AR109295A1 - Compuestos tricíclicos que contienen nitrógeno y usos de los mismos en medicina - Google Patents
Compuestos tricíclicos que contienen nitrógeno y usos de los mismos en medicinaInfo
- Publication number
- AR109295A1 AR109295A1 ARP170102212A ARP170102212A AR109295A1 AR 109295 A1 AR109295 A1 AR 109295A1 AR P170102212 A ARP170102212 A AR P170102212A AR P170102212 A ARP170102212 A AR P170102212A AR 109295 A1 AR109295 A1 AR 109295A1
- Authority
- AR
- Argentina
- Prior art keywords
- independently
- alkyl
- deuterium
- hydroxy
- amino
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- 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
- A61K31/41—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
- A61K31/415—1,2-Diazoles
-
- 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
- A61K31/41—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
-
- 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
- A61K31/41—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
- A61K31/42—Oxazoles
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
- 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
- C07D413/12—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Reproductive Health (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Compuestos tricíclicos que contienen nitrógeno que actúan como moduladores del FXR, o un estereoisómero, un isómero geométrico, un tautómero, un N-óxido, un hidrato, un solvato, un metabolito, una sal aceptable para uso farmacéutico o un profármaco del mismo, y el uso del compuesto para el tratamiento de enfermedades y/o condiciones mediadas por FXR. Además una composición farmacéutica que contiene el compuesto descripto en la presente y un método para el tratamiento de enfermedades y/o condiciones mediadas por FXR que comprende la administración del compuesto o la composición farmacéutica del mismo. Reivindicación 1: Un compuesto que presenta la fórmula (1), o un esteroisómero, un isómero geométrico, un tautómero, un N-óxido, un hidrato, un solvato, un metabolito, una sal aceptable para uso farmacéutico o un profármaco del mismo, donde: T es -NH-, -O-, -S-, -C(=O)- o -CH₂-; cada uno de X e Y es de modo independiente un enlace, -O-, -S(=O)ₜ, -NRˣ-, -CRʸRᶻ- o -C(=O)-, o -X-Y- es -CHRʰ-CHRᵏ- o -CRʸ=CRᶻ-; cada Rˣ es de modo independiente hidrógeno, deuterio, alquilo, aminoalquilo, haloalquilo, cicloalquilo, heterociclilo, arilo, arilo halo sustituido o arilalquilo; cada uno de Rʸ y Rᶻ es de modo independiente hidrógeno, deuterio, F, Cl, Br, I, hidroxi, amino, nitro, ciano, alquilo, haloalquilo, hidroxialquilo, aminoalquilo, alcoxi, alquilamino, alquenilo, alquinilo, cicloalquilo, heterociclilo, arilo, arilo halo sustituido o arilalquilo; o Rʸ y Rᶻ junto con el átomo de carbono adyacente al que están unidos, de modo independiente y opcional forma un anillo de cicloalcano o un anillo heterocíclico, y donde el anillo de cicloalcano y anillo heterocíclico es de modo independiente y opcionalmente sustituido con sustituyentes seleccionados de F, Cl, Br, I, hidroxi, amino, nitro, ciano, metilo, etilo, isopropilo y trifluorometilo; cada Rʰ y Rᵏ es de modo independiente hidrógeno, deuterio, F, Cl, Br, I, hidroxi, amino, nitro, ciano, metilo, etilo, isopropilo o trifluorometilo; o Rʰ y Rᵏ, junto con el átomo de carbón al cual están unido, forman un anillo de cicloalcano o un anillo heterocíclico, donde el anillo cicloalcano y anillo heterocíclico es de modo independiente y opcionalmente sustituido por sustituyentes seleccionados de F, Cl, Br, I, hidroxi, amino, nitro, ciano, metilo, etilo, isopropilo y trifluorometilo; cada Rᵃ y Rᵇ es de modo independiente hidrógeno, deuterio o C₁₋₃ alquilo; cada Rᶜ es de modo independiente hidrógeno, deuterio, F, Cl, Br, I, oxo, hidroxi, amino, nitro, ciano, metilo, etilo, n-propilo, isopropilo, difluorometilo, trifluorometilo, difluorometoxi, trifluorometoxi, hidroximetilo, aminometilo, metilamino, dimetilamino, metoximetilo, isopropoximetilo, vinilo, etinilo, ciclopropilo, ciclobutilo, ciclopentilo, ciclohexilo, azetidinilo, tetrahidrofuranilo, pirrolidinilo, piperidinilo, piperazinilo, tetrahidropiranilo, morfolinilo, tiomorfolinilo, fenilo, tiazolilo, tienilo, oxazolilo, triazolilo, tetrazolilo, piridinilo, pirimidinilo, -COOH, -C(=O)O-C₁₋₃ alquilo, -C(=O)NHS(=O)₂-C₁₋₃ alquilo, -C(=O)NHS(=O)₂-fenilo, -C(=O)NH-C₁₋₃ alquilen-S(=O)₂OH, -C(=O)NH-C₁₋₃ alquilen-C(=O)OH, -S(=O)₂NH₂, -S(=O)₂OH, -S(=O)₂-C₁₋₃ alquilo, -C(=O)NH₂ o -C(=O)N(CH₃)₂; cada R¹ es de modo independiente hidrógeno, deuterio, F, Cl, Br, I, hidroxi, amino, nitro, ciano, alquilo, haloalquilo, hidroxialquilo, aminoalquilo, alcoxi, alquilamino, haloalcoxi, alcoxialquilo, alquenilo, alquinilo, cicloalquilo, cicloalcoxi, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, arilo halo sustituido, arilalquilo, heteroarilo, -L¹-C(=O)OR⁸, -L¹-S(=O)ₜR⁹, -O-L²-C(=O)OR⁸, -O-L²-S(=O)ₜR⁹, -C(=O)NR¹⁰R¹¹, -C(=O)N(R¹⁰)S(=O)₂R⁹, -C(=NR¹⁰)NR¹⁰R¹¹, -C(=O)N(R¹⁰)-L³-S(=O)₂OR⁸, -C(=O)N(R¹⁰)C(=O)OR⁸ o -C(=O)N(R¹⁰)-L³-C(=O)OR⁸; o dos R¹ adyacentes, junto con los átomos del anillo al cual están unidos, de modo independiente y opcional forman un anillo carbocíclico, anillo heterocíclico, anillo aromático o anillo heteroaromático, y donde cada R¹ está de modo independiente y opcionalmente sustituido por uno o más R¹²; cada R⁸ es de modo independiente hidrógeno, deuterio, alquilo, aminoalquilo, alquenilo, alquinilo, haloalquilo, cicloalquilo, heterociclilo o arilo; cada R⁹ es de modo independiente hidrógeno, deuterio, hidroxi, amino, alquilo, aminoalquilo, alquenilo, alquinilo, haloalquilo, cicloalquilo, heterociclilo, arilo o -NR¹⁰R¹¹; cada R¹⁰ y R¹¹ es de modo independiente hidrógeno, deuterio, alquilo, aminoalquilo, alquenilo, alquinilo, haloalquilo, cicloalquilo, heterociclilo o arilo; o R¹⁰ y R¹¹, junto con el átomo de nitrógeno al cual están unido, de modo independiente y opcional forman un anillo heterocíclico o anillo heteroaromático; cada R¹² es de modo independiente hidrógeno, deuterio, F, Cl, Br, I, oxo, hidroxi, amino, nitro, ciano, alquilo, haloalquilo, alcoxi, alquilamino, alquenilo, alquinilo, cicloalquilo, heterociclilo, arilo o heteroarilo; cada L¹ es de modo independiente un enlace, -NH-, -C(=O)-, C₁₋₃ alquileno, C₂₋₄ alquenileno o C₂₋₄ alquinileno; cada L² es de modo independiente C₁₋₃ alquileno, C₂₋₄ alquenileno o C₂₋₄ alquinileno; cada L³ es de modo independiente un enlace o C₁₋₃ alquileno; Z es un compuesto seleccionado del grupo de fórmulas (2); cada L es de modo independiente un enlace, -O-, -S-, -NH-, -CH₂-, -CH₂-CH₂-, -O-CH₂-, -O-CH₂-CH₂- o -CH₂-O-CH₂-; cada R², R³, R⁴, R⁵ y R⁶ es de modo independiente hidrógeno, deuterio, F, Cl, Br, I, hidroxi, amino, nitro, ciano, C₁₋₃ alquilo, C₁₋₃ haloalquilo, C₁₋₃ alcoxi or C₁₋₃ haloalcoxi; cada R⁷ es de modo independiente hidrógeno, deuterio, F, Cl, Br, I, hidroxi, amino, nitro, ciano, C₁₋₆ alquilo, C₁₋₆ hidroxialquilo, C₁₋₆ haloalquilo, C₁₋₆ alcoxi, C₁₋₆ alquilamino, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₃₋₆ cicloalquilo o C₂₋₆ heterociclilo, y donde el C₃₋₆ cicloalquilo y C₂₋₆ heterociclilo está de modo independiente y opcionalmente sustituido por sustituyentes seleccionados de F, Cl, Br, I, hidroxi, amino, nitro y ciano; m es 0, 1, 2, 3 ó 4; n es 0, 1 ó 2; y cada t es de modo independiente 0, 1 ó 2; con la condición que un compuesto que tiene la fórmula (I) no sea un compuesto seleccionado del grupo de fórmulas (3).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610640043 | 2016-08-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR109295A1 true AR109295A1 (es) | 2018-11-14 |
Family
ID=61072781
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP170102212A AR109295A1 (es) | 2016-08-05 | 2017-08-04 | Compuestos tricíclicos que contienen nitrógeno y usos de los mismos en medicina |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US10562910B2 (es) |
| EP (1) | EP3494118B1 (es) |
| JP (1) | JP6983225B2 (es) |
| KR (1) | KR102368298B1 (es) |
| CN (1) | CN107686486B (es) |
| AR (1) | AR109295A1 (es) |
| AU (1) | AU2017306605B2 (es) |
| CA (1) | CA3030377C (es) |
| ES (1) | ES2950412T3 (es) |
| TW (1) | TW201808283A (es) |
| WO (1) | WO2018024224A1 (es) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
| CR20170181A (es) | 2014-10-06 | 2017-05-31 | Exicure Inc | Compuestos anti-tnf |
| CA2981503C (en) | 2015-03-31 | 2023-09-19 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as fxr/tgr5 agonists and methods of use thereof |
| NZ748641A (en) | 2016-06-13 | 2020-04-24 | Gilead Sciences Inc | Fxr (nr1h4) modulating compounds |
| CA2968836C (en) | 2016-06-13 | 2025-09-02 | Gilead Sciences, Inc. | FXR MODULATING COMPOUNDS (NR1H4) |
| MX2019003790A (es) | 2016-10-04 | 2019-09-26 | Enanta Pharm Inc | Analogos de isoxazol como agonistas de fxr y metodos de uso de los mismos. |
| WO2018081285A1 (en) | 2016-10-26 | 2018-05-03 | Enanta Pharmaceuticals, Inc. | Urea-containing isoxazole derivatives as fxr agonists and methods of use thereof |
| SI4122464T1 (sl) | 2017-03-28 | 2024-07-31 | Gilead Sciences, Inc. | Terapevtske kombinacije za zdravljenje bolezni jeter |
| CN111630051B (zh) * | 2017-11-01 | 2023-12-26 | 百时美施贵宝公司 | 作为法尼醇x受体调节剂的烯烃螺环化合物 |
| 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 |
| PT3911647T (pt) | 2019-01-15 | 2024-03-04 | Gilead Sciences Inc | Composto de isoxazole como agonista de fxr e composições farmacêuticas que o contenham |
| 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 |
| WO2020231917A1 (en) | 2019-05-13 | 2020-11-19 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as fxr agonists and methods of use thereof |
| CN110028443B (zh) * | 2019-05-29 | 2022-03-04 | 济南周行医药科技有限公司 | 一种调节fxr活性的三环化合物类药物中间体的制备方法 |
| US20220265614A1 (en) | 2019-07-23 | 2022-08-25 | Novartis Ag | Treatment comprising fxr agonists |
| EP4003349A1 (en) | 2019-07-23 | 2022-06-01 | Novartis AG | Combination treatment of liver diseases using fxr agonists |
| CA3153062A1 (en) | 2019-09-03 | 2021-03-11 | Novartis Ag | Treatment of liver disease or disorder comprising actrii receptor antagonists |
| 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 |
| US12492211B2 (en) | 2019-11-29 | 2025-12-09 | Sunshine Lake Pharma Co., Ltd. | Crystalline form of nitrogen-containing tricyclic compound and use thereof |
| CN112876490A (zh) * | 2019-11-29 | 2021-06-01 | 广东东阳光药业有限公司 | 含氮三环化合物的晶型及其用途 |
