CN102325767B - 7-苯氧基色满羧酸衍生物 - Google Patents
7-苯氧基色满羧酸衍生物 Download PDFInfo
- Publication number
- CN102325767B CN102325767B CN200980157228.9A CN200980157228A CN102325767B CN 102325767 B CN102325767 B CN 102325767B CN 200980157228 A CN200980157228 A CN 200980157228A CN 102325767 B CN102325767 B CN 102325767B
- Authority
- CN
- China
- Prior art keywords
- phenoxy
- chloro
- chroman
- mmol
- ylcarbamoyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 *CC(*)=*[C@@]1C=CC=CC1*=* Chemical compound *CC(*)=*[C@@]1C=CC=CC1*=* 0.000 description 40
- HUKXEWCAVBAUHR-GPAPLHSASA-N CC(C(CCOC1=CC2Oc(cc3)ccc3C(Nc3cccc([C@H]4C(C)=C(C)C=CC4)n3)=O)C1=CC2C#N)=O Chemical compound CC(C(CCOC1=CC2Oc(cc3)ccc3C(Nc3cccc([C@H]4C(C)=C(C)C=CC4)n3)=O)C1=CC2C#N)=O HUKXEWCAVBAUHR-GPAPLHSASA-N 0.000 description 1
- ZZDFQYJEMVJHHH-UHFFFAOYSA-N CC(C)c(nc1)ccc1-c1cccc(C(F)(F)F)c1 Chemical compound CC(C)c(nc1)ccc1-c1cccc(C(F)(F)F)c1 ZZDFQYJEMVJHHH-UHFFFAOYSA-N 0.000 description 1
- XWWTXFBOGABHDC-UHFFFAOYSA-N CC(C)c(nc1)cnc1-c(cc1)ccc1Cl Chemical compound CC(C)c(nc1)cnc1-c(cc1)ccc1Cl XWWTXFBOGABHDC-UHFFFAOYSA-N 0.000 description 1
- BFPRNDMHEWAFIR-UHFFFAOYSA-N CC(C)c(nc1)cnc1-c1cc(Cl)cc(CC(C)c2cncc(-c(cc3)ccc3Cl)c2)c1 Chemical compound CC(C)c(nc1)cnc1-c1cc(Cl)cc(CC(C)c2cncc(-c(cc3)ccc3Cl)c2)c1 BFPRNDMHEWAFIR-UHFFFAOYSA-N 0.000 description 1
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- KAAGQYIXHIYLQO-UHFFFAOYSA-N Cc1cccc(-c(cc2)cc(C(F)(F)F)c2Cl)n1 Chemical compound Cc1cccc(-c(cc2)cc(C(F)(F)F)c2Cl)n1 KAAGQYIXHIYLQO-UHFFFAOYSA-N 0.000 description 1
- SRVMPHBAKWMILJ-UHFFFAOYSA-N Cc1cccc(-c(cc2)cc(Cl)c2Cl)n1 Chemical compound Cc1cccc(-c(cc2)cc(Cl)c2Cl)n1 SRVMPHBAKWMILJ-UHFFFAOYSA-N 0.000 description 1
- KACAHPIWIDWGOV-UHFFFAOYSA-N Cc1cccc(-c(cc2)cc(F)c2F)n1 Chemical compound Cc1cccc(-c(cc2)cc(F)c2F)n1 KACAHPIWIDWGOV-UHFFFAOYSA-N 0.000 description 1
- JPYGBWPUMISAFG-UHFFFAOYSA-N Cc1cccc(-c(cc2)ccc2OC)n1 Chemical compound Cc1cccc(-c(cc2)ccc2OC)n1 JPYGBWPUMISAFG-UHFFFAOYSA-N 0.000 description 1
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- RTULCYKTDLBWTG-UHFFFAOYSA-N Cc1cncc(-c(cc2)ccc2Cl)n1 Chemical compound Cc1cncc(-c(cc2)ccc2Cl)n1 RTULCYKTDLBWTG-UHFFFAOYSA-N 0.000 description 1
- JRZOHDFTOWXRGY-UHFFFAOYSA-N Cc1cncc(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound Cc1cncc(-c2ccc(C(F)(F)F)cc2)n1 JRZOHDFTOWXRGY-UHFFFAOYSA-N 0.000 description 1
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- NAHFRAWWEFFLOS-UHFFFAOYSA-N Cc1cncc(-c2cccc(Cl)c2)n1 Chemical compound Cc1cncc(-c2cccc(Cl)c2)n1 NAHFRAWWEFFLOS-UHFFFAOYSA-N 0.000 description 1
- FARFUCSNDMWUHU-UHFFFAOYSA-N Cc1cncc(-c2ccccc2)n1 Chemical compound Cc1cncc(-c2ccccc2)n1 FARFUCSNDMWUHU-UHFFFAOYSA-N 0.000 description 1
- VJSQWGSMYCWLGI-UHFFFAOYSA-N Cc1nc(-c(c(OC)c2)ccc2Cl)ccc1 Chemical compound Cc1nc(-c(c(OC)c2)ccc2Cl)ccc1 VJSQWGSMYCWLGI-UHFFFAOYSA-N 0.000 description 1
- CWIBMJIQUPLCNN-UHFFFAOYSA-N Cc1nc(-c(cc2)ccc2F)ccc1 Chemical compound Cc1nc(-c(cc2)ccc2F)ccc1 CWIBMJIQUPLCNN-UHFFFAOYSA-N 0.000 description 1
- LEHZXSVXIWYEQV-UHFFFAOYSA-N Cc1nc(-c2ccccc2Cl)ccc1 Chemical compound Cc1nc(-c2ccccc2Cl)ccc1 LEHZXSVXIWYEQV-UHFFFAOYSA-N 0.000 description 1
- WKKWHHMPJSUMMX-UHFFFAOYSA-N Cc1nccc(-c(cc2)ccc2Cl)n1 Chemical compound Cc1nccc(-c(cc2)ccc2Cl)n1 WKKWHHMPJSUMMX-UHFFFAOYSA-N 0.000 description 1
- RYMJOBFRSDYUCR-UHFFFAOYSA-N N#Cc(c(Oc(cc1)ccc1C(Nc1cccc(-c(cc2)ccc2Cl)n1)=O)c1)cc2c1OCCC2C(O)=O Chemical compound N#Cc(c(Oc(cc1)ccc1C(Nc1cccc(-c(cc2)ccc2Cl)n1)=O)c1)cc2c1OCCC2C(O)=O RYMJOBFRSDYUCR-UHFFFAOYSA-N 0.000 description 1
- UNKJAMRRDYLMGN-UHFFFAOYSA-N N#Cc(c(Oc(cc1)ccc1C(Nc1nc(-c(ccc(Cl)c2)c2Cl)ccc1)=O)c1)cc2c1OCCC2C(O)=O Chemical compound N#Cc(c(Oc(cc1)ccc1C(Nc1nc(-c(ccc(Cl)c2)c2Cl)ccc1)=O)c1)cc2c1OCCC2C(O)=O UNKJAMRRDYLMGN-UHFFFAOYSA-N 0.000 description 1
- PVWKKIYDXWUOGR-UHFFFAOYSA-N OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2ccc(cc(C(F)(F)F)cc3)c3n2)=O)c2)Cl)c2OCC1)=O Chemical compound OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2ccc(cc(C(F)(F)F)cc3)c3n2)=O)c2)Cl)c2OCC1)=O PVWKKIYDXWUOGR-UHFFFAOYSA-N 0.000 description 1
- IHORHPUSNSCVRX-UHFFFAOYSA-N OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2cccc(-c(cc3)cc(C(F)(F)F)c3Cl)n2)=O)c2)Cl)c2OCC1)=O Chemical compound OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2cccc(-c(cc3)cc(C(F)(F)F)c3Cl)n2)=O)c2)Cl)c2OCC1)=O IHORHPUSNSCVRX-UHFFFAOYSA-N 0.000 description 1
- IVTOKRFTFFBYSW-UHFFFAOYSA-N OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2cnc(cc(cc3)Cl)c3n2)=O)c2)Cl)c2OCC1)=O Chemical compound OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2cnc(cc(cc3)Cl)c3n2)=O)c2)Cl)c2OCC1)=O IVTOKRFTFFBYSW-UHFFFAOYSA-N 0.000 description 1
- SLWTWMSGXZMDED-UHFFFAOYSA-N OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2cnc(ccc(Cl)c3)c3n2)=O)c2)Cl)c2OCC1)=O Chemical compound OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2cnc(ccc(Cl)c3)c3n2)=O)c2)Cl)c2OCC1)=O SLWTWMSGXZMDED-UHFFFAOYSA-N 0.000 description 1
- JHGPUDIYXDMHKJ-UHFFFAOYSA-N OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2nc(-c3cc(Cl)ccc3)cnc2)=O)c2)Cl)c2OCC1)=O Chemical compound OC(C1c(cc(c(Oc(cc2)ccc2C(Nc2nc(-c3cc(Cl)ccc3)cnc2)=O)c2)Cl)c2OCC1)=O JHGPUDIYXDMHKJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P27/14—Decongestants or antiallergics
-
- 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
- A61P37/02—Immunomodulators
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Otolaryngology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13998108P | 2008-12-22 | 2008-12-22 | |
| US61/139,981 | 2008-12-22 | ||
| PCT/US2009/068672 WO2010075200A1 (en) | 2008-12-22 | 2009-12-18 | 7-phenoxychroman carboxylic acid derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102325767A CN102325767A (zh) | 2012-01-18 |
| CN102325767B true CN102325767B (zh) | 2014-05-14 |
Family
ID=42060604
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980157228.9A Expired - Fee Related CN102325767B (zh) | 2008-12-22 | 2009-12-18 | 7-苯氧基色满羧酸衍生物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8785445B2 (https=) |
| EP (1) | EP2379535B1 (https=) |
| JP (1) | JP5575799B2 (https=) |
| CN (1) | CN102325767B (https=) |
| CA (1) | CA2748099C (https=) |
| TW (1) | TWI469977B (https=) |
| WO (1) | WO2010075200A1 (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2307397B1 (en) * | 2008-06-25 | 2014-08-20 | Array Biopharma, Inc. | 6-substituted phenoxychroman carboxylic acid derivatives |
| ES2663222T3 (es) | 2008-12-19 | 2018-04-11 | Vertex Pharmaceuticals Incorporated | Derivados de pirazina útiles como inhibidores de la quinasa ATR |
| US9630956B2 (en) | 2010-05-12 | 2017-04-25 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| JP2013526540A (ja) * | 2010-05-12 | 2013-06-24 | バーテックス ファーマシューティカルズ インコーポレイテッド | Atrキナーゼ阻害剤として有用な化合物 |
| WO2013049859A1 (en) | 2011-09-30 | 2013-04-04 | Vertex Pharmaceuticals Incorporated | Treating pancreatic cancer and non-small cell lung cancer with atr inhibitors |
| SG10201606774UA (en) | 2011-09-30 | 2016-10-28 | Vertex Pharma | Processes for making compounds useful as inhibitors of atr kinase |
| CA2869309C (en) | 2012-04-05 | 2021-02-09 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase and combination therapies thereof |
| US8975398B2 (en) | 2012-05-11 | 2015-03-10 | Abbvie Inc. | NAMPT inhibitors |
| TWI654180B (zh) | 2012-06-29 | 2019-03-21 | 美商艾佛艾姆希公司 | 殺真菌之雜環羧醯胺 |
| US8999632B2 (en) | 2012-10-04 | 2015-04-07 | Vertex Pharmaceuticals Incorporated | Method for measuring ATR inhibition mediated increases in DNA damage |
| ES2991300T3 (es) * | 2015-02-13 | 2024-12-03 | Inserm Institut Nat De La Sante Et De Larecherche Medicale | Antagonistas de PTGDR-1 y/o PTGDR-2 para prevenir y/o tratar lupus eritematoso sistémico |
| HK1258570A1 (zh) | 2015-09-30 | 2019-11-15 | Vertex Pharmaceuticals Inc. | 使用dna损伤剂及atr抑制剂的组合治疗癌症的方法 |
| WO2021063735A1 (en) | 2019-10-02 | 2021-04-08 | Basf Se | New bicyclic pyridine derivatives |
| CN111228247B (zh) * | 2019-12-05 | 2023-01-31 | 青海大学 | 一种用于治疗包虫病的含苯亚甲基丙酮药物及其制备方法 |
| US20250270173A1 (en) * | 2022-04-19 | 2025-08-28 | Gilgamesh Pharmaceuticals, Inc. | Pyridine derivatives for treating psychiatric disorders |
Citations (3)
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| WO2004058164A2 (en) * | 2002-12-20 | 2004-07-15 | Tularik, Inc. | Asthma and allergic inflammation modulators |
| WO2008024746A1 (en) * | 2006-08-21 | 2008-02-28 | Array Biopharma, Inc. | 4-substituted phenoxyphenylacetic acid derivatives |
| CN102131794A (zh) * | 2008-06-25 | 2011-07-20 | 阵列生物制药公司 | 6-取代的苯氧基色满羧酸衍生物 |
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| US20070119975A1 (en) * | 2001-11-28 | 2007-05-31 | Hunnicutt S B | Method and Apparatus for Reducing the Precipitation Rate of an Irrigation Sprinkler |
| GB0611781D0 (en) | 2006-06-14 | 2006-07-26 | Argenta Discovery Ltd | 2-Oxo-2H-Chromene Compounds |
| US8039484B2 (en) * | 2006-10-31 | 2011-10-18 | Merck Sharp & Dohme Corp. | Antidiabetic bicyclic compounds |
| US7960567B2 (en) * | 2007-05-02 | 2011-06-14 | Amgen Inc. | Compounds and methods useful for treating asthma and allergic inflammation |
| WO2009061730A2 (en) | 2007-11-05 | 2009-05-14 | Array Biopharma Inc. | 4-heteroaryl-substituted phenoxyphenylacetic acid |
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- 2009-12-18 CA CA2748099A patent/CA2748099C/en not_active Expired - Fee Related
- 2009-12-18 CN CN200980157228.9A patent/CN102325767B/zh not_active Expired - Fee Related
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- 2009-12-18 JP JP2011542470A patent/JP5575799B2/ja not_active Expired - Fee Related
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004058164A2 (en) * | 2002-12-20 | 2004-07-15 | Tularik, Inc. | Asthma and allergic inflammation modulators |
| CN1767823A (zh) * | 2002-12-20 | 2006-05-03 | 安姆根有限公司 | 哮喘和过敏性炎症调节剂 |
| WO2008024746A1 (en) * | 2006-08-21 | 2008-02-28 | Array Biopharma, Inc. | 4-substituted phenoxyphenylacetic acid derivatives |
| CN102131794A (zh) * | 2008-06-25 | 2011-07-20 | 阵列生物制药公司 | 6-取代的苯氧基色满羧酸衍生物 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102325767A (zh) | 2012-01-18 |
| EP2379535A1 (en) | 2011-10-26 |
| TW201028402A (en) | 2010-08-01 |
| EP2379535B1 (en) | 2016-06-15 |
| US8785445B2 (en) | 2014-07-22 |
| CA2748099A1 (en) | 2010-07-01 |
| JP2012513398A (ja) | 2012-06-14 |
| CA2748099C (en) | 2017-02-28 |
| WO2010075200A1 (en) | 2010-07-01 |
| US20120101103A1 (en) | 2012-04-26 |
| JP5575799B2 (ja) | 2014-08-20 |
| TWI469977B (zh) | 2015-01-21 |
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