MA34767B1 - Compositions et procédés pour la modulation de fxr - Google Patents
Compositions et procédés pour la modulation de fxrInfo
- Publication number
- MA34767B1 MA34767B1 MA36062A MA36062A MA34767B1 MA 34767 B1 MA34767 B1 MA 34767B1 MA 36062 A MA36062 A MA 36062A MA 36062 A MA36062 A MA 36062A MA 34767 B1 MA34767 B1 MA 34767B1
- Authority
- MA
- Morocco
- Prior art keywords
- compositions
- methods
- fxr modulation
- fxr
- present
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title 1
- 150000001413 amino acids Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 102000005962 receptors Human genes 0.000 abstract 1
- 108020003175 receptors Proteins 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- 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
- A61K31/46—8-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
- C07D451/06—Oxygen atoms
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- 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
- C07D471/02—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 two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Emergency Medicine (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Endocrinology (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Communicable Diseases (AREA)
- Gynecology & Obstetrics (AREA)
- Ophthalmology & Optometry (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Tropical Medicine & Parasitology (AREA)
- Vascular Medicine (AREA)
- Psychiatry (AREA)
- Dermatology (AREA)
Abstract
La présente invention concerne des composés de Formule (I), un stéréoisomère, énantiomère, sel pharmaceutiquement acceptable ou son conjugué acide aminé ; les variables étant telles que définies présentement ; et leurs compositions pharmaceutiques qui sont utiles comme modulateurs de l'activité de récepteurs du Farnésoïde X (FXR).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201061425189P | 2010-12-20 | 2010-12-20 | |
| US201161554297P | 2011-11-01 | 2011-11-01 | |
| PCT/US2011/062724 WO2012087519A1 (fr) | 2010-12-20 | 2011-11-30 | Compositions et procédés pour la modulation de fxr |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA34767B1 true MA34767B1 (fr) | 2013-12-03 |
Family
ID=45349296
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA36062A MA34767B1 (fr) | 2010-12-20 | 2013-06-28 | Compositions et procédés pour la modulation de fxr |
Country Status (39)
| Country | Link |
|---|---|
| US (2) | US9150568B2 (fr) |
| EP (1) | EP2655370B1 (fr) |
| JP (1) | JP5740483B2 (fr) |
| KR (1) | KR101626046B1 (fr) |
| CN (1) | CN103443099B (fr) |
| AP (1) | AP3414A (fr) |
| AR (1) | AR084425A1 (fr) |
| AU (1) | AU2011345233B2 (fr) |
| BR (1) | BR112013015452B1 (fr) |
| CA (1) | CA2819825C (fr) |
| CL (1) | CL2013001677A1 (fr) |
| CO (1) | CO6801729A2 (fr) |
| CR (1) | CR20130307A (fr) |
| CU (1) | CU24152B1 (fr) |
| CY (1) | CY1119530T1 (fr) |
| DK (1) | DK2655370T3 (fr) |
| EA (1) | EA025569B1 (fr) |
| ES (1) | ES2645728T3 (fr) |
| GT (1) | GT201300159A (fr) |
| HR (1) | HRP20171615T1 (fr) |
| HU (1) | HUE034150T2 (fr) |
| IL (1) | IL226853A (fr) |
| JO (1) | JO3297B1 (fr) |
| LT (1) | LT2655370T (fr) |
| MA (1) | MA34767B1 (fr) |
| MX (1) | MX338845B (fr) |
| MY (1) | MY163216A (fr) |
| NZ (1) | NZ613234A (fr) |
| PE (1) | PE20140207A1 (fr) |
| PH (1) | PH12013501256A1 (fr) |
| PL (1) | PL2655370T3 (fr) |
| PT (1) | PT2655370T (fr) |
| RS (1) | RS56335B1 (fr) |
| SG (1) | SG191046A1 (fr) |
| SI (1) | SI2655370T1 (fr) |
| TW (1) | TWI427078B (fr) |
| UY (1) | UY33815A (fr) |
| WO (1) | WO2012087519A1 (fr) |
| ZA (1) | ZA201304044B (fr) |
Families Citing this family (115)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014500318A (ja) * | 2010-12-20 | 2014-01-09 | アイアールエム・リミテッド・ライアビリティ・カンパニー | ファルネソイドx受容体を調節するための組成物および方法 |
| CU24152B1 (es) * | 2010-12-20 | 2016-02-29 | Irm Llc | 1,2 oxazol-8-azabiciclo[3,2,1]octano 8 il como moduladores de fxr |
| EP2545964A1 (fr) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Nouveaux composés se liant au fxr (nr1 h4) et modulant son activité |
| AU2013266398A1 (en) | 2012-05-22 | 2015-01-22 | Genentech, Inc. | N-substituted benzamides and their use in the treatment of pain |
| CN103007081B (zh) * | 2012-11-27 | 2013-12-04 | 鞠法红 | 一种治疗非酒精性脂肪肝的中药组合物 |
| WO2014138692A1 (fr) | 2013-03-07 | 2014-09-12 | Califia Bio, Inc. | Inhibiteurs de kinases de lignée mixte et procédés thérapeutiques |
| TN2016000143A1 (en) * | 2013-11-05 | 2017-10-06 | Novartis Ag | Compositions and methods for modulating farnesoid x receptors. |
| US10208081B2 (en) | 2014-11-26 | 2019-02-19 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as FXR/TGR5 agonists and methods of use thereof |
| EP3034499A1 (fr) | 2014-12-17 | 2016-06-22 | Gilead Sciences, Inc. | Nouveaux composés de modulation (FXR NR1H4) |
| EP3034501A1 (fr) | 2014-12-17 | 2016-06-22 | Gilead Sciences, Inc. | Hydroxy contenant des composés de modulation (FXR NR1H4) |
| RU2017125365A (ru) * | 2014-12-18 | 2019-01-21 | Новартис Аг | Производные азабициклооктана в качестве агонистов fxr для применения при лечении заболеваний печени и желудочно-кишечных заболеваний |
| TWI698430B (zh) | 2015-02-13 | 2020-07-11 | 南北兄弟藥業投資有限公司 | 三環化合物及其在藥物中的應用 |
| JP6785788B2 (ja) | 2015-03-31 | 2020-11-18 | エナンタ ファーマシューティカルズ インコーポレイテッド | Fxr/tgr5アゴニストとしての胆汁酸誘導体およびその使用方法 |
| CN106146483A (zh) * | 2015-04-23 | 2016-11-23 | 上海迪诺医药科技有限公司 | 杂环类法尼酯衍生物x受体调节剂 |
| CN106946867B (zh) * | 2016-01-06 | 2019-11-12 | 广州市恒诺康医药科技有限公司 | Fxr受体调节剂及其制备方法和用途 |
| WO2017133521A1 (fr) * | 2016-02-01 | 2017-08-10 | 山东轩竹医药科技有限公司 | Agoniste du récepteur fxr |