| AU2020390308A1 (en) * | 2019-11-29 | 2022-06-09 | Sunshine Lake Pharma Co., Ltd. | Amorphous form of nitrogen-containing tricyclic compound and use thereof |
| CN112876493B (zh) * | 2019-11-29 | 2023-05-09 | 广东东阳光药业有限公司 | 含氮三环化合物的盐及其用途 |
| US20230060422A1 (en) | 2019-12-20 | 2023-03-02 | Novartis Ag | Combination treatment of liver diseases using integrin inhibitors |
| WO2022101853A1 (en) | 2020-11-16 | 2022-05-19 | Novartis Ag | Method of determining liver fibrosis |
| CN115974885A (zh) * | 2021-10-15 | 2023-04-18 | 广东东阳光药业有限公司 | 含氮三环化合物的新晶型及其用途 |
| US20250268871A1 (en) * | 2021-10-15 | 2025-08-28 | Sunshine Lake Pharma Co., Ltd. | New crystal form of nitrogen-containing tricyclic compound and use thereof |
| US20240409549A1 (en) | 2021-10-15 | 2024-12-12 | Sunshine Lake Pharma Co., Ltd. | New crystal form and use of nitrogenous tricyclic compound |
| US20250262191A1 (en) * | 2021-10-15 | 2025-08-21 | Sunshine Lake Pharma Co., Ltd. | New crystal form of nitrogen-containing tricyclic compound and use thereof |
| WO2024140868A1 (zh) * | 2022-12-30 | 2024-07-04 | 广东东阳光药业股份有限公司 | 三环化合物的晶型及其用途 |
| CN118772166B (zh) * | 2023-04-10 | 2026-04-28 | 广东东阳光药业股份有限公司 | 含氮三环化合物的新晶型及其用途 |
| TWI896037B (zh) * | 2023-07-17 | 2025-09-01 | 大陸商上海樞境生物科技有限公司 | 雙環[5,6]咪唑嘧啶酮類衍生物、其製備方法和應用 |
Family Cites Families (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US801249A (en) * | 1904-03-10 | 1905-10-10 | Edward Keagy | Concrete-block mold. |
| JP2002532729A (ja) | 1998-12-23 | 2002-10-02 | グラクソ グループ リミテッド | 核内受容体のリガンドのアッセイ |
| IL146732A0 (en) * | 1999-06-03 | 2002-07-25 | Nippon Suisan Kaisha Ltd | Tricyclic fused heterocycle compounds, process for preparing the same and use thereof |
| ATE381542T1 (de) | 2001-08-13 | 2008-01-15 | Phenex Pharmaceuticals Ag | Nr1h4-kern-rezeptor-bindende verbindungen |
| JP2006515838A (ja) | 2002-11-22 | 2006-06-08 | スミスクライン ビーチャム コーポレーション | ファルネソイドx受容体アゴニスト |
| JP5081161B2 (ja) | 2005-12-19 | 2012-11-21 | スミスクライン ビーチャム コーポレーション | ファルネソイドx受容体アゴニスト |
| CA2640476A1 (en) | 2006-02-03 | 2007-08-16 | 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 |
| BRPI0712262A2 (pt) * | 2006-05-24 | 2012-07-10 | Lilly Co Eli | agonistas de fxr |
| US8106077B2 (en) | 2006-05-24 | 2012-01-31 | Eli Lilly And Company | Compounds and methods for modulating FXR |
| EP1894928A1 (en) | 2006-08-29 | 2008-03-05 | PheneX Pharmaceuticals AG | Heterocyclic fxr binding compounds |
| EP1894924A1 (en) | 2006-08-29 | 2008-03-05 | Phenex Pharmaceuticals AG | Heterocyclic FXR binding compounds |
| CL2007003035A1 (es) | 2006-10-24 | 2008-05-16 | Smithkline Beechman Corp | Compuestos derivados de isoxazol sustituidos, agonistas de receptores farnesoid x; procedimiento de preparacion; composicion farmaceutica que lo comprende; y uso del compuesto en el tratamiento de la obesidad, diabetes mellitus, fibrosis en organos, |
| KR20090094125A (ko) * | 2006-12-08 | 2009-09-03 | 엑셀리시스, 인코포레이티드 | Lxr 및 fxr 조절자 |
| WO2008157270A1 (en) * | 2007-06-13 | 2008-12-24 | Smithkline Beecham Corporation | Farnesoid x receptor agonists |
| CA2690406A1 (en) | 2007-07-02 | 2009-01-08 | Glaxosmithkline Llc | Farnesoid x receptor agonists |
| TW200906823A (en) | 2007-07-16 | 2009-02-16 | Lilly Co Eli | Compounds and methods for modulating FXR |
| EP2128158A1 (en) * | 2008-05-26 | 2009-12-02 | Phenex Pharmaceuticals AG | Heterocyclic cyclopropyl-substituted FXR binding compounds |
| EP2289883A1 (en) | 2009-08-19 | 2011-03-02 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
| JP2014500319A (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 |
| WO2012087520A1 (en) | 2010-12-20 | 2012-06-28 | Irm Llc | 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 |
| EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
| CN104513213A (zh) | 2013-09-28 | 2015-04-15 | 山东亨利医药科技有限责任公司 | Fxr激动剂 |
| CN104045635A (zh) | 2014-06-23 | 2014-09-17 | 华东理工大学 | 3,4,5-三取代异恶唑类化合物及其用途 |
| 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 |
| US20170368038A1 (en) | 2014-12-18 | 2017-12-28 | Novartis Ag | Azabicyclooctane derivatives as fxr agonists for use in the treatment of liver and gastrointestinal diseases |
| WO2016103037A1 (en) * | 2014-12-22 | 2016-06-30 | Akarna Therapeutics, Ltd. | Fused bicyclic compounds for the treatment of disease |
| 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 |
| 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 |
| CN107531721B (zh) * | 2015-04-30 | 2020-07-17 | 诺华股份有限公司 | 用于调节法尼醇x受体的稠合的三环吡唑衍生物 |
| 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 |
| WO2017128896A1 (zh) | 2016-01-26 | 2017-08-03 | 江苏豪森药业集团有限公司 | Fxr激动剂及其制备方法和应用 |
| 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 |
| CN107021957A (zh) | 2016-02-01 | 2017-08-08 | 山东轩竹医药科技有限公司 | Fxr受体激动剂 |
| CN107021958A (zh) | 2016-02-01 | 2017-08-08 | 山东轩竹医药科技有限公司 | Fxr受体激动剂 |
| TW201741307A (zh) | 2016-02-22 | 2017-12-01 | 艾洛斯生物製藥公司 | Fxr調節劑及其使用方法 |
| US10080741B2 (en) | 2016-04-26 | 2018-09-25 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use thereof |
| WO2017189663A1 (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 |
| WO2017201152A1 (en) | 2016-05-18 | 2017-11-23 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as fxr agonists and methods of use thereof |
| WO2017201155A1 (en) | 2016-05-18 | 2017-11-23 | Enanta Pharmaceuticals, Inc. | lSOXAZOLE 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 |
| AR108711A1 (es) | 2016-06-13 | 2018-09-19 | Gilead Sciences Inc | Compuestos moduladores de fxr (nr1h4) |
| NZ748641A (en) | 2016-06-13 | 2020-04-24 | Gilead Sciences Inc | Fxr (nr1h4) modulating compounds |
| MA55632A (fr) | 2016-08-23 | 2022-02-16 | Ardelyx Inc | Procédé de preparation de modulateurs du récepteur hormonal pour le traitement d'états et de troubles métaboliques |
| US11091482B2 (en) | 2016-08-23 | 2021-08-17 | Ardelyx, Inc. | Isoxazolyl-carbonyloxy azabicyclo[3.2.1]octanyl compounds as FXR activators |
| 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 |
| MX2019003790A (es) | 2016-10-04 | 2019-09-26 | Enanta Pharm Inc | Analogos de isoxazol como agonistas de fxr y metodos de uso de los mismos. |
| CN107973790A (zh) | 2016-10-22 | 2018-05-01 | 合帕吉恩治疗公司 | 杂环fxr调节剂 |
| WO2018081285A1 (en) | 2016-10-26 | 2018-05-03 | 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 |
| 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 |
| CN106632294A (zh) | 2016-12-15 | 2017-05-10 | 宁波百纳西药业有限公司 | 一种螺环化合物及其药物用途 |
| CN109071468B (zh) | 2017-01-20 | 2022-09-02 | 四川科伦博泰生物医药股份有限公司 | 一种杂环化合物及其制备方法和用途 |
| CN108341822B (zh) | 2017-01-23 | 2021-04-16 | 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应用 |
| CN108264506B (zh) | 2018-01-17 | 2021-01-26 | 中国药科大学 | 异黄酮衍生物、其制备方法和医药用途 |
| 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 |
-
2017
- 2017-08-01 TW TW106125961A patent/TW201808283A/zh unknown
- 2017-08-02 US US16/322,945 patent/US10562910B2/en active Active
- 2017-08-02 KR KR1020197005041A patent/KR102368298B1/ko active Active
- 2017-08-02 WO PCT/CN2017/095724 patent/WO2018024224A1/en not_active Ceased
- 2017-08-02 CA CA3030377A patent/CA3030377C/en active Active
- 2017-08-02 JP JP2019506117A patent/JP6983225B2/ja active Active
- 2017-08-02 AU AU2017306605A patent/AU2017306605B2/en active Active
- 2017-08-02 CN CN201710653056.0A patent/CN107686486B/zh active Active
- 2017-08-02 EP EP17836406.3A patent/EP3494118B1/en active Active
- 2017-08-02 ES ES17836406T patent/ES2950412T3/es active Active
- 2017-08-04 AR ARP170102212A patent/AR109295A1/es active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| EP3494118A1 (en) | 2019-06-12 |
| CA3030377A1 (en) | 2018-02-08 |
| JP2019524784A (ja) | 2019-09-05 |
| CN107686486A (zh) | 2018-02-13 |
| KR102368298B1 (ko) | 2022-02-28 |
| CA3030377C (en) | 2023-12-12 |
| ES2950412T3 (es) | 2023-10-09 |
| JP6983225B2 (ja) | 2021-12-17 |
| AU2017306605A1 (en) | 2019-02-14 |
| US10562910B2 (en) | 2020-02-18 |
| WO2018024224A1 (en) | 2018-02-08 |
| EP3494118A4 (en) | 2020-02-26 |
| TW201808283A (zh) | 2018-03-16 |
| US20190169203A1 (en) | 2019-06-06 |
| AU2017306605B2 (en) | 2021-08-05 |
| EP3494118B1 (en) | 2023-06-21 |
| CN107686486B (zh) | 2020-12-22 |
| KR20190035766A (ko) | 2019-04-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR109295A1 (es) | Compuestos tricíclicos que contienen nitrógeno y usos de los mismos en medicina | |
| AR116993A2 (es) | Compuestos heterociclos bicíclicos y sus usos en terapia | |
| AR103574A1 (es) | Compuestos tricíclicos y usos de lo mismos en medicina | |
| MX2020010737A (es) | Derivados de sulfamoilarilamida ciclados y su uso como medicamentos para el tratamiento de la hepatitis b. | |
| AR097024A1 (es) | Derivados sustituidos de quinazolin-4-ona | |
| UY36112A (es) | Compuestos de imidazo[4,5-c]quinolin-2-ona y su uso para tratar cáncer | |
| AR101189A1 (es) | Heterociclos nitrogenados antiproliferativos y sus métodos de uso | |
| PE20190709A1 (es) | Derivado de pirazolopiridinaque tiene el efecto agonista del receptor de glp-1 | |
| AR100438A1 (es) | Pirazolopiridinas y pirazolopirimidinas | |
| AR090994A1 (es) | Uracilos sustituidos biciclicamente y uso de los mismos | |
| AR100691A1 (es) | Esteroides neuroactivos, composiciones, y usos de los mismos | |
| AR089143A1 (es) | Triazolopiridinas sustituidas con actividad inhibidora de ttk | |
| MX366123B (es) | Sulfamoil-arilamidas y el uso de las mismas como medicamentos para el tratamiento de la hepatitis b. | |
| AR094300A1 (es) | Derivados de quinolonas | |
| MD20170016A2 (ro) | Compuşi aminopirimidinici ca inhibitori JAK | |
| MX353412B (es) | Derivados de n-fenil-carboxamida y su uso como medicamentos para el tratamiento de la hepatitis b. | |
| AR098666A1 (es) | Compuestos de biarilacetamida y sus métodos de uso | |
| AR094550A1 (es) | Inhibidores de btk | |
| AR100810A1 (es) | Inhibidores de fosfatidilinositol 3-quinasa | |
| AR107042A1 (es) | Inhibidores de la tirosina quinasa de bruton y métodos de su uso | |
| MX389014B (es) | Formas cristalinas de un compuesto inhibidor de jak | |
| AR092809A1 (es) | 3,5-diaminopirazol como inhibidor de quinasa | |
| CR20190261A (es) | Inhibidores de la tirosina quinasa de bruton | |
| EA201401082A1 (ru) | Фармацевтические препараты, содержащие антагонисты ccr3 | |
| AR097756A1 (es) | Derivados de fenilalanina sustituidos |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration |