MX2009013946A - Agonistas del receptor de farnesoide x. - Google Patents
Agonistas del receptor de farnesoide x.Info
- Publication number
- MX2009013946A MX2009013946A MX2009013946A MX2009013946A MX2009013946A MX 2009013946 A MX2009013946 A MX 2009013946A MX 2009013946 A MX2009013946 A MX 2009013946A MX 2009013946 A MX2009013946 A MX 2009013946A MX 2009013946 A MX2009013946 A MX 2009013946A
- Authority
- MX
- Mexico
- Prior art keywords
- fxr
- compounds
- relates
- present
- farnesoid
- Prior art date
Links
Classifications
-
- 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
- C07D413/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- C07D413/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D417/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
Abstract
La presente invención se refiere a receptores de farnesoide X (FXR, NR1H4) FXR es un miembro de la clase receptora nuclear de los factores de transcripción activos del ligando. Más particularmente, la presente invención se refiere a compuestos útiles como agonistas para FXR, formulaciones farmacéuticas que comprenden dichos compuestos, y el uso terapéutico de los mismos. Los compuestos novedosos de isoxazol se describen como parte de las composiciones farmacéuticas para el tratamiento de un padecimiento portado por la actividad disminuida del FXR, tal como obesidad, diabetes, enfermedad del hígado colestático, fibrosis del hígado, y síndrome metabólico.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US94754807P | 2007-07-02 | 2007-07-02 | |
PCT/US2008/066817 WO2009005998A1 (en) | 2007-07-02 | 2008-06-13 | Farnesoid x receptor agonists |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009013946A true MX2009013946A (es) | 2010-03-10 |
Family
ID=40226450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009013946A MX2009013946A (es) | 2007-07-02 | 2008-06-13 | Agonistas del receptor de farnesoide x. |
Country Status (11)
Country | Link |
---|---|
US (1) | US20110034507A1 (es) |
EP (1) | EP2173174A4 (es) |
JP (1) | JP2010532363A (es) |
KR (1) | KR20100044810A (es) |
CN (1) | CN101877966A (es) |
AU (1) | AU2008270784A1 (es) |
BR (1) | BRPI0812851A2 (es) |
CA (1) | CA2690406A1 (es) |
EA (1) | EA200901662A1 (es) |
MX (1) | MX2009013946A (es) |
WO (1) | WO2009005998A1 (es) |
Families Citing this family (70)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2010127452A1 (en) * | 2009-05-04 | 2010-11-11 | The Royal Institution For The Advancement Of Learning/Mcgill University | 5-oxo-ete receptor antagonist compounds |
EP2289883A1 (en) | 2009-08-19 | 2011-03-02 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
JP5990187B2 (ja) | 2010-12-16 | 2016-09-07 | ニヴァリス・セラピューティクス・インコーポレーテッド | S−ニトロソグルタチオン還元酵素阻害薬としての新規な置換二環芳香族化合物 |
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 |
CN102120734B (zh) * | 2011-01-30 | 2013-08-07 | 南京理工大学 | 激活醇作为烷基化试剂制备2-(n-烷基)氨基苯并噻唑衍生物的方法 |
EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
WO2013037482A1 (en) | 2011-09-15 | 2013-03-21 | Phenex Pharmaceuticals Ag | Farnesoid x receptor agonists for cancer treatment and prevention |
EP2799425A1 (en) | 2013-04-29 | 2014-11-05 | Esteve Química, S.A. | Preparation process of an agonist of the thrombopoietin receptor |
RS61540B1 (sr) | 2013-09-11 | 2021-04-29 | Inst Nat Sante Rech Med | Postupci i farmaceutske kompozicije za tretiranje infekcije hepatitis b virusa |
WO2015106164A1 (en) | 2014-01-10 | 2015-07-16 | Rgenix, Inc. | Lxr agonists and uses thereof |
JP2017528471A (ja) * | 2014-09-24 | 2017-09-28 | ギリアード サイエンシーズ, インコーポレイテッド | 肝疾患を処置する方法 |
EP3006939A1 (en) | 2014-10-06 | 2016-04-13 | Gilead Sciences, Inc. | Histidine-rich Glycoprotein as a marker for hepatic Farnesoid X receptor activation |
US10208081B2 (en) | 2014-11-26 | 2019-02-19 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as FXR/TGR5 agonists and methods of use thereof |
EP3034501A1 (en) | 2014-12-17 | 2016-06-22 | Gilead Sciences, Inc. | Hydroxy containing FXR (NR1H4) modulating compounds |