| CA3012583A1 (fr) * | 2016-02-08 | 2017-08-17 | Redx Pharma Plc | Composes heterocycliques, en particulier derives de 2-oxo -4,4,5,5,6,6,7,7-octahydrobenzoxazole, et leur utilisation en tant que composes antibacteriens |
| EP3419625B1 (fr) * | 2016-02-22 | 2021-04-07 | Novartis AG | Méthodes d'utilisation d'agonistes de fxr |
| US11110083B2 (en) * | 2016-02-22 | 2021-09-07 | Novartis Ag | Methods for treating liver disorders using FXR agonists |
| HK1257648A1 (zh) | 2016-02-22 | 2019-10-25 | Novartis Ag | Fxr促效剂之使用方法 |
| WO2017189652A1 (fr) | 2016-04-26 | 2017-11-02 | Enanta Pharmaceuticals, Inc. | Dérivés d'isoxazole utilisés comme agonistes de fxr et leurs procédés d'utilisation |
| US10080742B2 (en) | 2016-04-26 | 2018-09-25 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use thereof |
| WO2017189663A1 (fr) | 2016-04-26 | 2017-11-02 | Enanta Pharmaceuticals, Inc. | Dérivés d'isoxazole utilisés comme agonistes de fxr et leurs méthodes d'utilisation |
| US10138228B2 (en) | 2016-05-18 | 2018-11-27 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use therof |
| WO2017201155A1 (fr) * | 2016-05-18 | 2017-11-23 | Enanta Pharmaceuticals, Inc. | Dérivés d'isoxazole utilisés comme agonistes de fxr et leurs méthodes d'utilisation |
| WO2017201150A1 (fr) * | 2016-05-18 | 2017-11-23 | Enanta Pharmaceuticals, Inc. | Analogues de l'isoxazole comme agonistes de fxr et leurs procédés d'utilisation |
| CA2968836C (fr) | 2016-06-13 | 2025-09-02 | Gilead Sciences, Inc. | Composes modulant fxr (nr1h4) |
| AR108711A1 (es) * | 2016-06-13 | 2018-09-19 | Gilead Sciences Inc | Compuestos moduladores de fxr (nr1h4) |
| JP6678779B2 (ja) | 2016-06-13 | 2020-04-08 | ギリアード サイエンシーズ, インコーポレイテッド | Fxr(nr1h4)調節化合物 |
| TW201808283A (zh) | 2016-08-05 | 2018-03-16 | 廣東東陽光藥業有限公司 | 含氮三環化合物及其在藥物中的應用 |
| JP7093341B2 (ja) | 2016-08-23 | 2022-06-29 | アルデリックス, インコーポレイテッド | 代謝異常状態及び代謝障害を治療するためのホルモン受容体調節薬 |
| WO2018039384A1 (fr) * | 2016-08-23 | 2018-03-01 | Ardelyx, Inc. | Composés d'isoxazolyl-carbonyloxy azabicyclo [3.2.1] octane en tant qu'activateurs de fxr |
| CN108495850B (zh) | 2016-08-31 | 2021-11-26 | 江苏恒瑞医药股份有限公司 | 氧代吡啶酰胺类衍生物、其制备方法及其在医药上的应用 |
| JOP20190040A1 (ar) * | 2016-09-14 | 2019-03-10 | Novartis Ag | توليفة من ناهضات fxr |
| CA3036757A1 (fr) * | 2016-09-14 | 2018-03-22 | Novartis Ag | Nouveaux regimes d'agonistes de fxr |
| CN108430998B (zh) * | 2016-09-28 | 2021-07-09 | 四川科伦博泰生物医药股份有限公司 | 氮杂双环衍生物及其制备方法和用途 |
| CN109906223A (zh) * | 2016-10-04 | 2019-06-18 | 英安塔制药有限公司 | 异噁唑类似物作为fxr激动剂及其使用方法 |
| US10597391B2 (en) | 2016-10-26 | 2020-03-24 | Enanta Pharmaceuticals, Inc. | Urea-containing isoxazole derivatives as FXR agonists and methods of use thereof |
| CN108017636A (zh) * | 2016-11-04 | 2018-05-11 | 合帕吉恩治疗公司 | 作为fxr调节剂的含氮杂环化合物 |
| WO2018153933A1 (fr) | 2017-02-21 | 2018-08-30 | Genfit | Combinaison d'un agoniste ppar avec un agoniste fxr |
| EP4122464B1 (fr) | 2017-03-28 | 2024-05-15 | Gilead Sciences, Inc. | Combinaisons thérapeutiques pour le traitement des maladies du foie |
| HRP20220026T1 (hr) | 2017-04-12 | 2022-04-01 | Il Dong Pharmaceutical Co., Ltd. | Derivati izoksazola kao agonisti nuklearnog receptora i njihove uporabe |
| WO2018190643A1 (fr) * | 2017-04-12 | 2018-10-18 | Il Dong Pharmaceutical Co., Ltd. | Dérivés d'isoxazole en tant qu'agonistes du récepteur nucléaire et leur utilisation |
| CN109265471B (zh) * | 2017-06-30 | 2021-06-04 | 轩竹生物科技有限公司 | Fxr受体激动剂 |
| CA3068928C (fr) * | 2017-07-06 | 2022-05-31 | Xuanzhu (Hainan) Biopharmaceutical Co., Ltd. | Agoniste fxr |
| CN109320517B (zh) * | 2017-07-31 | 2021-08-17 | 轩竹生物科技有限公司 | Fxr受体激动剂 |
| AR114930A1 (es) * | 2017-09-12 | 2020-11-11 | Novartis Ag | Composición farmacéutica |
| WO2019055808A1 (fr) * | 2017-09-14 | 2019-03-21 | Ardelyx, Inc. | Modulateurs du récepteur hormonal pour le traitement d'états et de troubles métaboliques mutagènes et fibrotiques |
| AU2018360577A1 (en) * | 2017-11-01 | 2020-06-18 | Bristol-Myers Squibb Company | Bridged bicyclic compounds as farnesoid X receptor modulators |
| WO2019089664A1 (fr) | 2017-11-01 | 2019-05-09 | Bristol-Myers Squibb Company | Composés multicycliques en tant que modulateurs du récepteur farnésoïde x |
| WO2019089670A1 (fr) * | 2017-11-01 | 2019-05-09 | Bristol-Myers Squibb Company | Composés d'alcène utilisés en tant que modulateurs du récepteur farnésoïde x |
| BR112020008157A2 (pt) * | 2017-11-01 | 2020-10-06 | Bristol-Myers Squibb Company | compostos espirocíclicos como moduladores do receptor farnesoide x |
| EP3704112B1 (fr) | 2017-11-01 | 2023-09-27 | Bristol-Myers Squibb Company | Composés alkène-spirocycliques en tant que modulateurs du récepteur de farnésoïde x |
| TW201936189A (zh) * | 2017-11-30 | 2019-09-16 | 瑞士商諾華公司 | 用於使用fxr激動劑之方法 |
| WO2019118571A1 (fr) | 2017-12-12 | 2019-06-20 | Enanta Pharmaceuticals, Inc. | Analogues de l'isoxazole utilisés en tant qu'agonistes de fxr et leurs procédés d'utilisation |
| WO2019120088A1 (fr) | 2017-12-22 | 2019-06-27 | 四川科伦博泰生物医药股份有限公司 | Dérivé d'isoxazole, son procédé de préparation et son utilisation |
| CN110128432B (zh) | 2018-02-02 | 2021-03-02 | 广东东阳光药业有限公司 | 含氮三环化合物及其在药物中的应用 |
| US10829486B2 (en) | 2018-02-14 | 2020-11-10 | Enanta Pharmacueticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use thereof |
| US11787828B2 (en) | 2018-03-22 | 2023-10-17 | Viking Therapeutics, Inc. | Crystalline forms and methods of producing crystalline forms of a compound |
| CN110357875B (zh) * | 2018-04-10 | 2022-06-21 | 浙江海正药业股份有限公司 | 氮杂双环辛烷类衍生物、其制备方法及其在医药上的用途 |
| KR20210015849A (ko) | 2018-05-31 | 2021-02-10 | 노파르티스 아게 | 트로피펙소르 및 세니크리비록을 포함하는 조합물 |
