MA53665B1 - Agonistes du récepteur farnésoïde x et leurs utilisations - Google Patents
Agonistes du récepteur farnésoïde x et leurs utilisationsInfo
- Publication number
- MA53665B1 MA53665B1 MA53665A MA53665A MA53665B1 MA 53665 B1 MA53665 B1 MA 53665B1 MA 53665 A MA53665 A MA 53665A MA 53665 A MA53665 A MA 53665A MA 53665 B1 MA53665 B1 MA 53665B1
- Authority
- MA
- Morocco
- Prior art keywords
- farnesoid
- receptor agonists
- compounds
- methods
- receptor
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Biotechnology (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
L'invention concerne des composés qui sont des agonistes du récepteur farnésoïde X, des procédés de fabrication de tels composés, des compositions pharmaceutiques et des médicaments comprenant de tels composés, et des méthodes d'utilisation de tels composés dans le traitement d'états, de maladies ou de troubles associés à l'activité du récepteur farnésoïde X.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862733004P | 2018-09-18 | 2018-09-18 | |
| US201862733006P | 2018-09-18 | 2018-09-18 | |
| US201962881560P | 2019-08-01 | 2019-08-01 | |
| EP19862391.0A EP3852748B1 (fr) | 2018-09-18 | 2019-09-17 | Agonistes du récepteur farnésoïde x et leurs utilisations |
| PCT/US2019/051603 WO2020061113A1 (fr) | 2018-09-18 | 2019-09-17 | Agonistes du récepteur farnésoïde x et leurs utilisations |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA53665A MA53665A (fr) | 2021-07-28 |
| MA53665B1 true MA53665B1 (fr) | 2025-09-30 |
Family
ID=69887982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA53665A MA53665B1 (fr) | 2018-09-18 | 2019-09-17 | Agonistes du récepteur farnésoïde x et leurs utilisations |
Country Status (20)
| Country | Link |
|---|---|
| US (4) | US11084817B2 (fr) |
| EP (2) | EP4596543A3 (fr) |
| JP (1) | JP7554739B2 (fr) |
| KR (2) | KR102810978B1 (fr) |
| CN (1) | CN113056271B (fr) |
| AU (2) | AU2019344903B2 (fr) |
| BR (1) | BR112021004919A2 (fr) |
| CA (1) | CA3112411A1 (fr) |
| CL (1) | CL2021000632A1 (fr) |
| DK (1) | DK3852748T3 (fr) |
| FI (1) | FI3852748T3 (fr) |
| IL (1) | IL281475B2 (fr) |
| LT (1) | LT3852748T (fr) |
| MA (1) | MA53665B1 (fr) |
| MX (1) | MX2021003110A (fr) |
| PH (1) | PH12021550605A1 (fr) |
| PT (1) | PT3852748T (fr) |
| SG (1) | SG11202102651SA (fr) |
| TW (1) | TWI833805B (fr) |
| WO (1) | WO2020061113A1 (fr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018170182A1 (fr) * | 2017-03-15 | 2018-09-20 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| IL269068B (en) | 2017-03-15 | 2022-09-01 | Metacrine Inc | Paranoid x receptor agonists and uses thereof |
| WO2020061113A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| IL293892A (en) | 2020-01-15 | 2022-08-01 | Inserm Institut National De La Sant? Et De La Rech M?Dicale | Use of fxr agonists for treating an infection by hepatitis d virus |
| IL296539A (en) * | 2020-03-18 | 2022-11-01 | Metacrine Inc | Farnesoid x receptor agonists for the treatment of disease |
| EP4121012A1 (fr) * | 2020-03-18 | 2023-01-25 | Metacrine, Inc. | Formulations d'un agoniste du récepteur farnésoïde x |
| BR112022018596A2 (pt) * | 2020-03-18 | 2023-03-07 | Metacrine Inc | Formas cristalinas de um agonista de receptor farnesoide x |
| US20240100125A1 (en) | 2021-01-14 | 2024-03-28 | Enyo Pharma | Synergistic effect of a fxr agonist and ifn for the treatment of hbv infection |
