JP2006516976A5 - - Google Patents
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- JP2006516976A5 JP2006516976A5 JP2006500936A JP2006500936A JP2006516976A5 JP 2006516976 A5 JP2006516976 A5 JP 2006516976A5 JP 2006500936 A JP2006500936 A JP 2006500936A JP 2006500936 A JP2006500936 A JP 2006500936A JP 2006516976 A5 JP2006516976 A5 JP 2006516976A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- use according
- noradrenaline reuptake
- methyl
- bowel syndrome
- 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.)
- Ceased
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- -1 imidazole-5-yl - Chemical class 0.000 claims description 19
- 208000002551 irritable bowel syndrome Diseases 0.000 claims description 18
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 14
- 239000003369 serotonin 5-HT3 receptor antagonist Substances 0.000 claims description 11
- VHGCDTVCOLNTBX-QGZVFWFLSA-N atomoxetine Chemical compound O([C@H](CCNC)C=1C=CC=CC=1)C1=CC=CC=C1C VHGCDTVCOLNTBX-QGZVFWFLSA-N 0.000 claims description 10
- 229960002430 atomoxetine Drugs 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 208000023505 abnormal feces Diseases 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 229950001588 ramosetron Drugs 0.000 claims description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 7
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- GZXONPGTMHLBKQ-UTONKHPSSA-N 2,3-dihydroindol-1-yl-[(5r)-4,5,6,7-tetrahydro-3h-benzimidazol-5-yl]methanone;hydrochloride Chemical compound Cl.C1CC2=CC=CC=C2N1C(=O)[C@H]1CC(NC=N2)=C2CC1 GZXONPGTMHLBKQ-UTONKHPSSA-N 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- YWPHCCPCQOJSGZ-LLVKDONJSA-N (2r)-2-[(2-ethoxyphenoxy)methyl]morpholine Chemical compound CCOC1=CC=CC=C1OC[C@@H]1OCCNC1 YWPHCCPCQOJSGZ-LLVKDONJSA-N 0.000 claims description 5
- FELGMEQIXOGIFQ-CYBMUJFWSA-N (3r)-9-methyl-3-[(2-methylimidazol-1-yl)methyl]-2,3-dihydro-1h-carbazol-4-one Chemical compound CC1=NC=CN1C[C@@H]1C(=O)C(C=2C(=CC=CC=2)N2C)=C2CC1 FELGMEQIXOGIFQ-CYBMUJFWSA-N 0.000 claims description 5
- 206010000060 Abdominal distension Diseases 0.000 claims description 5
- HCYAFALTSJYZDH-UHFFFAOYSA-N Desimpramine Chemical compound C1CC2=CC=CC=C2N(CCCNC)C2=CC=CC=C21 HCYAFALTSJYZDH-UHFFFAOYSA-N 0.000 claims description 5
- WUKZPHOXUVCQOR-UHFFFAOYSA-N N-(1-azabicyclo[2.2.2]octan-3-yl)-6-chloro-4-methyl-3-oxo-1,4-benzoxazine-8-carboxamide Chemical compound C1N(CC2)CCC2C1NC(=O)C1=CC(Cl)=CC2=C1OCC(=O)N2C WUKZPHOXUVCQOR-UHFFFAOYSA-N 0.000 claims description 5
- PHVGLTMQBUFIQQ-UHFFFAOYSA-N Nortryptiline Chemical compound C1CC2=CC=CC=C2C(=CCCNC)C2=CC=CC=C21 PHVGLTMQBUFIQQ-UHFFFAOYSA-N 0.000 claims description 5
- 229960003550 alosetron Drugs 0.000 claims description 5
- FLZQKRKHLSUHOR-UHFFFAOYSA-N alosetron Chemical compound CC1=NC=N[C]1CN1C(=O)C(C=2C(=CC=CC=2)N2C)=C2CC1 FLZQKRKHLSUHOR-UHFFFAOYSA-N 0.000 claims description 5
- 229950005951 azasetron Drugs 0.000 claims description 5
- UKTAZPQNNNJVKR-KJGYPYNMSA-N chembl2368925 Chemical compound C1=CC=C2C(C(O[C@@H]3C[C@@H]4C[C@H]5C[C@@H](N4CC5=O)C3)=O)=CNC2=C1 UKTAZPQNNNJVKR-KJGYPYNMSA-N 0.000 claims description 5
- 229960003914 desipramine Drugs 0.000 claims description 5
- 229960003413 dolasetron Drugs 0.000 claims description 5
- 229960003727 granisetron Drugs 0.000 claims description 5
- MFWNKCLOYSRHCJ-BTTYYORXSA-N granisetron Chemical compound C1=CC=C2C(C(=O)N[C@H]3C[C@H]4CCC[C@@H](C3)N4C)=NN(C)C2=C1 MFWNKCLOYSRHCJ-BTTYYORXSA-N 0.000 claims description 5
- 229950007467 indisetron Drugs 0.000 claims description 5
- MHNNVDILNTUWNS-XYYAHUGASA-N indisetron Chemical group C1=CC=C2C(C(=O)N[C@H]3C[C@H]4CN(C[C@@H](C3)N4C)C)=NNC2=C1 MHNNVDILNTUWNS-XYYAHUGASA-N 0.000 claims description 5
- QSLMDECMDJKHMQ-GSXCWMCISA-N maprotiline Chemical compound C12=CC=CC=C2[C@@]2(CCCNC)C3=CC=CC=C3[C@@H]1CC2 QSLMDECMDJKHMQ-GSXCWMCISA-N 0.000 claims description 5
- 229960004090 maprotiline Drugs 0.000 claims description 5
- 229960001158 nortriptyline Drugs 0.000 claims description 5
- 229960005343 ondansetron Drugs 0.000 claims description 5
- FDXQKWSTUZCCTM-UHFFFAOYSA-N oxaprotiline Chemical compound C12=CC=CC=C2C2(CC(O)CNC)C3=CC=CC=C3C1CC2 FDXQKWSTUZCCTM-UHFFFAOYSA-N 0.000 claims description 5
- 229960002131 palonosetron Drugs 0.000 claims description 5
- CPZBLNMUGSZIPR-NVXWUHKLSA-N palonosetron Chemical compound C1N(CC2)CCC2[C@@H]1N1C(=O)C(C=CC=C2CCC3)=C2[C@H]3C1 CPZBLNMUGSZIPR-NVXWUHKLSA-N 0.000 claims description 5
- NTHPAPBPFQJABD-LLVKDONJSA-N ramosetron Chemical compound C12=CC=CC=C2N(C)C=C1C(=O)[C@H]1CC(NC=N2)=C2CC1 NTHPAPBPFQJABD-LLVKDONJSA-N 0.000 claims description 5
- 229960003770 reboxetine Drugs 0.000 claims description 5
- CBQGYUDMJHNJBX-RTBURBONSA-N reboxetine Chemical compound CCOC1=CC=CC=C1O[C@H](C=1C=CC=CC=1)[C@@H]1OCCNC1 CBQGYUDMJHNJBX-RTBURBONSA-N 0.000 claims description 5
- 229960003688 tropisetron Drugs 0.000 claims description 5
- UIVFDCIXTSJXBB-ITGUQSILSA-N tropisetron Chemical compound C1=CC=C[C]2C(C(=O)O[C@H]3C[C@H]4CC[C@@H](C3)N4C)=CN=C21 UIVFDCIXTSJXBB-ITGUQSILSA-N 0.000 claims description 5
- 229960001255 viloxazine Drugs 0.000 claims description 5
- 206010012735 Diarrhoea Diseases 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- SPKBYQZELVEOLL-QDMKHBRRSA-N chembl2111147 Chemical compound N([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C1=CC(Cl)=CC2=C1OC(C)(C)C2 SPKBYQZELVEOLL-QDMKHBRRSA-N 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 229950004681 zacopride Drugs 0.000 claims description 4
- 229950001074 zatosetron Drugs 0.000 claims description 4
- GJJFMKBJSRMPLA-HIFRSBDPSA-N (1R,2S)-2-(aminomethyl)-N,N-diethyl-1-phenyl-1-cyclopropanecarboxamide Chemical compound C=1C=CC=CC=1[C@@]1(C(=O)N(CC)CC)C[C@@H]1CN GJJFMKBJSRMPLA-HIFRSBDPSA-N 0.000 claims description 3
- PWWDCRQZITYKDV-UHFFFAOYSA-N 1-benzyl-2-piperazin-1-ylbenzimidazole Chemical compound C1CNCCN1C1=NC2=CC=CC=C2N1CC1=CC=CC=C1 PWWDCRQZITYKDV-UHFFFAOYSA-N 0.000 claims description 3
- DBXKJORICFHAQA-UHFFFAOYSA-N 2-[(2-methylimidazol-1-yl)methyl]benzo[f]thiochromen-1-one;hydrochloride Chemical compound Cl.CC1=NC=CN1CC1=CSC2=CC=C(C=CC=C3)C3=C2C1=O DBXKJORICFHAQA-UHFFFAOYSA-N 0.000 claims description 3
- FEROPKNOYKURCJ-UHFFFAOYSA-N 4-amino-N-(1-azabicyclo[2.2.2]octan-3-yl)-5-chloro-2-methoxybenzamide Chemical compound COC1=CC(N)=C(Cl)C=C1C(=O)NC1C(CC2)CCN2C1 FEROPKNOYKURCJ-UHFFFAOYSA-N 0.000 claims description 3
- DHSSDEDRBUKTQY-UHFFFAOYSA-N 6-prop-2-enyl-4,5,7,8-tetrahydrothiazolo[4,5-d]azepin-2-amine Chemical compound C1CN(CC=C)CCC2=C1N=C(N)S2 DHSSDEDRBUKTQY-UHFFFAOYSA-N 0.000 claims description 3
- JJZXGTBGAPUCHC-PBWFPOADSA-N [(1r,5s)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-ethyl-2-oxobenzimidazole-1-carboxylate Chemical compound C1[C@@H](N2C)CC[C@@H]2CC1OC(=O)N1C2=CC=CC=C2N(CC)C1=O JJZXGTBGAPUCHC-PBWFPOADSA-N 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 3
- 229950009727 lerisetron Drugs 0.000 claims description 3
- 229960000600 milnacipran Drugs 0.000 claims description 3
- AFOFVIBWSLOHFR-GOOCMWNKSA-N n-[(1r,5s)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl]-2-oxo-3-propan-2-ylbenzimidazole-1-carboxamide Chemical compound C1[C@@H](N2C)CC[C@@H]2CC1NC(=O)N1C2=CC=CC=C2N(C(C)C)C1=O AFOFVIBWSLOHFR-GOOCMWNKSA-N 0.000 claims description 3
- KOYCUQMOCJHRJC-MLOZCBHJSA-N n-[(1s,5r)-3,9-dimethyl-3,9-diazabicyclo[3.3.1]nonan-7-yl]-1h-indazole-3-carboxamide;hydron;dichloride Chemical compound Cl.Cl.C1=CC=C2C(C(=O)NC3C[C@H]4CN(C[C@@H](C3)N4C)C)=NNC2=C1 KOYCUQMOCJHRJC-MLOZCBHJSA-N 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 208000024891 symptom Diseases 0.000 claims description 3
- 229950008418 talipexole Drugs 0.000 claims description 3
- PNVNVHUZROJLTJ-UHFFFAOYSA-N venlafaxine Chemical compound C1=CC(OC)=CC=C1C(CN(C)C)C1(O)CCCCC1 PNVNVHUZROJLTJ-UHFFFAOYSA-N 0.000 claims description 3
- 229960004688 venlafaxine Drugs 0.000 claims description 3
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
- 239000002767 noradrenalin uptake inhibitor Substances 0.000 claims 9
- 239000003814 drug Substances 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- 229940126569 noradrenaline reuptake inhibitor Drugs 0.000 claims 5
- 229950007654 itasetron Drugs 0.000 claims 4
- RWXRJSRJIITQAK-ZSBIGDGJSA-N itasetron Chemical compound C12=CC=CC=C2NC(=O)N1C(=O)N[C@H](C1)C[C@H]2CC[C@@H]1N2C RWXRJSRJIITQAK-ZSBIGDGJSA-N 0.000 claims 4
- 230000008485 antagonism Effects 0.000 claims 3
- MJCKISCWHDATBN-UHFFFAOYSA-N 4-amino-5-chloro-n-[(1-ethyl-4,5-dihydroimidazol-2-yl)methyl]-2-methoxybenzamide Chemical compound CCN1CCN=C1CNC(=O)C1=CC(Cl)=C(N)C=C1OC MJCKISCWHDATBN-UHFFFAOYSA-N 0.000 claims 2
- JCOJXICRPMRJPO-UHFFFAOYSA-N N-pent-3-yn-2-yloxybenzamide Chemical compound C(C1=CC=CC=C1)(=O)NOC(C#CC)C JCOJXICRPMRJPO-UHFFFAOYSA-N 0.000 claims 2
- 229950007840 bemesetron Drugs 0.000 claims 2
- MNJNPLVXBISNSX-WDNDVIMCSA-N bemesetron Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C1=CC(Cl)=CC(Cl)=C1 MNJNPLVXBISNSX-WDNDVIMCSA-N 0.000 claims 2
- 230000005764 inhibitory process Effects 0.000 claims 2
- 229950002371 lintopride Drugs 0.000 claims 2
- 210000003097 mucus Anatomy 0.000 claims 2
- 230000000966 norepinephrine reuptake Effects 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- 230000001078 anti-cholinergic effect Effects 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000010006 flight Effects 0.000 claims 1
- QMEZUZOCLYUADC-UHFFFAOYSA-N hydrate;dihydrochloride Chemical compound O.Cl.Cl QMEZUZOCLYUADC-UHFFFAOYSA-N 0.000 claims 1
- 239000002966 varnish Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 description 4
- 206010010774 Constipation Diseases 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- YLHAMFZCYBVACR-UHFFFAOYSA-N Cl.C1=CC=CC2=C3C(=O)C=CSC3=CC=C21 Chemical compound Cl.C1=CC=CC2=C3C(=O)C=CSC3=CC=C21 YLHAMFZCYBVACR-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 208000024330 bloating Diseases 0.000 description 1
- 230000013872 defecation Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 201000000117 functional diarrhea Diseases 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229950003039 renzapride Drugs 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US44007703P | 2003-01-13 | 2003-01-13 | |
| US49248003P | 2003-08-04 | 2003-08-04 | |
| PCT/US2004/000807 WO2004062623A2 (en) | 2003-01-13 | 2004-01-13 | Method of treating functional bowel disorders |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011061194A Division JP2011157372A (ja) | 2003-01-13 | 2011-03-18 | 機能性腸障害を処置する方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006516976A JP2006516976A (ja) | 2006-07-13 |
| JP2006516976A5 true JP2006516976A5 (https=) | 2010-11-25 |
Family
ID=32718145
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006500936A Ceased JP2006516976A (ja) | 2003-01-13 | 2004-01-13 | 機能性腸障害を処置する方法 |
| JP2011061194A Pending JP2011157372A (ja) | 2003-01-13 | 2011-03-18 | 機能性腸障害を処置する方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011061194A Pending JP2011157372A (ja) | 2003-01-13 | 2011-03-18 | 機能性腸障害を処置する方法 |
Country Status (13)
| Country | Link |
|---|---|
| US (8) | US20040147509A1 (https=) |
| EP (2) | EP1558081A4 (https=) |
| JP (2) | JP2006516976A (https=) |
| KR (1) | KR20050111318A (https=) |
| CN (1) | CN100353946C (https=) |
| AU (1) | AU2004204825B2 (https=) |
| BR (1) | BRPI0406749A (https=) |
| CA (1) | CA2512983A1 (https=) |
| MX (1) | MXPA05007381A (https=) |
| NZ (1) | NZ541008A (https=) |
| PL (1) | PL378367A1 (https=) |
| WO (1) | WO2004062623A2 (https=) |
| ZA (1) | ZA200505817B (https=) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0216027D0 (en) | 2002-07-10 | 2002-08-21 | Arachnova Therapeutics Ltd | New therapeutic use |
| US20040048874A1 (en) * | 2001-05-22 | 2004-03-11 | Bardsley Hazel Judith | New therapeutic use of 4-(2-fluorophenyl)-6-methyl-2-(1-piperazinyl)thieno[2,3-D]pyrimidine |
| NZ541009A (en) * | 2003-01-13 | 2007-09-28 | Dynogen Pharmaceuticals Inc | Method of treating nausea, vomiting, retching or any combination thereof |
| MXPA05007381A (es) * | 2003-01-13 | 2006-02-10 | Dynogen Pharmaceuticals Inc | Metodo para el tratamiento de transtornos funcionales del intestino. |
| EP1539181B1 (en) * | 2003-04-04 | 2007-06-27 | Dynogen Pharmaceuticals Inc. | Method of treating lower urinary tract disorders |
| DE602006012811D1 (de) * | 2005-01-28 | 2010-04-22 | Astellas Pharma Inc | Verfahren zum screening eines therapeutischen wirkstoffs für darmirritationssyndrome |
| US20060293309A1 (en) * | 2005-03-28 | 2006-12-28 | Dynogen Pharmaceuticals, Inc. | Method of treating disorders and conditions using peripherally-restricted antagonists and inhibitors |
| WO2007000046A1 (en) * | 2005-06-27 | 2007-01-04 | Holburn Biomedical Corporation | Methods for diagnosing functional bowel disease |
| US20070010543A1 (en) * | 2005-07-01 | 2007-01-11 | Dynogen Pharmaceuticals, Inc. | Compositions and methods for treating gastrointestinal hypomotility and associated disorders |
| NZ568064A (en) * | 2005-10-07 | 2011-11-25 | Colocaps Pty Ltd | Preparation for the treatment of diarrhoea comprising loperamide and a bulking agent selected from husks, mucilage, or brans |
| US7441298B2 (en) * | 2005-12-02 | 2008-10-28 | Irobot Corporation | Coverage robot mobility |
| GB0524668D0 (en) * | 2005-12-02 | 2006-01-11 | Novartis Ag | Organic compounds |
| US20070254899A1 (en) * | 2006-03-31 | 2007-11-01 | Dynogen Pharmaceuticals, Inc. | Soluble salts of thieno[2,3-d]pyrimidine derivatives |
| TW200838534A (en) * | 2007-02-07 | 2008-10-01 | Astellas Pharma Inc | Treatment for irritable bowel syndrome |
| WO2010024306A1 (ja) * | 2008-08-28 | 2010-03-04 | アステラス製薬株式会社 | 過敏性腸症候群の治療方法 |
| ES2579616T3 (es) * | 2011-10-18 | 2016-08-12 | Helsinn Healthcare Sa | Combinaciones terapéuticas de netupitant y palonosetrón |
| JOP20130213B1 (ar) | 2012-07-17 | 2021-08-17 | Takeda Pharmaceuticals Co | معارضات لمستقبلht3-5 |
| JP6154025B2 (ja) | 2012-12-24 | 2017-06-28 | ニューロガストルクス,インコーポレイテッド | Gi管障害を治療するための方法 |
| WO2015200369A1 (en) | 2014-06-24 | 2015-12-30 | Neurogastrx, Inc. | Prodrugs of metopimazine |
| JP7055017B2 (ja) * | 2014-09-29 | 2022-04-15 | 武田薬品工業株式会社 | 結晶形の1-(1-メチル-1h-ピラゾール-4-イル)-n-((1r,5s,7s)-9-メチル-3-オキサ-9-アザビシクロ[3.3.1]ノナン-7-イル)-1h-インドール-3-カルボキサミド |
| US10836757B1 (en) | 2020-04-02 | 2020-11-17 | Neurogastrx, Inc. | Polymorphic forms of metopimazine |
| US20240003872A1 (en) * | 2020-11-15 | 2024-01-04 | Aphios Corporation | Methods for assaying and measuring the efficacy of anti-nausea compounds |
| CN113412817B (zh) * | 2021-05-31 | 2022-07-12 | 成都中医药大学附属医院 | 提高成模率减少死亡率的ibs-d实验动物模型方法 |
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-
2004
- 2004-01-13 MX MXPA05007381A patent/MXPA05007381A/es not_active Application Discontinuation
- 2004-01-13 EP EP04701811A patent/EP1558081A4/en not_active Withdrawn
- 2004-01-13 PL PL378367A patent/PL378367A1/pl not_active Application Discontinuation
- 2004-01-13 JP JP2006500936A patent/JP2006516976A/ja not_active Ceased
- 2004-01-13 US US10/757,364 patent/US20040147509A1/en not_active Abandoned
- 2004-01-13 EP EP10075488A patent/EP2286817A3/en not_active Withdrawn
- 2004-01-13 AU AU2004204825A patent/AU2004204825B2/en not_active Ceased
- 2004-01-13 CA CA002512983A patent/CA2512983A1/en not_active Abandoned
- 2004-01-13 WO PCT/US2004/000807 patent/WO2004062623A2/en not_active Ceased
- 2004-01-13 KR KR1020057012930A patent/KR20050111318A/ko not_active Withdrawn
- 2004-01-13 BR BR0406749-5A patent/BRPI0406749A/pt not_active IP Right Cessation
- 2004-01-13 CN CNB2004800042278A patent/CN100353946C/zh not_active Expired - Fee Related
- 2004-01-13 NZ NZ541008A patent/NZ541008A/en unknown
- 2004-05-03 US US10/838,789 patent/US20040254168A1/en not_active Abandoned
- 2004-05-07 US US10/841,319 patent/US20040259862A1/en not_active Abandoned
- 2004-05-07 US US10/841,318 patent/US20040254170A1/en not_active Abandoned
- 2004-05-07 US US10/841,317 patent/US20040254169A1/en not_active Abandoned
- 2004-06-11 US US10/866,593 patent/US20050032780A1/en not_active Abandoned
-
2005
- 2005-04-29 US US11/119,357 patent/US20050192270A1/en not_active Abandoned
- 2005-07-20 ZA ZA200505817A patent/ZA200505817B/en unknown
-
2006
- 2006-05-26 US US11/441,905 patent/US20060217391A1/en not_active Abandoned
-
2011
- 2011-03-18 JP JP2011061194A patent/JP2011157372A/ja active Pending
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