ECSP045261A - Inhibidores de la cisteín-proteasa catepsina - Google Patents
Inhibidores de la cisteín-proteasa catepsinaInfo
- Publication number
- ECSP045261A ECSP045261A EC2004005261A ECSP045261A ECSP045261A EC SP045261 A ECSP045261 A EC SP045261A EC 2004005261 A EC2004005261 A EC 2004005261A EC SP045261 A ECSP045261 A EC SP045261A EC SP045261 A ECSP045261 A EC SP045261A
- Authority
- EC
- Ecuador
- Prior art keywords
- inhibitors
- catepsina
- cistein
- proteasa
- compounds
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000006386 Bone Resorption Diseases 0.000 abstract 1
- 108090000712 Cathepsin B Proteins 0.000 abstract 1
- 102000004225 Cathepsin B Human genes 0.000 abstract 1
- 108090000625 Cathepsin K Proteins 0.000 abstract 1
- 102000004171 Cathepsin K Human genes 0.000 abstract 1
- 108090000624 Cathepsin L Proteins 0.000 abstract 1
- 102000004172 Cathepsin L Human genes 0.000 abstract 1
- 108090000613 Cathepsin S Proteins 0.000 abstract 1
- 102100035654 Cathepsin S Human genes 0.000 abstract 1
- 208000001132 Osteoporosis Diseases 0.000 abstract 1
- 230000024279 bone resorption Effects 0.000 abstract 1
- 239000002852 cysteine proteinase inhibitor Substances 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
Classifications
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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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- A61K31/00—Medicinal preparations containing organic active ingredients
- 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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- A61K31/18—Sulfonamides
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- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4174—Arylalkylimidazoles, e.g. oxymetazolin, naphazoline, miconazole
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/24—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
- C07C255/25—Aminoacetonitriles
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- 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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- C07D—HETEROCYCLIC COMPOUNDS
- 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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- 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
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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
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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
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- C07D213/63—One oxygen atom
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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
- C07D213/60—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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract
Esta invención se refiere a una nueva clase de compuestos que son inhibidores de cisteín-proteasa, incluyendo pero sin limitación, inhibidores de catepsinas K, L, S y B. Estos compuestos son útiles para tratar enfermedades en las que está indicada la inhibición de la resorción ósea, tales como la osteoporosis.
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 |
|---|---|
| ECSP045261A true ECSP045261A (es) | 2004-10-26 |
Family
ID=27807943
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2004005261A ECSP045261A (es) | 2002-03-05 | 2004-09-01 | Inhibidores de la cisteín-proteasa catepsina |
Country Status (27)
| Country | Link |
|---|---|
| US (6) | US20030232863A1 (es) |
| EP (1) | EP1482924B1 (es) |
| JP (2) | JP4201716B2 (es) |
| KR (1) | KR100975784B1 (es) |
| CN (1) | CN100430052C (es) |
| AT (1) | ATE395911T1 (es) |
| AU (1) | AU2003219953B8 (es) |
| BR (1) | BRPI0308208B8 (es) |
| CA (1) | CA2477657C (es) |
| CL (1) | CL2003001743A1 (es) |
| CY (1) | CY1111130T1 (es) |
| DE (1) | DE60321141D1 (es) |
| DK (1) | DK1482924T3 (es) |