| WO2022229302A1 (fr) | 2021-04-28 | 2022-11-03 | Enyo Pharma | Potentialisation forte d'effets d'agonistes de tlr3 à l'aide d'agonistes de fxr en tant que traitement combiné |
| CN116554121A (zh) * | 2023-05-05 | 2023-08-08 | 济南悟通生物科技有限公司 | 一种2-异丁基噻唑的合成方法 |
Family Cites Families (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CZ20013767A3 (cs) | 1999-05-17 | 2002-04-17 | Novo Nordisk A/S | Sloučenina, farmaceutický prostředek, pouľití sloučeniny a způsob léčení |
| US6645980B1 (en) | 2000-05-25 | 2003-11-11 | Sepracor Inc. | Heterocyclic analgesic compounds and methods of use thereof |
| CA2372887A1 (fr) | 1999-05-25 | 2000-11-30 | Sepracor Inc. | Composes heterocycliques analgesiques et procedes d'utilisation de ces derniers |
| US6511980B2 (en) | 2000-05-05 | 2003-01-28 | Ortho Mcneil Pharmaceutical, Inc. | Substituted diamine derivatives useful as motilin antagonists |
| JP2004509866A (ja) | 2000-09-25 | 2004-04-02 | アクテリオン ファマシューティカルズ リミテッド | 置換アミノ−アザ−シクロアルカン |
| FR2815032B1 (fr) | 2000-10-10 | 2003-08-08 | Pf Medicament | Nouveaux derives d'aminophenyle piperazine ou d'amino phenyle piperide inhibiteurs de proteines prenyl transferase ainsi que leurs preparations |
| FR2825706B1 (fr) | 2001-06-06 | 2003-12-12 | Pf Medicament | Nouveaux derives de benzothienyle ou d'indole, leur preparation et leur utilisation comme inhibiteurs de proteines prenyl transferase |
| FR2839974B1 (fr) | 2002-05-24 | 2004-07-16 | Pf Medicament | Derives de phenyl-furane ou de phenyl-thiophene,leur preparation et leur application a titre de medicament |
| WO2004009549A2 (fr) | 2002-07-18 | 2004-01-29 | Actelion Pharmaceuticals Ltd | Piperidines utiles pour traiter des maladies du systeme nerveux central |
| BR0314126A (pt) | 2002-09-20 | 2005-06-28 | Pfizer Prod Inc | Ligandos de amida acìclica e sulfonamida para o receptor de estrogênio |
| AU2003290796A1 (en) | 2002-11-14 | 2004-06-15 | The Scripps Research Institute | Non-steroidal fxr agonists |
| US20050143449A1 (en) | 2002-11-15 | 2005-06-30 | The Salk Institute For Biological Studies | Non-steroidal farnesoid X receptor modulators and methods for the use thereof |
| AU2003298654A1 (en) | 2002-11-15 | 2004-06-15 | The Salk Institute For Biological Studies | Structure of the farnesoid x receptor ligand binding domain and methods of use therefor |
| GB0309781D0 (en) | 2003-04-29 | 2003-06-04 | Glaxo Group Ltd | Compounds |
| US7759348B2 (en) | 2003-07-30 | 2010-07-20 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| US7335658B2 (en) | 2003-07-30 | 2008-02-26 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| US7754711B2 (en) | 2003-07-30 | 2010-07-13 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| WO2005058822A1 (fr) | 2003-12-17 | 2005-06-30 | Actelion Pharmaceuticals Ltd | Cycloalcanes amines substitues |
| WO2005097760A1 (fr) | 2004-03-26 | 2005-10-20 | Rigel Pharmaceuticals, Inc. | Composes antiviraux heterocycliques comportant des groupes fonctionnels metabolisables et leurs utilisations |
| WO2005113522A1 (fr) | 2004-05-07 | 2005-12-01 | Janssen Pharmaceutica, N.V. | Inhibiteurs carboxamides d'azole de systèmes bactériens de sécrétion de protéine de type iii |
| JP2006199656A (ja) | 2005-01-24 | 2006-08-03 | Kowa Co | アミド基を有する環状アミン化合物 |
| MY144229A (en) | 2006-01-26 | 2011-08-15 | Xenon Pharmaceuticals Inc | Pyridazine derivatives and their use as therapeutic agents |
