MA27295A1 - Inhibiteurs de la cathepsine protease a cysteine - Google Patents
Inhibiteurs de la cathepsine protease a cysteineInfo
- Publication number
- MA27295A1 MA27295A1 MA27826A MA27826A MA27295A1 MA 27295 A1 MA27295 A1 MA 27295A1 MA 27826 A MA27826 A MA 27826A MA 27826 A MA27826 A MA 27826A MA 27295 A1 MA27295 A1 MA 27295A1
- Authority
- MA
- Morocco
- Prior art keywords
- protease inhibitors
- cysteine cathepsin
- cathepsin protease
- inhibitors
- compounds
- Prior art date
Links
- 102000005600 Cathepsins Human genes 0.000 title abstract 2
- 108010084457 Cathepsins Proteins 0.000 title abstract 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 title 1
- 235000018417 cysteine Nutrition 0.000 title 1
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 title 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- 102000005927 Cysteine Proteases Human genes 0.000 abstract 1
- 108010005843 Cysteine Proteases Proteins 0.000 abstract 1
- 208000001132 Osteoporosis Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000030991 negative regulation of bone resorption Effects 0.000 abstract 1
Classifications
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- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/17—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and doubly-bound oxygen atoms bound to the same acyclic carbon skeleton
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/20—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
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- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/4164—1,3-Diazoles
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- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
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- C07C255/25—Aminoacetonitriles
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- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
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- C07C255/29—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton containing cyano groups and acylated amino groups bound to the carbon skeleton
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- C07C259/10—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to carbon atoms of six-membered aromatic rings
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- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
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- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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- 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
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Abstract
Cette invention concerne une nouvelle classe de composés qui sont des inhibiteurs de cystéines protéases, y compris mais sans y être limités, des inhibiteurs des cathepsines K, L, S et B. Ces composés sont utiles pour traiter des maladies dans lesquelles l'inhibition de la résorption osseuse est indiquée, telles que l'ostéoporose.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36181802P | 2002-03-05 | 2002-03-05 | |
| US40870402P | 2002-09-06 | 2002-09-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA27295A1 true MA27295A1 (fr) | 2005-05-02 |
Family
ID=27807943
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA27826A MA27295A1 (fr) | 2002-03-05 | 2004-08-17 | Inhibiteurs de la cathepsine protease a cysteine |
Country Status (27)
| Country | Link |
|---|---|
| US (6) | US7375134B2 (fr) |
| EP (1) | EP1482924B1 (fr) |
| JP (2) | JP4201716B2 (fr) |
| KR (1) | KR100975784B1 (fr) |
| CN (1) | CN100430052C (fr) |
| AT (1) | ATE395911T1 (fr) |
| AU (1) | AU2003219953B8 (fr) |
| BR (1) | BRPI0308208B8 (fr) |
| CA (1) | CA2477657C (fr) |
| CL (1) | CL2003001743A1 (fr) |
| CY (1) | CY1111130T1 (fr) |
| DE (1) | DE60321141D1 (fr) |
| DK (1) | DK1482924T3 (fr) |
| EC (1) | ECSP045261A (fr) |
| ES (1) | ES2305452T3 (fr) |
| HR (1) | HRP20040800B1 (fr) |
| IL (2) | IL163748A0 (fr) |
| IS (1) | IS2549B (fr) |
| MA (1) | MA27295A1 (fr) |
| MX (1) | MXPA04008621A (fr) |
| NO (1) | NO335099B1 (fr) |
| NZ (1) | NZ534583A (fr) |
| PL (1) | PL215865B1 (fr) |
| PT (1) | PT1482924E (fr) |
| RU (1) | RU2312861C2 (fr) |
| SI (1) | SI1482924T1 (fr) |
| WO (1) | WO2003075836A2 (fr) |
Families Citing this family (128)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9937531B2 (en) | 2009-03-10 | 2018-04-10 | Bookit Oy Ajanvarauspalvelu | Method and system for delivery of goods |
| WO2003063822A2 (fr) | 2002-02-01 | 2003-08-07 | Pfizer Products Inc. | Procede de fabrication de dispersions medicamenteuses amorphes solides homogenes sechees par pulverisation au moyen d'un appareil de sechage par pulverisation modifie |
| KR100975784B1 (ko) * | 2002-03-05 | 2010-08-17 | 머크 프로스트 캐나다 리미티드 | 카텝신 시스테인 프로테아제 억제제 |
| JPWO2003077948A1 (ja) * | 2002-03-19 | 2005-07-14 | 興和株式会社 | ミエローマ系腫瘍予防・治療剤及びその診断方法 |
| CN1809536A (zh) * | 2003-04-24 | 2006-07-26 | 麦克公司 | Akt活性抑制剂 |
| AU2004266740B2 (en) * | 2003-08-21 | 2010-08-26 | Merck Frosst Canada Ltd | Cathepsin cysteine protease inhibitors |
| CN1842515A (zh) * | 2003-08-27 | 2006-10-04 | 默克弗罗斯特加拿大有限公司 | 组织蛋白酶抑制剂 |
| KR20060079143A (ko) * | 2003-09-18 | 2006-07-05 | 액시스 파마슈티컬스 인코포레이티드 | 시스테인 프로테아제 억제제로서의 할로알킬 함유 화합물 |
| JP4769192B2 (ja) | 2003-10-24 | 2011-09-07 | アベンティス・ファーマスーティカルズ・インコーポレイテツド | カテプシン阻害剤としての新規な化合物及び組成物 |
| US7687524B2 (en) | 2003-12-12 | 2010-03-30 | Merck Frosst Canada & Co. | Cathepsin cysteine protease inhibitors |
| CN1921907A (zh) * | 2004-01-08 | 2007-02-28 | 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 |
| US7429674B2 (en) | 2004-04-14 | 2008-09-30 | Merck & Co. Inc.. | Process for preparing fluoroleucine alkyl esters |
| AU2005271620B2 (en) * | 2004-08-04 | 2011-03-24 | Merck Frosst Canada Ltd | Diastereoselective reductive amination process |
| BRPI0515470A (pt) * | 2004-09-17 | 2008-07-22 | Schering Ag | processos e intermediários para preparação de inibidores de cisteìna protease |
| TW200619206A (en) * | 2004-09-29 | 2006-06-16 | Anormed Inc | Chemokine-binding heterocyclic compound salts, and methods of use thereof |
| AR055283A1 (es) * | 2004-11-23 | 2007-08-15 | Merck Frosst Canada Ltd | Inhibidores de cisteinproteasa de catepsina |
| EP1817275A1 (fr) | 2004-12-01 | 2007-08-15 | Schering Aktiengesellschaft | Composes contenant un haloalkyle, utilises comme inhibiteurs de cysteine proteases |
| EP1819667B1 (fr) * | 2004-12-02 | 2012-10-17 | ViroBay, Inc. | Composes de sulfonamide utilises comme inhibiteurs des cysteine proteases |
| US20090005323A1 (en) * | 2005-01-19 | 2009-01-01 | Michael David Percival | Cathepsin K Inhibitors and Obesity |
| EP1841730A4 (fr) * | 2005-01-19 | 2010-10-27 | Merck Frosst Canada Ltd | Inhibiteurs de la cathepsine k et atherosclerose |
| US20080138635A1 (en) * | 2005-03-02 | 2008-06-12 | Zhikuan Chen | Conjugated Organic Molecules for Molecular Electronic Devices |
| DK1855674T3 (da) * | 2005-03-02 | 2014-10-20 | Merck Sharp & Dohme | Sammensætning til hæmning af cathepsin k |
| BRPI0609695A2 (pt) * | 2005-03-21 | 2011-10-18 | Applera Corp | composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, método para tratar uma doença e uma paciente sofrendo uma terapia |
| EP1866277B1 (fr) * | 2005-03-22 | 2014-06-25 | Virobay, Inc. | Composes contenant du sulfonyle en tant qu'inhibiteurs de cysteine proteases |
| US20090099264A1 (en) | 2005-06-02 | 2009-04-16 | Merck Frosst Canada Ltd. | Fluoroalkylamine Derivatives as Cathepsin Inhibtors |
| EP1908466B1 (fr) | 2005-07-19 | 2014-02-19 | Daiichi Sankyo Company, Limited | Dérivé d'une propanamide substituée et composition pharmaceutique contenant celui-ci |
| US20090264479A1 (en) * | 2005-07-26 | 2009-10-22 | Cameron Black | Papain Family Cysteine Protease Inhibitors for the Treatment of Parasitic Diseases |
| RU2478620C2 (ru) * | 2006-06-01 | 2013-04-10 | Санофи-Авентис | Спироциклические нитрилы в качестве ингибиторов протеазы |
| US7622593B2 (en) * | 2006-06-27 | 2009-11-24 | The Procter & Gamble Company | Human protein tyrosine phosphatase inhibitors and methods of use |
| JP5351030B2 (ja) * | 2006-10-04 | 2013-11-27 | 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阻害剤としてのジフルオロ含有化合物 |
| US7893112B2 (en) | 2006-10-04 | 2011-02-22 | Virobay, Inc. | Di-fluoro containing compounds as cysteine protease inhibitors |
| CN101616908B (zh) * | 2006-12-29 | 2014-09-10 | Abbvie德国有限责任两合公司 | 羧酰胺化合物及它们作为钙蛋白酶抑制剂的用途 |
| WO2008106059A1 (fr) | 2007-02-26 | 2008-09-04 | Merck & Co., Inc. | Formulations pour inhibiteurs de la cathepsine k |
| CN101668736B (zh) * | 2007-04-02 | 2013-06-12 | 默克弗罗斯特加拿大有限公司 | 用于制备组织蛋白酶k抑制剂的酰胺化反应 |
| KR20100023948A (ko) | 2007-06-08 | 2010-03-04 | 닛뽕 케미파 가부시키가이샤 | 뇌동맥류의 치료 또는 예방약 |
| 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 |
| CA2706746C (fr) * | 2007-11-29 | 2016-02-23 | Merck Frosst Canada Ltd. | Inhibiteurs de cysteine-proteases pour le traitement de maladies parasitaires |
| WO2009096198A1 (fr) * | 2008-02-01 | 2009-08-06 | Pharma Ip Limited Liability Intermediary Corporations | Nouveau derive de biaryle |
| WO2009123623A1 (fr) * | 2008-04-01 | 2009-10-08 | Virobay, Inc. | Composés contenant un di-fluoro en tant qu’inhibiteurs de cystéine protéase |
| US20090291945A1 (en) * | 2008-04-09 | 2009-11-26 | Teijin Pharma Limited | Cysteine protease inhibitors |
| WO2009140105A2 (fr) * | 2008-05-14 | 2009-11-19 | Merck & Co., Inc. | Préparations pour inhibiteurs de la cathepsine k |
| PE20120911A1 (es) * | 2009-04-20 | 2012-08-06 | Hoffmann La Roche | Derivados de prolina como inhibidores de catepsina |
| 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 |
| US9051304B2 (en) * | 2009-12-22 | 2015-06-09 | AbbVie Deutschland GmbH & Co. KG | Carboxamide compounds and their use as calpain inhibitors V |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| WO2012112363A1 (fr) | 2011-02-14 | 2012-08-23 | Merck Sharp & Dohme Corp. | Inhibiteurs de cystéine protéases, les cathepsines |
| WO2012148555A1 (fr) * | 2011-03-02 | 2012-11-01 | Merck Sharp & Dohme Corp. | Procédé d'amidation |
| US8680152B2 (en) | 2011-05-02 | 2014-03-25 | Virobay, Inc. | Cathepsin inhibitors for the treatment of bone cancer and bone cancer pain |
| AU2012257779A1 (en) * | 2011-05-16 | 2013-11-28 | Bayer Intellectual Property Gmbh | Use of cathepsin K inhibition for the treatment and/or prophylaxis of pulmonary hypertension and/or heart failure |
| WO2013105022A2 (fr) | 2012-01-09 | 2013-07-18 | Novartis Ag | Compositions organiques pour traiter des maladies associées à la bêta-caténine |
| CN107652289B (zh) | 2012-06-13 | 2020-07-21 | 因塞特控股公司 | 作为fgfr抑制剂的取代的三环化合物 |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| US20140199495A1 (en) | 2013-01-11 | 2014-07-17 | Floor Iptech Ab | Digital printing and embossing |
| CA2899030C (fr) | 2013-02-19 | 2021-03-09 | Novartis Ag | Derives de benzothiophene et compositions correspondantes en tant qu'agents de degradation selectifs des recepteurs des strogenes |
| MX364895B (es) | 2013-03-13 | 2019-05-10 | Forma Therapeutics Inc | Nuevos compuestos y composiciones para la inhibicion de fasn. |
| JP6449244B2 (ja) | 2013-04-19 | 2019-01-09 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Fgfr抑制剤としての二環式複素環 |
| EP2996678A1 (fr) | 2013-05-16 | 2016-03-23 | Sandoz AG | Comprimé à charge médicamenteuse accrue d'odanacatib |
| EP2808012A1 (fr) | 2013-05-29 | 2014-12-03 | ratiopharm GmbH | Procédé de production de forme posologique comportant de l'odanacatib |
| WO2014199644A1 (fr) | 2013-06-14 | 2014-12-18 | 生化学工業株式会社 | DÉRIVÉ α-OXOACYL AMINO-CAPROLACTAM |
| JP6226437B2 (ja) | 2013-06-14 | 2017-11-08 | 生化学工業株式会社 | α−オキソアシルアミノカプロラクタム体 |
| WO2015006177A1 (fr) * | 2013-07-11 | 2015-01-15 | Merck Sharp & Dohme Corp. | Formulations pour inhibiteurs de la cathepsine k avec de la vitamine d |
| EP3055314B1 (fr) * | 2013-10-08 | 2018-09-12 | Merck Sharp & Dohme Corp. | Inhibiteurs de cysteine protease de type cathepsine |
| WO2015092634A1 (fr) | 2013-12-16 | 2015-06-25 | Novartis Ag | Composés et compositions de 1,2,3,4-tétrahydroisoquinoléine en tant qu'antagonistes et agents de dégradation sélectifs des récepteurs des œstrogènes |
| JO3517B1 (ar) | 2014-01-17 | 2020-07-05 | Novartis Ag | ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2 |
| ES2699351T3 (es) | 2014-01-17 | 2019-02-08 | Novartis Ag | Derivados de 1-piridazin/triazin-3-il-piper(-azina)/idina/pirolidina y composiciones de las mismas para inhibir la actividad de SHP2 |
| ES2699354T3 (es) | 2014-01-17 | 2019-02-08 | Novartis Ag | Derivados de 1-(triazin-3-il/piridazin-3-il)-piper(-azin)idina y composiciones de las mismas para inhibir la actividad de SHP2 |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| CZ2014941A3 (cs) | 2014-12-19 | 2016-06-29 | Zentiva, K.S. | Příprava vysoce čistého intermediátu pro syntézu Odanacatibu |
| WO2016134294A1 (fr) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| ES2751669T3 (es) | 2015-02-20 | 2020-04-01 | Incyte Corp | Heterociclos bicíclicos como inhibidores FGFR |
| WO2016151499A1 (fr) | 2015-03-25 | 2016-09-29 | Novartis Ag | Dérivés n-hétérocycliques formylés utilisés en tant qu'inhibiteurs de fgfr4 |
| CN107787323B (zh) | 2015-06-19 | 2020-09-01 | 诺华股份有限公司 | 用于抑制shp2活性的化合物和组合物 |
| JP6718889B2 (ja) | 2015-06-19 | 2020-07-08 | ノバルティス アーゲー | Shp2の活性を阻害するための化合物および組成物 |
| WO2016203404A1 (fr) | 2015-06-19 | 2016-12-22 | Novartis Ag | Composés et compositions pour inhiber l'activité de shp2 |
| EP3342765B1 (fr) * | 2015-08-29 | 2021-09-15 | Sunshine Lake Pharma Co., Ltd. | Inhibiteur de cathepsine k et son application |
| EP3380455A1 (fr) * | 2015-11-26 | 2018-10-03 | H. Hoffnabb-La Roche Ag | Inhibiteurs de trypanosomes |
| CN106866502B (zh) * | 2015-12-10 | 2020-10-09 | 广东东阳光药业有限公司 | 组织蛋白酶k抑制剂及其用途 |
| ES2849560T3 (es) | 2016-05-04 | 2021-08-19 | Genoscience Pharma Sas | Derivados de 2,4-diamino-quinolina sustituidos para su uso en el tratamiento de enfermedades proliferativas |
| RU2744988C2 (ru) | 2016-06-14 | 2021-03-17 | Новартис Аг | Соединения и композиции для подавления активности shp2 |
| PL3575284T3 (pl) * | 2017-01-24 | 2021-12-27 | Astellas Pharma Inc. | Związek prolinamidu podstawiony fenylodifluorometylem |
| KR101916396B1 (ko) | 2017-02-20 | 2018-11-08 | 서울대학교 산학협력단 | 항암제 또는 항균제로 사용될 수 있는 단백질분해효소 저해제 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| TWI851542B (zh) | 2017-09-11 | 2024-08-11 | 美商克魯松藥物公司 | Shp2之八氫環戊烷并[c]吡咯別構抑制劑 |
| FI4046987T3 (fi) | 2017-12-05 | 2025-10-03 | Academisch Ziekenhuis Leiden | Katepsiini-inhibiittoreita |
| NL2020021B1 (en) * | 2017-12-05 | 2019-06-13 | Academisch Ziekenhuis Leiden | Cathepsin inhibitors |
| US11299478B2 (en) | 2018-03-28 | 2022-04-12 | Hanlim Pharmaceutical Co., Ltd. | 2-cyanopyrimidin-4-yl carbamate or urea derivative or salt thereof, and pharmaceutical composition including same |
| PE20210919A1 (es) | 2018-05-04 | 2021-05-19 | Incyte Corp | Sales de un inhibidor de fgfr |
| CN119241541A (zh) | 2018-05-04 | 2025-01-03 | 因赛特公司 | Fgfr抑制剂的固体形式和其制备方法 |
| FI3853234T3 (fi) | 2018-09-18 | 2025-07-28 | Nikang Therapeutics Inc | Fuusioituja trisyklisiä rengasjohdannaisia SRC-homologia-2-fosfataasin estäjinä |
| WO2020068867A1 (fr) | 2018-09-25 | 2020-04-02 | Black Diamond Therapeutics, Inc. | Dérivés de quinazoline utilisés en tant qu'inhibiteur de tyrosine kinase, compositions, leurs procédés de préparation et leur utilisation |
| CN113164776A (zh) | 2018-09-25 | 2021-07-23 | 黑钻治疗公司 | 酪氨酸激酶抑制剂组合物、其制备方法和使用方法 |
| EP3856345A1 (fr) | 2018-09-29 | 2021-08-04 | Novartis AG | Procédé de fabrication d'un composé pour inhiber l'activité de shp2 |
| TWI767148B (zh) | 2018-10-10 | 2022-06-11 | 美商弗瑪治療公司 | 抑制脂肪酸合成酶(fasn) |
| EP3873214A4 (fr) | 2018-10-29 | 2022-07-13 | Forma Therapeutics, Inc. | Formes solides de (4-(2-fluoro-4-(1-méthyl-1h-benzo[d]imidazol-5-yl)benzoyl)pipérazin-1-yl)(1-hydroxycyclopropyl)méthanone |
| WO2020185532A1 (fr) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Méthodes de traitement du cancer au moyen d'un inhibiteur de fgfr |
