ZA200304331B - Organic compounds. - Google Patents
Organic compounds. Download PDFInfo
- Publication number
- ZA200304331B ZA200304331B ZA200304331A ZA200304331A ZA200304331B ZA 200304331 B ZA200304331 B ZA 200304331B ZA 200304331 A ZA200304331 A ZA 200304331A ZA 200304331 A ZA200304331 A ZA 200304331A ZA 200304331 B ZA200304331 B ZA 200304331B
- Authority
- ZA
- South Africa
- Prior art keywords
- halogen
- alkyl
- formula
- hydrogen
- compounds
- Prior art date
Links
- 150000002894 organic compounds Chemical class 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 66
- 229910052739 hydrogen Inorganic materials 0.000 claims description 57
- 239000001257 hydrogen Substances 0.000 claims description 57
- -1 phenyloxy Chemical group 0.000 claims description 40
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 37
- 125000001424 substituent group Chemical group 0.000 claims description 29
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 24
- 150000002367 halogens Chemical class 0.000 claims description 23
- 229910052736 halogen Inorganic materials 0.000 claims description 22
- 150000002431 hydrogen Chemical class 0.000 claims description 17
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 8
- 125000004104 aryloxy group Chemical group 0.000 claims description 7
- 241001465754 Metazoa Species 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000005554 pyridyloxy group Chemical group 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 4
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 4
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 244000144972 livestock Species 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 241000607479 Yersinia pestis Species 0.000 claims 4
- 240000007594 Oryza sativa Species 0.000 claims 2
- 244000045947 parasite Species 0.000 claims 2
- 244000294411 Mirabilis expansa Species 0.000 claims 1
- 235000015429 Mirabilis expansa Nutrition 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 235000013536 miso Nutrition 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 7
- 229910052794 bromium Inorganic materials 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 229910052801 chlorine Inorganic materials 0.000 description 7
- 229910052731 fluorine Inorganic materials 0.000 description 7
- 239000011737 fluorine Substances 0.000 description 7
- 125000001153 fluoro group Chemical group F* 0.000 description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 150000008361 aminoacetonitriles Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 244000079386 endoparasite Species 0.000 description 3
- 125000004438 haloalkoxy group Chemical group 0.000 description 3
- 125000001188 haloalkyl group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 244000000013 helminth Species 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 230000000361 pesticidal effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000006039 1-hexenyl group Chemical group 0.000 description 1
- 125000005978 1-naphthyloxy group Chemical group 0.000 description 1
- 125000004797 2,2,2-trichloroethoxy group Chemical group ClC(CO*)(Cl)Cl 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000005979 2-naphthyloxy group Chemical group 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241000244206 Nematoda Species 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000006193 alkinyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000005366 cycloalkylthio group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 description 1
- 125000005347 halocycloalkyl group Chemical group 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- FXWHFKOXMBTCMP-WMEDONTMSA-N milbemycin Natural products COC1C2OCC3=C/C=C/C(C)CC(=CCC4CC(CC5(O4)OC(C)C(C)C(OC(=O)C(C)CC(C)C)C5O)OC(=O)C(C=C1C)C23O)C FXWHFKOXMBTCMP-WMEDONTMSA-N 0.000 description 1
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical class O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 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
- A61K31/275—Nitriles; Isonitriles
-
- 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
- A61K31/275—Nitriles; Isonitriles
- A61K31/277—Nitriles; Isonitriles having a ring, e.g. verapamil
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Paper (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH24892000 | 2000-12-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200304331B true ZA200304331B (en) | 2004-04-28 |
Family
ID=4569596
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200304331A ZA200304331B (en) | 2000-12-20 | 2003-06-03 | Organic compounds. |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US7700656B2 (pt) |
| EP (1) | EP1392281B1 (pt) |
| JP (1) | JP2004521097A (pt) |
| KR (1) | KR100850252B1 (pt) |
| CN (1) | CN1531426A (pt) |
| AR (1) | AR035523A1 (pt) |
| AT (1) | ATE354360T1 (pt) |
| AU (2) | AU3458802A (pt) |
| BR (1) | BR0116326A (pt) |
| CA (1) | CA2432388C (pt) |
| CY (1) | CY1106509T1 (pt) |
| DE (1) | DE60126838T2 (pt) |
| DK (1) | DK1392281T3 (pt) |
| ES (1) | ES2281453T3 (pt) |
| MX (1) | MXPA03005701A (pt) |
| NZ (1) | NZ526538A (pt) |
| PT (1) | PT1392281E (pt) |
| RU (1) | RU2286775C2 (pt) |
| TW (1) | TWI292712B (pt) |
| WO (1) | WO2002049641A2 (pt) |
| ZA (1) | ZA200304331B (pt) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR035531A1 (es) * | 2001-01-22 | 2004-06-02 | Novartis Ag | Composicion para el control de plagas endoparasiticas en ganados y animales domesticos, un metodo para su control y el uso de dicha composicion para la preparacion de medicamentos |
| AR036054A1 (es) | 2001-06-15 | 2004-08-04 | Novartis Ag | Uso de compuestos de aminoacetonitrilo para el control de plagas, una composicion y un proceso para dicho control y una composicion farmaceutica contra parasitos |
| WO2003004474A1 (en) * | 2001-07-06 | 2003-01-16 | Syngenta Participations Ag | Pesticidally active aminoacetonitriles |
| AR037746A1 (es) * | 2001-12-06 | 2004-12-01 | Novartis Ag | Compuestos derivados de amidoacetonitrilo, un procedimiento para su preparacion, un procedimiento para la preparacion de compuestos intermediarios, una composicion para combatir parasitos, un procedimiento para combatir dichos parasitos, y el empleo de dichos derivados para la preparacion de una com |
| TW200305556A (en) * | 2002-03-21 | 2003-11-01 | Novartis Ag | Organic compounds |
| TW200400932A (en) * | 2002-06-19 | 2004-01-16 | Novartis Ag | Organic compounds |
| TW200409760A (en) * | 2002-09-11 | 2004-06-16 | Novartis Ag | Organic compounds |
| GB0402677D0 (en) * | 2003-11-06 | 2004-03-10 | Novartis Ag | Organic compounds |
| TW200613251A (en) * | 2004-06-10 | 2006-05-01 | Novartis Ag | Organic compounds |
| WO2006043654A1 (ja) * | 2004-10-22 | 2006-04-27 | Nihon Nohyaku Co., Ltd. | アセトニトリル誘導体及び有害生物防除剤並びにその使用方法 |
| JP5112074B2 (ja) * | 2004-11-09 | 2013-01-09 | ノバルティス アーゲー | アミドアセトニトリル化合物のラセミ体からのアミドアセトニトリル化合物の鏡像異性体の調製方法 |
| US20080227863A1 (en) * | 2005-07-25 | 2008-09-18 | Novartis Ag | Organic Compounds |
| DE102006025874A1 (de) | 2006-06-02 | 2007-12-06 | Bayer Cropscience Ag | Alkoxyalkyl-substituierte cyclische Ketoenole |
| WO2008062005A1 (en) * | 2006-11-24 | 2008-05-29 | Novartis Ag | The use of aminoacetonitril compounds in the control of endoparasites in warm- blood animals. |
| PL2118055T3 (pl) * | 2007-02-09 | 2014-01-31 | Zoetis Uk Ltd | Środki przeciwpasożytnicze |
| MX2009008028A (es) * | 2007-02-21 | 2009-08-07 | Pfizer Ltd | Agentes antiparasitarios. |
| RS60858B1 (sr) * | 2007-05-15 | 2020-10-30 | Boehringer Ingelheim Animal Health Usa Inc | Ariloazol-2-il cijanoetilamino jedinjenja, postupci dobijanja i postupci njihove primene |
| WO2010048191A1 (en) | 2008-10-21 | 2010-04-29 | Merial Limited | Thioamide compounds, method of making and method of using thereof |
| AU2009313920B2 (en) | 2008-11-14 | 2014-10-23 | Boehringer Ingelheim Animal Health USA Inc. | Enantiomerically enriched aryloazol- 2 -yl cyanoethylamino paraciticidal compounds |
| UY33282A (es) * | 2010-03-25 | 2011-09-30 | Novartis Ag | Composiciones endoparasiticidas |
| CN108524480A (zh) | 2011-03-02 | 2018-09-14 | 国立大学法人东京大学 | 体内寄生虫防除剂 |
| AU2012342433A1 (en) * | 2011-11-25 | 2014-06-12 | Bayer Intellectual Property Gmbh | Use of aryl and hetaryl carboxamides as endoparasiticides |
| AU2013219467B2 (en) * | 2012-02-14 | 2016-07-07 | Nippon Soda Co., Ltd. | Aryloxyacetamide compound and pesticide |
| CN105496999A (zh) * | 2012-08-06 | 2016-04-20 | 皮特尼制药股份有限公司 | 治疗mTOR通路相关的疾病的化合物 |
| US8822689B2 (en) | 2012-09-19 | 2014-09-02 | Merial Limited | Aryloazol-2-yl cyanoethylamino compounds, method of making and method of using thereof |
| AR094961A1 (es) | 2013-03-15 | 2015-09-09 | Lilly Co Eli | 1-hidroxi-benzooxaboroles como agentes antiparasitarios |
| EP2821412A1 (en) * | 2013-07-01 | 2015-01-07 | Universität Zürich | Organometallic 2-cyano-2-aminobenzoate-propyl derivates and their use as anthelmintics |
| WO2015037747A1 (en) * | 2013-09-13 | 2015-03-19 | Nihon Nohyaku Co., Ltd. | Anticancer agent comprising aminoacetonitrile compound as active ingredient |
| EP3235815A1 (de) | 2016-04-19 | 2017-10-25 | Philipps-Universität Marburg | Wirkstoffe gegen parasitäre helminthen |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3457294A (en) | 1966-04-22 | 1969-07-22 | Abbott Lab | N-(substituted-benzoyl) aminoaceto- and aminopropionitriles |
| FR1520925A (fr) | 1966-04-22 | 1968-04-12 | Abbott Lab | Nouveaux benzoylamino-nitriles |
| US4515731A (en) | 1975-08-25 | 1985-05-07 | Monsanto Company | Asymmetric catalysis |
| GB8517279D0 (en) | 1985-07-08 | 1985-08-14 | Ici Plc | Benzamide derivatives |
| JP2994182B2 (ja) * | 1992-07-23 | 1999-12-27 | 石原産業株式会社 | アミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 |
| US6239077B1 (en) | 1998-05-01 | 2001-05-29 | Nihon Nohyaku Co., Ltd. | Aminoacetonitrile derivative agricultural and horticultural insecticide containing the same and use thereof |
| AR035531A1 (es) * | 2001-01-22 | 2004-06-02 | Novartis Ag | Composicion para el control de plagas endoparasiticas en ganados y animales domesticos, un metodo para su control y el uso de dicha composicion para la preparacion de medicamentos |
| JP4124661B2 (ja) | 2001-05-15 | 2008-07-23 | ノバルティス アクチエンゲゼルシャフト | ベンズアミドアセトニトリルおよび駆虫薬としてのその用途 |
| AR036054A1 (es) | 2001-06-15 | 2004-08-04 | Novartis Ag | Uso de compuestos de aminoacetonitrilo para el control de plagas, una composicion y un proceso para dicho control y una composicion farmaceutica contra parasitos |
| WO2003004474A1 (en) * | 2001-07-06 | 2003-01-16 | Syngenta Participations Ag | Pesticidally active aminoacetonitriles |
| AR038156A1 (es) * | 2002-01-21 | 2004-12-29 | Novartis Ag | Compuestos de amidoacetonitrilo, proceso para su preparacion, composicion para controlar los parasitos, y uso de estos compuestos para preparar una composicion farmaceutica |
-
2001
- 2001-12-18 US US10/433,811 patent/US7700656B2/en not_active Expired - Lifetime
- 2001-12-18 EP EP01985421A patent/EP1392281B1/en not_active Expired - Lifetime
- 2001-12-18 TW TW090131306A patent/TWI292712B/zh not_active IP Right Cessation
- 2001-12-18 DK DK01985421T patent/DK1392281T3/da active
- 2001-12-18 AU AU3458802A patent/AU3458802A/xx active Pending
- 2001-12-18 CN CNA018210155A patent/CN1531426A/zh active Pending
- 2001-12-18 MX MXPA03005701A patent/MXPA03005701A/es active IP Right Grant
- 2001-12-18 AT AT01985421T patent/ATE354360T1/de active
- 2001-12-18 CA CA2432388A patent/CA2432388C/en not_active Expired - Lifetime
- 2001-12-18 JP JP2002550981A patent/JP2004521097A/ja active Pending
- 2001-12-18 PT PT01985421T patent/PT1392281E/pt unknown
- 2001-12-18 NZ NZ526538A patent/NZ526538A/en not_active IP Right Cessation
- 2001-12-18 BR BR0116326-4A patent/BR0116326A/pt not_active IP Right Cessation
- 2001-12-18 AU AU2002234588A patent/AU2002234588B2/en not_active Expired
- 2001-12-18 DE DE60126838T patent/DE60126838T2/de not_active Expired - Lifetime
- 2001-12-18 KR KR1020037007242A patent/KR100850252B1/ko not_active IP Right Cessation
- 2001-12-18 RU RU2003122196/15A patent/RU2286775C2/ru active
- 2001-12-18 WO PCT/EP2001/014926 patent/WO2002049641A2/en active IP Right Grant
- 2001-12-18 ES ES01985421T patent/ES2281453T3/es not_active Expired - Lifetime
- 2001-12-18 AR ARP010105864A patent/AR035523A1/es not_active Application Discontinuation
-
2003
- 2003-06-03 ZA ZA200304331A patent/ZA200304331B/en unknown
-
2007
- 2007-04-12 CY CY20071100511T patent/CY1106509T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN1531426A (zh) | 2004-09-22 |
| CA2432388C (en) | 2010-06-08 |
| AU3458802A (en) | 2002-07-01 |
| NZ526538A (en) | 2005-12-23 |
| US7700656B2 (en) | 2010-04-20 |
| WO2002049641A2 (en) | 2002-06-27 |
| TWI292712B (en) | 2008-01-21 |
| CA2432388A1 (en) | 2002-06-27 |
| EP1392281A2 (en) | 2004-03-03 |
| US20040082624A1 (en) | 2004-04-29 |
| RU2003122196A (ru) | 2005-03-20 |
| BR0116326A (pt) | 2004-07-06 |
| ATE354360T1 (de) | 2007-03-15 |
| CY1106509T1 (el) | 2012-01-25 |
| RU2286775C2 (ru) | 2006-11-10 |
| MXPA03005701A (es) | 2003-10-06 |
| DK1392281T3 (da) | 2007-06-11 |
| KR100850252B1 (ko) | 2008-08-04 |
| AR035523A1 (es) | 2004-06-02 |
| DE60126838T2 (de) | 2007-11-08 |
| KR20030061414A (ko) | 2003-07-18 |
| DE60126838D1 (de) | 2007-04-05 |
| AU2002234588B2 (en) | 2005-03-24 |
| EP1392281B1 (en) | 2007-02-21 |
| JP2004521097A (ja) | 2004-07-15 |
| WO2002049641A3 (en) | 2003-12-04 |
| PT1392281E (pt) | 2007-05-31 |
| ES2281453T3 (es) | 2007-10-01 |
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