| AU2007229637A1 (en) | 2006-03-28 | 2007-10-04 | Novartis Ag | Amide derivatives and their application for the treatment of G protein related diseases |
| US20080081824A1 (en) | 2006-09-29 | 2008-04-03 | Bristol-Myers Squibb Company | Substituted piperidines as modulators of chemokine receptor activity |
| WO2008065500A2 (fr) | 2006-11-30 | 2008-06-05 | Pfizer Products Inc. | Hétéroaryl amides comme inhibiteurs du transport de la glycine de type i |
| NZ585370A (en) | 2007-12-19 | 2012-09-28 | Boehringer Ingelheim Int | Viral polymerase inhibitors |
| WO2010001869A1 (fr) | 2008-06-30 | 2010-01-07 | 武田薬品工業株式会社 | Composé de benzène tétrasubstitué et son utilisation |
| JP2010077109A (ja) | 2008-08-28 | 2010-04-08 | Takeda Chem Ind Ltd | 複素環化合物およびその用途 |
| WO2011008915A1 (fr) | 2009-07-15 | 2011-01-20 | Abbott Laboratories | Pyrrolopyridines inhibiteurs de kinases |
| JP2012532914A (ja) | 2009-07-15 | 2012-12-20 | メルク セローノ ソシエテ アノニム | テトラゾール誘導体 |
| FR2963005B1 (fr) | 2010-07-23 | 2012-08-17 | Sanofi Aventis | Derives d'oxadiazoles et de pyridazines, leur preparation et leur application en therapeutique |
| EP3872076A1 (fr) | 2011-03-23 | 2021-09-01 | Trevena, Inc. | Ligands de récepteurs opïoides, et leurs procédés d'utilisation et de production |
| EP2545964A1 (fr) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Nouveaux composés se liant au fxr (nr1 h4) et modulant son activité |
| CN103648634B (zh) | 2011-07-13 | 2016-05-18 | M技术株式会社 | 控制了微晶粒径的微粒的制造方法 |
| RU2543485C2 (ru) | 2013-02-26 | 2015-03-10 | Андрей Александрович Иващенко | Гетероциклические агонисты рецепторов желчных кислот tgr5, фармацевтическая композиция, способы их получения и применения |
| GB201316824D0 (en) | 2013-09-23 | 2013-11-06 | R & D Vernalis Ltd | New Chemical Entities |
| EP3116878A4 (fr) | 2014-03-13 | 2018-02-14 | Salk Institute for Biological Studies | Agonistes fxr et leurs procédés de fabrication et d'utilisation |
| AU2015229055B2 (en) | 2014-03-13 | 2019-09-12 | Salk Institute For Biological Studies | Analogs of fexaramine and methods of making and using |
| US20150258052A1 (en) | 2014-03-13 | 2015-09-17 | Salk Institute For Biological Studies | Methods of using fexaramine and agents that increase sympathetic nervous system activity to promote browning of white adipose tissue |
| US10077268B2 (en) | 2014-03-13 | 2018-09-18 | Salk Institute For Biological Studies | FXR agonists and methods for making and using |
| US10301268B2 (en) | 2014-03-13 | 2019-05-28 | The Salk Institute For Biological Studies | Analogs of fexaramine and methods of making and using |
| US20180116993A1 (en) | 2015-01-22 | 2018-05-03 | Xiamen University | Modulators of farnesoid x receptor and methods for the use thereof |
| CA2979399A1 (fr) | 2015-03-13 | 2016-09-22 | Salk Institute For Biological Studies | Traitement de diabetes auto-immuns latents des adultes a agonistes de recepteur x farnesoide pour activer les recepteurs intestinaux |
| WO2017018751A1 (fr) | 2015-07-24 | 2017-02-02 | 동국대학교 산학협력단 | Nouveau composé présentant une activité inhibitrice de blt et composition, destiné à prévenir ou à traiter des maladies inflammatoires, contenant ce dernier en tant que principe actif |
| WO2017049176A1 (fr) * | 2015-09-16 | 2017-03-23 | Metacrine, Inc. | Agonistes du récepteur x farnésoïde et leurs utilisations |