| AU2020250933A1 (en) | 2019-04-05 | 2021-10-28 | Centre Hospitalier Régional Et Universitaire De Brest | Protease-activated receptor-2 inhibitors for the treatment of sensory neuropathy induced by a marine neurotoxic poisoning |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CN114787150A (zh) | 2019-08-15 | 2022-07-22 | 黑钻治疗公司 | 炔基喹唑啉化合物 |
| WO2021067374A1 (fr) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
| GEP20247679B (en) | 2019-10-14 | 2024-10-10 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| IL293001A (en) | 2019-12-04 | 2022-07-01 | Incyte Corp | Derivatives of fgfr repressors |
| CA3163875A1 (fr) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Heterocycles tricycliques en tant qu'inhibiteurs de fgfr |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2021195206A1 (fr) | 2020-03-24 | 2021-09-30 | Black Diamond Therapeutics, Inc. | Formes polymorphes et utilisations associées |
| WO2022043558A1 (fr) | 2020-08-31 | 2022-03-03 | Advanced Accelerator Applications International Sa | Méthode de traitement de cancers exprimant le psma |
| WO2022043556A1 (fr) | 2020-08-31 | 2022-03-03 | Novartis Ag | Composition pharmaceutique stable |
| US20230321285A1 (en) | 2020-08-31 | 2023-10-12 | Advanced Accelerator Applications International Sa | Method of treating psma-expressing cancers |
| CN114539111A (zh) * | 2020-11-19 | 2022-05-27 | 深圳信立泰药业股份有限公司 | 奥当卡替的盐及其制备方法和医药用途 |
| WO2022140472A1 (fr) | 2020-12-22 | 2022-06-30 | Nikang Therapeutics, Inc. | Composés pour la dégradation de la kinase 2 dépendante des cyclines par l'intermédiaire d'une voie de l'ubiquitine-protéosome |
| WO2022152821A1 (fr) | 2021-01-13 | 2022-07-21 | Monte Rosa Therapeutics Ag | Composés d'isoindolinone |
| WO2022170052A1 (fr) | 2021-02-05 | 2022-08-11 | Black Diamond Therapeutics, Inc. | Dérivés de quinazoline, dérivés de pyridopyrimidine, dérivés de pyrimidopyrimidine et leurs utilisations |
| JP2024513575A (ja) | 2021-04-12 | 2024-03-26 | インサイト・コーポレイション | Fgfr阻害剤及びネクチン-4標的化剤を含む併用療法 |
| EP4323349A1 (fr) | 2021-04-14 | 2024-02-21 | Monte Rosa Therapeutics AG | Composés amide d'isoindolinone utilisés pour traiter des maladies associées à gspt1 |
| WO2022219407A1 (fr) | 2021-04-14 | 2022-10-20 | Monte Rosa Therapeutics Ag | Composés d'iso-indolinone |
| AR126101A1 (es) | 2021-06-09 | 2023-09-13 | Incyte Corp | Heterociclos tricíclicos como inhibidores de fgfr |
| WO2022261160A1 (fr) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr |
| TW202317589A (zh) | 2021-07-14 | 2023-05-01 | 美商尼坎醫療公司 | 作為kras抑制劑的伸烷基衍生物 |
| US12331026B2 (en) | 2022-03-28 | 2025-06-17 | Nikang Therapeutics, Inc. | Sulfonamido derivatives as cyclin-dependent kinase 2 inhibitors |
| EP4536363A1 (fr) | 2022-06-08 | 2025-04-16 | Nikang Therapeutics, Inc. | Dérivés de sulfamide utilisés en tant qu'inhibiteurs de kinase 2 dépendant de la cycline |
| EP4615833A1 (fr) | 2022-11-11 | 2025-09-17 | Nikang Therapeutics, Inc. | Composés bifonctionnels contenant des dérivés de pyrimidine 2,5-substitués pour dégrader la kinase 2 dépendante des cyclines par l'intermédiaire d'une voie ubiquitine-protéasome |
| WO2025072462A1 (fr) | 2023-09-27 | 2025-04-03 | Nikang Therapeutics, Inc. | Dérivés sulfonamides utilisés en tant qu'inhibiteurs de la kinase 2 dépendante de la cycline |
| TW202527955A (zh) | 2023-11-27 | 2025-07-16 | 美商尼坎醫療公司 | 用於經由泛素蛋白酶體途徑降解週期蛋白依賴性激酶2和週期蛋白依賴性激酶4的含有2,5-取代的嘧啶衍生物的雙功能化合物 |
| WO2025117981A1 (fr) | 2023-12-02 | 2025-06-05 | Nikang Therapeutics, Inc. | Composés bifonctionnels contenant des dérivés de pyrimidine 2,5-substitués pour dégrader la kinase 2 dépendante de la cycline par l'intermédiaire d'un système ubiquitine/protéasome |
| WO2025212828A1 (fr) | 2024-04-03 | 2025-10-09 | Nikang Therapeutics, Inc. | Composés bifonctionnels contenant des dérivés de pyrimidine 2,5-substitués pour dégrader la kinase cycline-dépendante 2 et la kinase cycline-dépendante 4 par l'intermédiaire de la voie ubiquitine-protéasome |
| WO2025240536A1 (fr) | 2024-05-15 | 2025-11-20 | Nikang Therapeutics, Inc. | Composés bifonctionnels contenant des dérivés de pyrimidine 2,5-substitués pour dégrader la kinase 2 dépendante d'une cycline et/ou la kinase 4 dépendante d'une cycline par l'intermédiaire de la voie ubiquitine-protéasome |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5187173A (en) * | 1991-12-27 | 1993-02-16 | Sterling Winthrop Inc. | 2-saccharinylmethyl and 4,5,6,7-tetrahydro-2-saccharinylmethyl phosphates, phosphonates and phosphinates useful as proteolytic enzyme inhibitors and compositions and method of use thereof |
| DZ2285A1 (fr) * | 1996-08-08 | 2002-12-25 | Smithkline Beecham Corp | Inhibiteurs de protéase de la cystéine. |
| KR100518690B1 (ko) * | 1997-11-05 | 2005-10-05 | 노파르티스 아게 | 디펩타이드 니트릴 |
| AU2560300A (en) | 1999-02-20 | 2000-09-04 | Astrazeneca Ab | Acetamido acetonitrile derivatives as inhibitors of cathepsin l and/or cathepsins |
| DK1178958T3 (da) * | 1999-03-15 | 2004-06-21 | Axys Pharm Inc | N-cyanomethylamider som proteaseinhibitorer |
| IL148630A0 (en) * | 1999-09-16 | 2002-09-12 | Axys Pharm Inc | Compounds and pharmaceutical compositions for inhibiting cathepsin s |
| GB0003111D0 (en) * | 2000-02-10 | 2000-03-29 | Novartis Ag | Organic compounds |
| WO2001077073A1 (fr) * | 2000-04-06 | 2001-10-18 | Merck Frosst Canada & Co. | Inhibiteurs de proteases a cysteine de type cathepsines |
| WO2001087828A1 (fr) * | 2000-05-15 | 2001-11-22 | Novartis Ag | Utilisation de peptidyl nitriles a substitution- n comme inhibiteurs des cathepsines de cysteine |
| ATE409482T1 (de) * | 2001-03-02 | 2008-10-15 | Merck Frosst Canada Ltd | Cathepsincystein-proteasehemmer |
| WO2003017598A1 (fr) * | 2001-08-15 | 2003-02-27 | The Board Of Governors For Higher Education, State Of Rhode Island And Providence Plantations | Procede et dispositif de memoire cache du protocole scsi vers le protocole ip |
| AU2002352663B2 (en) * | 2001-11-13 | 2007-06-21 | Axys Pharmaceuticals, Inc. | Cyanoalkylamino derivatives as protease inhibitors |
| KR100975784B1 (ko) | 2002-03-05 | 2010-08-17 | 머크 프로스트 캐나다 리미티드 | 카텝신 시스테인 프로테아제 억제제 |
| KR20060079143A (ko) * | 2003-09-18 | 2006-07-05 | 액시스 파마슈티컬스 인코포레이티드 | 시스테인 프로테아제 억제제로서의 할로알킬 함유 화합물 |
| AR055283A1 (es) * | 2004-11-23 | 2007-08-15 | Merck Frosst Canada Ltd | Inhibidores de cisteinproteasa de catepsina |
| US20090099264A1 (en) * | 2005-06-02 | 2009-04-16 | Merck Frosst Canada Ltd. | Fluoroalkylamine Derivatives as Cathepsin Inhibtors |
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