RU2005103618A - Ингибирующие циклооксигеназу-2 (цог-2) производные пиридина - Google Patents
Ингибирующие циклооксигеназу-2 (цог-2) производные пиридина Download PDFInfo
- Publication number
- RU2005103618A RU2005103618A RU2005103618/04A RU2005103618A RU2005103618A RU 2005103618 A RU2005103618 A RU 2005103618A RU 2005103618/04 A RU2005103618/04 A RU 2005103618/04A RU 2005103618 A RU2005103618 A RU 2005103618A RU 2005103618 A RU2005103618 A RU 2005103618A
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- RU
- Russia
- Prior art keywords
- alkyl
- methyl
- group
- phenyl
- methylsulfonyl
- Prior art date
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- 102000010907 Cyclooxygenase 2 Human genes 0.000 title claims 5
- 108010037462 Cyclooxygenase 2 Proteins 0.000 title claims 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims 72
- 229910052739 hydrogen Inorganic materials 0.000 claims 20
- 229910052799 carbon Inorganic materials 0.000 claims 19
- 150000001875 compounds Chemical class 0.000 claims 18
- 125000001153 fluoro group Chemical group F* 0.000 claims 15
- 125000003545 alkoxy group Chemical group 0.000 claims 13
- 229910052736 halogen Inorganic materials 0.000 claims 13
- 150000002367 halogens Chemical class 0.000 claims 13
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 9
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 6
- 229910052757 nitrogen Inorganic materials 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 239000001301 oxygen Substances 0.000 claims 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 3
- -1 4- (6 - {[(1,3-dimethyl-1H-pyrazol-4-yl) methyl] amino} -4-ethyl-2-pyridinyl) benzene Chemical compound 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000003386 piperidinyl group Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims 2
- 241001465754 Metazoa Species 0.000 claims 2
- 208000027866 inflammatory disease Diseases 0.000 claims 2
- 230000001404 mediated effect Effects 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 229940124530 sulfonamide Drugs 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- KJROYZQXANQCCB-UHFFFAOYSA-N 2-(4-methylsulfonylphenyl)-6-(pyridin-2-ylmethoxy)-4-(trifluoromethyl)pyridine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=CC(C(F)(F)F)=CC(OCC=2N=CC=CC=2)=N1 KJROYZQXANQCCB-UHFFFAOYSA-N 0.000 claims 1
- UEGXVPGOZGJIMA-UHFFFAOYSA-N 4-ethyl-2-[(1-methylpyrazol-4-yl)methylamino]-6-(4-methylsulfonylphenyl)pyridine-3-carbonitrile Chemical compound N#CC=1C(CC)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=NC=1NCC=1C=NN(C)C=1 UEGXVPGOZGJIMA-UHFFFAOYSA-N 0.000 claims 1
- GJGCELHMLIVVEN-UHFFFAOYSA-N 4-ethyl-2-[(5-methylpyridin-2-yl)methylamino]-6-(4-methylsulfonylphenyl)pyridine-3-carbonitrile Chemical compound N#CC=1C(CC)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=NC=1NCC1=CC=C(C)C=N1 GJGCELHMLIVVEN-UHFFFAOYSA-N 0.000 claims 1
- CXVYZIFUAOQBKB-UHFFFAOYSA-N 4-ethyl-2-[(6-methylpyridin-3-yl)methylamino]-6-(4-methylsulfonylphenyl)pyridine-3-carbonitrile Chemical compound N#CC=1C(CC)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=NC=1NCC1=CC=C(C)N=C1 CXVYZIFUAOQBKB-UHFFFAOYSA-N 0.000 claims 1
- QLEFRAISEMFOGS-UHFFFAOYSA-N 4-ethyl-6-(4-methylsulfonylphenyl)-2-(pyridin-2-ylmethoxy)pyridine-3-carbonitrile Chemical compound N#CC=1C(CC)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=NC=1OCC1=CC=CC=N1 QLEFRAISEMFOGS-UHFFFAOYSA-N 0.000 claims 1
- LLQNNOXVGDGVCI-UHFFFAOYSA-N 4-ethyl-6-(4-methylsulfonylphenyl)-2-(pyridin-2-ylmethylamino)pyridine-3-carbonitrile Chemical compound N#CC=1C(CC)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=NC=1NCC1=CC=CC=N1 LLQNNOXVGDGVCI-UHFFFAOYSA-N 0.000 claims 1
- JPRMYQBDXDYHMB-UHFFFAOYSA-N 4-ethyl-6-(4-methylsulfonylphenyl)-2-[(4-methyl-1,3-thiazol-2-yl)methylamino]pyridine-3-carbonitrile Chemical compound N#CC=1C(CC)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=NC=1NCC1=NC(C)=CS1 JPRMYQBDXDYHMB-UHFFFAOYSA-N 0.000 claims 1
- LSJNJEUKEDFUOS-UHFFFAOYSA-N 4-ethyl-6-(4-methylsulfonylphenyl)-n-(oxan-4-ylmethyl)pyridin-2-amine Chemical compound N=1C(C=2C=CC(=CC=2)S(C)(=O)=O)=CC(CC)=CC=1NCC1CCOCC1 LSJNJEUKEDFUOS-UHFFFAOYSA-N 0.000 claims 1
- WOPITVVKVRKXAR-UHFFFAOYSA-N 4-ethyl-n-[(2-ethyl-1,2,4-triazol-3-yl)methyl]-6-(4-methylsulfonylphenyl)pyridin-2-amine Chemical compound N=1C(C=2C=CC(=CC=2)S(C)(=O)=O)=CC(CC)=CC=1NCC1=NC=NN1CC WOPITVVKVRKXAR-UHFFFAOYSA-N 0.000 claims 1
- ZYYZFEFYWDMJKQ-UHFFFAOYSA-N 4-methyl-n-[(1-methylpyrazol-3-yl)methyl]-6-(4-methylsulfonylphenyl)pyridin-2-amine Chemical compound N=1C(C=2C=CC(=CC=2)S(C)(=O)=O)=CC(C)=CC=1NCC=1C=CN(C)N=1 ZYYZFEFYWDMJKQ-UHFFFAOYSA-N 0.000 claims 1
- TXHSNZYVIKJKHL-UHFFFAOYSA-N 4-methyl-n-[(1-methylpyrazol-4-yl)methyl]-6-(4-methylsulfonylphenyl)pyridin-2-amine Chemical compound N=1C(C=2C=CC(=CC=2)S(C)(=O)=O)=CC(C)=CC=1NCC=1C=NN(C)C=1 TXHSNZYVIKJKHL-UHFFFAOYSA-N 0.000 claims 1
- RHAKELPGMNNZMY-UHFFFAOYSA-N 4-methyl-n-[(2-methylpyrazol-3-yl)methyl]-6-(4-methylsulfonylphenyl)pyridin-2-amine Chemical compound N=1C(C=2C=CC(=CC=2)S(C)(=O)=O)=CC(C)=CC=1NCC1=CC=NN1C RHAKELPGMNNZMY-UHFFFAOYSA-N 0.000 claims 1
- PKHKNWQIBCZJMC-UHFFFAOYSA-N 4-methyl-n-[(3-methyl-1,2-oxazol-4-yl)methyl]-6-(4-methylsulfonylphenyl)pyridin-2-amine Chemical compound CC1=NOC=C1CNC1=CC(C)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 PKHKNWQIBCZJMC-UHFFFAOYSA-N 0.000 claims 1
- JQYGMWSNHGUYFH-UHFFFAOYSA-N 6-(4-methylsulfonylphenyl)-n-(pyridin-2-ylmethyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=CC(C(F)(F)F)=CC(NCC=2N=CC=CC=2)=N1 JQYGMWSNHGUYFH-UHFFFAOYSA-N 0.000 claims 1
- VFQRMDNTBZLTOG-UHFFFAOYSA-N 6-(4-methylsulfonylphenyl)-n-[(2-methyl-1,2,4-triazol-3-yl)methyl]-4-(trifluoromethyl)pyridin-2-amine Chemical compound CN1N=CN=C1CNC1=CC(C(F)(F)F)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 VFQRMDNTBZLTOG-UHFFFAOYSA-N 0.000 claims 1
- ZRBRLFRIMWOPNI-UHFFFAOYSA-N 6-(4-methylsulfonylphenyl)-n-pentan-3-yl-4-(trifluoromethyl)pyridin-2-amine Chemical compound CCC(CC)NC1=CC(C(F)(F)F)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 ZRBRLFRIMWOPNI-UHFFFAOYSA-N 0.000 claims 1
- IFLNYNOUGIZZSM-AKAXFMLLSA-N C1C[C@@H](C)CC[C@H]1NC1=CC(C(F)(F)F)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 Chemical compound C1C[C@@H](C)CC[C@H]1NC1=CC(C(F)(F)F)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 IFLNYNOUGIZZSM-AKAXFMLLSA-N 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- IMXXUEDKOYSPGU-UHFFFAOYSA-N n-(cyclohexylmethyl)-6-(4-methylsulfonylphenyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=CC(C(F)(F)F)=CC(NCC2CCCCC2)=N1 IMXXUEDKOYSPGU-UHFFFAOYSA-N 0.000 claims 1
- KTOVEMBDIBZSDA-UHFFFAOYSA-N n-(cyclopentylmethyl)-6-(4-methylsulfonylphenyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=CC(C(F)(F)F)=CC(NCC2CCCC2)=N1 KTOVEMBDIBZSDA-UHFFFAOYSA-N 0.000 claims 1
- CREBKKWJYADUSK-UHFFFAOYSA-N n-[(1,3-dimethylpyrazol-4-yl)methyl]-4-methyl-6-(4-methylsulfonylphenyl)pyridin-2-amine Chemical compound CC1=NN(C)C=C1CNC1=CC(C)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 CREBKKWJYADUSK-UHFFFAOYSA-N 0.000 claims 1
- RULFYBHOHILGIR-UHFFFAOYSA-N n-[(1,3-dimethylpyrazol-4-yl)methyl]-6-(4-methylsulfonylphenyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound CC1=NN(C)C=C1CNC1=CC(C(F)(F)F)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 RULFYBHOHILGIR-UHFFFAOYSA-N 0.000 claims 1
- ZPHKVHNHVVZLMJ-UHFFFAOYSA-N n-[(1,5-dimethylpyrazol-4-yl)methyl]-4-methyl-6-(4-methylsulfonylphenyl)pyridin-2-amine Chemical compound C1=NN(C)C(C)=C1CNC1=CC(C)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 ZPHKVHNHVVZLMJ-UHFFFAOYSA-N 0.000 claims 1
- JVSGYWWKSKBLRR-UHFFFAOYSA-N n-[(1,5-dimethylpyrazol-4-yl)methyl]-6-(4-methylsulfonylphenyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound C1=NN(C)C(C)=C1CNC1=CC(C(F)(F)F)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 JVSGYWWKSKBLRR-UHFFFAOYSA-N 0.000 claims 1
- JOPYSMUAZPPAPM-UHFFFAOYSA-N n-[(2-ethyl-1,2,4-triazol-3-yl)methyl]-4-methyl-6-(4-methylsulfonylphenyl)pyridin-2-amine Chemical compound CCN1N=CN=C1CNC1=CC(C)=CC(C=2C=CC(=CC=2)S(C)(=O)=O)=N1 JOPYSMUAZPPAPM-UHFFFAOYSA-N 0.000 claims 1
- JBPUBVBADITRBO-UHFFFAOYSA-N n-[(3-methyl-1,2,4-oxadiazol-5-yl)methyl]-6-(4-methylsulfonylphenyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound CC1=NOC(CNC=2N=C(C=C(C=2)C(F)(F)F)C=2C=CC(=CC=2)S(C)(=O)=O)=N1 JBPUBVBADITRBO-UHFFFAOYSA-N 0.000 claims 1
- UVKYPAUEYUYGBR-UHFFFAOYSA-N n-[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]-6-(4-methylsulfonylphenyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound O1C(C)=NC(CNC=2N=C(C=C(C=2)C(F)(F)F)C=2C=CC(=CC=2)S(C)(=O)=O)=N1 UVKYPAUEYUYGBR-UHFFFAOYSA-N 0.000 claims 1
- VKISWSRIBFIRHN-UHFFFAOYSA-N n-cycloheptyl-6-(4-methylsulfonylphenyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=CC(C(F)(F)F)=CC(NC2CCCCCC2)=N1 VKISWSRIBFIRHN-UHFFFAOYSA-N 0.000 claims 1
- HOGXDMUYFQWDIN-UHFFFAOYSA-N n-cyclohexyl-6-(4-methylsulfonylphenyl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=CC(C(F)(F)F)=CC(NC2CCCCC2)=N1 HOGXDMUYFQWDIN-UHFFFAOYSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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| AU2008333845C1 (en) | 2007-12-07 | 2014-01-16 | Vertex Pharmaceuticals Incorporated | Solid forms of 3-(6-(1-(2,2-difluorobenzo[d][1,3] dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl) benzoic acid |
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| LT3150198T (lt) | 2010-04-07 | 2021-12-10 | Vertex Pharmaceuticals Incorporated | 3-(6-(1-(2,2-difluorbenzo[d][1,3]dioksol-5-il) ciklopropankarboksamido)-3-metilpiridin-2-il)benzoinės rūgšties farmacinė kompozicija ir jos įvedimas |
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| BR112016010403A2 (pt) | 2013-11-12 | 2017-08-08 | Vertex Pharma | Processo de preparação de composições farmacêuticas para o tratamento de doenças mediadas por cftr |
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| EP1363908A4 (en) | 2001-01-24 | 2004-05-06 | Auckland Uniservices Ltd | ANTI-CANCER COMPLEXES 2,3-DIHYDRO-1H-PYRROLO 3,2-F] COBALT AND CHROME QUINOLINE |
| US6960595B2 (en) * | 2001-03-23 | 2005-11-01 | Bristol-Myers Squibb Pharma Company | 5-6 to 5-7 Heterobicycles as factor Xa inhibitors |
| US6756498B2 (en) | 2001-04-27 | 2004-06-29 | Smithkline Beecham Corporation | Process for the preparation of chemical compounds |
| GB0112803D0 (en) | 2001-05-25 | 2001-07-18 | Glaxo Group Ltd | Pyrimidine derivatives |
| GB0112810D0 (en) | 2001-05-25 | 2001-07-18 | Glaxo Group Ltd | Pyrimidine derivatives |
| GB0112802D0 (en) | 2001-05-25 | 2001-07-18 | Glaxo Group Ltd | Pyrimidine derivatives |
| IL159058A0 (en) | 2001-06-12 | 2004-05-12 | Neurogen Corp | 2,5-diarylpyrazines, 2,5-diarylpyridines and 2,5-diarylpyrimidines as crf1 receptor modulators |
| SE0102439D0 (sv) | 2001-07-05 | 2001-07-05 | Astrazeneca Ab | New compounds |
| GB0119477D0 (en) | 2001-08-09 | 2001-10-03 | Glaxo Group Ltd | Pyrimidine derivatives |
| GB0119472D0 (en) | 2001-08-09 | 2001-10-03 | Astrazeneca Ab | Compounds |
| US6667311B2 (en) | 2001-09-11 | 2003-12-23 | Albany Molecular Research, Inc. | Nitrogen substituted biaryl purine derivatives as potent antiproliferative agents |
| GB0206200D0 (en) | 2002-03-15 | 2002-05-01 | Glaxo Group Ltd | Pharmaceutical compositions |
| US6861249B1 (en) | 2002-04-09 | 2005-03-01 | David Kent | Microbial spray for animal waste |
| DE60305053T2 (de) | 2002-08-19 | 2006-08-31 | Glaxo Group Ltd., Greenford | Pyrimidinderivate als selektive cox-2-inhibitoren |
| GB0221443D0 (en) | 2002-09-16 | 2002-10-23 | Glaxo Group Ltd | Pyridine derivates |
| GB0227443D0 (en) | 2002-11-25 | 2002-12-31 | Glaxo Group Ltd | Pyrimidine derivatives |
| GB0319037D0 (en) | 2003-08-13 | 2003-09-17 | Glaxo Group Ltd | 7-Azaindole Derivatives |
-
2002
- 2002-09-16 GB GBGB0221443.5A patent/GB0221443D0/en not_active Ceased
-
2003
- 2003-09-12 ES ES03795019T patent/ES2343316T3/es not_active Expired - Lifetime
- 2003-09-12 RU RU2005103618/04A patent/RU2005103618A/ru not_active Application Discontinuation
- 2003-09-12 WO PCT/EP2003/011065 patent/WO2004024691A1/en not_active Ceased
- 2003-09-12 AR ARP030103312A patent/AR041246A1/es not_active Application Discontinuation
- 2003-09-12 BR BR0313718-0A patent/BR0313718A/pt not_active IP Right Cessation
- 2003-09-12 CN CNA038218496A patent/CN1681788A/zh active Pending
- 2003-09-12 MX MXPA05002886A patent/MXPA05002886A/es not_active Application Discontinuation
- 2003-09-12 KR KR1020057004428A patent/KR20050046782A/ko not_active Withdrawn
- 2003-09-12 NZ NZ538201A patent/NZ538201A/en unknown
- 2003-09-12 AT AT03795019T patent/ATE462694T1/de not_active IP Right Cessation
- 2003-09-12 PL PL03376023A patent/PL376023A1/xx not_active Application Discontinuation
- 2003-09-12 AU AU2003276063A patent/AU2003276063A1/en not_active Abandoned
- 2003-09-12 US US10/527,799 patent/US7446117B2/en not_active Expired - Fee Related
- 2003-09-12 EP EP03795019A patent/EP1546107B1/en not_active Expired - Lifetime
- 2003-09-12 DE DE60331931T patent/DE60331931D1/de not_active Expired - Lifetime
- 2003-09-12 CA CA002493497A patent/CA2493497A1/en not_active Abandoned
- 2003-09-12 JP JP2004535518A patent/JP4630063B2/ja not_active Expired - Fee Related
- 2003-09-15 TW TW092125337A patent/TW200404541A/zh unknown
-
2005
- 2005-01-20 IS IS7659A patent/IS7659A/is unknown
- 2005-01-24 IL IL16646005A patent/IL166460A0/xx unknown
- 2005-02-08 NO NO20050662A patent/NO20050662L/no not_active Application Discontinuation
- 2005-02-09 ZA ZA200501174A patent/ZA200501174B/xx unknown
- 2005-03-16 MA MA28149A patent/MA27436A1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO20050662L (no) | 2005-04-15 |
| WO2004024691A1 (en) | 2004-03-25 |
| AR041246A1 (es) | 2005-05-11 |
| EP1546107B1 (en) | 2010-03-31 |
| MXPA05002886A (es) | 2005-05-27 |
| ZA200501174B (en) | 2006-11-29 |
| CN1681788A (zh) | 2005-10-12 |
| JP4630063B2 (ja) | 2011-02-09 |
| CA2493497A1 (en) | 2004-03-25 |
| ATE462694T1 (de) | 2010-04-15 |
| US20060040988A1 (en) | 2006-02-23 |
| KR20050046782A (ko) | 2005-05-18 |
| IS7659A (is) | 2005-01-20 |
| EP1546107A1 (en) | 2005-06-29 |
| ES2343316T3 (es) | 2010-07-28 |
| GB0221443D0 (en) | 2002-10-23 |
| AU2003276063A1 (en) | 2004-04-30 |
| NZ538201A (en) | 2007-03-30 |
| MA27436A1 (fr) | 2005-07-01 |
| PL376023A1 (en) | 2005-12-12 |
| BR0313718A (pt) | 2005-07-12 |
| TW200404541A (en) | 2004-04-01 |
| DE60331931D1 (de) | 2010-05-12 |
| IL166460A0 (en) | 2006-01-15 |
| JP2006507247A (ja) | 2006-03-02 |
| US7446117B2 (en) | 2008-11-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA92 | Acknowledgement of application withdrawn (lack of supplementary materials submitted) |
Effective date: 20070926 |