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
- HXZZSPIFRSTFTR-UHFFFAOYSA-N CC(C)c1ccc(-c2cccc(C(F)(F)F)c2)nc1 Chemical compound CC(C)c1ccc(-c2cccc(C(F)(F)F)c2)nc1 HXZZSPIFRSTFTR-UHFFFAOYSA-N 0.000 description 1
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- HPCSFXAXSHEIEB-UHFFFAOYSA-N CC(C)c1nccc(-c2cc(Cl)ccc2)c1 Chemical compound CC(C)c1nccc(-c2cc(Cl)ccc2)c1 HPCSFXAXSHEIEB-UHFFFAOYSA-N 0.000 description 1
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- QWCHLCFKKWFSEB-UHFFFAOYSA-N Cc(nc1-c(cc2)ccc2Cl)ccc1F Chemical compound Cc(nc1-c(cc2)ccc2Cl)ccc1F QWCHLCFKKWFSEB-UHFFFAOYSA-N 0.000 description 1
- WMICEVGEHISPFU-UHFFFAOYSA-N Cc1cc(C)nc(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound Cc1cc(C)nc(-c2ccc(C(F)(F)F)cc2)n1 WMICEVGEHISPFU-UHFFFAOYSA-N 0.000 description 1
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- RMYDVWDSGGRLPF-UHFFFAOYSA-N Cc1ccc(-c2ccccc2Cl)nc1 Chemical compound Cc1ccc(-c2ccccc2Cl)nc1 RMYDVWDSGGRLPF-UHFFFAOYSA-N 0.000 description 1
- 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
- MQTHNMLVTZISOF-UHFFFAOYSA-N Cc1cccc(-c(ccc(Cl)c2)c2Cl)n1 Chemical compound Cc1cccc(-c(ccc(Cl)c2)c2Cl)n1 MQTHNMLVTZISOF-UHFFFAOYSA-N 0.000 description 1
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- ANPYCKIROSSZPQ-UHFFFAOYSA-N Cc1cccc(-c(ccc(F)c2)c2F)n1 Chemical compound Cc1cccc(-c(ccc(F)c2)c2F)n1 ANPYCKIROSSZPQ-UHFFFAOYSA-N 0.000 description 1
- SRFCKMCMDGAXCG-UHFFFAOYSA-N Cc1cccc(-c2cc(F)cc(F)c2)n1 Chemical compound Cc1cccc(-c2cc(F)cc(F)c2)n1 SRFCKMCMDGAXCG-UHFFFAOYSA-N 0.000 description 1
- KLGSWQCVIUWCIH-UHFFFAOYSA-N Cc1cccc(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound Cc1cccc(-c2ccc(C(F)(F)F)cc2)n1 KLGSWQCVIUWCIH-UHFFFAOYSA-N 0.000 description 1
- PWWSLTGKRGOQGI-UHFFFAOYSA-N Cc1cccc(-c2cccc(C(F)(F)F)c2)n1 Chemical compound Cc1cccc(-c2cccc(C(F)(F)F)c2)n1 PWWSLTGKRGOQGI-UHFFFAOYSA-N 0.000 description 1
- 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
- BEYGAJFXQGUQLF-UHFFFAOYSA-N Cc1cncc(-c2cccc(C(F)(F)F)c2)n1 Chemical compound Cc1cncc(-c2cccc(C(F)(F)F)c2)n1 BEYGAJFXQGUQLF-UHFFFAOYSA-N 0.000 description 1
- 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
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Otolaryngology (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 |
|---|---|---|---|---|
| CN103450138B (zh) * | 2008-06-25 | 2015-04-08 | 阵列生物制药公司 | 制备6-取代的苯氧基色满羧酸衍生物的中间体 |
| ES2921576T3 (es) | 2008-12-19 | 2022-08-29 | Vertex Pharma | Compuestos útiles como inhibidores de la quinasa ATR |
| NZ603477A (en) | 2010-05-12 | 2014-09-26 | Vertex Pharma | Compounds useful as inhibitors of atr kinase |
| US9334244B2 (en) | 2010-05-12 | 2016-05-10 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| CN108685922A (zh) | 2011-09-30 | 2018-10-23 | 沃泰克斯药物股份有限公司 | 用atr抑制剂治疗胰腺癌和非小细胞肺癌 |
| CN106496173A (zh) | 2011-09-30 | 2017-03-15 | 沃泰克斯药物股份有限公司 | 用于制备可用作atr激酶抑制剂的化合物的方法 |
| CN108478577A (zh) | 2012-04-05 | 2018-09-04 | 沃泰克斯药物股份有限公司 | 可用作atr激酶抑制剂的化合物及其组合疗法 |
| AR091023A1 (es) | 2012-05-11 | 2014-12-30 | Abbvie Inc | Inhibidores del nampt |
| 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 |
| DK2904406T3 (en) | 2012-10-04 | 2018-06-18 | Vertex Pharma | METHOD OF DETERMINING THE ATR INHIBITION, INCREASED DNA DAMAGE |
| JP6770522B2 (ja) * | 2015-02-13 | 2020-10-14 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | 全身性エリテマトーデスを予防し、及び/又は、治療するためのptgdr−1及び/又はptgdr−2アンタゴニスト |
| AU2016331955B2 (en) | 2015-09-30 | 2022-07-21 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of DNA damaging agents and ATR inhibitors |
| 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 |
| WO2023205116A1 (en) * | 2022-04-19 | 2023-10-26 | Gilgamesh Pharmaceuticals, Inc. | Pyridine derivatives for treating psychiatric disorders |
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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 |
| WO2008054675A2 (en) | 2006-10-31 | 2008-05-08 | Merck & Co., Inc. | 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 CN CN200980157228.9A patent/CN102325767B/zh not_active Expired - Fee Related
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- 2009-12-18 EP EP09793682.7A patent/EP2379535B1/en active Active
- 2009-12-18 WO PCT/US2009/068672 patent/WO2010075200A1/en not_active Ceased
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| Publication number | Priority date | Publication date | Assignee | Title |
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| 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
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|---|---|
| EP2379535A1 (en) | 2011-10-26 |
| CA2748099A1 (en) | 2010-07-01 |
| CN102325767A (zh) | 2012-01-18 |
| US20120101103A1 (en) | 2012-04-26 |
| CA2748099C (en) | 2017-02-28 |
| TW201028402A (en) | 2010-08-01 |
| WO2010075200A1 (en) | 2010-07-01 |
| TWI469977B (zh) | 2015-01-21 |
| JP2012513398A (ja) | 2012-06-14 |
| JP5575799B2 (ja) | 2014-08-20 |
| EP2379535B1 (en) | 2016-06-15 |
| US8785445B2 (en) | 2014-07-22 |
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