WO2008149965A1 - ピリドン化合物 - Google Patents
ピリドン化合物 Download PDFInfo
- Publication number
- WO2008149965A1 WO2008149965A1 PCT/JP2008/060417 JP2008060417W WO2008149965A1 WO 2008149965 A1 WO2008149965 A1 WO 2008149965A1 JP 2008060417 W JP2008060417 W JP 2008060417W WO 2008149965 A1 WO2008149965 A1 WO 2008149965A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- good
- receptor agonist
- group
- pyridone
- compound
- Prior art date
Links
- -1 Pyridone compound Chemical class 0.000 title abstract 2
- 101150109738 Ptger4 gene Proteins 0.000 abstract 3
- 230000000694 effects Effects 0.000 abstract 3
- 239000000018 receptor agonist Substances 0.000 abstract 3
- 229940044601 receptor agonist Drugs 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical group OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 abstract 2
- 208000005764 Peripheral Arterial Disease Diseases 0.000 abstract 1
- 208000030831 Peripheral arterial occlusive disease Diseases 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 230000017531 blood circulation Effects 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
- 150000003568 thioethers Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/69—Two or more oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D413/10—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 carbon chain containing aromatic rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA2693552A CA2693552A1 (en) | 2007-06-07 | 2008-06-06 | Pyridone compound |
| CN200880018253A CN101679262A (zh) | 2007-06-07 | 2008-06-06 | 吡啶酮化合物 |
| MX2009013355A MX2009013355A (es) | 2007-06-07 | 2008-06-06 | Compuesto de piridona. |
| EP08765230A EP2154130A4 (en) | 2007-06-07 | 2008-06-06 | pyridone |
| JP2009517901A JPWO2008149965A1 (ja) | 2007-06-07 | 2008-06-06 | ピリドン化合物 |
| US12/663,246 US20100179137A1 (en) | 2007-06-07 | 2008-06-06 | Pyridone compound |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007-151243 | 2007-06-07 | ||
| JP2007151243 | 2007-06-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2008149965A1 true WO2008149965A1 (ja) | 2008-12-11 |
Family
ID=40093769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2008/060417 WO2008149965A1 (ja) | 2007-06-07 | 2008-06-06 | ピリドン化合物 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20100179137A1 (ja) |
| EP (1) | EP2154130A4 (ja) |
| JP (1) | JPWO2008149965A1 (ja) |
| KR (1) | KR20100031725A (ja) |
| CN (1) | CN101679262A (ja) |
| CA (1) | CA2693552A1 (ja) |
| MX (1) | MX2009013355A (ja) |
| TW (1) | TW200911245A (ja) |
| WO (1) | WO2008149965A1 (ja) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009154190A1 (ja) | 2008-06-17 | 2009-12-23 | アステラス製薬株式会社 | ピリドン化合物 |
| US8592629B2 (en) | 2010-07-12 | 2013-11-26 | Pfizer Limited | Sulfonamide derivatives as Nav 1.7 inhibitors |
| US8685977B2 (en) | 2010-07-12 | 2014-04-01 | Pfizer Limited | Chemical compounds |
| US8772293B2 (en) | 2010-07-09 | 2014-07-08 | Pfizer Limited | Chemical compounds |
| JP2022031717A (ja) * | 2014-12-19 | 2022-02-22 | ガイストリッヒ・ファルマ・アーゲー | オキサチアジン様化合物を作製する方法 |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2593433B1 (en) | 2010-07-12 | 2014-11-26 | Pfizer Limited | N-sulfonylbenzamides as inhibitors of voltage-gated sodium channels |
| WO2012007868A2 (en) | 2010-07-12 | 2012-01-19 | Pfizer Limited | Chemical compounds |
| WO2012007869A2 (en) | 2010-07-12 | 2012-01-19 | Pfizer Limited | Chemical compounds |
| EP2773641B1 (en) | 2011-10-31 | 2017-09-27 | Xenon Pharmaceuticals Inc. | Biaryl ether sulfonamides and their use as therapeutic agents |
| JP6014154B2 (ja) | 2011-10-31 | 2016-10-25 | ゼノン・ファーマシューティカルズ・インコーポレイテッドXenon Pharmaceuticals Inc. | ベンゼンスルホンアミド化合物および治療剤としてのそれらの使用 |
| HK1209100A1 (en) | 2012-05-22 | 2016-03-24 | 基因泰克有限公司 | N-substituted benzamides and their use in the treatment of pain |
| JP6309519B2 (ja) * | 2012-07-06 | 2018-04-11 | ジェネンテック, インコーポレイテッド | N置換ベンズアミド及びその使用方法 |
| JP6096370B2 (ja) | 2013-03-14 | 2017-03-15 | ジェネンテック, インコーポレイテッド | 置換トリアゾロピリジンとその使用方法 |
| EP2970156B1 (en) | 2013-03-15 | 2018-07-25 | Genentech, Inc. | Substituted benzoxazoles and methods of use thereof |
| EA201691085A1 (ru) | 2013-11-27 | 2017-02-28 | Дженентек, Инк. | Замещенные бензамиды и способы их применения |
| US10005724B2 (en) | 2014-07-07 | 2018-06-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| CR20170591A (es) | 2015-05-22 | 2018-05-07 | Genentech Inc | Benzamidas sustituidas y métodos para utilizarlas |
| MA42683A (fr) | 2015-08-27 | 2018-07-04 | Genentech Inc | Composés thérapeutiques et leurs méthodes utilisation |
| KR20180067561A (ko) | 2015-09-28 | 2018-06-20 | 제넨테크, 인크. | 치료 화합물 및 그의 사용 방법 |
| JP2018535234A (ja) | 2015-11-25 | 2018-11-29 | ジェネンテック, インコーポレイテッド | ナトリウムチャネル遮断薬として有用な置換ベンズアミド |
| JP2019513714A (ja) | 2016-03-30 | 2019-05-30 | ジェネンテック, インコーポレイテッド | 置換ベンズアミド及びその使用方法 |
| CA3039853A1 (en) | 2016-10-17 | 2018-04-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| MA47106A (fr) | 2016-12-21 | 2019-10-30 | Amgen Inc | Formulations d'anticorps anti-tnf alpha |
| CN110546148A (zh) | 2017-03-24 | 2019-12-06 | 基因泰克公司 | 作为钠通道抑制剂的4-哌啶-n-(嘧啶-4-基)色满-7-磺酰胺衍生物 |
| WO2019165290A1 (en) | 2018-02-26 | 2019-08-29 | Genentech, Inc. | Pyridine-sulfonamide compounds and their use against pain and related conditions |
| CN111936494A (zh) | 2018-03-30 | 2020-11-13 | 豪夫迈·罗氏有限公司 | 作为钠通道抑制剂的取代的氢-吡啶并-吖嗪 |
| TW202003490A (zh) | 2018-05-22 | 2020-01-16 | 瑞士商赫孚孟拉羅股份公司 | 治療性化合物及其使用方法 |
Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0535980A1 (en) | 1991-10-02 | 1993-04-07 | Sumitomo Chemical Company, Limited | 2-Pyridone derivatives, a process for their preparation and their use as fungicides |
| JPH05194398A (ja) * | 1991-10-02 | 1993-08-03 | Sumitomo Chem Co Ltd | アクリル酸誘導体、その製造法およびそれを有効成分として含有する植物病害防除剤 |
| WO2001087842A1 (en) * | 2000-05-18 | 2001-11-22 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyridones useful for selective inhibition of the coagulation cascade |
| WO2003059884A1 (en) | 2001-12-21 | 2003-07-24 | X-Ceptor Therapeutics, Inc. | Modulators of lxr |
| WO2005116010A1 (en) | 2004-05-26 | 2005-12-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
| WO2006014207A1 (en) | 2004-07-02 | 2006-02-09 | Allergan, Inc. | Prostaglandin analogs |
| WO2006052630A1 (en) | 2004-11-04 | 2006-05-18 | Allergan, Inc. | Therapeutic substituted piperidone compounds |
| WO2006080323A1 (ja) | 2005-01-27 | 2006-08-03 | Asahi Kasei Pharma Corporation | ヘテロ6員環化合物及びその用途 |
| JP2006520758A (ja) * | 2003-03-26 | 2006-09-14 | メルク フロスト カナダ リミテツド | Ep4受容体作動薬としてのプロスタグランジン類縁体 |
| JP2006526637A (ja) * | 2003-06-02 | 2006-11-24 | アラーガン、インコーポレイテッド | 医薬としての8−アザプロスタグランジンカーボネートおよびチオカーボネート類似体 |
| WO2007014454A1 (en) | 2005-08-03 | 2007-02-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
| WO2007014462A1 (en) | 2005-08-03 | 2007-02-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006526337A (ja) * | 2003-05-09 | 2006-11-16 | 松下電器産業株式会社 | 再生装置及びダイジェスト再生方法 |
| WO2009154190A1 (ja) * | 2008-06-17 | 2009-12-23 | アステラス製薬株式会社 | ピリドン化合物 |
-
2008
- 2008-06-06 TW TW097121177A patent/TW200911245A/zh unknown
- 2008-06-06 EP EP08765230A patent/EP2154130A4/en not_active Withdrawn
- 2008-06-06 US US12/663,246 patent/US20100179137A1/en not_active Abandoned
- 2008-06-06 WO PCT/JP2008/060417 patent/WO2008149965A1/ja active Application Filing
- 2008-06-06 KR KR1020107000252A patent/KR20100031725A/ko not_active Withdrawn
- 2008-06-06 CA CA2693552A patent/CA2693552A1/en not_active Abandoned
- 2008-06-06 CN CN200880018253A patent/CN101679262A/zh active Pending
- 2008-06-06 JP JP2009517901A patent/JPWO2008149965A1/ja not_active Withdrawn
- 2008-06-06 MX MX2009013355A patent/MX2009013355A/es not_active Application Discontinuation
Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0535980A1 (en) | 1991-10-02 | 1993-04-07 | Sumitomo Chemical Company, Limited | 2-Pyridone derivatives, a process for their preparation and their use as fungicides |
| JPH05194398A (ja) * | 1991-10-02 | 1993-08-03 | Sumitomo Chem Co Ltd | アクリル酸誘導体、その製造法およびそれを有効成分として含有する植物病害防除剤 |
| WO2001087842A1 (en) * | 2000-05-18 | 2001-11-22 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyridones useful for selective inhibition of the coagulation cascade |
| WO2003059884A1 (en) | 2001-12-21 | 2003-07-24 | X-Ceptor Therapeutics, Inc. | Modulators of lxr |
| JP2006520758A (ja) * | 2003-03-26 | 2006-09-14 | メルク フロスト カナダ リミテツド | Ep4受容体作動薬としてのプロスタグランジン類縁体 |
| JP2006526637A (ja) * | 2003-06-02 | 2006-11-24 | アラーガン、インコーポレイテッド | 医薬としての8−アザプロスタグランジンカーボネートおよびチオカーボネート類似体 |
| WO2005116010A1 (en) | 2004-05-26 | 2005-12-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
| WO2006014207A1 (en) | 2004-07-02 | 2006-02-09 | Allergan, Inc. | Prostaglandin analogs |
| WO2006052630A1 (en) | 2004-11-04 | 2006-05-18 | Allergan, Inc. | Therapeutic substituted piperidone compounds |
| WO2006080323A1 (ja) | 2005-01-27 | 2006-08-03 | Asahi Kasei Pharma Corporation | ヘテロ6員環化合物及びその用途 |
| WO2007014454A1 (en) | 2005-08-03 | 2007-02-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
| WO2007014462A1 (en) | 2005-08-03 | 2007-02-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
Non-Patent Citations (14)
| Title |
|---|
| "Pharmaceutical Research and Development", vol. 7, 1990, HIROKAWA PUBLISHING COMPANY, pages: 163 - 198 |
| "Protective Groups in Organic Synthesis", 2007 |
| AM. J. PHYSIOL., vol. 279, 2000, pages F755 |
| BIOCHEM. PHARMACOL., vol. 61, 2001, pages 1153 |
| BR. J. PHARMACOL., vol. 2001, no. 134, pages 313 |
| CIRCULATION, vol. 104, 2001, pages 1176 |
| EUR. J. VASE. ENDOVASC. SURG, vol. 33, no. 1, 2007, pages L |
| GASTROENTEROLOGY, vol. 117, 1999, pages 1352 |
| KID. INT., vol. 56, 1999, pages 589 |
| PHSIOL. REV., vol. 79, 1999, pages 1193 |
| PROC. NATL. ACAD. SCI. U.S.A., vol. 99, 2002, pages 4580 |
| PROG. MED., vol. 5, 1985, pages 2157 - 2161 |
| PROSTAGLANDINS, vol. 52, 1996, pages 175 |
| See also references of EP2154130A4 |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009154190A1 (ja) | 2008-06-17 | 2009-12-23 | アステラス製薬株式会社 | ピリドン化合物 |
| US8772293B2 (en) | 2010-07-09 | 2014-07-08 | Pfizer Limited | Chemical compounds |
| US8592629B2 (en) | 2010-07-12 | 2013-11-26 | Pfizer Limited | Sulfonamide derivatives as Nav 1.7 inhibitors |
| US8685977B2 (en) | 2010-07-12 | 2014-04-01 | Pfizer Limited | Chemical compounds |
| JP2022031717A (ja) * | 2014-12-19 | 2022-02-22 | ガイストリッヒ・ファルマ・アーゲー | オキサチアジン様化合物を作製する方法 |
| JP7449913B2 (ja) | 2014-12-19 | 2024-03-14 | ガイストリッヒ・ファルマ・アーゲー | オキサチアジン様化合物を作製する方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| TW200911245A (en) | 2009-03-16 |
| CN101679262A (zh) | 2010-03-24 |
| EP2154130A4 (en) | 2011-09-07 |
| EP2154130A1 (en) | 2010-02-17 |
| JPWO2008149965A1 (ja) | 2010-08-26 |
| CA2693552A1 (en) | 2008-12-11 |
| MX2009013355A (es) | 2010-02-22 |
| KR20100031725A (ko) | 2010-03-24 |
| US20100179137A1 (en) | 2010-07-15 |
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