AR078552A1 - Derivados de feniloxadiazol como agentes inhibidores de las pgds - Google Patents
Derivados de feniloxadiazol como agentes inhibidores de las pgdsInfo
- Publication number
- AR078552A1 AR078552A1 ARP100103650A ARP100103650A AR078552A1 AR 078552 A1 AR078552 A1 AR 078552A1 AR P100103650 A ARP100103650 A AR P100103650A AR P100103650 A ARP100103650 A AR P100103650A AR 078552 A1 AR078552 A1 AR 078552A1
- Authority
- AR
- Argentina
- Prior art keywords
- compound
- formula
- acid addition
- addition salts
- phenyloxadiazol
- Prior art date
Links
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
- C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
-
- 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
-
- 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
-
- 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
- A61P11/02—Nasal agents, e.g. decongestants
-
- 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
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- 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
- A61P5/00—Drugs for disorders of the endocrine system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/06—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Otolaryngology (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Se refiere a una composicion farmacéutica que comprende el compuesto, compuestos intermedios y a un procedimiento para fabricar dichos compuestos, y al uso del compuesto para tratar trastornos inflamatorios y/o alérgicos, particularmente trastornos tales como rinitis alérgica, asma, enfermedad pulmonar obstructiva cronica (COPD) y degeneracion macular relacionada con la edad (AMD) Reivindicacion 1: Un compuesto de formula (1) en la que R1 es hidrogeno o alquilo C1-6, R2 es hidrogeno, halogeno o alquilo de C1-3, y R3 es hidroxialquilo; o una de sus sales farmacéuticamente aceptables. Reivindicacion 17: Un compuesto de formula 2 o una de sus sales de adicion de ácidos. Reivindicacion 18: Un compuesto de formula 3 o una de sus sales de adicion de ácidos. Reivindicacion 19: Un compuesto de formula 4. Reivindicacion 20: Un compuesto de formula 5. Reivindicacion 22: El compuesto segun la reivindicacion 21 que es de formula 6 o una de sus sales de adicion de ácidos.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24969309P | 2009-10-08 | 2009-10-08 | |
| FR1056094 | 2010-07-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR078552A1 true AR078552A1 (es) | 2011-11-16 |
Family
ID=43606440
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100103650A AR078552A1 (es) | 2009-10-08 | 2010-10-07 | Derivados de feniloxadiazol como agentes inhibidores de las pgds |
Country Status (21)
| Country | Link |
|---|---|
| US (5) | US9469627B2 (es) |
| EP (1) | EP2486024B1 (es) |
| JP (2) | JP5753176B2 (es) |
| KR (1) | KR101701135B1 (es) |
| CN (3) | CN102666508A (es) |
| AR (1) | AR078552A1 (es) |
| AU (1) | AU2010303439B2 (es) |
| BR (1) | BR112012007635B1 (es) |
| CA (1) | CA2776242C (es) |
| DK (1) | DK2486024T3 (es) |
| ES (1) | ES2543011T3 (es) |
| HK (1) | HK1173441A1 (es) |
| IL (1) | IL218967A (es) |
| MA (1) | MA33725B1 (es) |
| MX (1) | MX2012003021A (es) |
| NZ (1) | NZ599099A (es) |
| RU (2) | RU2572608C2 (es) |
| SG (1) | SG179199A1 (es) |
| TW (1) | TWI508960B (es) |
| UY (1) | UY32938A (es) |
| WO (1) | WO2011044307A1 (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2776242C (en) * | 2009-10-08 | 2014-09-02 | Sanofi | Phenyloxadiazole derivatives as pgds inhibitors |
| US9320723B2 (en) * | 2010-05-03 | 2016-04-26 | University Of Rochester | Methods of treating thyroid eye disease |
| BR112018012469B1 (pt) | 2015-12-17 | 2020-11-24 | Astex Therapeutics Limited | compostos quinolina-3-carboxamidas como inibidores da h-pgds, composição farmacêutica compreendendo os ditos compostos e uso terapêutico dos mesmos. |
| JOP20190072A1 (ar) | 2016-10-13 | 2019-04-07 | Glaxosmithkline Ip Dev Ltd | مشتقات 1، 3 سيكلوبوتان ثنائي الاستبدال أو آزيتيدين كمثبطات للإنزيم المخلق للبروستاجلاندين d المكون للدم |
| EP3630738B1 (en) * | 2017-05-22 | 2023-07-19 | Egis Gyógyszergyár Zrt. | Process for the production of ozanimod |
| UY37764A (es) | 2017-06-13 | 2019-01-02 | Glaxosmithkline Ip Dev Ltd | Nuevos compuestos inhibidores de la prostaglandina d sintasa hematopoyética (h-pgds) |
| CA3085293A1 (en) | 2017-12-13 | 2019-06-20 | Glaxosmithkline Intellectual Property Development Limited | Fused pyridines which act as inhibitors of h-pgds |
| JP2022506850A (ja) | 2018-11-08 | 2022-01-17 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッド | 化学化合物 |
| WO2021256569A1 (ja) | 2020-06-19 | 2021-12-23 | 佐藤製薬株式会社 | Ｈ－ｐｇｄｓを阻害する縮環化合物 |
| WO2023113023A1 (ja) * | 2021-12-17 | 2023-06-22 | 佐藤製薬株式会社 | Ｈ－ｐｇｄｓを阻害するアザインドール誘導体 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5176132A (en) | 1989-05-31 | 1993-01-05 | Fisons Plc | Medicament inhalation device and formulation |
| DE10117823A1 (de) * | 2001-04-10 | 2002-10-17 | Merck Patent Gmbh | Oxalsäurederivate |
| MXPA04009095A (es) * | 2002-03-19 | 2004-12-06 | Ono Pharmaceutical Co | Compuesto de acido carboxilico y agente farmaceutico que comprende el compuesto como ingrediente activo. |
| KR20050035885A (ko) | 2002-08-16 | 2005-04-19 | 아벤티스 파마슈티칼스 인크. | 마이크로솜성 프로스타글란딘 ｅ 신타제 또는 조혈성 프로스타글란딘 ｄ 신타제의 활성을 감소시키는 능력에 대해 화합물 또는 제제를 검정하는 방법 |
| GB0222023D0 (en) | 2002-09-21 | 2002-10-30 | Aventis Pharma Ltd | Inhaler |
| WO2005094805A1 (ja) | 2004-04-01 | 2005-10-13 | Institute Of Medicinal Molecular Design. Inc. | イミン誘導体及びアミド誘導体 |
| EP1745047B1 (en) * | 2004-04-21 | 2010-03-24 | Schering Corporation | Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine adenosine-a2a- receptor antagonists |
| JP5209181B2 (ja) * | 2005-03-15 | 2013-06-12 | 富士フイルム株式会社 | 化合物、組成物、位相差板、楕円偏光板および液晶表示装置 |
| TW200720255A (en) | 2005-07-13 | 2007-06-01 | Taiho Pharmaceutical Co Ltd | Benzoimidazole compound capable of inhibiting prostaglandin d synthetase |
| JP2007051121A (ja) * | 2005-07-22 | 2007-03-01 | Taiho Yakuhin Kogyo Kk | プロスタグランジンｄ合成酵素を阻害するピリミジン化合物 |
| CN100556905C (zh) * | 2005-09-08 | 2009-11-04 | 国家南方农药创制中心江苏基地 | 吡唑酰胺类化合物及其中间体和以该类化合物为活性成分的有害生物防治剂 |
| NZ566877A (en) | 2005-09-29 | 2010-05-28 | Sanofi Aventis | Phenyl-1,2,4-oxadiazolone derivatives, processes for their preparation and their use as pharmaceuticals |
| DOP2006000210A (es) * | 2005-10-04 | 2007-06-15 | Aventis Pharma Inc | Compuestos de pirimidina amida como inhibidores de pgds |
| EP2129660A2 (en) | 2006-12-19 | 2009-12-09 | Pfizer Products Inc. | Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases |
| WO2008104869A1 (en) * | 2007-02-26 | 2008-09-04 | Pfizer Products Inc. | Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases |
| NZ579892A (en) | 2007-03-30 | 2012-03-30 | Sanofi Aventis | Pyrimidine hydrazide compounds as prostaglandin D synthase inhibitors |
| GB0706793D0 (en) | 2007-04-05 | 2007-05-16 | Evotec Ag | Compounds |
| TW201034675A (en) * | 2008-12-18 | 2010-10-01 | Sanofi Aventis | Method for treating macular degeneration |
| US9058931B2 (en) | 2009-01-12 | 2015-06-16 | The United States Of America, As Represented By The Secretary Of The Navy | Composite electrode structure |
| CA2776242C (en) * | 2009-10-08 | 2014-09-02 | Sanofi | Phenyloxadiazole derivatives as pgds inhibitors |
-
2010
- 2010-10-07 CA CA2776242A patent/CA2776242C/en active Active
- 2010-10-07 ES ES10765724.9T patent/ES2543011T3/es active Active
- 2010-10-07 BR BR112012007635-3A patent/BR112012007635B1/pt active IP Right Grant
- 2010-10-07 MX MX2012003021A patent/MX2012003021A/es not_active Application Discontinuation
- 2010-10-07 NZ NZ599099A patent/NZ599099A/xx unknown
- 2010-10-07 RU RU2012118756/04A patent/RU2572608C2/ru active
- 2010-10-07 RU RU2015151129A patent/RU2015151129A/ru not_active Application Discontinuation
- 2010-10-07 AR ARP100103650A patent/AR078552A1/es unknown
- 2010-10-07 SG SG2012018933A patent/SG179199A1/en unknown
- 2010-10-07 CN CN201080055808XA patent/CN102666508A/zh active Pending
- 2010-10-07 DK DK10765724.9T patent/DK2486024T3/en active
- 2010-10-07 CN CN201711114032.4A patent/CN107875155A/zh active Pending
- 2010-10-07 JP JP2012533302A patent/JP5753176B2/ja active Active
- 2010-10-07 TW TW099134129A patent/TWI508960B/zh active
- 2010-10-07 WO PCT/US2010/051727 patent/WO2011044307A1/en active Application Filing
- 2010-10-07 AU AU2010303439A patent/AU2010303439B2/en active Active
- 2010-10-07 CN CN201710240652.6A patent/CN106943407A/zh active Pending
- 2010-10-07 EP EP20100765724 patent/EP2486024B1/en active Active
- 2010-10-07 KR KR1020127008972A patent/KR101701135B1/ko active IP Right Grant
- 2010-10-08 UY UY0001032938A patent/UY32938A/es not_active Application Discontinuation
-
2012
- 2012-04-01 IL IL218967A patent/IL218967A/en active IP Right Grant
- 2012-04-04 US US13/439,511 patent/US9469627B2/en active Active
- 2012-05-04 MA MA34835A patent/MA33725B1/fr unknown
-
2013
- 2013-01-15 HK HK13100596.3A patent/HK1173441A1/xx unknown
-
2015
- 2015-05-20 JP JP2015102335A patent/JP5897186B2/ja active Active
-
2016
- 2016-09-07 US US15/258,892 patent/US9937175B2/en active Active
-
2018
- 2018-02-23 US US15/903,337 patent/US20190000845A1/en not_active Abandoned
- 2018-09-20 US US16/137,241 patent/US20190262338A1/en not_active Abandoned
-
2022
- 2022-11-22 US US17/992,553 patent/US20230190747A1/en not_active Abandoned
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |