RU2006113691A - Применение 4-анилин-3-хинолинкарбонитрилов для лечения хронической миелогенной лейкемии (cml) - Google Patents
Применение 4-анилин-3-хинолинкарбонитрилов для лечения хронической миелогенной лейкемии (cml) Download PDFInfo
- Publication number
- RU2006113691A RU2006113691A RU2006113691/14A RU2006113691A RU2006113691A RU 2006113691 A RU2006113691 A RU 2006113691A RU 2006113691/14 A RU2006113691/14 A RU 2006113691/14A RU 2006113691 A RU2006113691 A RU 2006113691A RU 2006113691 A RU2006113691 A RU 2006113691A
- Authority
- RU
- Russia
- Prior art keywords
- methoxy
- amino
- methoxyphenyl
- dichloro
- carbonitrile
- Prior art date
Links
- 230000001684 chronic effect Effects 0.000 title 1
- 208000032839 leukemia Diseases 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 25
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 20
- 239000008194 pharmaceutical composition Substances 0.000 claims 10
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000004432 carbon atom Chemical group C* 0.000 claims 8
- 150000003839 salts Chemical class 0.000 claims 8
- 208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 claims 5
- 208000010833 Chronic myeloid leukaemia Diseases 0.000 claims 5
- 208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 claims 5
- 230000002401 inhibitory effect Effects 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- WCXVZXSLSCQTGU-UHFFFAOYSA-N 4-(2,4-dichloro-5-ethoxyanilino)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinoline-3-carbonitrile Chemical compound C1=C(Cl)C(OCC)=CC(NC=2C3=CC(OC)=C(OCC4CCN(C)CC4)C=C3N=CC=2C#N)=C1Cl WCXVZXSLSCQTGU-UHFFFAOYSA-N 0.000 claims 2
- NPTUGALLOCBPCM-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-ethoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCC3CCN(C)CC3)C(OCC)=CC2=C1NC1=CC(OC)=C(Cl)C=C1Cl NPTUGALLOCBPCM-UHFFFAOYSA-N 0.000 claims 2
- JQGPWNQWNMMMAS-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-ethoxy-7-[2-(1-methylpiperidin-4-yl)ethoxy]quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCCC3CCN(C)CC3)C(OCC)=CC2=C1NC1=CC(OC)=C(Cl)C=C1Cl JQGPWNQWNMMMAS-UHFFFAOYSA-N 0.000 claims 2
- PCSXTJQETYJEOI-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-ethoxy-7-[2-(4-methylpiperazin-1-yl)ethoxy]quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCCN3CCN(C)CC3)C(OCC)=CC2=C1NC1=CC(OC)=C(Cl)C=C1Cl PCSXTJQETYJEOI-UHFFFAOYSA-N 0.000 claims 2
- OSJKQGUEJYZHQM-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-ethoxy-7-[3-(1-methylpiperidin-4-yl)propoxy]quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCCCC3CCN(C)CC3)C(OCC)=CC2=C1NC1=CC(OC)=C(Cl)C=C1Cl OSJKQGUEJYZHQM-UHFFFAOYSA-N 0.000 claims 2
- FEPWXPAVJHFWGS-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-ethoxy-7-[3-(4-ethylpiperazin-1-yl)propoxy]quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCCCN3CCN(CC)CC3)C(OCC)=CC2=C1NC1=CC(OC)=C(Cl)C=C1Cl FEPWXPAVJHFWGS-UHFFFAOYSA-N 0.000 claims 2
- SNJXHAGNHXWXDO-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-ethoxy-7-[3-(4-methylpiperazin-1-yl)propoxy]quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCCCN3CCN(C)CC3)C(OCC)=CC2=C1NC1=CC(OC)=C(Cl)C=C1Cl SNJXHAGNHXWXDO-UHFFFAOYSA-N 0.000 claims 2
- TXAYKQMEBQBGLR-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinoline-3-carbonitrile Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=CC(OC)=C(OCC4CCN(C)CC4)C=C3N=CC=2C#N)=C1Cl TXAYKQMEBQBGLR-UHFFFAOYSA-N 0.000 claims 2
- FCIILWHQWNLPJU-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-methoxy-7-[2-(1-methylpiperidin-4-yl)ethoxy]quinoline-3-carbonitrile Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=CC(OC)=C(OCCC4CCN(C)CC4)C=C3N=CC=2C#N)=C1Cl FCIILWHQWNLPJU-UHFFFAOYSA-N 0.000 claims 2
- UNVLTPQRCHRNDB-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-methoxy-7-[2-(4-methylpiperazin-1-yl)ethoxy]quinoline-3-carbonitrile Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=CC(OC)=C(OCCN4CCN(C)CC4)C=C3N=CC=2C#N)=C1Cl UNVLTPQRCHRNDB-UHFFFAOYSA-N 0.000 claims 2
- QXWCRBMAGJJKTO-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-methoxy-7-[3-(1-methylpiperidin-4-yl)propoxy]quinoline-3-carbonitrile Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=CC(OC)=C(OCCCC4CCN(C)CC4)C=C3N=CC=2C#N)=C1Cl QXWCRBMAGJJKTO-UHFFFAOYSA-N 0.000 claims 2
- SUGCHLACYQMXHH-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-6-methoxy-7-[3-(4-propylpiperazin-1-yl)propoxy]quinoline-3-carbonitrile Chemical compound C1CN(CCC)CCN1CCCOC1=CC2=NC=C(C#N)C(NC=3C(=CC(Cl)=C(OC)C=3)Cl)=C2C=C1OC SUGCHLACYQMXHH-UHFFFAOYSA-N 0.000 claims 2
- HOHWAQXKWAAULM-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-7-[(1-ethylpiperidin-4-yl)methoxy]-6-methoxyquinoline-3-carbonitrile Chemical compound C1CN(CC)CCC1COC1=CC2=NC=C(C#N)C(NC=3C(=CC(Cl)=C(OC)C=3)Cl)=C2C=C1OC HOHWAQXKWAAULM-UHFFFAOYSA-N 0.000 claims 2
- JYNBIMGGLJKDLR-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-7-[2-(4-ethylpiperazin-1-yl)ethoxy]-6-methoxyquinoline-3-carbonitrile Chemical compound C1CN(CC)CCN1CCOC1=CC2=NC=C(C#N)C(NC=3C(=CC(Cl)=C(OC)C=3)Cl)=C2C=C1OC JYNBIMGGLJKDLR-UHFFFAOYSA-N 0.000 claims 2
- BIEFBSIFAKMKOT-UHFFFAOYSA-N 4-(2,4-dichloro-5-methoxyanilino)-7-[3-(4-ethylpiperazin-1-yl)propoxy]-6-methoxyquinoline-3-carbonitrile Chemical compound C1CN(CC)CCN1CCCOC1=CC2=NC=C(C#N)C(NC=3C(=CC(Cl)=C(OC)C=3)Cl)=C2C=C1OC BIEFBSIFAKMKOT-UHFFFAOYSA-N 0.000 claims 2
- ONVKFNZGEFTWQD-UHFFFAOYSA-N 4-(2,4-dichloroanilino)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCC3CCN(C)CC3)C(OC)=CC2=C1NC1=CC=C(Cl)C=C1Cl ONVKFNZGEFTWQD-UHFFFAOYSA-N 0.000 claims 2
- YCFQNCQMGGRGHM-UHFFFAOYSA-N 4-(2,4-dimethylanilino)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCC3CCN(C)CC3)C(OC)=CC2=C1NC1=CC=C(C)C=C1C YCFQNCQMGGRGHM-UHFFFAOYSA-N 0.000 claims 2
- ZPKGDYKWVKCDJQ-UHFFFAOYSA-N 4-(2-chloro-5-methoxyanilino)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinoline-3-carbonitrile Chemical compound COC1=CC=C(Cl)C(NC=2C3=CC(OC)=C(OCC4CCN(C)CC4)C=C3N=CC=2C#N)=C1 ZPKGDYKWVKCDJQ-UHFFFAOYSA-N 0.000 claims 2
- YAFBWUKWKZZPIF-UHFFFAOYSA-N 6-methoxy-4-(5-methoxy-2,4-dimethylanilino)-7-[(1-methylpiperidin-4-yl)methoxy]quinoline-3-carbonitrile Chemical compound C1=C(C)C(OC)=CC(NC=2C3=CC(OC)=C(OCC4CCN(C)CC4)C=C3N=CC=2C#N)=C1C YAFBWUKWKZZPIF-UHFFFAOYSA-N 0.000 claims 2
- YQWRDEHPSFGGHV-UHFFFAOYSA-N 6-methoxy-4-(5-methoxy-2-methylanilino)-7-[(1-methylpiperidin-4-yl)methoxy]quinoline-3-carbonitrile Chemical compound COC1=CC=C(C)C(NC=2C3=CC(OC)=C(OCC4CCN(C)CC4)C=C3N=CC=2C#N)=C1 YQWRDEHPSFGGHV-UHFFFAOYSA-N 0.000 claims 2
- BWLSIYJKVFXNFV-UHFFFAOYSA-N 6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]-4-(3,4,5-trimethoxyanilino)quinoline-3-carbonitrile Chemical compound N#CC1=CN=C2C=C(OCC3CCN(C)CC3)C(OC)=CC2=C1NC1=CC(OC)=C(OC)C(OC)=C1 BWLSIYJKVFXNFV-UHFFFAOYSA-N 0.000 claims 2
- 229940122924 Src inhibitor Drugs 0.000 claims 2
- UBPYILGKFZZVDX-UHFFFAOYSA-N bosutinib Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=CC(OC)=C(OCCCN4CCN(C)CC4)C=C3N=CC=2C#N)=C1Cl UBPYILGKFZZVDX-UHFFFAOYSA-N 0.000 claims 2
- 229940043355 kinase inhibitor Drugs 0.000 claims 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 claims 2
- 239000005517 L01XE01 - Imatinib Substances 0.000 claims 1
- 229940080856 gleevec Drugs 0.000 claims 1
- KTUFNOKKBVMGRW-UHFFFAOYSA-N imatinib Chemical compound C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4706—4-Aminoquinolines; 8-Aminoquinolines, e.g. chloroquine, primaquine
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51781903P | 2003-11-06 | 2003-11-06 | |
| US60/517,819 | 2003-11-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2006113691A true RU2006113691A (ru) | 2007-12-20 |
Family
ID=34590192
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2006113691/14A RU2006113691A (ru) | 2003-11-06 | 2004-11-03 | Применение 4-анилин-3-хинолинкарбонитрилов для лечения хронической миелогенной лейкемии (cml) |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US7417148B2 (https=) |
| EP (1) | EP1680119A1 (https=) |
| JP (1) | JP2007533655A (https=) |
| KR (1) | KR20060118461A (https=) |
| CN (1) | CN1874776A (https=) |
| AU (1) | AU2004289243B2 (https=) |
| BR (1) | BRPI0416289A (https=) |
| CA (1) | CA2543163A1 (https=) |
| CO (1) | CO5690608A2 (https=) |
| CR (1) | CR8350A (https=) |
| EC (1) | ECSP066548A (https=) |
| IL (1) | IL175424A0 (https=) |
| MX (1) | MXPA06004744A (https=) |
| NO (1) | NO20062255L (https=) |
| RU (1) | RU2006113691A (https=) |
| SG (1) | SG146681A1 (https=) |
| WO (1) | WO2005046693A1 (https=) |
| ZA (1) | ZA200603596B (https=) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1680119A1 (en) * | 2003-11-06 | 2006-07-19 | Wyeth | 4-anilino-3-quinolinecarbonitriles for the treatment of chronic myelogenous leukemia (cml) |
| CN103705517A (zh) | 2005-06-17 | 2014-04-09 | 得克萨斯大学体系董事会 | Src激酶抑制剂对溶骨性病变的抑制 |
| CN101252931A (zh) * | 2005-06-24 | 2008-08-27 | 惠氏公司 | 用于治疗癌症的4-苯胺基-3-喹啉甲腈 |
| US20080119463A1 (en) * | 2006-11-16 | 2008-05-22 | Wyeth | 4-Anilino-3-quinolinecarbonitriles for the treatment of acute myelogenous leukemia (AML) |
| WO2008060283A1 (en) * | 2006-11-16 | 2008-05-22 | Wyeth | 4-anilino-3-quinolinecarbonitriles for the treatment of acute myelogenous leukemia (aml) |
| WO2008064004A2 (en) * | 2006-11-16 | 2008-05-29 | Wyeth | 4-anilino-3-quinolinecarbonitriles for the treatment of acute myelogenous leukemia (aml) |
| CA2964162C (en) * | 2007-06-01 | 2019-12-31 | Wyeth Llc | Treatment of imatinib resistant leukemia using 4-aminoquinoline-3-carbonitriles having mutation in the bcrabl gene |
| WO2013187967A1 (en) | 2012-06-15 | 2013-12-19 | Institute For Cancer Research D/B/A The Research Institute Of Fox Case Cancer Center ("Fox Chase Cancer Center") | Sensitization of cancer cells to dna damage by inhibiting kinases essential for dna damage checkpoint control |
| JP6280546B2 (ja) | 2012-06-26 | 2018-02-14 | デル マー ファーマシューティカルズ | ジアンヒドロガラクチトール、ジアセチルジアンヒドロガラクチトール、ジブロモズルシトール、又はこれらの類似体若しくは誘導体を用いた、遺伝子多型又はａｈｉ１の調節不全若しくは変異を有する患者におけるチロシンキナーゼインヒビター抵抗性悪性腫瘍を処置するための方法 |
| WO2015123758A1 (en) | 2014-02-20 | 2015-08-27 | Apotex Inc. | Bosutinib forms and preparation methods thereof |
| EP3246046A4 (en) | 2015-01-13 | 2018-12-05 | Kyoto University | Agent for preventing and/or treating amyotrophic lateral sclerosis |
| US10722484B2 (en) | 2016-03-09 | 2020-07-28 | K-Gen, Inc. | Methods of cancer treatment |
| EP3953450A1 (en) | 2019-04-09 | 2022-02-16 | Massachusetts Institute Of Technology | A micro physiological model for neuronal and muscular diseases and disorders |
| WO2022053130A1 (en) | 2020-09-09 | 2022-03-17 | Sid Alex Group, S.R.O. | Antago-mir-155 for treatment of v-src, c-src-tyrosine kinase-induced cancers |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6002008A (en) * | 1997-04-03 | 1999-12-14 | American Cyanamid Company | Substituted 3-cyano quinolines |
| TWI275390B (en) | 2002-04-30 | 2007-03-11 | Wyeth Corp | Process for the preparation of 7-substituted-3- quinolinecarbonitriles |
| TW200423938A (en) * | 2003-02-21 | 2004-11-16 | Wyeth Corp | 4-[(2,4-dichloro-5-methoxyphenyl)amino]-6-alkoxy-3-quinolinecarbonitriles for the treatment of ischemic injury |
| EP1680119A1 (en) * | 2003-11-06 | 2006-07-19 | Wyeth | 4-anilino-3-quinolinecarbonitriles for the treatment of chronic myelogenous leukemia (cml) |
-
2004
- 2004-11-03 EP EP04800721A patent/EP1680119A1/en not_active Withdrawn
- 2004-11-03 RU RU2006113691/14A patent/RU2006113691A/ru unknown
- 2004-11-03 KR KR1020067008812A patent/KR20060118461A/ko not_active Withdrawn
- 2004-11-03 AU AU2004289243A patent/AU2004289243B2/en not_active Expired
- 2004-11-03 BR BRPI0416289-7A patent/BRPI0416289A/pt not_active Application Discontinuation
- 2004-11-03 US US10/980,097 patent/US7417148B2/en not_active Expired - Lifetime
- 2004-11-03 JP JP2006539641A patent/JP2007533655A/ja active Pending
- 2004-11-03 SG SG200807148-2A patent/SG146681A1/en unknown
- 2004-11-03 MX MXPA06004744A patent/MXPA06004744A/es active IP Right Grant
- 2004-11-03 CN CNA2004800323110A patent/CN1874776A/zh active Pending
- 2004-11-03 CA CA002543163A patent/CA2543163A1/en not_active Abandoned
- 2004-11-03 WO PCT/US2004/036722 patent/WO2005046693A1/en not_active Ceased
-
2006
- 2006-04-20 CR CR8350A patent/CR8350A/es not_active Application Discontinuation
- 2006-05-04 IL IL175424A patent/IL175424A0/en unknown
- 2006-05-05 EC EC2006006548A patent/ECSP066548A/es unknown
- 2006-05-05 ZA ZA200603596A patent/ZA200603596B/xx unknown
- 2006-05-19 NO NO20062255A patent/NO20062255L/no not_active Application Discontinuation
- 2006-05-26 CO CO06051033A patent/CO5690608A2/es not_active Application Discontinuation
-
2008
- 2008-06-16 US US12/139,834 patent/US7919625B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US7919625B2 (en) | 2011-04-05 |
| NO20062255L (no) | 2006-08-01 |
| IL175424A0 (en) | 2008-04-13 |
| US20050101780A1 (en) | 2005-05-12 |
| BRPI0416289A (pt) | 2007-01-23 |
| US7417148B2 (en) | 2008-08-26 |
| SG146681A1 (en) | 2008-10-30 |
| MXPA06004744A (es) | 2006-07-05 |
| CA2543163A1 (en) | 2005-05-26 |
| EP1680119A1 (en) | 2006-07-19 |
| CN1874776A (zh) | 2006-12-06 |
| CO5690608A2 (es) | 2006-10-31 |
| CR8350A (es) | 2006-10-06 |
| US20100029677A1 (en) | 2010-02-04 |
| ZA200603596B (en) | 2009-12-30 |
| AU2004289243A1 (en) | 2005-05-26 |
| AU2004289243B2 (en) | 2010-07-22 |
| KR20060118461A (ko) | 2006-11-23 |
| JP2007533655A (ja) | 2007-11-22 |
| WO2005046693A1 (en) | 2005-05-26 |
| ECSP066548A (es) | 2006-10-17 |
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| FA91 | Application withdrawn (on applicant's request) |
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| FA91 | Application withdrawn (on applicant's request) |
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