MX2017011650A - Inhibidores de kv1.3 y su aplicacion medica. - Google Patents
Inhibidores de kv1.3 y su aplicacion medica.Info
- Publication number
- MX2017011650A MX2017011650A MX2017011650A MX2017011650A MX2017011650A MX 2017011650 A MX2017011650 A MX 2017011650A MX 2017011650 A MX2017011650 A MX 2017011650A MX 2017011650 A MX2017011650 A MX 2017011650A MX 2017011650 A MX2017011650 A MX 2017011650A
- Authority
- MX
- Mexico
- Prior art keywords
- group
- alkyl
- hydrogen
- nr4r5
- heterocycloalkyl
- Prior art date
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- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
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- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
- A61K31/37—Coumarins, e.g. psoralen
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4741—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having oxygen as a ring hetero atom, e.g. tubocuraran derivatives, noscapine, bicuculline
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- 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
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- C07D491/12—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 three hetero rings
- C07D491/14—Ortho-condensed systems
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- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
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- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
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- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
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- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
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- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
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- Immunology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
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- Hematology (AREA)
- Biomedical Technology (AREA)
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- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Obesity (AREA)
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Abstract
La presente invención se refiere a un compuesto de la fórmula general (II) o una sal o solvato del mismo, así como a usos médicos que implican los mismos, en donde (ver Fórmula) A1 se selecciona del grupo que consiste en N y C-R8; A2 se selecciona del grupo que consiste en N y C-R3; A3 se selecciona del grupo que consiste en N y C-R9; A4 y A5 y A6 se seleccionan independientemente del grupo que consiste en N y C-R1; R1 se selecciona del grupo que consiste en hidrógeno, alquilo (C1-C3), halógeno, alcoxi (C1-C3) y haloalquilo (C1-C3); R2 se selecciona del grupo que consiste en hidrógeno, halógeno y alquilo (C1-C3); R3 se selecciona del grupo que consiste en hidrógeno, alquilo (C1-C3), NR4R5, alquil (C1-C3)-NR4R5 y ciano, en donde R4 y R5 se seleccionan independientemente del grupo que consiste en hidrógeno, cicloalquilo (C3-C5), heterocicloalquilo (C3-C5) y alquilo (C1-C3), o R4 y R5, junto con el átomo de nitrógeno al que están unidos, forman un anillo heterocíclico de 5 a 7 miembros, que comprende opcionalmente, además del átomo de nitrógeno antes mencionado, un grupo heteroátomo adicional seleccionado del grupo que consiste en O y NR6, en donde R6 se selecciona del grupo que consiste en hidrógeno, metilo, acetilo y formilo; Y se selecciona del grupo que consiste en O y S; R8 se selecciona del grupo que consiste en alquilo (C1-C4), cicloalquilo (C3-C5) y heterocicloalquilo (C3-C5); y R9 se selecciona del grupo que consiste en hidrógeno, alquilo (C1-C3) y alcoxi (C1-C3); en donde determinados compuestos particulares son excluidos por condiciones, y métodos para producir este tipo de compuestos.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15159080 | 2015-03-13 | ||
| PCT/EP2016/055451 WO2016146583A1 (en) | 2015-03-13 | 2016-03-14 | Kv1.3 inhibitors and their medical application |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX2017011650A true MX2017011650A (es) | 2018-02-09 |
| MX373022B MX373022B (es) | 2020-05-26 |
Family
ID=52736854
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2017011650A MX373022B (es) | 2015-03-13 | 2016-03-14 | Inhibidores de kv1.3 y su aplicacion medica. |
Country Status (28)
| Country | Link |
|---|---|
| US (4) | US10822345B2 (es) |
| EP (1) | EP3268374B1 (es) |
| JP (1) | JP6506409B2 (es) |
| KR (1) | KR20170137056A (es) |
| CN (1) | CN107548397B (es) |
| AU (1) | AU2016232338B2 (es) |
| BR (1) | BR112017019439A2 (es) |
| CA (1) | CA2979503A1 (es) |
| CY (1) | CY1122470T1 (es) |
| DK (1) | DK3268374T3 (es) |
| EA (1) | EA037194B1 (es) |
| ES (1) | ES2762938T3 (es) |
| HK (1) | HK1243997B (es) |
| HR (1) | HRP20192258T1 (es) |
| IL (1) | IL254391B (es) |
| LT (1) | LT3268374T (es) |
| MX (1) | MX373022B (es) |
| PH (1) | PH12017501652B1 (es) |
| PL (1) | PL3268374T3 (es) |
| PT (1) | PT3268374T (es) |
| RS (1) | RS59758B1 (es) |
| SG (1) | SG11201707284PA (es) |
| SI (1) | SI3268374T1 (es) |
| SM (1) | SMT201900704T1 (es) |
| TW (1) | TWI701249B (es) |
| UA (1) | UA121493C2 (es) |
| WO (1) | WO2016146583A1 (es) |
| ZA (1) | ZA201705561B (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3133065A1 (en) | 2015-08-21 | 2017-02-22 | Merck Patent GmbH | Compounds for optically active devices |
| EP3363793A1 (en) | 2017-02-15 | 2018-08-22 | Merck Patent GmbH | Hydrophobic compounds for optically active devices |
| EP3363786A1 (en) | 2017-02-15 | 2018-08-22 | Merck Patent GmbH | Compounds for optically active devices |
| CA3075985A1 (en) | 2017-09-20 | 2019-03-28 | Lead Discovery Center Gmbh | Coumarin derivatives, processes for their preparation and uses thereof for the treatment of cancer |
| US10703735B2 (en) | 2018-07-25 | 2020-07-07 | Lead Discovery Center Gmbh | 4-phenyl-coumarin derivatives, processes for their preparation and uses thereof for the treatment of cancer |
| CA3111649A1 (en) * | 2018-09-07 | 2020-03-12 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Tricyclic compounds acting on crbn proteins |
| JP7525507B2 (ja) | 2019-03-20 | 2024-07-30 | リード ディスカバリー センター ゲーエムベーハー | キノリン誘導体、それらの調製のための方法及びがんの治療のためのその使用 |
| KR20230012616A (ko) | 2020-05-20 | 2023-01-26 | 에이엠오 아일랜드 | 광학 활성 장치에 사용하기 위한 아자쿠마린 및 아자티오쿠마린 유도체 |
| CN115960112B (zh) * | 2023-02-03 | 2024-02-20 | 北京大学深圳医院(北京大学深圳临床医学院) | 一种花椒毒醇衍生物及其制备方法和应用 |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS5729765A (en) | 1980-10-08 | 1982-02-17 | Yuuichi Yanagi | Melting of snow on roof |
| US6861405B2 (en) | 2001-06-12 | 2005-03-01 | Yale University | Compositions and methods relating to glucose metabolism, weight control, and food intake |
| AUPS127202A0 (en) | 2002-03-20 | 2002-04-18 | Walter And Eliza Hall Institute Of Medical Research, The | Therapeutic ion channel blocking agents and methods of use thereof |
| US7772408B1 (en) | 2002-08-29 | 2010-08-10 | The Regents Of The University Of California | Substituted 5-alkoxypsoralens as inhibitors of potassium channel activity in lymphocytes and other cells |
| AU2003288925A1 (en) | 2002-10-08 | 2004-05-04 | Massachusetts Institute Of Technology | Compounds for modulation of cholesterol transport |
| ITPD20020325A1 (it) | 2002-12-18 | 2004-06-19 | Consorzio Interuniversitario Nazionale La Chimic | Sintesi di aniline funzionalizzate mono-n-sostituite. |
| CN100486245C (zh) | 2003-07-31 | 2009-05-06 | 中兴通讯股份有限公司 | 一种支持多媒体消息版权保护的多媒体消息业务实现方法 |
| US7557138B2 (en) | 2004-10-04 | 2009-07-07 | The Regents Of The University Of California | 5-phenoxyalkoxypsoralens and methods for selective inhibition of the voltage gated Kv1.3 potassium channel |
| US8063093B2 (en) | 2005-03-15 | 2011-11-22 | Andrew J Harvey | Potassium channel blockers and uses thereof |
| EP1928463A2 (en) | 2005-08-17 | 2008-06-11 | Solvay Pharmaceuticals GmbH | Method of using potassium channel inhibiting compounds |
| US20100239562A1 (en) | 2006-05-22 | 2010-09-23 | The Johns Hopkins University | Kv CHANNELS IN NEURODEGENERATION AND NEUROPROTECTION |
| NZ575685A (en) | 2006-10-04 | 2012-04-27 | Bionomics Ltd | Novel benzofuran potassium channel blockers and uses thereof |
| US8217189B2 (en) | 2006-10-04 | 2012-07-10 | Bionomics Limited | Chromenone potassium channel blockers and uses thereof |
| CN101307056B (zh) * | 2007-05-16 | 2011-04-27 | 中国科学院上海药物研究所 | 线型呋喃香豆素衍生物、其制备方法和用途、以及包含该衍生物的药物组合物 |
| WO2009043117A1 (en) | 2007-10-04 | 2009-04-09 | Bionomics Limited | Novel aryl potassium channel blockers and uses thereof |
| US9114102B2 (en) | 2007-11-07 | 2015-08-25 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Method of inhibiting ABCG2 and related treatments |
| EP2303850A4 (en) | 2008-06-13 | 2012-10-31 | Bionomics Ltd | NEW KALIUM CHANNEL BLOCKS AND APPLICATIONS THEREOF |
| GB0815782D0 (en) | 2008-08-29 | 2008-10-08 | Xention Ltd | Novel potassium channel blockers |
| ES2345527B1 (es) | 2008-10-08 | 2011-09-08 | Hospital Clinic I Provincial De Barcelona | Sustancias bloqueadoras de los canales kv 1.3 para el tratamiento de enfermedades asociadas a hiperplasia de la intima. |
| TW201026708A (en) | 2008-12-12 | 2010-07-16 | Solvay Pharm Bv | Spiro azepane-oxazolidinones as Kv1.3 potassium channel blockers |
| WO2010130638A1 (en) | 2009-05-14 | 2010-11-18 | Evotec Ag | Sulfonamide compounds, pharmaceutical compositions and uses thereof |
| CA2774327C (en) | 2009-09-15 | 2019-01-15 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Pharmaceutical compositions which inhibit fkbp52-mediated regulation of androgen receptor function and methods of using same |
| CN102091067B (zh) | 2009-12-09 | 2013-04-10 | 中国科学院上海药物研究所 | 呋喃香豆素类化合物在制备药物中的新用途 |
| WO2011073277A1 (en) | 2009-12-16 | 2011-06-23 | Evotec Ag | PIPERIDINE ARYL SULFONAMIDE DERIVATIVES AS Kv1.3 MODULATORS |
| WO2011073269A1 (en) | 2009-12-16 | 2011-06-23 | Evotec Ag | Piperidine aryl sulfonamide derivatives as kv1.3 modulators |
| WO2011073273A1 (en) | 2009-12-16 | 2011-06-23 | Evotec Ag | Benzoxazine aryl sulfonamide derivatives as kv1.3 modulators |
| US9737585B2 (en) | 2011-03-02 | 2017-08-22 | Bioincept, Llc | Compositions and methods for treatment of intracellular damage and bacterial infection |
| WO2012170917A2 (en) | 2011-06-09 | 2012-12-13 | The Regents Of The University Of California | Reduction of microglia-mediated neurotoxicity by kv1.3 inhibition |
| WO2013052507A1 (en) | 2011-10-03 | 2013-04-11 | The Regents Of The University Of California | TREATMENT OF OBESITY AND OBESITY-RELATED DISORDERS BY PHARMACOLOGICAL TARGETING OF Kv1.3 POTASSIUM CHANNELS |
| CN108779456B (zh) * | 2016-03-31 | 2022-04-05 | 东丽株式会社 | 蛋白质的制造方法 |
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