EP3034499A1 (en) | 2014-12-17 | 2016-06-22 | Gilead Sciences, Inc. | Novel FXR (NR1H4) modulating compounds |
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 |
SG10201910670RA (en) | 2015-03-31 | 2020-01-30 | Enanta Pharm Inc | Bile acid derivatives as fxr/tgr5 agonists and methods of use thereof |
WO2017133521A1 (zh) * | 2016-02-01 | 2017-08-10 | 山东轩竹医药科技有限公司 | Fxr受体激动剂 |
ES2902404T3 (es) | 2016-02-22 | 2022-03-28 | Novartis Ag | Métodos para utilizar agonistas de fxr. |
WO2017189652A1 (en) | 2016-04-26 | 2017-11-02 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as fxr agonists and methods of use thereof |
WO2017189651A1 (en) | 2016-04-26 | 2017-11-02 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as fxr agonists and methods of use thereof |
US10080743B2 (en) | 2016-04-26 | 2018-09-25 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use thereof |
US10138228B2 (en) | 2016-05-18 | 2018-11-27 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use therof |
US10149835B2 (en) | 2016-05-18 | 2018-12-11 | Elmore Patent Law Group, P.C. | Isoxazole derivatives as FXR agonists and methods of use thereof |
US10144729B2 (en) | 2016-05-18 | 2018-12-04 | Enanta Pharmaceuticals, Inc. | Isoxazole analogs as FXR agonists and methods of use thereof |
ES2921432T3 (es) | 2016-06-13 | 2022-08-25 | Gilead Sciences Inc | Derivados de azetidina como moduladores de FXR (NR1H4) |
CA2968836A1 (en) | 2016-06-13 | 2017-12-13 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
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 |
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 |
BR112019006651A2 (pt) | 2016-10-04 | 2019-07-02 | Enanta Pharm Inc | análogos de isoxazol como agonistas de fxr e métodos de uso do mesmo |
WO2018081285A1 (en) | 2016-10-26 | 2018-05-03 | Enanta Pharmaceuticals, Inc. | Urea-containing isoxazole derivatives as fxr agonists and methods of use thereof |
US10654797B2 (en) | 2016-11-03 | 2020-05-19 | North & South Brother Pharmacy Investment Company Limited | Solid forms of an adamantyl compound, compositions and uses 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 |
CN108218852A (zh) * | 2016-12-15 | 2018-06-29 | 宁波百纳西药业有限公司 | 一种螺环化合物、其制备方法、组合物及用途 |
MX2019009908A (es) | 2017-02-21 | 2019-10-14 | Genfit | Combinacion de un agonista de ppar con un agonista de fxr. |
PL3600309T3 (pl) | 2017-03-28 | 2022-11-07 | Gilead Sciences, Inc. | Skojarzenia terapeutyczne do leczenia chorób wątroby |
EP3600293A1 (en) | 2017-03-30 | 2020-02-05 | Institut National de la Sante et de la Recherche Medicale (INSERM) | Methods and pharmaceutical compositions for reducing persistence and expression of episomal viruses |
WO2018190643A1 (en) * | 2017-04-12 | 2018-10-18 | Il Dong Pharmaceutical Co., Ltd. | An isoxazole derivatives as nuclear receptor agonists and used thereof |
RU2741306C1 (ru) | 2017-04-12 | 2021-01-25 | Ил Дон Фармасьютикал Ко., Лтд. | Производные изоксазола в качестве агонистов ядерных рецепторов и их применение |
AU2018272359B2 (en) * | 2017-05-26 | 2022-03-03 | Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. | Lactam compound as FXR receptor agonist |
CN109575008B (zh) * | 2017-09-29 | 2020-11-17 | 轩竹生物科技有限公司 | Fxr受体激动剂 |
SG11202003830SA (en) | 2017-11-01 | 2020-05-28 | Bristol Myers Squibb Co | Alkene spirocyclic compounds as farnesoid x receptor modulators |
CN111511731B (zh) | 2017-11-01 | 2023-05-23 | 百时美施贵宝公司 | 作为法尼醇x受体调节剂的烯烃化合物 |
EP3704107B1 (en) | 2017-11-01 | 2023-04-12 | Bristol-Myers Squibb Company | Multicyclic compounds as farnesoid x receptor modulators |
EP3704113B1 (en) | 2017-11-01 | 2023-10-11 | Bristol-Myers Squibb Company | Bridged bicyclic compounds as farnesoid x receptor modulators |
EA202091101A1 (ru) | 2017-11-01 | 2020-08-06 | Бристол-Маерс Сквибб Компани | Спироциклические соединения в качестве модуляторов фарнезоидного x-рецептора |
US10689391B2 (en) | 2017-12-12 | 2020-06-23 | Enanta Pharmaceuticals, Inc. | Isoxazole analogs as FXR agonists and methods of use thereof |
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 |
WO2019160813A1 (en) | 2018-02-14 | 2019-08-22 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as fxr agonists and methods of use thereof |
CN108586294A (zh) * | 2018-05-29 | 2018-09-28 | 王若锴 | 一种脲类衍生物及其在防治炎症中的应用 |
KR102605291B1 (ko) * | 2018-09-07 | 2023-11-23 | 메드샤인 디스커버리 아이엔씨. | 트리사이클릭 퓨란에 의해 치환된 피페리디온 화합물 |
CN109096195A (zh) * | 2018-09-27 | 2018-12-28 | 上海雅本化学有限公司 | 一种艾曲波帕的制备方法 |
KR20210097158A (ko) * | 2018-11-26 | 2021-08-06 | 씨에스피씨 종콰이 팔마씨우티컬 테크놀로지 (스자좡) 컴퍼니 리미티드 | Fxr 작용제의 고체 형태, 결정 형태, 및 결정 형태 a, 및 이의 제조방법 및 이의 적용 |
CA3124702A1 (en) | 2019-01-15 | 2020-07-23 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
AR118050A1 (es) | 2019-02-15 | 2021-09-15 | Bristol Myers Squibb Co | Compuestos bicíclicos sustituidos como moduladores del receptor farnesoide x |
JP2022519906A (ja) | 2019-02-19 | 2022-03-25 | ギリアード サイエンシーズ, インコーポレイテッド | Fxrアゴニストの固体形態 |
US11555032B2 (en) | 2019-05-13 | 2023-01-17 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use thereof |
WO2020249064A1 (en) * | 2019-06-14 | 2020-12-17 | Nanjing Ruijie Pharma Co., Ltd. | Compounds for modulating fxr |
AU2020312735A1 (en) | 2019-07-18 | 2021-12-16 | Enyo Pharma | Method for decreasing adverse-effects of interferon |
CN110804025B (zh) * | 2019-11-29 | 2022-02-08 | 扬州工业职业技术学院 | 一种卤代苯异噁唑衍生物及其制备方法与应用 |
CN110922368B (zh) * | 2019-11-29 | 2022-08-16 | 扬州工业职业技术学院 | 一种氯代苯异噁唑氨基苯甲酸衍生物及其制备方法与应用 |
WO2021108974A1 (en) * | 2019-12-03 | 2021-06-10 | Gannex Pharma Co., Ltd | Compounds for modulating activity of fxr and uses thereof |
CN113105443B (zh) * | 2020-01-13 | 2022-10-04 | 中国药科大学 | 异噁唑类fxr受体激动剂、其制备方法和医药用途 |
IL293892A (en) | 2020-01-15 | 2022-08-01 | Inserm Institut National De La Sant? Et De La Rech M?Dicale | Use of fxr agonists to treat hepatitis d virus infection |
WO2022077161A1 (en) * | 2020-10-12 | 2022-04-21 | Gannex Pharma Co., Ltd. | Compounds for modulating activity of fxr and uses thereof |
CN114315815A (zh) * | 2020-10-12 | 2022-04-12 | 甘莱制药有限公司 | 用于调节fxr活性的化合物及其应用 |
AU2022209084A1 (en) | 2021-01-14 | 2023-08-10 | Centre Leon Bérard | 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 |
CA3213217A1 (en) | 2021-04-28 | 2022-11-03 | Raphael Darteil | Strong potentiation of tlr3 agonists effects using fxr agonists as a combined treatment |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9919411D0 (en) * | 1999-08-18 | 1999-10-20 | Zeneca Ltd | Chemical compounds |
ATE381542T1 (de) * | 2001-08-13 | 2008-01-15 | Phenex Pharmaceuticals Ag | Nr1h4-kern-rezeptor-bindende verbindungen |
AU2003290700A1 (en) * | 2002-11-22 | 2004-06-18 | Smithkline Beecham Corporation | Farnesoid x receptor agonists |
-
2008
- 2008-06-13 CA CA2690406A patent/CA2690406A1/en not_active Abandoned
- 2008-06-13 BR BRPI0812851-0A2A patent/BRPI0812851A2/pt not_active IP Right Cessation
- 2008-06-13 MX MX2009013946A patent/MX2009013946A/es not_active Application Discontinuation
- 2008-06-13 EP EP08770928A patent/EP2173174A4/en not_active Withdrawn
- 2008-06-13 CN CN2008801047900A patent/CN101877966A/zh active Pending
- 2008-06-13 AU AU2008270784A patent/AU2008270784A1/en not_active Abandoned
- 2008-06-13 KR KR1020107002455A patent/KR20100044810A/ko not_active Application Discontinuation
- 2008-06-13 US US12/665,772 patent/US20110034507A1/en not_active Abandoned
- 2008-06-13 JP JP2010514955A patent/JP2010532363A/ja not_active Withdrawn
- 2008-06-13 EA EA200901662A patent/EA200901662A1/ru unknown
- 2008-06-13 WO PCT/US2008/066817 patent/WO2009005998A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
BRPI0812851A2 (pt) | 2014-09-30 |
KR20100044810A (ko) | 2010-04-30 |
EP2173174A1 (en) | 2010-04-14 |
WO2009005998A1 (en) | 2009-01-08 |
AU2008270784A1 (en) | 2009-01-08 |
EP2173174A4 (en) | 2010-08-04 |
EA200901662A1 (ru) | 2010-06-30 |
US20110034507A1 (en) | 2011-02-10 |
CA2690406A1 (en) | 2009-01-08 |
CN101877966A (zh) | 2010-11-03 |
JP2010532363A (ja) | 2010-10-07 |
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