02 |
| US20020052378A1 (en) | 2002-05-02 |
| DE60132975D1 (de) | 2008-04-10 |
| EP1248612A1 (de) | 2002-10-16 |
| WO2001049288A1 (en) | 2001-07-12 |
| US6525036B2 (en) | 2003-02-25 |
| WO2001049288A9 (en) | 2001-10-25 |
| AU779855B2 (en) | 2005-02-17 |
| DE60132975T2 (de) | 2009-02-26 |
| AU2631401A (en) | 2001-07-16 |
| EP1248612B1 (de) | 2008-02-27 |
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| Date | Code | Title | Description |
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| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |