ES2210990T3 - Uso pesticida y parasiticida de compuestos de tiazolo-/4,5-b) piridina 2-tio substituidos. - Google Patents
Uso pesticida y parasiticida de compuestos de tiazolo-/4,5-b) piridina 2-tio substituidos.Info
- Publication number
- ES2210990T3 ES2210990T3 ES99308947T ES99308947T ES2210990T3 ES 2210990 T3 ES2210990 T3 ES 2210990T3 ES 99308947 T ES99308947 T ES 99308947T ES 99308947 T ES99308947 T ES 99308947T ES 2210990 T3 ES2210990 T3 ES 2210990T3
- Authority
- ES
- Spain
- Prior art keywords
- carbon atoms
- groups
- atoms
- carbon
- pyridine
- 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.)
- Expired - Lifetime
Links
- 239000000575 pesticide Substances 0.000 title claims abstract description 9
- 150000001875 compounds Chemical class 0.000 title claims description 68
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title description 7
- 230000000590 parasiticidal effect Effects 0.000 title description 6
- 239000002297 parasiticide Substances 0.000 title description 4
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- 241000244206 Nematoda Species 0.000 claims description 23
- 125000004429 atom Chemical group 0.000 claims description 23
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 22
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 125000003545 alkoxy group Chemical group 0.000 claims description 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 13
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 125000005347 halocycloalkyl group Chemical group 0.000 claims description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
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- FGIFJNOQNLEKSX-UHFFFAOYSA-N 2-(3,4,4-trifluorobut-3-enylsulfanyl)-[1,3]thiazolo[4,5-b]pyridine Chemical compound C1=CC=C2SC(SCCC(F)=C(F)F)=NC2=N1 FGIFJNOQNLEKSX-UHFFFAOYSA-N 0.000 claims description 6
- WKAGJPPVUAWOTF-UHFFFAOYSA-N 2-(difluoromethylsulfanyl)-[1,3]thiazolo[4,5-b]pyridine Chemical compound C1=CC=C2SC(SC(F)F)=NC2=N1 WKAGJPPVUAWOTF-UHFFFAOYSA-N 0.000 claims description 6
- QQYFYWQEODMNSL-UHFFFAOYSA-N 2-[bromo(difluoro)methyl]sulfanyl-[1,3]thiazolo[4,5-b]pyridine Chemical compound C1=CC=C2SC(SC(F)(Br)F)=NC2=N1 QQYFYWQEODMNSL-UHFFFAOYSA-N 0.000 claims description 6
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
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- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 235000019770 animal feed premixes Nutrition 0.000 description 1
- 230000000767 anti-ulcer Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 229940097012 bacillus thuringiensis Drugs 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- 150000008047 benzoylureas Chemical class 0.000 description 1
- WGQKYBSKWIADBV-UHFFFAOYSA-O benzylaminium Chemical compound [NH3+]CC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-O 0.000 description 1
- 239000003124 biologic agent Substances 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 239000012888 bovine serum Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 235000012730 carminic acid Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- AZSZCFSOHXEJQE-UHFFFAOYSA-N dibromodifluoromethane Chemical compound FC(F)(Br)Br AZSZCFSOHXEJQE-UHFFFAOYSA-N 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000001984 ectoparasiticidal effect Effects 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000002158 endotoxin Substances 0.000 description 1
- 229940013764 fipronil Drugs 0.000 description 1
- RYLHNOVXKPXDIP-UHFFFAOYSA-N flufenoxuron Chemical compound C=1C=C(NC(=O)NC(=O)C=2C(=CC=CC=2F)F)C(F)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl RYLHNOVXKPXDIP-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000004459 forage Substances 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 210000002216 heart Anatomy 0.000 description 1
- 229940056881 imidacloprid Drugs 0.000 description 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000012678 infectious agent Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002949 juvenile hormone Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229960001614 levamisole Drugs 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 230000001617 migratory effect Effects 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
- 235000019713 millet Nutrition 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 1
- PUPKPAZSFZOLOR-UHFFFAOYSA-N n,n-dimethylformamide;toluene Chemical compound CN(C)C=O.CC1=CC=CC=C1 PUPKPAZSFZOLOR-UHFFFAOYSA-N 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- HXTSPGYEPSIZKP-UHFFFAOYSA-N phenol;tin Chemical class [Sn].OC1=CC=CC=C1 HXTSPGYEPSIZKP-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229960005141 piperazine Drugs 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000004540 pour-on Substances 0.000 description 1
- 235000014483 powder concentrate Nutrition 0.000 description 1
- 229960002957 praziquantel Drugs 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229960005134 pyrantel Drugs 0.000 description 1
- YSAUAVHXTIETRK-AATRIKPKSA-N pyrantel Chemical compound CN1CCCN=C1\C=C\C1=CC=CS1 YSAUAVHXTIETRK-AATRIKPKSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 230000037387 scars Effects 0.000 description 1
- 230000000276 sedentary effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229940056729 sodium sulfate anhydrous Drugs 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19264898A | 1998-11-16 | 1998-11-16 | |
| US192648 | 1998-11-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2210990T3 true ES2210990T3 (es) | 2004-07-01 |
Family
ID=22710500
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99308947T Expired - Lifetime ES2210990T3 (es) | 1998-11-16 | 1999-11-10 | Uso pesticida y parasiticida de compuestos de tiazolo-/4,5-b) piridina 2-tio substituidos. |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP1000946B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP4624510B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR20000035479A (cg-RX-API-DMAC7.html) |
| AR (1) | AR021272A1 (cg-RX-API-DMAC7.html) |
| AT (1) | ATE252106T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU5943699A (cg-RX-API-DMAC7.html) |
| BR (1) | BR9905615B1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2289363A1 (cg-RX-API-DMAC7.html) |
| DE (1) | DE69912067T2 (cg-RX-API-DMAC7.html) |
| DK (1) | DK1000946T3 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2210990T3 (cg-RX-API-DMAC7.html) |
| IL (1) | IL132831A (cg-RX-API-DMAC7.html) |
| NZ (1) | NZ500926A (cg-RX-API-DMAC7.html) |
| PL (1) | PL336563A1 (cg-RX-API-DMAC7.html) |
| SI (1) | SI1000946T1 (cg-RX-API-DMAC7.html) |
| TR (1) | TR199902807A3 (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA997122B (cg-RX-API-DMAC7.html) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6914068B2 (en) * | 2001-07-12 | 2005-07-05 | Basf Aktiengesellschaft | Thiazolo[4,5-b]pyridines as fungicides |
| ATE363829T1 (de) * | 2001-09-10 | 2007-06-15 | Basf Ag | Pestizide und parasitizide di- und trifluorsubstituierte alkenverbindungen |
| AU2003252536A1 (en) * | 2002-08-01 | 2004-02-23 | Basf Aktiengesellschaft | Pesticidal fluoroalkene derivatives |
| JP5540640B2 (ja) | 2009-10-07 | 2014-07-02 | 住友化学株式会社 | 複素環化合物及びその有害節足動物防除用途 |
| US20180282347A1 (en) * | 2014-12-02 | 2018-10-04 | Bayer Cropscience Aktiengesellschaft | Bicyclic compounds as pest control agents |
| CA3015345A1 (en) | 2016-02-23 | 2017-08-31 | Indiana University Research & Technology Corporation | Combination therapies for treatment of spinal muscular atrophy |
| US20230151025A1 (en) * | 2020-04-07 | 2023-05-18 | Bayer Aktiengesellschaft | Substituted thiazolopyridines, salts thereof and their use as herbicidally active substances |
| TW202328150A (zh) | 2021-09-07 | 2023-07-16 | 德商拜耳廠股份有限公司 | 經取代之噻唑并吡啶、其鹽及其作為除草活性物質之用途 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3137996A1 (de) * | 1981-09-24 | 1983-04-28 | Hoechst Ag, 6230 Frankfurt | Heterocyclische phenylaether, verfahren zu deren herstellung und diese enthaltende herbizide mittel |
| JPS60104067A (ja) * | 1983-11-09 | 1985-06-08 | Ishihara Sangyo Kaisha Ltd | Ν−ベンゾイル−ν’−フエニルウレア系化合物及びそれらを含有する殺虫剤 |
| GB9219634D0 (en) * | 1992-09-16 | 1992-10-28 | Ici Plc | Heterocyclic compounds |
| GB9219632D0 (en) * | 1992-09-16 | 1992-10-28 | Ici Plc | Heterocyclic compounds |
| US5496816A (en) * | 1994-03-14 | 1996-03-05 | Merck & Co., Inc. | Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment |
-
1999
- 1999-11-08 JP JP31680299A patent/JP4624510B2/ja not_active Expired - Fee Related
- 1999-11-09 IL IL132831A patent/IL132831A/en not_active IP Right Cessation
- 1999-11-09 NZ NZ500926A patent/NZ500926A/en unknown
- 1999-11-10 EP EP99308947A patent/EP1000946B1/en not_active Expired - Lifetime
- 1999-11-10 ES ES99308947T patent/ES2210990T3/es not_active Expired - Lifetime
- 1999-11-10 SI SI9930496T patent/SI1000946T1/xx unknown
- 1999-11-10 DE DE69912067T patent/DE69912067T2/de not_active Expired - Lifetime
- 1999-11-10 DK DK99308947T patent/DK1000946T3/da active
- 1999-11-10 AT AT99308947T patent/ATE252106T1/de active
- 1999-11-12 CA CA002289363A patent/CA2289363A1/en not_active Abandoned
- 1999-11-12 BR BRPI9905615-1A patent/BR9905615B1/pt not_active IP Right Cessation
- 1999-11-15 PL PL99336563A patent/PL336563A1/xx not_active Application Discontinuation
- 1999-11-15 AR ARP990105793A patent/AR021272A1/es unknown
- 1999-11-15 KR KR1019990050630A patent/KR20000035479A/ko not_active Withdrawn
- 1999-11-15 ZA ZA9907122A patent/ZA997122B/xx unknown
- 1999-11-16 TR TR1999/02807A patent/TR199902807A3/tr unknown
- 1999-11-16 AU AU59436/99A patent/AU5943699A/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CA2289363A1 (en) | 2000-05-16 |
| ATE252106T1 (de) | 2003-11-15 |
| AR021272A1 (es) | 2002-07-03 |
| SI1000946T1 (en) | 2004-04-30 |
| DE69912067T2 (de) | 2004-07-22 |
| TR199902807A2 (xx) | 2000-06-21 |
| DK1000946T3 (da) | 2004-02-23 |
| ZA997122B (en) | 2000-05-19 |
| NZ500926A (en) | 2001-04-27 |
| PL336563A1 (en) | 2000-05-22 |
| AU5943699A (en) | 2000-05-18 |
| JP4624510B2 (ja) | 2011-02-02 |
| TR199902807A3 (tr) | 2000-06-21 |
| IL132831A (en) | 2007-09-20 |
| EP1000946A3 (en) | 2001-09-12 |
| KR20000035479A (ko) | 2000-06-26 |
| EP1000946B1 (en) | 2003-10-15 |
| IL132831A0 (en) | 2001-03-19 |
| BR9905615A (pt) | 2000-11-07 |
| JP2000143668A (ja) | 2000-05-26 |
| EP1000946A2 (en) | 2000-05-17 |
| DE69912067D1 (de) | 2003-11-20 |
| BR9905615B1 (pt) | 2011-02-08 |
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