| CA3045644C (fr) | 2018-06-13 | 2024-01-16 | Pfizer Inc. | Antagonistes du recepteur glp-1 et leurs utilisations |
| WO2020001304A1 (fr) * | 2018-06-26 | 2020-01-02 | 轩竹(海南)医药科技有限公司 | Agoniste du récepteur fxr |
| WO2020011146A1 (fr) * | 2018-07-11 | 2020-01-16 | 中国医药研究开发中心有限公司 | Composés 1,2,4-oxadiazole, leur procédé de préparation et utilisation médicale associée |
| AU2019309727B2 (en) | 2018-07-25 | 2021-12-23 | Novartis Ag | NLRP3 inflammasome inhibitors |
| EP3981467A1 (fr) * | 2018-08-08 | 2022-04-13 | Inorbit Therapeutics Ab | Composés utiles dans la modulation du récepteur farnésoïde x et leurs procédés de fabrication et d'utilisation |
| US11254660B2 (en) | 2018-08-31 | 2022-02-22 | Pfizer Inc. | Combinations for treatment of NASH/NAFLD and related diseases |
| WO2020117962A1 (fr) | 2018-12-05 | 2020-06-11 | Viking Therapeutics, Inc. | Compositions pour le traitement de la fibrose et de l'inflammation |
| EP3911647B1 (fr) | 2019-01-15 | 2023-12-13 | Gilead Sciences, Inc. | Composé d'isoxazole comme agoniste de fxr et les compositions pharmaceutiques le comprenant. |
| WO2020156241A1 (fr) | 2019-01-31 | 2020-08-06 | 中国医药研究开发中心有限公司 | Composés cycliques aromatiques ou cycliques hétéroaromatiques, procédé de préparation correspondant et utilisation médicale associée |
| CN113727973B (zh) | 2019-02-15 | 2025-08-29 | 百时美施贵宝公司 | 可用作类法尼醇x受体调节剂的取代酰胺化合物 |
| AR118050A1 (es) | 2019-02-15 | 2021-09-15 | Bristol Myers Squibb Co | Compuestos bicíclicos sustituidos como moduladores del receptor farnesoide x |
| AU2020221371A1 (en) | 2019-02-15 | 2021-10-07 | Bristol-Myers Squibb Company | Substituted amide compounds useful as farnesoid x receptor modulators |
| CN113677666A (zh) | 2019-02-15 | 2021-11-19 | 百时美施贵宝公司 | 作为类法尼醇x受体调节剂的经取代的双环化合物 |
| AU2020225225B2 (en) | 2019-02-19 | 2022-12-22 | Gilead Sciences, Inc. | Solid forms of FXR agonists |
| JP2022524820A (ja) * | 2019-03-13 | 2022-05-10 | ノバルティス アーゲー | 医薬組成物 |
| CN111825667B (zh) * | 2019-04-19 | 2023-07-25 | 中国科学院上海药物研究所 | Fxr小分子激动剂及其制备方法和用途 |
| KR20250076664A (ko) | 2019-04-19 | 2025-05-29 | 상하이 인스티튜트 오브 마테리아 메디카 차이니즈 아카데미 오브 싸이언시즈 | Fxr 소분자 작용제 및 이의 제조 방법과 용도 |
| CN111825701B (zh) * | 2019-04-19 | 2023-12-08 | 正大天晴药业集团股份有限公司 | 含苯并噻唑的三环类fxr调节剂化合物 |
| WO2020231917A1 (fr) | 2019-05-13 | 2020-11-19 | Enanta Pharmaceuticals, Inc. | Dérivés d'isoxazole utilisés en tant qu'agonistes de fxr et leurs procédés d'utilisation |
| UY38687A (es) | 2019-05-17 | 2023-05-15 | Novartis Ag | Inhibidores del inflamasoma nlrp3, composiciones, combinaciones de los mismos y métodos para su uso |
| EP3972596B1 (fr) * | 2019-05-20 | 2025-07-16 | Pfizer Inc. | Combinaisons comprenant du benzodioxol en tant qu'agonistes de glp-1r destinées à être utilisées dans le traitement de la nash/nafld et de maladies associées |
