MX2016000731A - Derivados de espiro [2.4] heptano puenteado substituidos por piperazina, utilizados como agonistas del receptor alx. - Google Patents
Derivados de espiro [2.4] heptano puenteado substituidos por piperazina, utilizados como agonistas del receptor alx.Info
- Publication number
- MX2016000731A MX2016000731A MX2016000731A MX2016000731A MX2016000731A MX 2016000731 A MX2016000731 A MX 2016000731A MX 2016000731 A MX2016000731 A MX 2016000731A MX 2016000731 A MX2016000731 A MX 2016000731A MX 2016000731 A MX2016000731 A MX 2016000731A
- Authority
- MX
- Mexico
- Prior art keywords
- receptor agonists
- substituted bridged
- piperazine substituted
- bridged spiro
- heptane derivatives
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Virology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Epidemiology (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La presente invención se refiere a un derivado de espiro[2.4] heptano puenteado, substituido por piperazina de la fórmula (I), su preparación y su utilización como compuesto farmacéuticamente activo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IB2013055906 | 2013-07-18 | ||
PCT/EP2014/065351 WO2015007830A1 (en) | 2013-07-18 | 2014-07-17 | Piperazine substituted bridged spiro[2.4]heptane derivatives as alx receptor agonists |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2016000731A true MX2016000731A (es) | 2016-04-13 |
MX360699B MX360699B (es) | 2018-11-14 |
Family
ID=51205401
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2016000731A MX360699B (es) | 2013-07-18 | 2014-07-17 | Derivados de espiro [2.4] heptano puenteado substituidos por piperazina, utilizados como agonistas del receptor alx. |
Country Status (13)
Country | Link |
---|---|
US (1) | US9533964B2 (es) |
EP (1) | EP3022188B1 (es) |
JP (1) | JP6330038B2 (es) |
KR (1) | KR20160033747A (es) |
CN (1) | CN105377824B (es) |
AU (1) | AU2014292064B2 (es) |
BR (1) | BR112016001106A8 (es) |
CA (1) | CA2915757A1 (es) |
ES (1) | ES2639798T3 (es) |
MX (1) | MX360699B (es) |
RU (1) | RU2016105310A (es) |
TW (1) | TW201536289A (es) |
WO (1) | WO2015007830A1 (es) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015007830A1 (en) | 2013-07-18 | 2015-01-22 | Actelion Pharmaceuticals Ltd | Piperazine substituted bridged spiro[2.4]heptane derivatives as alx receptor agonists |
AR097279A1 (es) | 2013-08-09 | 2016-03-02 | Actelion Pharmaceuticals Ltd | Derivados de benzimidazolil-metil urea como agonistas del receptor de alx |
KR102375396B1 (ko) | 2014-05-13 | 2022-03-18 | 노파르티스 아게 | 연골형성을 유도하기 위한 화합물 및 조성물 |
JP6746614B2 (ja) | 2015-05-27 | 2020-08-26 | 杏林製薬株式会社 | ウレア誘導体、またはその薬理学的に許容される塩 |
BR112017024966A2 (pt) | 2015-05-27 | 2018-08-07 | Kyorin Seiyaku Kk | derivado de ureia ou sal farmacologicamente aceitável do mesmo |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0708765A4 (en) | 1993-07-16 | 1996-06-26 | Merck & Co Inc | PIPERAZINYLCAMPHER DERIVATIVES SUBSTITUTED AS OXYTOCIN ANTAGONISTS |
CA2399032A1 (en) | 2000-02-04 | 2001-08-09 | The Government Of The United States Of America | Ligands for fpr class receptors that induce a host immune response to a pathogen or inhibit hiv infection |
US20050164305A1 (en) | 2002-04-03 | 2005-07-28 | Bayer Healthcare Ag | Diagnostics and therapeutics for diseases associated with n-formyl peptide receptor like 1 (fprl1) |
BRPI0416272A (pt) | 2003-11-07 | 2007-01-09 | Acadia Pharm Inc | usos do receptor fprl1, e de compostos, uso profilático de compostos, métodos de triagem para um composto capaz de afetar uma ou mais atividades de um receptor fprl1, de tratamento ou prevenção de inflamação, de identificação de um composto de indução de vasodilatação, para antagonismo de uma resposta vasoconstrutiva a um sulfidopeptìdeo leucotrieno em um indivìduo, e para estimulação de proliferação celular em um indivìduo, e, composto |
AR069650A1 (es) | 2007-12-14 | 2010-02-10 | Actelion Pharmaceuticals Ltd | Derivados de aminopirazol como agonistas no peptidicos del receptor alx humano |
CN101903378B (zh) | 2007-12-18 | 2014-03-12 | 埃科特莱茵药品有限公司 | 氨基三唑衍生物 |
MX2011012264A (es) * | 2009-05-18 | 2011-12-12 | Actelion Pharmaceuticals Ltd | Derivados spiro[2.4]heptano puenteados como agonistas del receptor de lipoxina a(alx) y/o de formil peptido tipo 2 (fprl2). |
PL2440555T3 (pl) | 2009-06-09 | 2016-11-30 | Pochodne fluorowanego aminotriazolu | |
CN102803237B (zh) | 2009-06-12 | 2014-09-24 | 埃科特莱茵药品有限公司 | 作为alx受体激动剂的噁唑和噻唑衍生物 |
CA2803920A1 (en) | 2010-06-24 | 2011-12-29 | Richard Beard | Derivatives of cycloalkyl- and cycloalkenyl-1,2-dicarboxylic acid compounds having formyl peptide receptor like-1 (fprl-1) agonist or antagonist activity |
KR101905927B1 (ko) * | 2010-11-17 | 2018-10-08 | 이도르시아 파마슈티컬스 리미티드 | 가교된 스피로[2.4]헵탄 에스테르 유도체 |
AU2011340103A1 (en) | 2010-12-07 | 2013-07-25 | Actelion Pharmaceuticals Ltd. | Hydroxylated aminotriazole derivatives as ALX receptor agonists |
ES2526132T3 (es) | 2010-12-07 | 2015-01-07 | Actelion Pharmaceuticals Ltd. | Derivados de oxazolil-metiléter como agonistas del receptor de ALX |
AU2012282977A1 (en) | 2011-07-11 | 2014-02-06 | Allergan, Inc. | Polycyclic pyrrolidine-2,5-dione derivatives as -formyl peptide receptor like-1 (FPRLl-1) receptor modulators |
CN104284887B (zh) * | 2012-05-16 | 2016-06-22 | 埃科特莱茵药品有限公司 | 作为alx受体激动剂的经1-(对-甲苯基)环丙基取代的桥联螺[2.4]庚烷衍生物 |
MA37618B1 (fr) | 2012-05-16 | 2017-08-31 | Actelion Pharmaceuticals Ltd | Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx |
AU2014225992B2 (en) | 2013-03-06 | 2018-03-22 | Allergan, Inc. | Use of agonists of formyl peptide receptor 2 for treating ocular inflammatory diseases |
CN105007908B (zh) | 2013-03-06 | 2017-10-03 | 阿勒根公司 | 用于治疗皮肤病的甲酰基肽受体2的激动剂的用途 |
WO2015007830A1 (en) | 2013-07-18 | 2015-01-22 | Actelion Pharmaceuticals Ltd | Piperazine substituted bridged spiro[2.4]heptane derivatives as alx receptor agonists |
AR097279A1 (es) | 2013-08-09 | 2016-03-02 | Actelion Pharmaceuticals Ltd | Derivados de benzimidazolil-metil urea como agonistas del receptor de alx |
-
2014
- 2014-07-17 WO PCT/EP2014/065351 patent/WO2015007830A1/en active Application Filing
- 2014-07-17 BR BR112016001106A patent/BR112016001106A8/pt not_active IP Right Cessation
- 2014-07-17 KR KR1020167004127A patent/KR20160033747A/ko not_active Application Discontinuation
- 2014-07-17 TW TW103124607A patent/TW201536289A/zh unknown
- 2014-07-17 AU AU2014292064A patent/AU2014292064B2/en not_active Ceased
- 2014-07-17 JP JP2016526635A patent/JP6330038B2/ja not_active Expired - Fee Related
- 2014-07-17 RU RU2016105310A patent/RU2016105310A/ru unknown
- 2014-07-17 EP EP14739472.0A patent/EP3022188B1/en not_active Not-in-force
- 2014-07-17 CA CA2915757A patent/CA2915757A1/en not_active Abandoned
- 2014-07-17 US US14/905,768 patent/US9533964B2/en not_active Expired - Fee Related
- 2014-07-17 MX MX2016000731A patent/MX360699B/es active IP Right Grant
- 2014-07-17 ES ES14739472.0T patent/ES2639798T3/es active Active
- 2014-07-17 CN CN201480039969.8A patent/CN105377824B/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP3022188A1 (en) | 2016-05-25 |
WO2015007830A1 (en) | 2015-01-22 |
CA2915757A1 (en) | 2015-01-22 |
KR20160033747A (ko) | 2016-03-28 |
TW201536289A (zh) | 2015-10-01 |
BR112016001106A8 (pt) | 2017-12-26 |
BR112016001106A2 (es) | 2017-07-25 |
JP2016525107A (ja) | 2016-08-22 |
CN105377824B (zh) | 2017-08-04 |
CN105377824A (zh) | 2016-03-02 |
MX360699B (es) | 2018-11-14 |
AU2014292064B2 (en) | 2018-07-05 |
RU2016105310A (ru) | 2017-08-23 |
AU2014292064A1 (en) | 2016-03-03 |
EP3022188B1 (en) | 2017-06-07 |
ES2639798T3 (es) | 2017-10-30 |
US20160152584A1 (en) | 2016-06-02 |
US9533964B2 (en) | 2017-01-03 |
JP6330038B2 (ja) | 2018-05-23 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
GB | Transfer or rights |
Owner name: IDORSIA PHARMACEUTICALS LTD |
|
FG | Grant or registration |