PE20091627A1 - 4-hidroxipirimidina-5-carboxamidas sustituidas - Google Patents
4-hidroxipirimidina-5-carboxamidas sustituidasInfo
- Publication number
- PE20091627A1 PE20091627A1 PE2009000390A PE2009000390A PE20091627A1 PE 20091627 A1 PE20091627 A1 PE 20091627A1 PE 2009000390 A PE2009000390 A PE 2009000390A PE 2009000390 A PE2009000390 A PE 2009000390A PE 20091627 A1 PE20091627 A1 PE 20091627A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- hydroxypyrimidine
- compounds
- phenylethyl
- carbonyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 1-METHYL-1-PHENYLETHYL Chemical class 0.000 abstract 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- ZOSXLRUOBVSFQV-UHFFFAOYSA-N 6-oxo-1h-pyrimidine-5-carboxamide Chemical group NC(=O)C1=CN=CN=C1O ZOSXLRUOBVSFQV-UHFFFAOYSA-N 0.000 abstract 1
- 206010021143 Hypoxia Diseases 0.000 abstract 1
- 102000004079 Prolyl Hydroxylases Human genes 0.000 abstract 1
- 108010043005 Prolyl Hydroxylases Proteins 0.000 abstract 1
- 208000007502 anemia Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 208000028867 ischemia Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- 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
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/14—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 three or more hetero 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
- C07D405/14—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 three or more hetero rings
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE 4-HIDROXIPIRIMIDINA-5-CARBOXAMIDA SUSTITUIDAS DE FORMULA (I) DONDE A ES HETEROCICLILO OPCIONALMENTE SUSTITUIDO CON R9, DONDE R9 ES OH, HALOGENO, OXO, ALQUILO(C1-C6), ENTRE OTROS; R1 ES -ALQUIL(C1-C10), -ALQUIL(C1-C10)-CICLOALQUILO(C3-C10), -ALQUENIL(C2-C10), ENTRE OTROS; R2 ES H, -ALQUIL(C1-C10), -O-ALQUILARIL(C1-C10), ARILO, ENTRE OTROS; R3 ES H, OH, HALOGENO, ALCOXI(C1-C6), ENTRE OTROS; R4 ES H, -ALQUIL(C1-C10), -ALQUENIL(C2-C10), -CICLOALQUIL(C3-C10), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 2-(4-BROMOPIRIDIN-2-IL)-4-HIDROXI-N-(1-METIL-1-FENILETIL)PIRIMIDINA-5-CARBOXAMIDA, ACIDO 2-(4-HIDROXI-5-{[(1-METIL-1-FENILETIL)AMINO]CARBONIL}PIRIMIDIN-2-IL)ISONICOTINICO, ACIDO 6-(5-{[(4-FLUOROBENCIL)AMINO]CARBONIL}-4-HIDROXIPIRIMIDIN-2-IL)NICOTINICO, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PROLILHIDROXILASA DEL FACTOR INDUCIBLE POR HIPOXIA (HIF) PARA POTENCIAR LA PRODUCCION ENDOGENA DE ERITROPOYETINA SIENDO UTILES PARA EL TRATAMIENTO DE ANEMIA, ISQUEMIA
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6986408P | 2008-03-18 | 2008-03-18 | |
| US19291808P | 2008-09-23 | 2008-09-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20091627A1 true PE20091627A1 (es) | 2009-10-30 |
Family
ID=40627533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2009000390A PE20091627A1 (es) | 2008-03-18 | 2009-03-17 | 4-hidroxipirimidina-5-carboxamidas sustituidas |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US8278304B2 (es) |
| EP (1) | EP2257539B1 (es) |
| JP (1) | JP5557832B2 (es) |
| CN (1) | CN102036981B (es) |
| AR (1) | AR070925A1 (es) |
| AU (1) | AU2009225869B2 (es) |
| CA (1) | CA2718528C (es) |
| CL (1) | CL2009000639A1 (es) |
| ES (1) | ES2524883T3 (es) |
| MX (1) | MX2010010209A (es) |
| PE (1) | PE20091627A1 (es) |
| TW (1) | TW200944511A (es) |
| WO (1) | WO2009117269A1 (es) |
Families Citing this family (42)
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|---|---|---|---|---|
| CA2722772C (en) | 2008-04-28 | 2020-12-22 | Janssen Pharmaceutica N.V. | Benzoimidazoles as prolyl hydroxylase inhibitors |
| PE20110408A1 (es) * | 2008-07-18 | 2011-06-22 | Takeda Pharmaceutical | Derivados de benzazepina y sus usos como antagonistas de histamina h3 |
| AU2010213814B2 (en) | 2009-02-10 | 2015-07-30 | Janssen Pharmaceutica Nv | Quinazolinones as prolyl hydroxylase inhibitors |
| CN102802628A (zh) * | 2009-06-30 | 2012-11-28 | 默沙东公司 | 取代的4-羟基嘧啶-5-甲酰胺 |
| WO2011002623A1 (en) | 2009-06-30 | 2011-01-06 | Merck Sharp & Dohme Corp. | Substituted 4-hydroxypyrimidine-5-carboxamides |
| AR077999A1 (es) * | 2009-09-02 | 2011-10-05 | Vifor Int Ag | Antagonistas de pirimidin y triazin-hepcidina |
| PT2488486T (pt) | 2009-10-13 | 2019-11-05 | Ligand Pharm Inc | Compostos de moléculas pequenas de mimética de fator de crescimento hematopoiético e utilizações dos mesmos |
| WO2011048525A1 (en) * | 2009-10-20 | 2011-04-28 | Pfizer Inc. | Novel heteroaryl imidazoles and heteroaryl triazoles as gamma-secretase modulators |
| PH12012500770A1 (en) * | 2009-10-21 | 2016-05-13 | Daiichi Sankyo Co Ltd | 5-hydroxypyrimidine-4-carboxamide derivative |
| WO2011083314A1 (en) * | 2010-01-08 | 2011-07-14 | Takeda Pharmaceutical Company Limited | Benzazepine derivatives for the treatment of central nervous system disorders |
| WO2011133444A1 (en) | 2010-04-21 | 2011-10-27 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
| UY33469A (es) * | 2010-06-29 | 2012-01-31 | Irm Llc Y Novartis Ag | Composiciones y metodos para modular la via de señalizacion de wnt |
| WO2012021830A1 (en) | 2010-08-13 | 2012-02-16 | Janssen Pharmaceutica Nv | 4 - aminoquinazolin- 2 - yl - 1 - pyrrazole - 4 - carboxylic acid compounds as prolyl hydroxylase inhibitors |
| CN106478497B (zh) * | 2010-10-18 | 2020-05-08 | 拉夸里亚创药株式会社 | 作为ttx-s阻滞剂的芳胺衍生物 |
| GB201102659D0 (en) | 2011-02-15 | 2011-03-30 | Isis Innovation | Assay |
| MX2013015058A (es) | 2011-06-24 | 2014-01-20 | Amgen Inc | Antagonistas de melastatina 8 de potencial receptor transitorio y su uso en tratamientos. |
| MY157429A (en) * | 2011-06-24 | 2016-06-15 | Amgen Inc | Trpm8 antagonists and their use in treatments |
| GB201113101D0 (en) | 2011-07-28 | 2011-09-14 | Isis Innovation | Assay |
| WO2013036676A1 (en) | 2011-09-06 | 2013-03-14 | New York Blood Center, Inc. | Hiv inhibitors |
| WO2013040790A1 (en) * | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
| WO2013040789A1 (en) * | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
| US9079930B2 (en) | 2011-09-23 | 2015-07-14 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
| EP2758058B1 (en) * | 2011-09-23 | 2017-04-26 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
| ES2689481T3 (es) | 2011-10-25 | 2018-11-14 | Janssen Pharmaceutica Nv | Formulaciones de sal de meglumina de ácido 1-(5,6-dicloro-1h-benzo[d]imidazol-2-il)-1h-pirazol-4-carboxílico |
| CA2869135A1 (en) | 2012-03-30 | 2013-10-03 | Daiichi Sankyo Company, Limited | (2-heteroarylamino)succinic acid derivatives |
| CN103450194B (zh) * | 2012-06-05 | 2015-07-08 | 首都医科大学 | 四氢-β-咔啉-3-甲酰脂肪链胺、其制备、纳米结构、免疫抑制作用及应用 |
| US8952009B2 (en) | 2012-08-06 | 2015-02-10 | Amgen Inc. | Chroman derivatives as TRPM8 inhibitors |
| WO2014160810A1 (en) * | 2013-03-29 | 2014-10-02 | Takeda Pharmaceutical Company Limited | 6-(5-hydroxy-1h-pyrazol-1-yl)nicotinamide derivatives and their use as phd inhibitors |
| CN106061963B (zh) | 2013-12-20 | 2019-10-22 | 3-V生物科学股份有限公司 | 脂质合成的杂环调节剂和其组合 |
| JP2017114765A (ja) * | 2014-04-25 | 2017-06-29 | 大正製薬株式会社 | トリアゾリルで置換されたヘテロアリール化合物 |
| US10137107B2 (en) | 2014-09-19 | 2018-11-27 | New York Blood Center, Inc. | Substituted phenylpyrrolecarboxamides with therapeutic activity in HIV |
| CA2962922C (en) * | 2014-09-29 | 2021-10-26 | The Scripps Research Institute | Sphingosine-1-phosphate receptor modulators for treatment of cardiopulmonary disorders |
| WO2016054804A1 (en) * | 2014-10-10 | 2016-04-14 | Merck Sharp & Dohme Corp. | Substituted pyrimidines as inhibitors of hif prolyl hydroxylase |
| CN111349077B (zh) * | 2019-02-02 | 2022-06-28 | 杭州华东医药集团新药研究院有限公司 | 一种哒嗪衍生物及其制备方法和医药用途 |
| GB201908511D0 (en) * | 2019-06-13 | 2019-07-31 | Adorx Therapeutics Ltd | Hydroxamate compounds |
| AU2021350973B2 (en) * | 2020-09-25 | 2024-03-07 | Shanghai Meiyue Biotech Development Co., Ltd. | Pyrimidine carboxamide compound and application thereof |
| US20240051943A1 (en) * | 2020-12-21 | 2024-02-15 | Intervet Inc. | A process for the preparation of n-(bis(4-methoxyphenyl)methyl)-6-oxo-2-(pyridazin-3-yl)-1,6-dihydropyrimidine-5-carboxamide |
| CN114835687B (zh) * | 2021-04-02 | 2023-09-05 | 北京华森英诺生物科技有限公司 | AhR抑制剂 |
| IL308349A (en) | 2021-08-10 | 2024-01-01 | Abbvie Inc | NICOTINAMIDE RIPK1 INHIBITORS |
| US20250002491A1 (en) | 2021-10-04 | 2025-01-02 | Forx Therapeutics Ag | N,n-dimethyl-4-(7-(n-(1-methylcyclopropyl)sulfamoyl)-imidazo[1,5-a]pyridin-5-yl)piperazine-1-carboxamide derivatives and the corresponding pyrazolo[1,5-a]pyridine derivatives as parg inhibitors for the treatment of cancer |
| GB202301059D0 (en) * | 2023-01-25 | 2023-03-08 | Univ Oxford Innovation Ltd | PHD inhibitors |
| GB202301050D0 (en) * | 2023-01-25 | 2023-03-08 | Univ Oxford Innovation Ltd | PHD Inhibitors |
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| DE2853220A1 (de) * | 1978-12-09 | 1980-07-03 | Hoechst Ag | Neue amino-pyrimidin-carbanilide, verfahren zu ihrer herstellung, diese verbindungen enthaltende arzneimittel und ihre verwendung |
| ATE147384T1 (de) * | 1992-02-22 | 1997-01-15 | Hoechst Ag | 4-amino-2-ureido-pyrimidin-5-carbonsäureamide, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| CN102584799A (zh) * | 1999-09-16 | 2012-07-18 | 田边三菱制药株式会社 | 含氮的6-员芳香环化合物 |
| DE60025243T2 (de) * | 1999-10-12 | 2006-06-22 | Takeda Pharmaceutical Co. Ltd. | Pyrimidin-5-carboximidverbindungen, verfahren zur herstellung derselben und deren verwendung |
| US7273868B2 (en) * | 2000-04-28 | 2007-09-25 | Tanabe Seiyaku Co., Ltd. | Pyrazine derivatives |
| HUP0301802A3 (en) * | 2000-06-28 | 2009-04-28 | Teva Pharma | Process for producing carvedilol, crystalline carvedilol, process for producing it and pharmaceutical composition containing it |
| EP1366760B1 (en) * | 2001-02-15 | 2010-06-30 | Mitsubishi Tanabe Pharma Corporation | Tablets quickly disintegrated in oral cavity |
| HUP0303841A2 (hu) * | 2001-02-20 | 2004-03-01 | Bristol-Myers Squibb Company | 2,4-Diszubsztituált-5-pirimidinkarboxamid-származékok mint KCNQ káliumcsatorna modulátorok és ezeket tartalmazó gyógyszerkészítmények és előállításuk |
| EP1682532B1 (en) * | 2003-10-31 | 2007-06-27 | Warner-Lambert Company LLC | Pyrimidines as inhibitors of phosphoinositide-3-kinases (pi3k) |
| US7091202B2 (en) * | 2004-09-15 | 2006-08-15 | Bristol-Myers Squibb Company | 4-arylspirocycloalkyl-2-aminopyrimidine carboxamide KCNQ potassium channel modulators |
| WO2007031829A2 (en) * | 2005-09-15 | 2007-03-22 | Orchid Research Laboratories Limited | Novel pyrimidine carboxamides |
| AU2006326449A1 (en) * | 2005-12-14 | 2007-06-21 | E. I. Du Pont De Nemours And Company | Isoxazolines for controlling invertebrate pests |
| CN103382216B (zh) * | 2006-01-27 | 2016-04-20 | 菲布罗根有限公司 | 使低氧诱导因子(hif)稳定的氰基异喹啉化合物 |
| US20090176825A1 (en) * | 2006-05-16 | 2009-07-09 | Fitch Duke M | Prolyl hydroxylase inhibitors |
| JO2934B1 (en) * | 2006-06-23 | 2015-09-15 | سميث كلاين بيتشام كوربوريشن | Prolyl hydroxylase inhibitors |
| NZ623002A (en) * | 2006-06-26 | 2015-08-28 | Akebia Therapeutics Inc | Prolyl hydroxylase inhibitors and methods of use |
| CN101511783A (zh) * | 2006-09-08 | 2009-08-19 | 诺瓦提斯公司 | 用于治疗淋巴细胞相互作用介导的疾病的n-联芳(杂)芳基磺酰胺衍生物 |
-
2009
- 2009-03-09 JP JP2011500864A patent/JP5557832B2/ja active Active
- 2009-03-09 CN CN200980118093.5A patent/CN102036981B/zh active Active
- 2009-03-09 EP EP09722697.1A patent/EP2257539B1/en active Active
- 2009-03-09 CA CA2718528A patent/CA2718528C/en active Active
- 2009-03-09 AU AU2009225869A patent/AU2009225869B2/en active Active
- 2009-03-09 MX MX2010010209A patent/MX2010010209A/es not_active Application Discontinuation
- 2009-03-09 WO PCT/US2009/036501 patent/WO2009117269A1/en not_active Ceased
- 2009-03-09 ES ES09722697.1T patent/ES2524883T3/es active Active
- 2009-03-12 US US12/381,468 patent/US8278304B2/en active Active
- 2009-03-17 CL CL2009000639A patent/CL2009000639A1/es unknown
- 2009-03-17 AR ARP090100958A patent/AR070925A1/es unknown
- 2009-03-17 PE PE2009000390A patent/PE20091627A1/es not_active Application Discontinuation
- 2009-03-17 TW TW098108639A patent/TW200944511A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AR070925A1 (es) | 2010-05-12 |
| CL2009000639A1 (es) | 2009-07-17 |
| JP2011515402A (ja) | 2011-05-19 |
| ES2524883T3 (es) | 2014-12-15 |
| JP5557832B2 (ja) | 2014-07-23 |
| TW200944511A (en) | 2009-11-01 |
| AU2009225869A1 (en) | 2009-09-24 |
| US20090239876A1 (en) | 2009-09-24 |
| CA2718528C (en) | 2016-10-25 |
| CA2718528A1 (en) | 2009-09-24 |
| EP2257539B1 (en) | 2014-09-10 |
| US8278304B2 (en) | 2012-10-02 |
| EP2257539A1 (en) | 2010-12-08 |
| CN102036981B (zh) | 2015-04-08 |
| MX2010010209A (es) | 2010-10-05 |
| WO2009117269A1 (en) | 2009-09-24 |
| AU2009225869B2 (en) | 2014-01-23 |
| CN102036981A (zh) | 2011-04-27 |
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