| US20220241376A1 (en) | 2019-07-18 | 2022-08-04 | Enyo Pharma | Method for decreasing adverse-effects of interferon |
| AU2020316740A1 (en) | 2019-07-23 | 2022-01-27 | Novartis Ag | Treatment comprising FXR agonists |
| TW202114672A (zh) | 2019-07-23 | 2021-04-16 | 瑞士商諾華公司 | 使用fxr促效劑的肝臟疾病之組合治療 |
| WO2021044351A1 (fr) | 2019-09-06 | 2021-03-11 | Novartis Ag | Procédés de traitement d'une maladie hépatique à l'aide d'inhibiteurs de lta4h |
| JP2022548617A (ja) | 2019-09-19 | 2022-11-21 | ノバルティス アーゲー | Fxrアゴニストを含む処置 |
| JP2022550312A (ja) | 2019-09-30 | 2022-12-01 | ノバルティス アーゲー | Fxrアゴニストの使用を含む処置 |
| CN114728954B (zh) * | 2019-11-29 | 2023-10-17 | 广东东阳光药业股份有限公司 | Tropifexor的新晶型及其制备方法 |
| CN114728955A (zh) * | 2019-11-29 | 2022-07-08 | 广东东阳光药业有限公司 | Tropifexor的新晶型及其制备方法 |
| WO2021108974A1 (fr) | 2019-12-03 | 2021-06-10 | Gannex Pharma Co., Ltd | Composés pour moduler l'activité du fxr et leurs utilisations |
| AU2020402177A1 (en) | 2019-12-10 | 2022-06-16 | Pfizer Inc. | Solid forms of 2-((4-((s)-2-(5-chloropyridin-2-yl)-2-methylbenzo(d) (1,3)dioxol-4-yl)piperidin-1-yl)methyl)-1-(((s)-oxetan-2-yl)methyl)-1h-benzo(d) imidazole-6-carboxylic acid, 1,3-dihydroxy-2-(hydroxymethyl)propan-2-amine salt |
| CN114929219A (zh) | 2019-12-20 | 2022-08-19 | 诺华股份有限公司 | 使用整联蛋白抑制剂组合治疗肝脏疾病 |
| WO2021133948A1 (fr) | 2019-12-23 | 2021-07-01 | Axcella Health Inc. | Compositions et méthodes pour le traitement de maladies et de troubles hépatiques |
| CN114945361A (zh) | 2020-01-15 | 2022-08-26 | 法国国家卫生及研究医学协会 | Fxr激动剂在治疗丁型肝炎病毒感染中的用途 |
| BR112022017578A2 (pt) | 2020-03-27 | 2022-10-18 | Pfizer | Tratamento do diabetes tipo 2 ou obesidade ou sobrepeso com ácido 2-[(4-{6-[(4-ciano-2-fluorobenzil)óxi]piridin-2-il}piperidin-1-il)metil]-1-[(2s)-oxetan-2-ilmetil]-1h-benzimidazol-6-carboxílico ou um sal farmacêutico do mesmo |
| WO2021233461A1 (fr) * | 2020-05-22 | 2021-11-25 | 苏州晶云药物科技股份有限公司 | Nouvelle forme cristalline d'un composé benzothiazole et son procédé de préparation |
| EP4161925A4 (fr) * | 2020-06-09 | 2024-09-04 | Viking Therapeutics, Inc. | Compositions et méthodes de traitement de troubles hépatiques |
| IL301285A (en) | 2020-09-10 | 2023-05-01 | Precirix N V | A portion of an antibody against FAP |
| CN114315830B (zh) * | 2020-09-30 | 2025-08-12 | 中国科学院上海药物研究所 | Fxr小分子激动剂及其制备方法和用途 |
| US20240100125A1 (en) | 2021-01-14 | 2024-03-28 | Enyo Pharma | Synergistic effect of a fxr agonist and ifn for the treatment of hbv infection |
| CN113024552B (zh) * | 2021-03-26 | 2022-08-05 | 厦门市博瑞来医药科技有限公司 | 一类新型非甾体fxr激动剂的合成及其应用 |
| EP4329761A1 (fr) | 2021-04-28 | 2024-03-06 | ENYO Pharma | Potentialisation forte d'effets d'agonistes de tlr3 à l'aide d'agonistes de fxr en tant que traitement combiné |
| CN113292555B (zh) * | 2021-04-28 | 2022-03-18 | 武汉纽瑞斯医药科技有限公司 | 一种Tropifexor的制备方法 |
