EA200970655A1 - 6-замещенные пиримидины, ингибирующие вич - Google Patents
6-замещенные пиримидины, ингибирующие вичInfo
- Publication number
- EA200970655A1 EA200970655A1 EA200970655A EA200970655A EA200970655A1 EA 200970655 A1 EA200970655 A1 EA 200970655A1 EA 200970655 A EA200970655 A EA 200970655A EA 200970655 A EA200970655 A EA 200970655A EA 200970655 A1 EA200970655 A1 EA 200970655A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- 6alkyl
- amino
- cyano
- substituted pyrimidine
- inhibiting hiv
- Prior art date
Links
- -1 6-substituted pyrimidine Chemical class 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 230000010076 replication Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D409/12—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 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
- C07D417/06—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 carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- General Chemical & Material Sciences (AREA)
- AIDS & HIV (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Ингибиторы репликации ВИЧ формулы (I), где Rпредставляет собой водород; арил; формил; Cалкилкарбонил; Cалкил; Cалкилоксикарбонил; R, R, Rи Rпредставляют собой водород; гидрокси; галоген; Сциклоалкил; Cалкилокси; карбоксил; Cалкилоксикарбонил; циано; нитро; амино; моно- или ди(Салкил)амино; полигалогенСалкил; полигалогенСалкилокси; -C(=O)R; необязательно замещенный Cалкил, Салкенил или Салкинил; Rи Rпредставляют собой гидрокси; галоген; Сциклоалкил; Cалкилокси; карбоксил; Cалкилоксикарбонил; формил; циано; нитро; амино; моно- или ди(Cалкил)амино; полигалогенСалкил; полигалогенСалкилокси; -C(=O)R; циано; -S(=O)R; -NH-S(=O)R; -NHC(=O)H; -C(=O)NHNH; -NHC(=O)R; Het; -Y-Het; необязательно замещенный Cалкил,, Салкенил или Cалкинил; Rпредставляет собой пиридил, -С(=O)NRR; -CH(ORR; -CH-NRR; -CH=NOR; -СН-O-Салкенил; -СН-O-Р(=O)(OR); -CH-O-C(=O)-NH; -С(=O)-R; X представляет собой -NR-, -О-, -СН-, -S-; фармацевтические композиции, содержащие эти соединения в качестве активного компонента, и способы получения указанных соединений и композиций.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06127325 | 2006-12-29 | ||
PCT/EP2007/064605 WO2008080964A1 (en) | 2006-12-29 | 2007-12-28 | Hiv inhibiting 6-substituted pyrimidines |
Publications (2)
Publication Number | Publication Date |
---|---|
EA200970655A1 true EA200970655A1 (ru) | 2009-12-30 |
EA020772B1 EA020772B1 (ru) | 2015-01-30 |
Family
ID=39283877
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200970655A EA020772B1 (ru) | 2006-12-29 | 2007-12-28 | 6-замещенные пиримидины, ингибирующие вич |
Country Status (13)
Country | Link |
---|---|
US (1) | US9006243B2 (ru) |
EP (1) | EP2114901B1 (ru) |
JP (1) | JP5185283B2 (ru) |
KR (1) | KR20090094073A (ru) |
CN (1) | CN101573343B (ru) |
AU (1) | AU2007341227C1 (ru) |
BR (1) | BRPI0720858B8 (ru) |
CA (1) | CA2674178C (ru) |
DK (1) | DK2114901T3 (ru) |
EA (1) | EA020772B1 (ru) |
ES (1) | ES2470570T3 (ru) |
MX (1) | MX2009007005A (ru) |
WO (1) | WO2008080964A1 (ru) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CO5271699A1 (es) | 2000-01-24 | 2003-04-30 | Pfizer Prod Inc | Procedimiento para el tratamiento de cardiomiopatia utilizando inhibidores de la glucogeno fosforilasa |
CN101031558B (zh) | 2004-09-30 | 2011-10-05 | 泰博特克药品有限公司 | 抑制人类免疫缺陷病毒的5-杂环基嘧啶 |
WO2006035069A1 (en) | 2004-09-30 | 2006-04-06 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 5-substituted pyrimidines |
RU2398768C2 (ru) * | 2005-02-18 | 2010-09-10 | Тиботек Фармасьютикалз Лтд. | Ингибирующие вич производные 2-(4-цианофениламино)-пиримидин-оксида |
KR20080114741A (ko) | 2006-03-30 | 2008-12-31 | 티보텍 파마슈티칼즈 리미티드 | Hiv를 억제하는 5-아미도 치환 피리미딘 |
WO2008080965A2 (en) | 2006-12-29 | 2008-07-10 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 5,6-substituted pyrimidines |
US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
PL2300013T5 (pl) | 2008-05-21 | 2025-04-28 | Takeda Pharmaceutical Company Limited | Pochodne fosforu jako inhibitor kinazy |
NZ603525A (en) | 2008-06-27 | 2015-02-27 | Celgene Avilomics Res Inc | Pyrimidine based compound and uses thereof |
US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
US11351168B1 (en) | 2008-06-27 | 2022-06-07 | Celgene Car Llc | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
JP5918693B2 (ja) | 2009-05-05 | 2016-05-18 | ダナ ファーバー キャンサー インスティテュート インコーポレイテッド | Egfr阻害剤及び疾患の治療方法 |
WO2011017079A1 (en) | 2009-07-27 | 2011-02-10 | Teva Pharmaceutical Industries Ltd. | Process for the preparation and purification of etravirine and intermediates thereof |
RU2013109393A (ru) | 2010-08-10 | 2014-09-20 | Сэлджин Авиаломикс Ресеарч, Инк. | Безилатная соль ингибитора втк |
TWI545115B (zh) | 2010-11-01 | 2016-08-11 | 阿維拉製藥公司 | 雜環化合物及其用途 |
JP5956999B2 (ja) | 2010-11-01 | 2016-07-27 | セルジーン アヴィロミクス リサーチ, インコーポレイテッド | ヘテロアリール化合物およびその使用 |
JP5957003B2 (ja) | 2010-11-10 | 2016-07-27 | セルジーン アヴィロミクス リサーチ, インコーポレイテッド | 変異体選択的egfr阻害剤およびその使用 |
CA2832504C (en) | 2011-05-04 | 2019-10-01 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
CN102260215A (zh) * | 2011-05-13 | 2011-11-30 | 复旦大学 | 一种二芳基嘧啶类衍生物及其制备方法和用途 |
EP2770830A4 (en) | 2011-10-28 | 2015-05-27 | Celgene Avilomics Res Inc | METHODS OF TREATING A DISEASE OR DISEASE ASSOCIATED WITH TYROSINE KINASE BTK (BRUTON'S TYROSINE KINASE) |
BR112014022790B1 (pt) | 2012-03-15 | 2022-04-19 | Celgene Car Llc | Sais de um inibidor de quinase de receptor de fator do crescimento epidermal, composição farmacêutica e usos do mesmo |
SG10201700804XA (en) | 2012-03-15 | 2017-03-30 | Celgene Avilomics Res Inc | Solid forms of an epidermal growth factor receptor kinase inhibitor |
WO2013169401A1 (en) | 2012-05-05 | 2013-11-14 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
CN102731414B (zh) * | 2012-07-04 | 2014-11-26 | 宁波九胜创新医药科技有限公司 | 4-[(4-氯-2-嘧啶基)氨基]苯腈的制备方法 |
CN102718720B (zh) * | 2012-07-04 | 2015-01-07 | 宁波九胜创新医药科技有限公司 | 4-[(4,6-二氯-2-嘧啶基)氨基]苯腈的制备方法 |
EP2935226A4 (en) | 2012-12-21 | 2016-11-02 | Celgene Avilomics Res Inc | HETEROARYL COMPOUNDS AND USES THEREOF |
PE20151274A1 (es) | 2013-02-08 | 2015-09-12 | Celgene Avilomics Res Inc | Inhibidores de erk y sus usos |
US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
US9492471B2 (en) | 2013-08-27 | 2016-11-15 | Celgene Avilomics Research, Inc. | Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase |
US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
DK3179858T3 (da) | 2014-08-13 | 2019-07-22 | Celgene Car Llc | Forme og sammensætninger af en ERK-inhibitor |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3459731A (en) | 1966-12-16 | 1969-08-05 | Corn Products Co | Cyclodextrin polyethers and their production |
CZ154398A3 (cs) | 1995-11-23 | 1998-08-12 | Janssen Pharmaceutica N.V. | Pevné směsi cyklodextrinů připravené vytlačováním taveniny |
NO311614B1 (no) | 1996-10-01 | 2001-12-17 | Janssen Pharmaceutica Nv | Substituerte diamino-1,3,5-triazinderivater |
IL138669A0 (en) * | 1998-03-27 | 2001-10-31 | Janssen Pharmaceutica Nv | Hiv inhibiting pyrimidine derivatives |
EP0945447A1 (en) | 1998-03-27 | 1999-09-29 | Janssen Pharmaceutica N.V. | Trisubstituted 1,3,5-triazine derivatives for treatment of HIV infections |
BRPI9915552B8 (pt) * | 1998-11-10 | 2021-05-25 | Janssen Pharmaceutica Nv | pirimidinas inibidoras da reprodução do hiv |
GB9828511D0 (en) | 1998-12-24 | 1999-02-17 | Zeneca Ltd | Chemical compounds |
AU783981C (en) | 2000-05-08 | 2007-05-03 | Janssen Pharmaceutica N.V. | HIV replication inhibitors |
NZ526472A (en) | 2000-12-21 | 2004-04-30 | Vertex Pharma | Pyrazole compounds useful as protein kinase inhibitors |
JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
AR039540A1 (es) * | 2002-05-13 | 2005-02-23 | Tibotec Pharm Ltd | Compuestos microbicidas con contenido de pirimidina o triazina |
KR20050084621A (ko) | 2002-11-15 | 2005-08-26 | 티보텍 파마슈티칼즈 리미티드 | 항감염성 화합물로서의 치환된 인돌피리디늄 |
CL2004000306A1 (es) * | 2003-02-20 | 2005-04-08 | Tibotec Pharm Ltd | Compuestos derivados de pirimidina sustituidas con indano; proceso para su preparacion; composicion farmaceutica que lo comprende; combinacion farmaceutica; y su uso para el tratamiento o profilaxis de una enfermedad infecciosa. |
US7504396B2 (en) | 2003-06-24 | 2009-03-17 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
WO2006035069A1 (en) * | 2004-09-30 | 2006-04-06 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 5-substituted pyrimidines |
CN101031558B (zh) | 2004-09-30 | 2011-10-05 | 泰博特克药品有限公司 | 抑制人类免疫缺陷病毒的5-杂环基嘧啶 |
BRPI0515935B8 (pt) * | 2004-09-30 | 2021-05-25 | Janssen Sciences Ireland Uc | pirimidinas heterociclil- ou 5-carbo substituídas para inibição de hiv, e composição farmacêutica |
CA2599228C (en) * | 2005-01-27 | 2014-05-13 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 2-( 4-cyanophenylamino) pyrimidine derivatives |
KR20080114741A (ko) | 2006-03-30 | 2008-12-31 | 티보텍 파마슈티칼즈 리미티드 | Hiv를 억제하는 5-아미도 치환 피리미딘 |
US8163745B2 (en) * | 2006-03-30 | 2012-04-24 | Tibotec Pharmaceuticals Ltd. | HIV inhibiting 5-(hydroxymethylene and aminomethylene) substituted pyrimidines |
WO2008080965A2 (en) | 2006-12-29 | 2008-07-10 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 5,6-substituted pyrimidines |
-
2007
- 2007-12-28 KR KR1020097009722A patent/KR20090094073A/ko not_active Withdrawn
- 2007-12-28 BR BRPI0720858A patent/BRPI0720858B8/pt not_active IP Right Cessation
- 2007-12-28 MX MX2009007005A patent/MX2009007005A/es active IP Right Grant
- 2007-12-28 EP EP20070858201 patent/EP2114901B1/en active Active
- 2007-12-28 EA EA200970655A patent/EA020772B1/ru not_active IP Right Cessation
- 2007-12-28 DK DK07858201T patent/DK2114901T3/da active
- 2007-12-28 CA CA2674178A patent/CA2674178C/en active Active
- 2007-12-28 CN CN200780048993.8A patent/CN101573343B/zh active Active
- 2007-12-28 JP JP2009543476A patent/JP5185283B2/ja active Active
- 2007-12-28 WO PCT/EP2007/064605 patent/WO2008080964A1/en active Application Filing
- 2007-12-28 ES ES07858201.2T patent/ES2470570T3/es active Active
- 2007-12-28 US US12/521,189 patent/US9006243B2/en active Active
- 2007-12-28 AU AU2007341227A patent/AU2007341227C1/en not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
BRPI0720858A2 (pt) | 2014-07-01 |
EA020772B1 (ru) | 2015-01-30 |
BRPI0720858B1 (pt) | 2020-01-21 |
AU2007341227B2 (en) | 2013-04-18 |
MX2009007005A (es) | 2009-07-09 |
BRPI0720858B8 (pt) | 2021-05-25 |
EP2114901B1 (en) | 2014-04-09 |
CN101573343A (zh) | 2009-11-04 |
EP2114901A1 (en) | 2009-11-11 |
AU2007341227C1 (en) | 2013-08-29 |
US9006243B2 (en) | 2015-04-14 |
ES2470570T3 (es) | 2014-06-24 |
DK2114901T3 (da) | 2014-06-30 |
AU2007341227A1 (en) | 2008-07-10 |
CA2674178C (en) | 2015-11-10 |
US20100016317A1 (en) | 2010-01-21 |
KR20090094073A (ko) | 2009-09-03 |
WO2008080964A1 (en) | 2008-07-10 |
CA2674178A1 (en) | 2008-07-10 |
JP2010514735A (ja) | 2010-05-06 |
JP5185283B2 (ja) | 2013-04-17 |
CN101573343B (zh) | 2016-02-24 |
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