| EC (1) | ECSP045261A (es) |
| ES (1) | ES2305452T3 (es) |
| HR (1) | HRP20040800B1 (es) |
| IL (2) | IL163748A0 (es) |
| IS (1) | IS2549B (es) |
| MA (1) | MA27295A1 (es) |
| MX (1) | MXPA04008621A (es) |
| NO (1) | NO335099B1 (es) |
| NZ (1) | NZ534583A (es) |
| PL (1) | PL215865B1 (es) |
| PT (1) | PT1482924E (es) |
| RU (1) | RU2312861C2 (es) |
| SI (1) | SI1482924T1 (es) |
| WO (1) | WO2003075836A2 (es) |
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 |
| MXPA04007433A (es) | 2002-02-01 | 2004-10-11 | Pfizer Prod Inc | Procedimiento para preparar dispersiones solidas amorfas homogeneas de farmaco secadas por pulverizacion utilizando un dispositivo de secado por pulverizacion modificado. |
| SI1482924T1 (sl) | 2002-03-05 | 2008-12-31 | Merck Frosst Canada Ltd | Katepsin cistein proteazni inhibitorji |
| US7745154B2 (en) * | 2002-03-19 | 2010-06-29 | Kowa Co., Ltd. | Preventives/remedies for myeloma tumor and method of diagnosing the same |
| ATE446752T1 (de) | 2003-04-24 | 2009-11-15 | Merck & Co Inc | Hemmer der akt aktivität |
| 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 |
| PT1663958E (pt) * | 2003-09-18 | 2015-06-01 | Virobay Inc | Compostos contendo haloalquilo como inibidores de protease de cisteína |
| NZ546504A (en) * | 2003-10-24 | 2009-01-31 | Aventis Pharma Inc | Novel keto-oxadiazole derivatives as cathepsin inhibitors |
| CA2548600A1 (en) * | 2003-12-12 | 2005-06-23 | Merck Frosst Canada & Co. | Cathepsin cysteine protease inhibitors |
| EP1715920A4 (en) * | 2004-01-08 | 2009-03-18 | Merck Frosst Canada Ltd | CATHEPSINCYSTEINPROTEASEHEMMER |
| US7429674B2 (en) | 2004-04-14 | 2008-09-30 | Merck & Co. Inc.. | Process for preparing fluoroleucine alkyl esters |
| US7183425B2 (en) | 2004-08-04 | 2007-02-27 | Merck Frosst Canada Ltd. | Diastereoselective reductive amination process |
| CN101068783A (zh) * | 2004-09-17 | 2007-11-07 | 拜耳先灵制药有限公司 | 用于制备半胱氨酸蛋白酶抑制剂的方法和中间体 |
| 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 (en) | 2004-12-01 | 2007-08-15 | Schering Aktiengesellschaft | Haloalkyl containing compounds as cysteine protease inhibitors |
| 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 |
| EP1841419A4 (en) * | 2005-01-19 | 2009-02-25 | Merck Frosst Canada Ltd | CATHEPSIN K AND ADIPOSITAS INHIBITORS |
| EP1841730A4 (en) * | 2005-01-19 | 2010-10-27 | Merck Frosst Canada Ltd | CATHEPSIN K INHIBITORS AND ATHEROSCLEROSIS |
| WO2006093467A1 (en) * | 2005-03-02 | 2006-09-08 | Agency For Science, Technology And Research | Conjugated organic molecules for molecular electronic devices |
| SI1855674T1 (sl) * | 2005-03-02 | 2014-10-30 | Merck Sharp & Dohme Corp. | Sestavek za inhibicijo katepsina k |
| 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 |
| US20090099264A1 (en) | 2005-06-02 | 2009-04-16 | Merck Frosst Canada Ltd. | Fluoroalkylamine Derivatives as Cathepsin Inhibtors |
| EP1908466B1 (en) | 2005-07-19 | 2014-02-19 | Daiichi Sankyo Company, Limited | Substituted propanamide derivative and pharmaceutical composition containing the same |
| EP1909784A4 (en) * | 2005-07-26 | 2010-04-21 | Merck Frosst Canada Ltd | CYSTEIN PROTEASE HEMMER OF THE PAPAIN FAMILY FOR THE TREATMENT OF PARASITIC ILLNESSES |
| WO2007137738A1 (de) * | 2006-06-01 | 2007-12-06 | Sanofi-Aventis | Spiro-cyclische nitrile als protease-inhibitoren |
| US7622593B2 (en) * | 2006-06-27 | 2009-11-24 | The Procter & Gamble Company | Human protein tyrosine phosphatase inhibitors and methods of use |
| 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 |
| PT2439205E (pt) * | 2006-12-29 | 2015-07-16 | Abbvie Deutschland | Compostos de carboxamida e seus usos como inibidores de calpaína |
| EP2132173B1 (en) | 2007-02-26 | 2015-10-07 | Merck Sharp & Dohme Corp. | Formulations for cathepsin k inhibitors |
| CA2682622A1 (en) * | 2007-04-02 | 2008-10-09 | Merck Frosst Canada Ltd. | Amidation process for the preparation of cathepsin k inhibitors |
| US20110092484A1 (en) | 2007-06-08 | 2011-04-21 | Nippon Chemiphar Co., Ltd. | Therapeutic or prophylactic agent for cerebral aneurysm |
| 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 |
| EP2225196B1 (en) * | 2007-11-29 | 2015-01-28 | Merck Canada Inc. | Cysteine protease inhibitors for the treatment of parasitic diseases |
| JPWO2009096198A1 (ja) * | 2008-02-01 | 2011-05-26 | 一般社団法人ファルマIp | 新規ビアリール誘導体 |
| EP2262370A4 (en) * | 2008-04-01 | 2011-08-31 | Virobay Inc | DIFLUOROUS COMPOUNDS AS A CYSTONE PROTEASE INHIBITOR |
| WO2009125861A1 (ja) * | 2008-04-09 | 2009-10-15 | 帝人ファーマ株式会社 | システインプロテアーゼ阻害剤 |
| EP2291079B1 (en) * | 2008-05-14 | 2013-04-24 | Merck Sharp & Dohme Corp. | Formulations for cathepsin k inhibitors |
| ES2436550T3 (es) * | 2009-04-20 | 2014-01-02 | F. Hoffmann-La Roche Ag | Nuevos 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 |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| WO2012112363A1 (en) * | 2011-02-14 | 2012-08-23 | Merck Sharp & Dohme Corp. | Cathepsin cysteine protease inhibitors |
| EP2681188A4 (en) * | 2011-03-02 | 2015-04-15 | Merck Sharp & Dohme | amidation |
| WO2012151319A1 (en) | 2011-05-02 | 2012-11-08 | Virobay, Inc. | Cathepsin inhibitors for the treatment of bone cancer and bone cancer pain |
| KR20140034821A (ko) | 2011-05-16 | 2014-03-20 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 폐고혈압 및/또는 심부전의 치료 및/또는 예방을 위한 카텝신 k 억제의 용도 |
| CA2860676A1 (en) | 2012-01-09 | 2013-07-18 | Novartis Ag | Organic compositions to treat beta-catenin-related diseases |
| US9611267B2 (en) | 2012-06-13 | 2017-04-04 | Incyte Holdings Corporation | Substituted tricyclic compounds as FGFR inhibitors |
| 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 |
| US9279058B2 (en) | 2013-01-11 | 2016-03-08 | Floor Iptech Ab | Digital embossing |
| EP2958907B1 (en) | 2013-02-19 | 2018-02-28 | Novartis AG | Benzothiophene derivatives and compositions thereof as selective estrogen receptor degraders |
| EP3587406B1 (en) | 2013-03-13 | 2021-01-27 | Forma Therapeutics, Inc. | 2-hydroxy-1-{4-[(4-phenylphenyl)carbonyl]piperazin-1-yl}ethan-1-one derivatives and related compounds as fatty acid synthase (fasn) inhibitors for the treatment of cancer |
| TWI649318B (zh) | 2013-04-19 | 2019-02-01 | 英塞特控股公司 | 作為fgfr抑制劑之雙環雜環 |
| WO2014184378A1 (en) | 2013-05-16 | 2014-11-20 | Sandoz Ag | Tablet with increased drug load of odanacatib |
| EP2808012A1 (en) | 2013-05-29 | 2014-12-03 | ratiopharm GmbH | Method for producing dosage form comprising odanacatib |
| 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 |
| WO2014199644A1 (ja) | 2013-06-14 | 2014-12-18 | 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誘導体 |
| WO2015006177A1 (en) * | 2013-07-11 | 2015-01-15 | Merck Sharp & Dohme Corp. | Formulations for cathepsin k inhibitors with vitamin d |
| EP3055314B1 (en) * | 2013-10-08 | 2018-09-12 | Merck Sharp & Dohme Corp. | Cathepsin cysteine protease inhibitors |
| WO2015092634A1 (en) | 2013-12-16 | 2015-06-25 | Novartis Ag | 1,2,3,4-tetrahydroisoquinoline compounds and compositions as selective estrogen receptor antagonists and degraders |
| US10093646B2 (en) | 2014-01-17 | 2018-10-09 | Novartis Ag | 1-pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and compositions thereof for inhibiting the activity of 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 |
| JO3517B1 (ar) | 2014-01-17 | 2020-07-05 | Novartis Ag | ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط 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 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| AU2016219822B2 (en) | 2015-02-20 | 2020-07-09 | Incyte Holdings Corporation | Bicyclic heterocycles as FGFR inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| US10189813B2 (en) | 2015-03-25 | 2019-01-29 | Novartis Ag | Formylated N-heterocyclic derivatives as FGFR4 inhibitors |
| EP3310779B1 (en) | 2015-06-19 | 2019-05-08 | Novartis AG | Compounds and compositions for inhibiting the activity of shp2 |
| ES2805232T3 (es) | 2015-06-19 | 2021-02-11 | Novartis Ag | Compuestos y composiciones para inhibir la actividad de SHP2 |
| ES2824576T3 (es) | 2015-06-19 | 2021-05-12 | Novartis Ag | Compuestos y composiciones para inhibir la actividad de SHP2 |
| EP3342765B1 (en) * | 2015-08-29 | 2021-09-15 | Sunshine Lake Pharma Co., Ltd. | Cathepsin k inhibitor and application thereof |
| WO2017089389A1 (en) * | 2015-11-26 | 2017-06-01 | F. Hoffmann-La Roche Ag | Trypanosomes inhibitors |
| 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 |
| CA3023032A1 (en) | 2016-05-04 | 2017-11-09 | Genoscience Pharma | Substituted 2,4-diamino-quinoline derivatives for use in the treatment of proliferative diseases |
| CN109415360B (zh) | 2016-06-14 | 2021-11-02 | 诺华股份有限公司 | 用于抑制shp2活性的化合物和组合物 |
| AU2018211735B2 (en) * | 2017-01-24 | 2021-08-12 | Astellas Pharma Inc. | Phenyldifluoromethyl-substituted prolinamide compound |
| 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 |
| TW202517628A (zh) | 2017-09-11 | 2025-05-01 | 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 |
| DK3720840T3 (da) | 2017-12-05 | 2022-03-21 | Academisch Ziekenhuis Leiden | Cathepsinhæmmere |
| NL2020021B1 (en) * | 2017-12-05 | 2019-06-13 | Academisch Ziekenhuis Leiden | Cathepsin inhibitors |
| JP7271566B2 (ja) | 2018-03-28 | 2023-05-11 | ハンリム ファーマシューティカル カンパニー リミテッド | 2-シアノピリミジン-4-イル カルバメート誘導体もしくはウレア誘導体またはその塩及びそれを含む医薬組成物 |
| ES2991427T3 (es) | 2018-05-04 | 2024-12-03 | Incyte Corp | Formas sólidas de un inhibidor de FGFR y procedimientos para preparar las mismas |
| TW201946630A (zh) | 2018-05-04 | 2019-12-16 | 美商英塞特公司 | Fgfr抑制劑之鹽 |
| CN112996795B (zh) | 2018-09-18 | 2024-11-12 | 尼坎治疗公司 | 作为src同源-2磷酸酶抑制剂的稠合的三环衍生物 |
| JP2022502496A (ja) | 2018-09-25 | 2022-01-11 | ブラック ダイアモンド セラピューティクス,インコーポレイティド | チロシンキナーゼ阻害剤組成物、作製方法、および使用方法 |
| WO2020068867A1 (en) | 2018-09-25 | 2020-04-02 | Black Diamond Therapeutics, Inc. | Quinazoline derivatives as tyrosine kinase inhibitor, compositions, methods of making them and their use |
| IL305106B2 (en) | 2018-09-29 | 2025-08-01 | Novartis Ag | Process of manufacture of a compound for inhibiting the activity of 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) |
| CN113382633A (zh) | 2018-10-29 | 2021-09-10 | 福马治疗股份有限公司 | (4-(2-氟-4-(1-甲基-1H-苯并[d]咪唑-5-基)苯甲酰基)哌嗪-1-基)(1-羟基环丙基)甲酮的固体形式 |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| WO2020201572A1 (en) | 2019-04-05 | 2020-10-08 | Université De Bretagne Occidentale | Protease-activated receptor-2 inhibitors for the treatment of sensory neuropathy induced by a marine neurotoxic poisoning |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021030711A1 (en) | 2019-08-15 | 2021-02-18 | Black Diamond Therapeutics, Inc. | Alkynyl quinazoline compounds |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| GEAP202415945A (en) | 2019-10-14 | 2024-04-25 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| CA3163875A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| AU2020395185A1 (en) | 2019-12-04 | 2022-06-02 | Incyte Corporation | Derivatives of an FGFR inhibitor |
| WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021195206A1 (en) | 2020-03-24 | 2021-09-30 | Black Diamond Therapeutics, Inc. | Polymorphic forms and related uses |
| WO2022043557A1 (en) | 2020-08-31 | 2022-03-03 | Advanced Accelerator Applications International Sa | Method of treating psma-expressing cancers |
| WO2022043556A1 (en) | 2020-08-31 | 2022-03-03 | Novartis Ag | Stable radiopharmaceutical composition |
| US20230338587A1 (en) | 2020-08-31 | 2023-10-26 | 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 (en) | 2020-12-22 | 2022-06-30 | Nikang Therapeutics, Inc. | Compounds for degrading cyclin-dependent kinase 2 via ubiquitin proteosome pathway |
| MX2023008296A (es) | 2021-01-13 | 2023-09-29 | Monte Rosa Therapeutics Inc | Compuestos de isoindolinona. |
| WO2022170052A1 (en) | 2021-02-05 | 2022-08-11 | Black Diamond Therapeutics, Inc. | Quinazoline derivatives, pyridopyrimidine derivatives, pyrimidopyrimidine derivatives, and uses thereof |
| EP4323405A1 (en) | 2021-04-12 | 2024-02-21 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| WO2022219407A1 (en) | 2021-04-14 | 2022-10-20 | Monte Rosa Therapeutics Ag | Isoindolinone compounds |
| WO2022219412A1 (en) | 2021-04-14 | 2022-10-20 | Monte Rosa Therapeutics Ag | Isoindolinone amide compounds useful to treat diseases associated with gspt1 |
| AR126101A1 (es) | 2021-06-09 | 2023-09-13 | Incyte Corp | Heterociclos tricíclicos como inhibidores de fgfr |
| CA3220274A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| WO2023284730A1 (en) | 2021-07-14 | 2023-01-19 | Nikang Therapeutics, Inc. | Alkylidene derivatives as kras inhibitors |
| IL315603A (en) | 2022-03-28 | 2024-11-01 | Nikang Therapeutics Inc | Sulfonamido derivatives as cycle-dependent KINASE 2 inhibitors |
| EP4536363A1 (en) | 2022-06-08 | 2025-04-16 | Nikang Therapeutics, Inc. | Sulfamide derivatives as cyclin-dependent kinase 2 inhibitors |
| TW202434563A (zh) | 2022-11-11 | 2024-09-01 | 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的含有2,5-取代的嘧啶衍生物之雙功能化合物 |
| WO2025072462A1 (en) | 2023-09-27 | 2025-04-03 | Nikang Therapeutics, Inc. | Sulfonamide derivatives as cyclin-dependent kinase 2 inhibitors |
| WO2025117616A1 (en) | 2023-11-27 | 2025-06-05 | Nikang Therapeutics, Inc. | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and cyclin-dependent kinase 4 via ubiquitin proteasome pathway |
| WO2025117981A1 (en) | 2023-12-02 | 2025-06-05 | Nikang Therapeutics, Inc. | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway |
| WO2025212828A1 (en) | 2024-04-03 | 2025-10-09 | Nikang Therapeutics, Inc. | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and cyclin-dependent kinase 4 via ubiquitin proteasome pathway |
| WO2025240536A1 (en) | 2024-05-15 | 2025-11-20 | Nikang Therapeutics, Inc. | Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and/or cyclin-dependent kinase 4 via ubiquitin proteasome pathway |
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. |
| NZ503889A (en) * | 1997-11-05 | 2002-07-26 | Novartis Ag | Dipeptide nitriles |
| WO2000049007A1 (en) | 1999-02-20 | 2000-08-24 | Astrazeneca Ab | Acetamido acetonitrile derivatives as inhibitors of cathepsin l and/or cathepsin s |
| EP1161415B1 (en) * | 1999-03-15 | 2005-07-13 | Axys Pharmaceuticals, Inc. | N-cyanomethylamides as protease inhibitors |
| WO2001019796A1 (en) * | 1999-09-16 | 2001-03-22 | Axys Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions as cathepsin s inhibitors |
| GB0003111D0 (en) * | 2000-02-10 | 2000-03-29 | Novartis Ag | Organic compounds |
| WO2001077073A1 (en) * | 2000-04-06 | 2001-10-18 | Merck Frosst Canada & Co. | Cathepsin cysteine 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 |
| US7012075B2 (en) * | 2001-03-02 | 2006-03-14 | Merck & Co., Inc. | Cathepsin cysteine protease inhibitors |
| WO2003017598A1 (en) * | 2001-08-15 | 2003-02-27 | The Board Of Governors For Higher Education, State Of Rhode Island And Providence Plantations | Scsi-to-ip cache storage device and method |
| US7371747B2 (en) * | 2001-11-13 | 2008-05-13 | Merck Frosst Canada & Co. | Cyanoalkylamino derivatives as protease inhibitors |
| SI1482924T1 (sl) * | 2002-03-05 | 2008-12-31 | Merck Frosst Canada Ltd | Katepsin cistein proteazni inhibitorji |
| PT1663958E (pt) * | 2003-09-18 | 2015-06-01 | Virobay Inc | Compostos contendo haloalquilo como inibidores de protease de cisteína |
| 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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