| MX2024002613A (es) | 2021-08-31 | 2024-03-22 | Pfizer | Formas solidas de acido 2-[(4-{6-[(4-ciano-2-fluorobencil)oxi]piri din-2-il}piperidin-1-il)metil]-1-[(2s)-oxetan-2-ilmetil]-1h-benci midazol-6-carboxilico, sal de 1,3-dihidroxi-2-(hidroximetil)propan -2-amina. |
| US12443426B2 (en) | 2021-12-07 | 2025-10-14 | Nutanix, Inc. | Techniques for switching device implementations for virtual devices |
| ES3029434T3 (en) * | 2022-03-16 | 2025-06-24 | Cascade Pharmaceuticals Inc | A fxr small molecule agonist, the preparation and use thereof |
| WO2023203135A1 (fr) | 2022-04-22 | 2023-10-26 | Precirix N.V. | Anticorps radiomarqué amélioré |
| WO2023213801A1 (fr) | 2022-05-02 | 2023-11-09 | Precirix N.V. | Pré-ciblage |
| WO2023228023A1 (fr) | 2022-05-23 | 2023-11-30 | Pfizer Inc. | Traitement du diabète de type 2 ou contrôle de la gestion du poids avec de l'acide 2-((4-((s)-2-(5-chloropyridin-2-yl)-2-méthylbenzo[d][1,3]dioxol-4-yl)pipéridin-1-yl)méthyl)-1-(((s)-oxétan-2-yl)méthyl)-1h-benzo[d]imidazole-6-carboxylique ou un sel pharmaceutique de celui-ci |
| TW202408494A (zh) * | 2022-06-30 | 2024-03-01 | 南韓商日東製藥股份有限公司 | 異噁唑衍生物及其鹽的新晶型以及包括其之醫藥組合物 |
| UY40374A (es) | 2022-08-03 | 2024-02-15 | Novartis Ag | Inhibidores de inflamasoma nlrp3 |
| EP4495125A1 (fr) * | 2023-07-19 | 2025-01-22 | Freie Universität Berlin | Procédé de synthèse sans catalyseur pour introduire un fragment trifluorométhoxy dans au moins un composé organique |
| WO2025099561A1 (fr) | 2023-11-07 | 2025-05-15 | Pfizer Inc. | Formulations de matrice à libération contrôlée orales d'acide 2-[(4-{6-[(4-cyano-2-fluorobenzyl)oxy]pyridin-2-yl}pipéridin-1-yl)méthyl]-1-[(2s)-oxétan-2-ylméthyl]-1h-benzimidazole-6-carboxylique ou d'un sel pharmaceutiquement acceptable de celui-ci |
| WO2025224648A1 (fr) | 2024-04-26 | 2025-10-30 | Pfizer Inc. | Compositions/formulations orales de l'acide 2-({4-[(2s)-2-(4-chloro-2-fluorophényl)-2-méthyl-1,3-benzodioxol-4-yl]pipéridin-1-yl}méthyl)-1-[(2s)-oxétan-2-ylméthyl]-1h-benzimidazole-6-carboxylique ou d'un sel pharmaceutiquement acceptable de celui-ci |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT72878B (en) | 1980-04-24 | 1983-03-29 | Merck & Co Inc | Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents |
| JPH0672123B2 (ja) | 1986-08-21 | 1994-09-14 | セントラル硝子株式会社 | トリフルオロメチル基を有するシクロヘキサンカルボン酸の製造方法 |
| US7319109B2 (en) | 2002-11-22 | 2008-01-15 | Smith Kline Beecham Corporation | Farnesoid X receptor agonists |
| JP2007524596A (ja) | 2003-02-28 | 2007-08-30 | トランスフォーム・ファーマシューティカルズ・インコーポレイテッド | 共結晶医薬組成物 |
| AU2006311422A1 (en) | 2005-11-09 | 2007-05-18 | Memory Pharmaceuticals Corporation | 1 h-indazoles, benzothiazoles, 1,2-benzoisoxazoles, 1,2-benzoisothiazoles, and chromones and preparation and uses thereof |
| BRPI0619126A2 (pt) | 2005-12-02 | 2011-09-13 | Pfizer Ltd | derivados espirocìclicos, composição farmacêutica e usos dos mesmos |
