BG63655B1 - Използване на аминотиазоли като микробициди - Google Patents
Използване на аминотиазоли като микробициди Download PDFInfo
- Publication number
- BG63655B1 BG63655B1 BG103520A BG10352099A BG63655B1 BG 63655 B1 BG63655 B1 BG 63655B1 BG 103520 A BG103520 A BG 103520A BG 10352099 A BG10352099 A BG 10352099A BG 63655 B1 BG63655 B1 BG 63655B1
- Authority
- BG
- Bulgaria
- Prior art keywords
- methyl
- formula
- alkyl
- technical materials
- chloro
- Prior art date
Links
- 230000003641 microbiacidal effect Effects 0.000 title claims description 11
- 229940124561 microbicide Drugs 0.000 title claims description 7
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical class NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 title claims description 4
- 239000000463 material Substances 0.000 claims abstract description 21
- 244000005700 microbiome Species 0.000 claims abstract description 13
- 230000006378 damage Effects 0.000 claims abstract description 12
- 150000003839 salts Chemical class 0.000 claims abstract description 8
- 239000002253 acid Substances 0.000 claims abstract description 7
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
- -1 microbicides Chemical class 0.000 claims description 58
- 238000002360 preparation method Methods 0.000 claims description 7
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 239000002855 microbicide agent Substances 0.000 claims description 4
- IYCKMNAVTMOAKD-UHFFFAOYSA-N 1,2-thiazol-3-amine Chemical compound NC=1C=CSN=1 IYCKMNAVTMOAKD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
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- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 11
- 150000002367 halogens Chemical class 0.000 abstract description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
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- 239000013543 active substance Substances 0.000 description 17
- 239000000203 mixture Substances 0.000 description 11
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- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
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- LKFXYYLRIUSARI-UHFFFAOYSA-N 1,3-thiazol-5-amine Chemical class NC1=CN=CS1 LKFXYYLRIUSARI-UHFFFAOYSA-N 0.000 description 3
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- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 2
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- SDMSCIWHRZJSRN-UHFFFAOYSA-N isoxathion Chemical compound O1N=C(OP(=S)(OCC)OCC)C=C1C1=CC=CC=C1 SDMSCIWHRZJSRN-UHFFFAOYSA-N 0.000 description 1
- DWKPPFQULDPWHX-VKHMYHEASA-N l-alanyl ester Chemical compound COC(=O)[C@H](C)N DWKPPFQULDPWHX-VKHMYHEASA-N 0.000 description 1
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- 159000000003 magnesium salts Chemical class 0.000 description 1
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- 235000019341 magnesium sulphate Nutrition 0.000 description 1
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- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 1
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- 239000001923 methylcellulose Substances 0.000 description 1
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- 230000000813 microbial effect Effects 0.000 description 1
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical compound 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
- 239000003750 molluscacide Substances 0.000 description 1
- 230000002013 molluscicidal effect Effects 0.000 description 1
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 description 1
- YZBLFMPOMVTDJY-CBYMMZEQSA-N moxidectin Chemical compound O1[C@H](C(\C)=C\C(C)C)[C@@H](C)C(=N/OC)\C[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 YZBLFMPOMVTDJY-CBYMMZEQSA-N 0.000 description 1
- 229960004816 moxidectin Drugs 0.000 description 1
- NADZXQJLRPBPFJ-UHFFFAOYSA-N n,4,6-trichloro-n-phenyl-1,3,5-triazin-2-amine Chemical compound N=1C(Cl)=NC(Cl)=NC=1N(Cl)C1=CC=CC=C1 NADZXQJLRPBPFJ-UHFFFAOYSA-N 0.000 description 1
- BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 description 1
- FTSDMYVLFMEZJS-UHFFFAOYSA-N n-(2,2,2-trichloroethyl)formamide Chemical compound ClC(Cl)(Cl)CNC=O FTSDMYVLFMEZJS-UHFFFAOYSA-N 0.000 description 1
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- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 235000015097 nutrients Nutrition 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
- PZXOQEXFMJCDPG-UHFFFAOYSA-N omethoate Chemical compound CNC(=O)CSP(=O)(OC)OC PZXOQEXFMJCDPG-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 description 1
- 229960000625 oxytetracycline Drugs 0.000 description 1
- 235000019366 oxytetracycline Nutrition 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000008060 phenylpyrroles Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 229940007042 proteus vulgaris Drugs 0.000 description 1
- FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 description 1
- QHGVXILFMXYDRS-UHFFFAOYSA-N pyraclofos Chemical compound C1=C(OP(=O)(OCC)SCCC)C=NN1C1=CC=C(Cl)C=C1 QHGVXILFMXYDRS-UHFFFAOYSA-N 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- MSHXTAQSSIEBQS-UHFFFAOYSA-N s-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydron;chloride Chemical compound [Cl-].NC(=O)SCC([NH+](C)C)CSC(N)=O MSHXTAQSSIEBQS-UHFFFAOYSA-N 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- CEYYIKYYFSTQRU-UHFFFAOYSA-M trimethyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)C CEYYIKYYFSTQRU-UHFFFAOYSA-M 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 230000003253 viricidal effect Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19654147A DE19654147A1 (de) | 1996-12-23 | 1996-12-23 | Verwendung von Aminoisothiazolen als Mikrobizide |
| PCT/EP1997/006854 WO1998027816A1 (de) | 1996-12-23 | 1997-12-09 | Verwendung von aminoisothiazolen als mikrobizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BG103520A BG103520A (en) | 2000-06-30 |
| BG63655B1 true BG63655B1 (bg) | 2002-08-30 |
Family
ID=7816104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BG103520A BG63655B1 (bg) | 1996-12-23 | 1999-06-22 | Използване на аминотиазоли като микробициди |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US6069161A (cs) |
| EP (1) | EP0946098B1 (cs) |
| JP (1) | JP2001508051A (cs) |
| KR (1) | KR20000062287A (cs) |
| CN (1) | CN1121140C (cs) |
| AT (1) | ATE204129T1 (cs) |
| AU (1) | AU742233B2 (cs) |
| BG (1) | BG63655B1 (cs) |
| BR (1) | BR9713614A (cs) |
| CA (1) | CA2275470A1 (cs) |
| CZ (1) | CZ292552B6 (cs) |
| DE (2) | DE19654147A1 (cs) |
| EA (1) | EA001604B1 (cs) |
| ES (1) | ES2163208T3 (cs) |
| HU (1) | HUP0000483A3 (cs) |
| IL (1) | IL130360A0 (cs) |
| NO (1) | NO313854B1 (cs) |
| NZ (1) | NZ336289A (cs) |
| PL (1) | PL334381A1 (cs) |
| TR (1) | TR199901454T2 (cs) |
| WO (1) | WO1998027816A1 (cs) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR9812042A (pt) * | 1997-09-08 | 2000-09-26 | Basf Ag | Uso de misturas |
| KR20010062209A (ko) * | 1999-12-10 | 2001-07-07 | 히가시 데쓰로 | 고내식성 막이 내부에 형성된 챔버를 구비하는 처리 장치 |
| US7048788B2 (en) * | 2003-08-05 | 2006-05-23 | Shunichi Yamazaki | Ship bottom paint using coal ash and diatomaceous earth |
| MX2007000095A (es) * | 2004-06-24 | 2007-03-21 | Vertex Pharma | Moduladores de transportadores con casete de union con atp. |
| JP5575179B2 (ja) * | 2011-06-07 | 2014-08-20 | ローム アンド ハース カンパニー | 安定な殺生物剤組成物 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4396413A (en) * | 1971-05-12 | 1983-08-02 | Rohm And Haas Company | Metal salt complexes of 3-isothiazolones as effective biocidal agents |
| US4032322A (en) * | 1976-06-18 | 1977-06-28 | Loren Kenneth Gibbons | Isothiazolylformamidine derivatives as herbicides |
| DE4328425A1 (de) * | 1993-08-24 | 1995-03-02 | Basf Ag | Acylamino-substituierte Isoxazol- bzw. Isothiazolderivate, Verfahren zu deren Herstellung und ihre Verwendung |
-
1996
- 1996-12-23 DE DE19654147A patent/DE19654147A1/de not_active Withdrawn
-
1997
- 1997-12-09 ES ES97952901T patent/ES2163208T3/es not_active Expired - Lifetime
- 1997-12-09 PL PL97334381A patent/PL334381A1/xx unknown
- 1997-12-09 AT AT97952901T patent/ATE204129T1/de not_active IP Right Cessation
- 1997-12-09 KR KR1019997005684A patent/KR20000062287A/ko not_active Abandoned
- 1997-12-09 AU AU56605/98A patent/AU742233B2/en not_active Ceased
- 1997-12-09 DE DE59704331T patent/DE59704331D1/de not_active Expired - Fee Related
- 1997-12-09 CZ CZ19992263A patent/CZ292552B6/cs not_active IP Right Cessation
- 1997-12-09 NZ NZ336289A patent/NZ336289A/xx unknown
- 1997-12-09 HU HU0000483A patent/HUP0000483A3/hu unknown
- 1997-12-09 CN CN97180949A patent/CN1121140C/zh not_active Expired - Fee Related
- 1997-12-09 IL IL13036097A patent/IL130360A0/xx unknown
- 1997-12-09 US US09/331,067 patent/US6069161A/en not_active Expired - Fee Related
- 1997-12-09 JP JP52830198A patent/JP2001508051A/ja not_active Withdrawn
- 1997-12-09 CA CA002275470A patent/CA2275470A1/en not_active Abandoned
- 1997-12-09 BR BR9713614-0A patent/BR9713614A/pt not_active Application Discontinuation
- 1997-12-09 WO PCT/EP1997/006854 patent/WO1998027816A1/de not_active Ceased
- 1997-12-09 TR TR1999/01454T patent/TR199901454T2/xx unknown
- 1997-12-09 EP EP97952901A patent/EP0946098B1/de not_active Expired - Lifetime
- 1997-12-09 EA EA199900539A patent/EA001604B1/ru not_active IP Right Cessation
-
1999
- 1999-06-22 BG BG103520A patent/BG63655B1/bg unknown
- 1999-06-22 NO NO19993079A patent/NO313854B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CN1121140C (zh) | 2003-09-17 |
| IL130360A0 (en) | 2000-06-01 |
| CN1241907A (zh) | 2000-01-19 |
| EP0946098A1 (de) | 1999-10-06 |
| ATE204129T1 (de) | 2001-09-15 |
| AU742233B2 (en) | 2001-12-20 |
| JP2001508051A (ja) | 2001-06-19 |
| ES2163208T3 (es) | 2002-01-16 |
| US6069161A (en) | 2000-05-30 |
| DE19654147A1 (de) | 1998-06-25 |
| NO993079D0 (no) | 1999-06-22 |
| CZ292552B6 (cs) | 2003-10-15 |
| EA001604B1 (ru) | 2001-06-25 |
| KR20000062287A (ko) | 2000-10-25 |
| NZ336289A (en) | 2000-03-27 |
| HUP0000483A2 (hu) | 2000-06-28 |
| AU5660598A (en) | 1998-07-17 |
| CZ226399A3 (cs) | 1999-10-13 |
| EA199900539A1 (ru) | 2000-02-28 |
| WO1998027816A1 (de) | 1998-07-02 |
| NO313854B1 (no) | 2002-12-16 |
| CA2275470A1 (en) | 1998-07-02 |
| EP0946098B1 (de) | 2001-08-16 |
| NO993079L (no) | 1999-06-22 |
| HUP0000483A3 (en) | 2001-02-28 |
| TR199901454T2 (xx) | 1999-08-23 |
| BR9713614A (pt) | 2000-04-11 |
| DE59704331D1 (de) | 2001-09-20 |
| PL334381A1 (en) | 2000-02-28 |
| BG103520A (en) | 2000-06-30 |
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