CN101868464B - 作为pi3抑制剂的噻吩并嘧啶衍生物 - Google Patents
作为pi3抑制剂的噻吩并嘧啶衍生物 Download PDFInfo
- Publication number
- CN101868464B CN101868464B CN2008801126921A CN200880112692A CN101868464B CN 101868464 B CN101868464 B CN 101868464B CN 2008801126921 A CN2008801126921 A CN 2008801126921A CN 200880112692 A CN200880112692 A CN 200880112692A CN 101868464 B CN101868464 B CN 101868464B
- Authority
- CN
- China
- Prior art keywords
- thieno
- morpholin
- ylmethyl
- indol
- diaza
- 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 CCCOCCNc1nc(*)nc2c1[s]c(*)c2 Chemical compound CCCOCCNc1nc(*)nc2c1[s]c(*)c2 0.000 description 8
- GWNSHRCBWQEQPK-UHFFFAOYSA-N C(COCC1)C1N1CCNCC1 Chemical compound C(COCC1)C1N1CCNCC1 GWNSHRCBWQEQPK-UHFFFAOYSA-N 0.000 description 1
- CKQRFDCOYHDOHL-UHFFFAOYSA-O CC(C)(C)[SH+](C)(C)[n](ccc1c2)c1ccc2F Chemical compound CC(C)(C)[SH+](C)(C)[n](ccc1c2)c1ccc2F CKQRFDCOYHDOHL-UHFFFAOYSA-O 0.000 description 1
- DGDMKKDWXPHWKA-HPDCSRJSSA-N CCC(C1)(C2)C1(CCNC1)[C@@H]1OCC2O Chemical compound CCC(C1)(C2)C1(CCNC1)[C@@H]1OCC2O DGDMKKDWXPHWKA-HPDCSRJSSA-N 0.000 description 1
- OSIZSRFJZJVILD-UHFFFAOYSA-N CN(C1)CC2NC1COC2 Chemical compound CN(C1)CC2NC1COC2 OSIZSRFJZJVILD-UHFFFAOYSA-N 0.000 description 1
- KAUWPAWTMFDVGL-UHFFFAOYSA-N CN1C(C2)CN2CC1 Chemical compound CN1C(C2)CN2CC1 KAUWPAWTMFDVGL-UHFFFAOYSA-N 0.000 description 1
- YKBHIAMXELZBES-UHFFFAOYSA-N CN1C(CC2)CN2CC1 Chemical compound CN1C(CC2)CN2CC1 YKBHIAMXELZBES-UHFFFAOYSA-N 0.000 description 1
- OQMSHITZFTVBHN-UHFFFAOYSA-N CN1CC(CC2)NC2C1 Chemical compound CN1CC(CC2)NC2C1 OQMSHITZFTVBHN-UHFFFAOYSA-N 0.000 description 1
- RIOMVCRDANXKNN-UHFFFAOYSA-N Cc1cc(c(N2CCOCC2)nc(C2CC2)n2)c2[s]1 Chemical compound Cc1cc(c(N2CCOCC2)nc(C2CC2)n2)c2[s]1 RIOMVCRDANXKNN-UHFFFAOYSA-N 0.000 description 1
- KJMVQYBTWHOTSI-UHFFFAOYSA-N Clc(nc1N2CCOCC2)nc2c1[s]c(CN(CC1)CCC11OCCO1)c2 Chemical compound Clc(nc1N2CCOCC2)nc2c1[s]c(CN(CC1)CCC11OCCO1)c2 KJMVQYBTWHOTSI-UHFFFAOYSA-N 0.000 description 1
- GJIJYVIKVNXYPY-UHFFFAOYSA-N Clc(nc1N2CCOCC2)nc2c1[s]c(CN1CC3(CCCC3)NCC1)c2 Chemical compound Clc(nc1N2CCOCC2)nc2c1[s]c(CN1CC3(CCCC3)NCC1)c2 GJIJYVIKVNXYPY-UHFFFAOYSA-N 0.000 description 1
- PXIYAYABWJJIJT-CYBMUJFWSA-N Clc1nc(N2CCOCC2)c2[s]c(CN3C[C@@H](CCC4)N4CC3)cc2n1 Chemical compound Clc1nc(N2CCOCC2)c2[s]c(CN3C[C@@H](CCC4)N4CC3)cc2n1 PXIYAYABWJJIJT-CYBMUJFWSA-N 0.000 description 1
- DSOLFSSRDLXUTP-UHFFFAOYSA-N O=C(CNCC1)N1C1CCOCC1 Chemical compound O=C(CNCC1)N1C1CCOCC1 DSOLFSSRDLXUTP-UHFFFAOYSA-N 0.000 description 1
- PFAKZIZFIXKDFP-UHFFFAOYSA-N O=Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1 Chemical compound O=Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1 PFAKZIZFIXKDFP-UHFFFAOYSA-N 0.000 description 1
- UJBGQWKTUHGOGV-UHFFFAOYSA-N OCC(CN(Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)CC1)C1N1CCC1 Chemical compound OCC(CN(Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)CC1)C1N1CCC1 UJBGQWKTUHGOGV-UHFFFAOYSA-N 0.000 description 1
- UJBGQWKTUHGOGV-XPCCGILXSA-N OC[C@@H](CN(Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)CC1)C1N1CCC1 Chemical compound OC[C@@H](CN(Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)CC1)C1N1CCC1 UJBGQWKTUHGOGV-XPCCGILXSA-N 0.000 description 1
- MZZALHIPUZSVKG-UHFFFAOYSA-N OCc1cc(nc(-c2c(cc[nH]3)c3cc(F)c2)nc2N3CCOCC3)c2[s]1 Chemical compound OCc1cc(nc(-c2c(cc[nH]3)c3cc(F)c2)nc2N3CCOCC3)c2[s]1 MZZALHIPUZSVKG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Communicable Diseases (AREA)
- Cardiology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Virology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0721059.8 | 2007-10-26 | ||
| GBGB0721095.8A GB0721095D0 (en) | 2007-10-26 | 2007-10-26 | Pharmaceutical compounds |
| GB07210958 | 2007-10-26 | ||
| PCT/GB2008/003621 WO2009053715A1 (en) | 2007-10-26 | 2008-10-27 | Thienopyrimidiene derivatives as pi3k inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101868464A CN101868464A (zh) | 2010-10-20 |
| CN101868464B true CN101868464B (zh) | 2013-11-13 |
Family
ID=38830047
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008801126921A Expired - Fee Related CN101868464B (zh) | 2007-10-26 | 2008-10-27 | 作为pi3抑制剂的噻吩并嘧啶衍生物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8293735B2 (enExample) |
| EP (1) | EP2205610B1 (enExample) |
| JP (1) | JP5675360B2 (enExample) |
| CN (1) | CN101868464B (enExample) |
| CA (1) | CA2701276A1 (enExample) |
| ES (1) | ES2442501T3 (enExample) |
| GB (1) | GB0721095D0 (enExample) |
| WO (1) | WO2009053715A1 (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030133939A1 (en) | 2001-01-17 | 2003-07-17 | Genecraft, Inc. | Binding domain-immunoglobulin fusion proteins |
| US7754208B2 (en) | 2001-01-17 | 2010-07-13 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
| EP2295080A3 (en) | 2005-07-25 | 2011-06-22 | Emergent Product Development Seattle, LLC | B-cell reduction using CD37-specific and CD20-specific binding molecules |
| CN105837690A (zh) | 2006-06-12 | 2016-08-10 | 新兴产品开发西雅图有限公司 | 具有效应功能的单链多价结合蛋白 |
| EP2214675B1 (en) | 2007-10-25 | 2013-11-20 | Genentech, Inc. | Process for making thienopyrimidine compounds |
| PE20091268A1 (es) | 2007-12-19 | 2009-09-19 | Amgen Inc | Derivados heterociclicos como inhibidores de pi3 quinasa |
| PT2132228E (pt) | 2008-04-11 | 2011-10-11 | Emergent Product Dev Seattle | Imunoterapia de cd37 e sua combinação com um quimioterápico bifuncional |
| TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| EP2451811A1 (en) * | 2009-05-27 | 2012-05-16 | F. Hoffmann-La Roche AG | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
| SG175708A1 (en) | 2009-05-27 | 2011-12-29 | Genentech Inc | Bicyclic pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
| GB201004200D0 (en) * | 2010-03-15 | 2010-04-28 | Univ Basel | Spirocyclic compounds and their use as therapeutic agents and diagnostic probes |
| EP3399026B1 (en) | 2010-06-14 | 2024-06-26 | The Scripps Research Institute | Reprogramming of cells to a new fate |
| AU2011343712B2 (en) | 2010-12-16 | 2015-09-17 | Genentech, Inc. | Tricyclic PI3k inhibitor compounds and methods of use |
| EP2548864B1 (en) | 2011-07-22 | 2014-02-19 | Université Joseph Fourier | Novel bis-indolic derivatives, a process for preparing the same and their uses as a drug |
| EP2852661A1 (en) | 2012-05-23 | 2015-04-01 | F. Hoffmann-La Roche AG | Compositions and methods of obtaining and using endoderm and hepatocyte cells |
| EP2890698B1 (en) * | 2012-08-30 | 2017-03-01 | F. Hoffmann-La Roche AG | Dioxino- and oxazin-[2,3-d]pyrimidine pi3k inhibitor compounds and methods of use |
| GB201402431D0 (en) * | 2014-02-12 | 2014-03-26 | Karus Therapeutics Ltd | Compounds |
| KR102784293B1 (ko) | 2015-09-21 | 2025-03-20 | 압테보 리서치 앤드 디벨롭먼트 엘엘씨 | Cd3 결합 폴리펩타이드 |
| US10591000B2 (en) * | 2016-05-24 | 2020-03-17 | Means Industries, Inc. | One-way clutch assembly and coupling member for therein wherein locking member dynamics with respect to strut laydown speed are enhanced |
| TW201825465A (zh) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| TW201815787A (zh) | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| TW201813963A (zh) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| AU2019416623B2 (en) * | 2018-12-27 | 2022-12-08 | Holosmedic | Novel compound and pharmaceutical composition comprising same for enhancing anticancer activity |
| KR102338609B1 (ko) * | 2019-05-20 | 2021-12-14 | 보령제약 주식회사 | 피리도-피리미딘 화합물 및 이를 유효성분으로 포함하는 pi3k 관련 질환의 예방 또는 치료용 약학적 조성물 |
| US20220227729A1 (en) | 2019-05-21 | 2022-07-21 | Bayer Aktiengesellschaft | Identification and use of kras inhibitors |
| CN114127062A (zh) * | 2019-05-31 | 2022-03-01 | 伊迪亚生物科学有限公司 | 作为DNA聚合酶Theta抑制剂的噻二唑基衍生物 |
| BR112022007998A2 (pt) * | 2019-10-31 | 2022-07-05 | Holosmedic | Novo composto e composição farmacêutica para prevenção ou tratamento de câncer que compreende os mesmos |
| CN112920199B (zh) * | 2020-06-02 | 2023-02-03 | 四川大学 | 一种哌嗪酮取代物或其衍生物及其制备方法和应用、药物组合物 |
| KR20240161147A (ko) | 2022-03-14 | 2024-11-12 | 슬랩 파마슈티컬스 엘엘씨 | 다중 사이클릭 화합물 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1470356A1 (de) * | 1964-01-15 | 1970-04-30 | Thomae Gmbh Dr K | Neue Thieno[3,2-d]pyrimidine und Verfahren zu ihrer Herstellung |
| BE754606A (fr) * | 1969-08-08 | 1971-02-08 | Thomae Gmbh Dr K | Nouvelles 2-aminoalcoylamino-thieno(3,2-d)pyrimidines et leurs procedesde fabrication |
| BE759493A (fr) * | 1969-11-26 | 1971-05-25 | Thomae Gmbh Dr K | Nouvelles 2-(5-nitro-2-furyl)-thieno(3,2-d) pyrimidines et procedes pour les fabriquer |
| US3763156A (en) * | 1970-01-28 | 1973-10-02 | Boehringer Sohn Ingelheim | 2-heterocyclic amino-4-morpholinothieno(3,2-d)pyrimidines |
| RO62428A (fr) | 1971-05-04 | 1978-01-15 | Thomae Gmbh Dr K | Procede pour la preparation des thyeno-(3,2-d)-pyrimidines |
| CH592668A5 (enExample) * | 1973-10-02 | 1977-10-31 | Delalande Sa | |
| GB1570494A (en) * | 1975-11-28 | 1980-07-02 | Ici Ltd | Thienopyrimidine derivatives and their use as pesticides |
| ZA782648B (en) * | 1977-05-23 | 1979-06-27 | Ici Australia Ltd | The prevention,control or eradication of infestations of ixodid ticks |
| AU3053999A (en) * | 1998-03-31 | 1999-10-25 | Kyowa Hakko Kogyo Co. Ltd. | Nitrogenous heterocyclic compounds |
| US6232320B1 (en) * | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| US6608053B2 (en) * | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| AU5261001A (en) | 2000-04-27 | 2001-11-12 | Imperial Cancer Research Technology Ltd | Condensed heteroaryl derivatives |
| US20020156601A1 (en) * | 2001-04-19 | 2002-10-24 | Tu Kevin Hsiaohsu | Event monitoring and detection system |
| WO2004017950A2 (en) | 2002-08-22 | 2004-03-04 | Piramed Limited | Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents |
| ES2217956B1 (es) | 2003-01-23 | 2006-04-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de 4-aminotieno(2,3-d)pirimidin-6-carbonitrilo. |
| GB0423653D0 (en) * | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
| GB0520657D0 (en) | 2005-10-11 | 2005-11-16 | Ludwig Inst Cancer Res | Pharmaceutical compounds |
| BRPI0710866A2 (pt) * | 2006-04-26 | 2012-08-14 | Hoffmann La Roche | compostos farmacÊuticos |
| CN101479274B (zh) * | 2006-04-26 | 2013-06-12 | 霍夫曼-拉罗奇有限公司 | 药用化合物 |
| RU2439074C2 (ru) * | 2006-04-26 | 2012-01-10 | Ф. Хоффманн-Ля Рош Аг | ПРОИЗВОДНОЕ ТИЕНО[3,2-d]ПИРИМИДИНА В КАЧЕСТВЕ ИНГИБИТОРА ФОСФАТИДИЛИНОЗИТОЛ-3-КИНАЗЫ (РI3К) |
| JP5291616B2 (ja) * | 2006-04-26 | 2013-09-18 | ジェネンテック, インコーポレイテッド | ホスホイノシチド3−キナーゼ抑制剤化合物およびその使用方法 |
| GB0608820D0 (en) * | 2006-05-04 | 2006-06-14 | Piramed Ltd | Pharmaceutical compounds |
| WO2008070740A1 (en) * | 2006-12-07 | 2008-06-12 | F.Hoffmann-La Roche Ag | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
| JP5500990B2 (ja) * | 2006-12-07 | 2014-05-21 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | ホスホイノシチド3−キナーゼ阻害剤化合物及び使用方法 |
| AU2008298948B2 (en) * | 2007-09-12 | 2014-09-04 | F. Hoffmann-La Roche Ag | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use |
| ES2399774T3 (es) * | 2007-09-24 | 2013-04-03 | Genentech, Inc. | Compuestos de tiazolopirimidina inhibidores de PI3K y métodos de uso |
| EP2214675B1 (en) * | 2007-10-25 | 2013-11-20 | Genentech, Inc. | Process for making thienopyrimidine compounds |
| EP2215090B1 (en) | 2007-10-26 | 2015-03-04 | F. Hoffmann-La Roche AG | Purine derivatives useful as pi3 kinase inhibitors |
| US8158624B2 (en) * | 2008-05-30 | 2012-04-17 | Genetech, Inc. | Purine PI3K inhibitor compounds and methods of use |
| SG175708A1 (en) * | 2009-05-27 | 2011-12-29 | Genentech Inc | Bicyclic pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
| EP2451811A1 (en) * | 2009-05-27 | 2012-05-16 | F. Hoffmann-La Roche AG | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
-
2007
- 2007-10-26 GB GBGB0721095.8A patent/GB0721095D0/en not_active Ceased
-
2008
- 2008-10-27 US US12/739,435 patent/US8293735B2/en not_active Expired - Fee Related
- 2008-10-27 WO PCT/GB2008/003621 patent/WO2009053715A1/en not_active Ceased
- 2008-10-27 CA CA2701276A patent/CA2701276A1/en not_active Abandoned
- 2008-10-27 CN CN2008801126921A patent/CN101868464B/zh not_active Expired - Fee Related
- 2008-10-27 ES ES08842778.6T patent/ES2442501T3/es active Active
- 2008-10-27 EP EP08842778.6A patent/EP2205610B1/en not_active Not-in-force
- 2008-10-27 JP JP2010530548A patent/JP5675360B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2205610A1 (en) | 2010-07-14 |
| JP2011500774A (ja) | 2011-01-06 |
| JP5675360B2 (ja) | 2015-02-25 |
| EP2205610B1 (en) | 2013-11-20 |
| CN101868464A (zh) | 2010-10-20 |
| GB0721095D0 (en) | 2007-12-05 |
| US8293735B2 (en) | 2012-10-23 |
| CA2701276A1 (en) | 2009-04-30 |
| WO2009053715A1 (en) | 2009-04-30 |
| US20110021496A1 (en) | 2011-01-27 |
| ES2442501T3 (es) | 2014-02-11 |
| WO2009053715A8 (en) | 2010-06-03 |
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