| US7863302B2 (en) * | 2006-02-03 | 2011-01-04 | Eli Lilly And Company | Compounds and methods for modulating FX-receptors |
| JP2007230909A (ja) * | 2006-03-01 | 2007-09-13 | Univ Of Tokyo | 置換イソキサゾール誘導体 |
| AR061101A1 (es) | 2006-05-24 | 2008-08-06 | Lilly Co Eli | Compuesto de fenil-triazolil- metoxi- arilo, su uso para la manufactura de un medicamento y composicion farmaceutica que lo comprende |
| EP1894924A1 (fr) * | 2006-08-29 | 2008-03-05 | Phenex Pharmaceuticals AG | Composés hétérocycliques de liason du FXR |
| KR20100044810A (ko) * | 2007-07-02 | 2010-04-30 | 글락소스미스클라인 엘엘씨 | 파네소이드 x 수용체 효능제 |
| TW200906823A (en) * | 2007-07-16 | 2009-02-16 | Lilly Co Eli | Compounds and methods for modulating FXR |
| MX2010004450A (es) | 2007-10-22 | 2010-05-05 | Schering Corp | Derivados heterociclo biciclicos y su uso como moduladores de la actividad de gpr119. |
| EP2289883A1 (fr) * | 2009-08-19 | 2011-03-02 | Phenex Pharmaceuticals AG | Nouveaux composés modulant l'activité du recepteur FXR (NR1H4) |
| WO2011053688A1 (fr) | 2009-10-29 | 2011-05-05 | Schering Corporation | Dérivés de pipéridine bicycliques pontés et leurs procédés d'utilisation |
| US20140039007A1 (en) | 2010-12-20 | 2014-02-06 | David C. Tully | Compositions and methods for modulating farnesoid x receptors |
| CU24152B1 (es) * | 2010-12-20 | 2016-02-29 | Irm Llc | 1,2 oxazol-8-azabiciclo[3,2,1]octano 8 il como moduladores de fxr |
| JP2014500318A (ja) | 2010-12-20 | 2014-01-09 | アイアールエム・リミテッド・ライアビリティ・カンパニー | ファルネソイドx受容体を調節するための組成物および方法 |
-
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- 2011-11-30 PE PE2013001456A patent/PE20140207A1/es active IP Right Grant
- 2011-11-30 PL PL11796872T patent/PL2655370T3/pl unknown
- 2011-11-30 CA CA2819825A patent/CA2819825C/fr active Active
- 2011-11-30 KR KR1020137019136A patent/KR101626046B1/ko not_active Expired - Fee Related
- 2011-11-30 SG SG2013043864A patent/SG191046A1/en unknown
- 2011-11-30 NZ NZ61323411A patent/NZ613234A/en not_active IP Right Cessation
- 2011-11-30 BR BR112013015452-7A patent/BR112013015452B1/pt not_active IP Right Cessation
- 2011-11-30 PT PT117968727T patent/PT2655370T/pt unknown
- 2011-11-30 PH PH1/2013/501256A patent/PH12013501256A1/en unknown
- 2011-11-30 SI SI201131307T patent/SI2655370T1/sl unknown
- 2011-11-30 WO PCT/US2011/062724 patent/WO2012087519A1/fr not_active Ceased
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2013
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- 2013-06-28 MA MA36062A patent/MA34767B1/fr unknown
- 2013-07-08 CO CO13160561A patent/CO6801729A2/es not_active Application Discontinuation
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2015
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2017
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