JP2009534358A - アデノシンａ３受容体アゴニスト - Google Patents
アデノシンａ３受容体アゴニスト Download PDFInfo
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- JP2009534358A JP2009534358A JP2009505894A JP2009505894A JP2009534358A JP 2009534358 A JP2009534358 A JP 2009534358A JP 2009505894 A JP2009505894 A JP 2009505894A JP 2009505894 A JP2009505894 A JP 2009505894A JP 2009534358 A JP2009534358 A JP 2009534358A
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- alkyl
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- nitrogen
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- 125000005843 halogen group Chemical group 0.000 claims description 28
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 27
- 125000005842 heteroatom Chemical group 0.000 claims description 27
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- 229910052760 oxygen Inorganic materials 0.000 claims description 25
- -1 carboxy, amino Chemical group 0.000 claims description 24
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- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
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- ZHVMTESWXXCMID-UYSODQMBSA-N tert-butyl N-[(1S,4R)-4-(2,6-dichloropurin-9-yl)cyclopent-2-en-1-yl]-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamate [(1S,4R)-4-(2,6-dichloropurin-9-yl)cyclopent-2-en-1-yl] ethyl carbonate Chemical compound C(C)OC(O[C@@H]1C=C[C@@H](C1)N1C2=NC(=NC(=C2N=C1)Cl)Cl)=O.C(=O)(OC(C)(C)C)N([C@@H]1C=C[C@@H](C1)N1C2=NC(=NC(=C2N=C1)Cl)Cl)C(=O)OC(C)(C)C ZHVMTESWXXCMID-UYSODQMBSA-N 0.000 description 1
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- JJOIPZNUMCWSCX-LCLWPZTBSA-N tert-butyl n-[(1s,2r,3s,4r)-4-[2-chloro-6-[(3-iodophenyl)methylamino]purin-9-yl]-2,3-dihydroxycyclopentyl]-n-[(2-methylpropan-2-yl)oxycarbonyl]carbamate Chemical compound O[C@@H]1[C@H](O)[C@@H](N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C[C@H]1N1C2=NC(Cl)=NC(NCC=3C=C(I)C=CC=3)=C2N=C1 JJOIPZNUMCWSCX-LCLWPZTBSA-N 0.000 description 1
- OGDBLCCEJZQMDU-NWDGAFQWSA-N tert-butyl n-[(1s,4r)-4-(2,6-dichloropurin-9-yl)cyclopent-2-en-1-yl]-n-[(2-methylpropan-2-yl)oxycarbonyl]carbamate Chemical compound C1=C[C@@H](N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C[C@H]1N1C2=NC(Cl)=NC(Cl)=C2N=C1 OGDBLCCEJZQMDU-NWDGAFQWSA-N 0.000 description 1
- XCAQIUOFDMREBA-UHFFFAOYSA-N tert-butyl n-[(2-methylpropan-2-yl)oxycarbonyl]carbamate Chemical compound CC(C)(C)OC(=O)NC(=O)OC(C)(C)C XCAQIUOFDMREBA-UHFFFAOYSA-N 0.000 description 1
- XAEVFMACVBKUEB-LCLWPZTBSA-N tert-butyl n-acetyl-n-[(1s,2r,3s,4r)-2,3-dihydroxy-4-[6-[(3-iodophenyl)methylamino]purin-9-yl]cyclopentyl]carbamate Chemical compound O[C@@H]1[C@H](O)[C@@H](N(C(=O)C)C(=O)OC(C)(C)C)C[C@H]1N1C2=NC=NC(NCC=3C=C(I)C=CC=3)=C2N=C1 XAEVFMACVBKUEB-LCLWPZTBSA-N 0.000 description 1
- OCNUBCIZNALWCA-LLHIFLOGSA-N tert-butyl n-acetyl-n-[(1s,2r,3s,4r)-4-(6-chloro-2-iodopurin-9-yl)-2,3-dihydroxycyclopentyl]carbamate Chemical compound O[C@@H]1[C@H](O)[C@@H](N(C(=O)C)C(=O)OC(C)(C)C)C[C@H]1N1C2=NC(I)=NC(Cl)=C2N=C1 OCNUBCIZNALWCA-LLHIFLOGSA-N 0.000 description 1
- CBXCDSJDUWOTCI-HWIPXOPOSA-N tert-butyl n-acetyl-n-[(1s,2r,3s,4r)-4-[6-[[5-chloro-2-[(3-methyl-1,2-oxazol-5-yl)methoxy]phenyl]methylamino]purin-9-yl]-2,3-dihydroxycyclopentyl]carbamate Chemical compound O[C@@H]1[C@H](O)[C@@H](N(C(=O)C)C(=O)OC(C)(C)C)C[C@H]1N1C2=NC=NC(NCC=3C(=CC=C(Cl)C=3)OCC=3ON=C(C)C=3)=C2N=C1 CBXCDSJDUWOTCI-HWIPXOPOSA-N 0.000 description 1
- LAZCAHRIJXWNQS-NWDGAFQWSA-N tert-butyl n-acetyl-n-[(1s,4r)-4-(6-chloropurin-9-yl)cyclopent-2-en-1-yl]carbamate Chemical compound C1=C[C@@H](N(C(=O)C)C(=O)OC(C)(C)C)C[C@H]1N1C2=NC=NC(Cl)=C2N=C1 LAZCAHRIJXWNQS-NWDGAFQWSA-N 0.000 description 1
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Classifications
-
- 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
- C07D403/08—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 alicyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0607944.6A GB0607944D0 (en) | 2006-04-21 | 2006-04-21 | Organic compounds |
| PCT/EP2007/053847 WO2007147659A1 (en) | 2006-04-21 | 2007-04-19 | Adenosine a3 receptor agonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009534358A true JP2009534358A (ja) | 2009-09-24 |
| JP2009534358A5 JP2009534358A5 (enExample) | 2011-03-10 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009505894A Pending JP2009534358A (ja) | 2006-04-21 | 2007-04-19 | アデノシンａ３受容体アゴニスト |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20090281126A1 (enExample) |
| EP (1) | EP2013199A1 (enExample) |
| JP (1) | JP2009534358A (enExample) |
| KR (1) | KR20080110845A (enExample) |
| CN (1) | CN101426785A (enExample) |
| AU (1) | AU2007263237B2 (enExample) |
| BR (1) | BRPI0710514A2 (enExample) |
| CA (1) | CA2649648A1 (enExample) |
| GB (1) | GB0607944D0 (enExample) |
| MX (1) | MX2008013520A (enExample) |
| RU (1) | RU2008145708A (enExample) |
| WO (1) | WO2007147659A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GT200500281A (es) * | 2004-10-22 | 2006-04-24 | Novartis Ag | Compuestos organicos. |
| GB0500785D0 (en) | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| GB0607953D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| HRP20120494T1 (hr) | 2006-04-21 | 2012-08-31 | Novartis Ag | Derivati purina za uporabu kao agonista adenozin a2a receptora |
| GB0607945D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607950D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607954D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607948D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| EP1889846A1 (en) | 2006-07-13 | 2008-02-20 | Novartis AG | Purine derivatives as A2a agonists |
| EP1903044A1 (en) | 2006-09-14 | 2008-03-26 | Novartis AG | Adenosine Derivatives as A2A Receptor Agonists |
| JP2010508835A (ja) * | 2006-11-10 | 2010-03-25 | ノバルティス アーゲー | シクロペンテンジオールモノアセテート誘導体 |
| KR20100068286A (ko) * | 2007-10-17 | 2010-06-22 | 노파르티스 아게 | 아데노신 ａ1 수용체 리간드로서의 퓨린 유도체 |
| AU2009231978C1 (en) | 2008-03-31 | 2014-01-30 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Purine derivatives as A3 adenosine receptor- selective agonists |
| US8916570B2 (en) | 2008-03-31 | 2014-12-23 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | A3 adenosine receptor agonists and antagonists |
| WO2010014921A2 (en) | 2008-08-01 | 2010-02-04 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | A3 adenosine receptor antagonists and partial agonists |
| US9181253B2 (en) | 2008-08-01 | 2015-11-10 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Adenosine receptor agonists, partial agonists, and antagonists |
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| WO2002055085A2 (en) * | 2001-01-16 | 2002-07-18 | Can-Fite Biopharma Ltd. | Use of an adenosine a3 receptor agonist for inhibition of viral replication |
| WO2005063246A1 (en) * | 2003-12-29 | 2005-07-14 | Can-Fite Biopharma Ltd. | Method for treatment of multiple sclerosis |
| WO2006011130A1 (en) * | 2004-07-28 | 2006-02-02 | Can-Fite Biopharma Ltd. | Adenosine a3 receptor agonists for the treatment of dry eye disorders including sjogren’s syndrome |
| JP2008526911A (ja) * | 2005-01-14 | 2008-07-24 | ノバルティス アクチエンゲゼルシャフト | Ａ２ａ受容体アゴニストとしてのプリン誘導体 |
| JP4904279B2 (ja) * | 2004-10-22 | 2012-03-28 | ノバルティス アーゲー | アデノシンａ−２ａ受容体アゴニストとして使用するためのプリン誘導体 |
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| GB1528382A (en) * | 1974-12-26 | 1978-10-11 | Teijin Ltd | Cyclopentene diols and acyl esters thereof and processes for their preparation |
| US4738954A (en) * | 1985-11-06 | 1988-04-19 | Warner-Lambert Company | Novel N6 -substituted-5'-oxidized adenosine analogs |
| US4954504A (en) * | 1986-11-14 | 1990-09-04 | Ciba-Geigy Corporation | N9 -cyclopentyl-substituted adenine derivatives having adenosine-2 receptor stimulating activity |
| US5688774A (en) * | 1993-07-13 | 1997-11-18 | The United States Of America As Represented By The Department Of Health And Human Services | A3 adenosine receptor agonists |
| JP2000502709A (ja) * | 1996-01-02 | 2000-03-07 | ローヌ―プーラン ローラー ファーマシューティカルズ インコーポレイテッド | ２，４―ジヒドロキシピリジン及び２，４―ジヒドロキシ―３―ニトロピリジンの製造方法 |
| US6376472B1 (en) * | 1996-07-08 | 2002-04-23 | Aventis Pharmaceuticals, Inc. | Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties |
| GB9813554D0 (en) * | 1998-06-23 | 1998-08-19 | Glaxo Group Ltd | Chemical compounds |
| CN1383427A (zh) * | 1998-12-31 | 2002-12-04 | 阿温蒂斯药物公司 | 制备n6－取代的脱氮杂一腺苷衍生物的方法 |
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| US6586413B2 (en) * | 1999-11-05 | 2003-07-01 | The United States Of America As Represented By The Department Of Health And Human Services | Methods and compositions for reducing ischemic injury of the heart by administering adenosine receptor agonists and antagonists |
| US20040162422A1 (en) * | 2001-03-20 | 2004-08-19 | Adrian Hall | Chemical compounds |
| EP1258247A1 (en) * | 2001-05-14 | 2002-11-20 | Aventis Pharma Deutschland GmbH | Adenosine analogues for the treatment of insulin resistance syndrome and diabetes |
| US7414036B2 (en) * | 2002-01-25 | 2008-08-19 | Muscagen Limited | Compounds useful as A3 adenosine receptor agonists |
| US7825102B2 (en) * | 2004-07-28 | 2010-11-02 | Can-Fite Biopharma Ltd. | Treatment of dry eye conditions |
| KR20070050484A (ko) * | 2004-09-09 | 2007-05-15 | 더 가브먼트 오브 더 유나이티드 스테이츠 오브 아메리카, 리프리젠티드 바이 더 세크러테리, 디파트먼트 오브 헬쓰 앤드 휴먼 서비씨즈 | Ａ1 및 ａ3 아데노신 수용체 아고니스트로서의 퓨린 유도체 |
| US7176172B2 (en) * | 2004-10-25 | 2007-02-13 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Quaternary ammonium polyol salts as anti-aging actives in personal care compositions |
| US20080051364A1 (en) * | 2004-11-08 | 2008-02-28 | Pninna Fishman | Therapeutic Treatment of Accelerated Bone Resorption |
| WO2006084281A1 (en) * | 2005-02-04 | 2006-08-10 | Millennium Pharmaceuticals, Inc. | Inhibitors of e1 activating enzymes |
| JP5339916B2 (ja) * | 2005-11-30 | 2013-11-13 | キャン−ファイト・バイオファーマ・リミテッド | 骨関節炎の治療におけるａ３アデノシン受容体アゴニストの使用 |
| DK1983990T3 (da) * | 2006-01-26 | 2011-07-11 | Us Gov Health & Human Serv | Allosteriske A3-adenosin-receptormodulatorer |
| HRP20120786T1 (hr) * | 2006-02-02 | 2012-11-30 | Millennium Pharmaceuticals, Inc. | Inhibitori aktivirajuä†eg enzima e1 |
| GB0607950D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607954D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| HRP20120494T1 (hr) * | 2006-04-21 | 2012-08-31 | Novartis Ag | Derivati purina za uporabu kao agonista adenozin a2a receptora |
| GB0607945D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607948D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607951D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| EP1889846A1 (en) * | 2006-07-13 | 2008-02-20 | Novartis AG | Purine derivatives as A2a agonists |
| US8008307B2 (en) * | 2006-08-08 | 2011-08-30 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of E1 activating enzymes |
| EP1903044A1 (en) * | 2006-09-14 | 2008-03-26 | Novartis AG | Adenosine Derivatives as A2A Receptor Agonists |
| JP2010508835A (ja) * | 2006-11-10 | 2010-03-25 | ノバルティス アーゲー | シクロペンテンジオールモノアセテート誘導体 |
| US20090181934A1 (en) * | 2007-10-17 | 2009-07-16 | Novartis Ag | Organic Compounds |
| KR20100068286A (ko) * | 2007-10-17 | 2010-06-22 | 노파르티스 아게 | 아데노신 ａ1 수용체 리간드로서의 퓨린 유도체 |
-
2006
- 2006-04-21 GB GBGB0607944.6A patent/GB0607944D0/en not_active Ceased
-
2007
- 2007-04-19 AU AU2007263237A patent/AU2007263237B2/en not_active Ceased
- 2007-04-19 JP JP2009505894A patent/JP2009534358A/ja active Pending
- 2007-04-19 EP EP07845239A patent/EP2013199A1/en not_active Withdrawn
- 2007-04-19 CA CA002649648A patent/CA2649648A1/en not_active Abandoned
- 2007-04-19 CN CNA2007800142903A patent/CN101426785A/zh active Pending
- 2007-04-19 BR BRPI0710514-2A patent/BRPI0710514A2/pt not_active IP Right Cessation
- 2007-04-19 WO PCT/EP2007/053847 patent/WO2007147659A1/en not_active Ceased
- 2007-04-19 RU RU2008145708/04A patent/RU2008145708A/ru not_active Application Discontinuation
- 2007-04-19 MX MX2008013520A patent/MX2008013520A/es not_active Application Discontinuation
- 2007-04-19 KR KR1020087025605A patent/KR20080110845A/ko not_active Withdrawn
- 2007-04-19 US US12/296,714 patent/US20090281126A1/en not_active Abandoned
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002055085A2 (en) * | 2001-01-16 | 2002-07-18 | Can-Fite Biopharma Ltd. | Use of an adenosine a3 receptor agonist for inhibition of viral replication |
| WO2005063246A1 (en) * | 2003-12-29 | 2005-07-14 | Can-Fite Biopharma Ltd. | Method for treatment of multiple sclerosis |
| WO2006011130A1 (en) * | 2004-07-28 | 2006-02-02 | Can-Fite Biopharma Ltd. | Adenosine a3 receptor agonists for the treatment of dry eye disorders including sjogren’s syndrome |
| JP4904279B2 (ja) * | 2004-10-22 | 2012-03-28 | ノバルティス アーゲー | アデノシンａ−２ａ受容体アゴニストとして使用するためのプリン誘導体 |
| JP2008526911A (ja) * | 2005-01-14 | 2008-07-24 | ノバルティス アクチエンゲゼルシャフト | Ａ２ａ受容体アゴニストとしてのプリン誘導体 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20080110845A (ko) | 2008-12-19 |
| RU2008145708A (ru) | 2010-05-27 |
| CN101426785A (zh) | 2009-05-06 |
| WO2007147659A1 (en) | 2007-12-27 |
| CA2649648A1 (en) | 2007-12-27 |
| US20090281126A1 (en) | 2009-11-12 |
| BRPI0710514A2 (pt) | 2011-08-16 |
| AU2007263237A1 (en) | 2007-12-27 |
| EP2013199A1 (en) | 2009-01-14 |
| GB0607944D0 (en) | 2006-05-31 |
| MX2008013520A (es) | 2008-10-29 |
| AU2007263237B2 (en) | 2010-09-30 |
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