CN104011012B - 白三烯b4拮抗剂化合物 - Google Patents
白三烯b4拮抗剂化合物 Download PDFInfo
- Publication number
- CN104011012B CN104011012B CN201380004537.9A CN201380004537A CN104011012B CN 104011012 B CN104011012 B CN 104011012B CN 201380004537 A CN201380004537 A CN 201380004537A CN 104011012 B CN104011012 B CN 104011012B
- Authority
- CN
- China
- Prior art keywords
- compound
- pharmaceutically acceptable
- propyl
- cells
- aaa
- 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 *[I+]CC12C3C1C3C*2 Chemical compound *[I+]CC12C3C1C3C*2 0.000 description 5
- JAPMJSVZDUYFKL-UHFFFAOYSA-N C1C2C1CCC2 Chemical compound C1C2C1CCC2 JAPMJSVZDUYFKL-UHFFFAOYSA-N 0.000 description 1
- CXOZQHPXKPDQGT-UHFFFAOYSA-N CC1C=CCC1 Chemical compound CC1C=CCC1 CXOZQHPXKPDQGT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/24—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
- C07C233/25—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261584975P | 2012-01-10 | 2012-01-10 | |
| US61/584975 | 2012-01-10 | ||
| US201261585799P | 2012-01-12 | 2012-01-12 | |
| US61/585799 | 2012-01-12 | ||
| PCT/US2013/020195 WO2013106238A1 (en) | 2012-01-10 | 2013-01-04 | Leukotriene b4 antagonist compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104011012A CN104011012A (zh) | 2014-08-27 |
| CN104011012B true CN104011012B (zh) | 2016-01-20 |
Family
ID=47604162
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380004537.9A Expired - Fee Related CN104011012B (zh) | 2012-01-10 | 2013-01-04 | 白三烯b4拮抗剂化合物 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US9187411B2 (enExample) |
| EP (1) | EP2802557B1 (enExample) |
| JP (1) | JP2015509917A (enExample) |
| KR (1) | KR20140099546A (enExample) |
| CN (1) | CN104011012B (enExample) |
| AU (1) | AU2013208260A1 (enExample) |
| BR (1) | BR112014016450A2 (enExample) |
| CA (1) | CA2857521C (enExample) |
| EA (1) | EA023067B1 (enExample) |
| ES (1) | ES2571452T3 (enExample) |
| IN (1) | IN2014MN01014A (enExample) |
| MX (1) | MX2014008452A (enExample) |
| WO (1) | WO2013106238A1 (enExample) |
| ZA (1) | ZA201404732B (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10370368B2 (en) | 2015-11-30 | 2019-08-06 | Merck Sharp & Dohme Corp. | Aryl acylsulfonamides as BLT1 antagonists |
| WO2017095722A1 (en) | 2015-11-30 | 2017-06-08 | Merck Sharp & Dohme Corp. | Aryl acylsulfonamides as blt1 antagonists |
| WO2017095724A1 (en) | 2015-11-30 | 2017-06-08 | Merck Sharp & Dohme Corp. | Aryl sulfonamides as blt1 antagonists |
| WO2017095725A1 (en) | 2015-11-30 | 2017-06-08 | Merck Sharp & Dohme Corp. | Aryl sulfonamides as blt1 antagonists |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0132366B1 (en) * | 1983-07-18 | 1990-01-03 | Eli Lilly And Company | Leukotriene antagonists |
| CN1035001C (zh) * | 1993-01-02 | 1997-05-28 | 伊莱利利公司 | 取代的苯基苯酚基白三烯拮抗物 |
| WO2001094333A2 (en) * | 2000-06-02 | 2001-12-13 | Eli Lilly & Company | Process for the preparation of benzoyl substituted bicyclic compounds and chiral benzopyran derivatives |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9027023D0 (en) | 1990-12-12 | 1991-01-30 | Wellcome Found | Anti-atherosclerotic aryl compounds |
| PH30449A (en) | 1991-11-25 | 1997-05-28 | Lilly Co Eli | Substituted phenyl phenol leukotriene antagonists |
| WO1996036347A1 (en) | 1995-05-17 | 1996-11-21 | Eli Lilly And Company | Use of leukotriene antagonists for alzheimer's disease |
| WO1998042346A1 (en) | 1997-03-21 | 1998-10-01 | Eli Lilly And Company | Leukotriene antagonists useful for treating ischemia reperfusion injury |
| WO2001034198A2 (en) | 1999-11-11 | 2001-05-17 | Eli Lilly And Company | Oncolytic combinations for the treatment of cancer |
| EP1231939A2 (en) | 1999-11-11 | 2002-08-21 | Eli Lilly And Company | Oncolytic combinations for the treatment of cancer |
| BR0110473A (pt) | 2000-05-09 | 2003-04-01 | Univ Creighton | Métodos para inibição de proliferação e indução de apoptose em células de câncer |
| CN1751037A (zh) | 2003-02-14 | 2006-03-22 | 伊莱利利公司 | 作为ppar调节剂的磺酰胺衍生物 |
-
2013
- 2013-01-04 CN CN201380004537.9A patent/CN104011012B/zh not_active Expired - Fee Related
- 2013-01-04 EP EP13701305.8A patent/EP2802557B1/en active Active
- 2013-01-04 WO PCT/US2013/020195 patent/WO2013106238A1/en not_active Ceased
- 2013-01-04 MX MX2014008452A patent/MX2014008452A/es unknown
- 2013-01-04 EA EA201491099A patent/EA023067B1/ru not_active IP Right Cessation
- 2013-01-04 JP JP2014552215A patent/JP2015509917A/ja not_active Withdrawn
- 2013-01-04 US US14/359,924 patent/US9187411B2/en not_active Expired - Fee Related
- 2013-01-04 BR BR112014016450A patent/BR112014016450A2/pt not_active IP Right Cessation
- 2013-01-04 AU AU2013208260A patent/AU2013208260A1/en not_active Abandoned
- 2013-01-04 KR KR1020147018769A patent/KR20140099546A/ko not_active Withdrawn
- 2013-01-04 ES ES13701305T patent/ES2571452T3/es active Active
- 2013-01-04 CA CA2857521A patent/CA2857521C/en not_active Expired - Fee Related
-
2014
- 2014-05-26 IN IN1014MUN2014 patent/IN2014MN01014A/en unknown
- 2014-06-26 ZA ZA2014/04732A patent/ZA201404732B/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0132366B1 (en) * | 1983-07-18 | 1990-01-03 | Eli Lilly And Company | Leukotriene antagonists |
| CN1035001C (zh) * | 1993-01-02 | 1997-05-28 | 伊莱利利公司 | 取代的苯基苯酚基白三烯拮抗物 |
| WO2001094333A2 (en) * | 2000-06-02 | 2001-12-13 | Eli Lilly & Company | Process for the preparation of benzoyl substituted bicyclic compounds and chiral benzopyran derivatives |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2857521C (en) | 2016-03-01 |
| CN104011012A (zh) | 2014-08-27 |
| IN2014MN01014A (enExample) | 2015-07-03 |
| CA2857521A1 (en) | 2013-07-18 |
| EP2802557A1 (en) | 2014-11-19 |
| ZA201404732B (en) | 2015-11-25 |
| MX2014008452A (es) | 2014-08-27 |
| EP2802557B1 (en) | 2016-04-06 |
| JP2015509917A (ja) | 2015-04-02 |
| WO2013106238A1 (en) | 2013-07-18 |
| KR20140099546A (ko) | 2014-08-12 |
| EA023067B1 (ru) | 2016-04-29 |
| BR112014016450A2 (pt) | 2019-09-24 |
| EA201491099A1 (ru) | 2014-11-28 |
| AU2013208260A1 (en) | 2014-06-05 |
| US20140343151A1 (en) | 2014-11-20 |
| US9187411B2 (en) | 2015-11-17 |
| ES2571452T3 (es) | 2016-05-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4534092B2 (ja) | 心不全治療剤 | |
| EP1536799B1 (en) | Novel 2-amino-4-oxoquinazolones as lxr nuclear receptor binding compounds with partial agonistic properties | |
| Soudijn et al. | Nicotinic acid receptor subtypes and their ligands | |
| Zhao et al. | Synaptotagmin VII regulates bone remodeling by modulating osteoclast and osteoblast secretion | |
| JPWO2002020055A1 (ja) | 心不全治療剤 | |
| CN104011012B (zh) | 白三烯b4拮抗剂化合物 | |
| JP3731827B2 (ja) | アミノメチルインダン、‐ベンゾフラン及び‐ベンゾチオフエン | |
| JP2006514614A (ja) | 11β−ヒドロキシステロイドデヒドロゲナーゼ1型および2型のインヒビター | |
| EP2567698B1 (en) | GPR 17 agonists and screening assay | |
| MXPA02007603A (es) | Usos terapeuticos de mediadores ppar. | |
| Kamata et al. | Melanin-Concentrating Hormone Receptor 1 Antagonists. Synthesis and Structure–Activity Relationships of Novel 3-(Aminomethyl) quinolines | |
| US6458845B1 (en) | Macrophage scavenger receptor antagonists | |
| Bertinaria et al. | Designing multitarget anti‐inflammatory agents: chemical modulation of the lumiracoxib structure toward dual thromboxane antagonists–COX‐2 inhibitors | |
| CA3050187A1 (en) | N-{[2-(piperidin-1-yl)phenyl](phenyl)methyl}-2-(3-oxo-3,4-dihydro-2h-1,4-benzoxa zin-7-yl)acetamide derivatives and related compounds as ror-gamma modulators for treating autoimmune diseases | |
| Du et al. | NCOR1 maintains the homeostasis of vascular smooth muscle cells and protects against aortic aneurysm | |
| WO2006043710A1 (ja) | 創薬標的タンパク質及び標的遺伝子、並びにスクリーニング方法 | |
| JP4255285B2 (ja) | インテグリン発現抑制を介した血管新生抑制剤の効果を検定する方法 | |
| TW482673B (en) | Vitronectin receptor antagonists | |
| Siebenbuerger et al. | Highly potent 17β-HSD2 inhibitors with a promising pharmacokinetic profile for targeted osteoporosis therapy | |
| JPWO2001019986A1 (ja) | ペプチドロイコトリエン受容体 | |
| CA2338122A1 (en) | Macrophage scavenger receptor antagonists | |
| JP2007523166A (ja) | Hm74の調節剤としてのフロセミド誘導体および炎症を処置するためのそれらの使用 | |
| CA2556801A1 (en) | Methods and agents for inhibiting dynamin-dependent endocytosis | |
| Christ et al. | Development and characterization of new inhibitors of the human and mouse hematopoietic prostaglandin D2 synthases | |
| Hakami et al. | Fibulin‐4 and latent‐transforming growth factor beta‐binding protein‐4 interactions with syndecan‐2 and syndecan‐3 are required for elastogenesis |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160120 Termination date: 20170104 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |