AU2004287847A1 - Imidazo(1,2-a)pyridine anxiolytics - Google Patents
Imidazo(1,2-a)pyridine anxiolytics Download PDFInfo
- Publication number
- AU2004287847A1 AU2004287847A1 AU2004287847A AU2004287847A AU2004287847A1 AU 2004287847 A1 AU2004287847 A1 AU 2004287847A1 AU 2004287847 A AU2004287847 A AU 2004287847A AU 2004287847 A AU2004287847 A AU 2004287847A AU 2004287847 A1 AU2004287847 A1 AU 2004287847A1
- Authority
- AU
- Australia
- Prior art keywords
- methyl
- imidazo
- pyridin
- tolyl
- ethanone
- 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.)
- Abandoned
Links
- 239000002249 anxiolytic agent Substances 0.000 title description 3
- 230000000949 anxiolytic effect Effects 0.000 title description 3
- 229940005530 anxiolytics Drugs 0.000 title description 2
- UTCSSFWDNNEEBH-UHFFFAOYSA-N imidazo[1,2-a]pyridine Chemical compound C1=CC=CC2=NC=CN21 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 134
- 238000000034 method Methods 0.000 claims abstract description 90
- 208000019901 Anxiety disease Diseases 0.000 claims abstract description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims description 37
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 28
- 102000004300 GABA-A Receptors Human genes 0.000 claims description 20
- 108090000839 GABA-A Receptors Proteins 0.000 claims description 20
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 15
- 229910052757 nitrogen Inorganic materials 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 14
- 206010010904 Convulsion Diseases 0.000 claims description 13
- 208000035475 disorder Diseases 0.000 claims description 11
- 239000004215 Carbon black (E152) Substances 0.000 claims description 9
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims description 8
- 150000003951 lactams Chemical class 0.000 claims description 8
- 208000002193 Pain Diseases 0.000 claims description 7
- 230000036407 pain Effects 0.000 claims description 7
- 125000003107 substituted aryl group Chemical group 0.000 claims description 7
- OLUHYENLUZPNBC-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-3-yl)-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound C1=CC(C)=CC=C1C1=C(CC(=O)C2OC3=CC=CC=C3OC2)N2C=C(C)C=CC2=N1 OLUHYENLUZPNBC-UHFFFAOYSA-N 0.000 claims description 6
- 208000007101 Muscle Cramp Diseases 0.000 claims description 6
- 208000005392 Spasm Diseases 0.000 claims description 6
- 206010047700 Vomiting Diseases 0.000 claims description 6
- 125000002252 acyl group Chemical group 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 208000020925 Bipolar disease Diseases 0.000 claims description 5
- 208000020401 Depressive disease Diseases 0.000 claims description 5
- 208000030814 Eating disease Diseases 0.000 claims description 5
- 208000019454 Feeding and Eating disease Diseases 0.000 claims description 5
- 208000010877 cognitive disease Diseases 0.000 claims description 5
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 5
- 235000014632 disordered eating Nutrition 0.000 claims description 5
- 208000030533 eye disease Diseases 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 230000002401 inhibitory effect Effects 0.000 claims description 5
- 230000000626 neurodegenerative effect Effects 0.000 claims description 5
- OUNYFBAGLBGQQZ-UHFFFAOYSA-N 1-(2-methylimidazo[1,2-a]pyridin-3-yl)-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound CC=1N=C2C=CC=CN2C=1C(=O)CC(N1C=C(C)C=CC1=N1)=C1C1=CC=C(C)C=C1 OUNYFBAGLBGQQZ-UHFFFAOYSA-N 0.000 claims description 4
- XSJHFVJQRATCHU-UHFFFAOYSA-N 1-(3-methoxythiophen-2-yl)-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound C1=CSC(C(=O)CC=2N3C=C(C)C=CC3=NC=2C=2C=CC(C)=CC=2)=C1OC XSJHFVJQRATCHU-UHFFFAOYSA-N 0.000 claims description 4
- AZHOOSUVNLYVGF-UHFFFAOYSA-N 1-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]-3-thiophen-2-ylpropan-2-one Chemical compound C1=CC(C)=CC=C1C1=C(CC(=O)CC=2SC=CC=2)N2C=C(C)C=CC2=N1 AZHOOSUVNLYVGF-UHFFFAOYSA-N 0.000 claims description 4
- PSWIEORCBJQVIO-UHFFFAOYSA-N 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]-1-(3-methylthiophen-2-yl)ethanone Chemical compound C1=CSC(C(=O)CC=2N3C=C(C)C=CC3=NC=2C=2C=CC(C)=CC=2)=C1C PSWIEORCBJQVIO-UHFFFAOYSA-N 0.000 claims description 4
- OKJRXJSPVFKYOS-UHFFFAOYSA-N 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]-1-thiophen-2-ylethanone Chemical compound C1=CC(C)=CC=C1C1=C(CC(=O)C=2SC=CC=2)N2C=C(C)C=CC2=N1 OKJRXJSPVFKYOS-UHFFFAOYSA-N 0.000 claims description 4
- 206010001488 Aggression Diseases 0.000 claims description 4
- 230000016571 aggressive behavior Effects 0.000 claims description 4
- 208000012761 aggressive behavior Diseases 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 230000003001 depressive effect Effects 0.000 claims description 4
- 208000020016 psychiatric disease Diseases 0.000 claims description 4
- OXAVKXNORMEZCS-UHFFFAOYSA-N 1-(1,5-dimethyltriazol-4-yl)-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound N1=NN(C)C(C)=C1C(=O)CC1=C(C=2C=CC(C)=CC=2)N=C2N1C=C(C)C=C2 OXAVKXNORMEZCS-UHFFFAOYSA-N 0.000 claims description 3
- OQNNRUOSICVMIE-UHFFFAOYSA-N 1-(1-benzothiophen-2-yl)-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound C1=CC(C)=CC=C1C1=C(CC(=O)C=2SC3=CC=CC=C3C=2)N2C=C(C)C=CC2=N1 OQNNRUOSICVMIE-UHFFFAOYSA-N 0.000 claims description 3
- RRSWPILKRQBBAT-UHFFFAOYSA-N 1-(2,5-dimethylpyrazol-3-yl)-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound CN1N=C(C)C=C1C(=O)CC1=C(C=2C=CC(C)=CC=2)N=C2N1C=C(C)C=C2 RRSWPILKRQBBAT-UHFFFAOYSA-N 0.000 claims description 3
- RPXQWDUZISYFIS-UHFFFAOYSA-N 1-(2,7-dimethylimidazo[1,2-a]pyridin-3-yl)-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound CC=1N=C2C=C(C)C=CN2C=1C(=O)CC(N1C=C(C)C=CC1=N1)=C1C1=CC=C(C)C=C1 RPXQWDUZISYFIS-UHFFFAOYSA-N 0.000 claims description 3
- PRFLQFGIQQKWRS-UHFFFAOYSA-N 1-(5,7-dimethylpyrazolo[1,5-a]pyrimidin-3-yl)-2-[2-(4-methoxyphenyl)-6-methylimidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound C1=CC(OC)=CC=C1C1=C(CC(=O)C2=C3N=C(C)C=C(C)N3N=C2)N2C=C(C)C=CC2=N1 PRFLQFGIQQKWRS-UHFFFAOYSA-N 0.000 claims description 3
- GXTBBKDPGINRKD-UHFFFAOYSA-N 1-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]-4-phenylbutan-2-one Chemical compound C1=CC(C)=CC=C1C1=C(CC(=O)CCC=2C=CC=CC=2)N2C=C(C)C=CC2=N1 GXTBBKDPGINRKD-UHFFFAOYSA-N 0.000 claims description 3
- RFRQGQNPUSODBI-UHFFFAOYSA-N 1-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]heptan-2-one Chemical compound N1=C2C=CC(C)=CN2C(CC(=O)CCCCC)=C1C1=CC=C(C)C=C1 RFRQGQNPUSODBI-UHFFFAOYSA-N 0.000 claims description 3
- GQDXBOTUVGHDOU-UHFFFAOYSA-N 1-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]propan-2-one Chemical compound N1=C2C=CC(C)=CN2C(CC(=O)C)=C1C1=CC=C(C)C=C1 GQDXBOTUVGHDOU-UHFFFAOYSA-N 0.000 claims description 3
- YQDFSZIKCJYNRJ-UHFFFAOYSA-N 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]-1-thiophen-3-ylethanone Chemical compound C1=CC(C)=CC=C1C1=C(CC(=O)C2=CSC=C2)N2C=C(C)C=CC2=N1 YQDFSZIKCJYNRJ-UHFFFAOYSA-N 0.000 claims description 3
- 230000004770 neurodegeneration Effects 0.000 claims description 3
- ZSJYHCQDWOQEHA-UHFFFAOYSA-N 1-cyclopentyl-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound C1=CC(C)=CC=C1C1=C(CC(=O)C2CCCC2)N2C=C(C)C=CC2=N1 ZSJYHCQDWOQEHA-UHFFFAOYSA-N 0.000 claims description 2
- DDSQLAZNSYYIAD-UHFFFAOYSA-N 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]-1-(4-methylthiadiazol-5-yl)ethanone Chemical compound N1=NSC(C(=O)CC=2N3C=C(C)C=CC3=NC=2C=2C=CC(C)=CC=2)=C1C DDSQLAZNSYYIAD-UHFFFAOYSA-N 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 3
- ZHOPGYKNRIPWPS-UHFFFAOYSA-N 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]-1-(1-methylpyrrol-2-yl)ethanone Chemical compound C1=CC(C)=CC=C1C1=C(CC(=O)C=2N(C=CC=2)C)N2C=C(C)C=CC2=N1 ZHOPGYKNRIPWPS-UHFFFAOYSA-N 0.000 claims 2
- RKYVBXKNNHDPNN-UHFFFAOYSA-N 1-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]ethanone Chemical compound N1=C2C=CC(C)=CN2C(C(=O)C)=C1C1=CC=C(C)C=C1 RKYVBXKNNHDPNN-UHFFFAOYSA-N 0.000 claims 1
- DPGUTUXFDZQNPH-UHFFFAOYSA-N 2-[6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl]-1-thiophen-2-ylethanone Chemical compound C1=CC(Cl)=CC=C1C1=C(CC(=O)C=2SC=CC=2)N2C=C(Cl)C=CC2=N1 DPGUTUXFDZQNPH-UHFFFAOYSA-N 0.000 claims 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 abstract description 7
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- 230000036506 anxiety Effects 0.000 abstract description 6
- 150000005234 imidazo[1,2-a]pyridines Chemical class 0.000 abstract description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 124
- 239000000243 solution Substances 0.000 description 70
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 69
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 64
- 235000019439 ethyl acetate Nutrition 0.000 description 57
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 56
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 50
- 238000001819 mass spectrum Methods 0.000 description 45
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 42
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- UVFOVSRWICIMNX-UHFFFAOYSA-N methyl 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetate Chemical compound N1=C2C=CC(C)=CN2C(CC(=O)OC)=C1C1=CC=C(C)C=C1 UVFOVSRWICIMNX-UHFFFAOYSA-N 0.000 description 25
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Landscapes
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51504303P | 2003-10-28 | 2003-10-28 | |
| US60/515,043 | 2003-10-28 | ||
| PCT/US2004/035822 WO2005044818A2 (en) | 2003-10-28 | 2004-10-28 | Imidazo[1,2-a]pyridine anxiolytics |
Publications (1)
| Publication Number | Publication Date |
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| AU2004287847A1 true AU2004287847A1 (en) | 2005-05-19 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2004287847A Abandoned AU2004287847A1 (en) | 2003-10-28 | 2004-10-28 | Imidazo(1,2-a)pyridine anxiolytics |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US7148353B2 (enExample) |
| EP (1) | EP1682549B1 (enExample) |
| JP (1) | JP2007509960A (enExample) |
| AT (1) | ATE482211T1 (enExample) |
| AU (1) | AU2004287847A1 (enExample) |
| CA (1) | CA2544213A1 (enExample) |
| DE (1) | DE602004029272D1 (enExample) |
| WO (1) | WO2005044818A2 (enExample) |
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| AU2006327217A1 (en) * | 2005-11-28 | 2007-06-28 | Mallinckrodt Inc. | Improved method of preparation for Imidazolepyridines |
| EP1803722A1 (en) * | 2006-01-03 | 2007-07-04 | Ferrer Internacional, S.A. | Imidazo[1,2-a]pyridin-3-yl-acetic acid hydrazides, processes for their preparation and pharmaceutical uses thereof |
| WO2009143156A2 (en) * | 2008-05-19 | 2009-11-26 | Sepracor Inc. | IMIDAZO[1,2-a]PYRIDINE COMPOUNDS |
| WO2011041713A2 (en) * | 2009-10-02 | 2011-04-07 | Glaxosmithkline Llc | Piperazinyl antiviral agents |
| EP2493889B1 (en) | 2009-10-30 | 2017-09-06 | Janssen Pharmaceutica, N.V. | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| US9556166B2 (en) * | 2011-05-12 | 2017-01-31 | Proteostasis Therapeutics, Inc. | Proteostasis regulators |
| MX344600B (es) | 2011-06-27 | 2016-12-20 | Janssen Pharmaceutica Nv | Derivados de 1-aril-4-metil-[1,2,4]triazolo[4,3-a]quinoxalina. |
| HK1206250A1 (en) | 2012-06-26 | 2016-01-08 | Janssen Pharmaceutica Nv | Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl-[1,2,4] triazolo [4,3-a] quinoxaline compounds and ped 10 inhibitors for use in the treatment of neurological or metabolic disorders |
| CN104411314B (zh) | 2012-07-09 | 2017-10-20 | 詹森药业有限公司 | 磷酸二酯酶10的抑制剂 |
| BR112015000675B1 (pt) * | 2012-07-13 | 2022-07-12 | UCB Biopharma SRL | Derivados de imidazopiridina como moduladores da atividade de tnf |
| TWI648281B (zh) * | 2013-10-17 | 2019-01-21 | 日商安斯泰來製藥股份有限公司 | 含硫二環式化合物 |
| TW201601632A (zh) | 2013-11-20 | 2016-01-16 | 杜邦股份有限公司 | １－芳基－３－烷基吡唑殺蟲劑 |
| AU2015284280C1 (en) | 2014-07-02 | 2020-02-13 | Fmc Corporation | Piperidinone herbicides |
| US9926316B2 (en) * | 2016-03-03 | 2018-03-27 | The Cleveland Clinic Foundation | Antitumor derivatives for differentiation therapy |
| CN107383005B (zh) * | 2017-09-11 | 2020-03-13 | 华东理工大学 | 6-甲基-2-(4-甲基苯基)咪唑并[1,2-a]吡啶-3-乙酸的制备方法 |
| CN113387946B (zh) * | 2021-05-17 | 2023-08-01 | 衡阳师范学院 | 一种超声辅助多组分合成2-苯基-3-芳胺甲基咪唑并吡啶衍生物的方法 |
Family Cites Families (12)
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|---|---|---|---|---|
| SU522187A1 (ru) * | 1975-03-12 | 1976-07-25 | Военная Краснознаменная академия химической защиты им.Маршала Советского Союза С.К.Тимошенко | Способ получени 3-ацил-2-алкил (арил)-имидазо (1,2 )пиридинов |
| FR2492382A1 (fr) * | 1980-10-22 | 1982-04-23 | Synthelabo | Derives d'imidazo (1,2-a) pyridine, leur preparation et leur application en therapeutique |
| FR2525601A1 (fr) | 1982-04-21 | 1983-10-28 | Synthelabo | Derives d'imidazo(1,2-a)pyridines, leur preparation et leur application en therapeutique |
| FR2568880B1 (fr) | 1984-08-07 | 1986-12-12 | Synthelabo | Derives d'acylaminomethyl-3 imidazo(1,2-a)pyridines, leur preparation et leur application en therapeutique |
| WO1986007059A2 (en) | 1985-05-25 | 1986-12-04 | Yoshitomi Pharmaceutical Industries, Ltd. | Oxodiazine compounds |
| FR2647451B1 (fr) | 1989-05-26 | 1994-08-05 | Sanofi Sa | Derives d'imidazo(1,2-a)pyridine, procede de preparation, compositions pharmaceutiques les contenant |
| US6514969B2 (en) * | 2000-08-16 | 2003-02-04 | Boehringer Ingelheim Pharma Kg | β-amyloid inhibitors, processes for preparing them, and their use in pharmaceutical compositions |
| DE10040016A1 (de) * | 2000-08-16 | 2002-02-28 | Boehringer Ingelheim Pharma | Neue beta-Amyloid Inhibitoren, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel |
| SE0100568D0 (sv) | 2001-02-20 | 2001-02-20 | Astrazeneca Ab | Compounds |
| SE0100567D0 (sv) | 2001-02-20 | 2001-02-20 | Astrazeneca Ab | Compounds |
| WO2003000682A1 (en) | 2001-06-25 | 2003-01-03 | Merck & Co., Inc. | (pyrimidyl)(phenyl)substituted fused heteroaryl p38 inhibiting and pkg kinase inhibiting compounds |
| CA2484631A1 (en) | 2002-05-13 | 2003-11-27 | Merck & Co., Inc. | Phenyl substituted imidazopyridines and phenyl substituted benzimidazoles |
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2004
- 2004-10-28 WO PCT/US2004/035822 patent/WO2005044818A2/en not_active Ceased
- 2004-10-28 AU AU2004287847A patent/AU2004287847A1/en not_active Abandoned
- 2004-10-28 CA CA002544213A patent/CA2544213A1/en not_active Abandoned
- 2004-10-28 AT AT04796657T patent/ATE482211T1/de not_active IP Right Cessation
- 2004-10-28 EP EP04796657A patent/EP1682549B1/en not_active Expired - Lifetime
- 2004-10-28 DE DE602004029272T patent/DE602004029272D1/de not_active Expired - Lifetime
- 2004-10-28 JP JP2006538253A patent/JP2007509960A/ja not_active Withdrawn
- 2004-10-28 US US10/976,331 patent/US7148353B2/en not_active Expired - Lifetime
- 2004-10-28 US US10/595,592 patent/US7723324B2/en active Active
-
2006
- 2006-09-15 US US11/532,402 patent/US7566725B2/en not_active Expired - Lifetime
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|---|---|
| US7566725B2 (en) | 2009-07-28 |
| EP1682549B1 (en) | 2010-09-22 |
| US20080096867A1 (en) | 2008-04-24 |
| JP2007509960A (ja) | 2007-04-19 |
| EP1682549A2 (en) | 2006-07-26 |
| US20070043074A1 (en) | 2007-02-22 |
| US7148353B2 (en) | 2006-12-12 |
| ATE482211T1 (de) | 2010-10-15 |
| WO2005044818A3 (en) | 2005-06-16 |
| US20050171144A1 (en) | 2005-08-04 |
| DE602004029272D1 (de) | 2010-11-04 |
| CA2544213A1 (en) | 2005-05-19 |
| US7723324B2 (en) | 2010-05-25 |
| WO2005044818A2 (en) | 2005-05-19 |
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