| JP2018532772A (ja) | 2015-09-16 | 2018-11-08 | メタクリン,インク. | ファルネソイドx受容体アゴニストおよびそれらの使用 |
| AU2016323992B2 (en) | 2015-09-16 | 2021-05-06 | Eli Lilly And Company | Farnesoid X receptor agonists and uses thereof |
| EP3350158A4 (fr) | 2015-09-16 | 2019-05-08 | Metacrine, Inc. | Agonistes du récepteur x farnésoïde et leurs utilisations |
| CN105477636B (zh) * | 2015-10-16 | 2019-09-17 | 厦门大学 | 使用阿维菌素及其衍生物治疗代谢疾病的方法 |
| CN107126419B (zh) | 2016-02-26 | 2020-06-19 | 石药集团中诺药业(石家庄)有限公司 | 一种奥贝胆酸片剂及其制备方法 |
| WO2017170182A1 (fr) | 2016-03-31 | 2017-10-05 | 株式会社Adeka | Composition photosensible et nouveau composé |
| IL269068B (en) | 2017-03-15 | 2022-09-01 | Metacrine Inc | Paranoid x receptor agonists and uses thereof |
| WO2018170182A1 (fr) | 2017-03-15 | 2018-09-20 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| WO2018170167A1 (fr) | 2017-03-15 | 2018-09-20 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| US20200131129A1 (en) | 2017-03-15 | 2020-04-30 | Metacrine, Inc. | Farnesoid x receptor agonists and uses thereof |
| US20200131142A1 (en) | 2017-03-15 | 2020-04-30 | Metacrine, Inc. | Farnesoid x receptor agonists and uses thereof |
| CZ2017298A3 (cs) | 2017-05-26 | 2018-12-05 | Zentiva, K.S. | Amorfní formy obeticholové kyseliny |
| WO2020060007A1 (fr) | 2018-09-17 | 2020-03-26 | 엘지전자 주식회사 | Procédé et dispositif sans fil pour gérer une session de pdu dans une communication mobile 5g |
| WO2020061116A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| CA3112414A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du recepteur farnesoide x pour le traitement d'une maladie |
| WO2020061113A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| WO2020061117A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| WO2020061118A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| BR112021004931A2 (pt) | 2018-09-18 | 2021-06-01 | Metacrine, Inc. | formas cristalinas de um agonista de receptor farnesoide x |
| US20220054469A1 (en) | 2018-09-18 | 2022-02-24 | Metacrine, Inc. | Farnesoid x receptor agonists and uses thereof |
| BR112022018596A2 (pt) | 2020-03-18 | 2023-03-07 | Metacrine Inc | Formas cristalinas de um agonista de receptor farnesoide x |
| IL296539A (en) | 2020-03-18 | 2022-11-01 | Metacrine Inc | Farnesoid x receptor agonists for the treatment of disease |
| EP4121012A1 (fr) | 2020-03-18 | 2023-01-25 | Metacrine, Inc. | Formulations d'un agoniste du récepteur farnésoïde x |
-
2019
- 2019-09-17 WO PCT/US2019/051603 patent/WO2020061113A1/fr not_active Ceased
- 2019-09-17 AU AU2019344903A patent/AU2019344903B2/en active Active
- 2019-09-17 BR BR112021004919-3A patent/BR112021004919A2/pt unknown
- 2019-09-17 TW TW108133441A patent/TWI833805B/zh active
- 2019-09-17 MA MA53665A patent/MA53665B1/fr unknown
- 2019-09-17 IL IL281475A patent/IL281475B2/en unknown
- 2019-09-17 US US16/573,993 patent/US11084817B2/en active Active
- 2019-09-17 LT LTEPPCT/US2019/051603T patent/LT3852748T/lt unknown
- 2019-09-17 SG SG11202102651SA patent/SG11202102651SA/en unknown
- 2019-09-17 JP JP2021513407A patent/JP7554739B2/ja active Active
- 2019-09-17 KR KR1020217011359A patent/KR102810978B1/ko active Active
- 2019-09-17 CA CA3112411A patent/CA3112411A1/fr active Pending
- 2019-09-17 MX MX2021003110A patent/MX2021003110A/es unknown
- 2019-09-17 DK DK19862391.0T patent/DK3852748T3/da active
- 2019-09-17 PT PT198623910T patent/PT3852748T/pt unknown
- 2019-09-17 EP EP25178478.1A patent/EP4596543A3/fr active Pending
- 2019-09-17 KR KR1020257016139A patent/KR20250073553A/ko active Pending
- 2019-09-17 FI FIEP19862391.0T patent/FI3852748T3/fi active
- 2019-09-17 CN CN201980075902.2A patent/CN113056271B/zh active Active
- 2019-09-17 EP EP19862391.0A patent/EP3852748B1/fr active Active
-
2021
- 2021-03-16 CL CL2021000632A patent/CL2021000632A1/es unknown
- 2021-03-17 PH PH12021550605A patent/PH12021550605A1/en unknown
- 2021-06-16 US US17/349,757 patent/US11773094B2/en active Active
-
2023
- 2023-07-17 US US18/353,659 patent/US20230382913A1/en not_active Abandoned
-
2024
- 2024-10-31 US US18/933,587 patent/US20250289821A1/en active Pending
-
2025
- 2025-05-22 AU AU2025203804A patent/AU2025203804A1/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA53665B1 (fr) | Agonistes du récepteur farnésoïde x et leurs utilisations | |
| MA58049B1 (fr) | Antagonistes du récepteur du sous-type 2 de la mélanocortine (mc2r) à pipéridine à double substitution gem et leurs utilisations | |
| MA31764B1 (fr) | Composés et compositions en tant que modulateurs de l'activité de gpr119 | |
| MA64509B1 (fr) | Composés hétérocycliques utilisés comme immunomodulateurs | |
| MA64121B1 (fr) | Composés hétérocycliques utilisés comme immunomodulateurs | |
| MA52288B1 (fr) | Modulateurs d'enzymes de modification de méthyle, compositions et utilisations de ceux-ci | |
| PH12019502058A1 (en) | Farnesoid x receptor agonists and uses thereof | |
| MA47392B1 (fr) | Bis-octahydrophénanthrène carboxamides et leurs conjugués protéiques | |
| MA30462B1 (fr) | Composes de pyridylamide antagonistes des canaux calciques de type t | |
| MA47043A1 (fr) | Composés indole carboxamides utiles comme inhibiteurs de kinase | |
| MA30339B1 (fr) | Azolopyrimidines inhibitrices de l'activite du recepteur cannabinoïde 1 | |
| MA56019A (fr) | Nouveaux composés et compositions pharmaceutiques associées pour le traitement de maladies | |
| MA40290A1 (fr) | Agents immunorégulateurs | |
| MA29931B1 (fr) | Inhibiteurs de la proteine d'activation de la 5-lipoxygenase (flap) | |
| MA33419B1 (fr) | Composés et compositions pour le traitement de maladies parasitaires | |
| MA28660B1 (fr) | Composes et compositions en tant que modulateurs de ppar | |
| MA46665B1 (fr) | Composés de tyrosine tyrosine de peptide cyclique couplés à un anticorps en tant que modulateurs des récepteurs du neuropeptide y | |
| MX2023003677A (es) | Inhibidores de hidroxiesteroide 17beta- deshidrogenasa 13 (hsd17b13) y usos de estos. | |
| MX2023003678A (es) | Inhibidores de hidroxiesteroide 17beta- deshidrogenasa 13 (hsd17b13) y usos de estos. | |
| MA43113A (fr) | Anticorps anti-htr a1 et méthodes d'utilisation de ceux-ci | |
| MA58646A1 (fr) | Tubulysines et conjugués tubulysines-protéines | |
| MA40875B1 (fr) | 2,4-diamino-quinoléine substituée servant de nouveaux agents anticancéreux | |
| MA46611A (fr) | Traitements combinés comprenant des imidazopyrazinones pour le traitement de troubles psychiatriques et/ou cognitifs | |
| WO2017177024A8 (fr) | Méthodes de traitement de troubles oculaires | |
| WO2019018451A3 (fr) | Compositions et méthodes de prévention et de traitement d'effets de proximité induits par rayonnement provoqués par un rayonnement ou une radiothérapie |