ATE175839T1 - Fungizide wirkstoffkombinationen - Google Patents
Fungizide wirkstoffkombinationenInfo
- Publication number
- ATE175839T1 ATE175839T1 AT95115677T AT95115677T ATE175839T1 AT E175839 T1 ATE175839 T1 AT E175839T1 AT 95115677 T AT95115677 T AT 95115677T AT 95115677 T AT95115677 T AT 95115677T AT E175839 T1 ATE175839 T1 AT E175839T1
- Authority
- AT
- Austria
- Prior art keywords
- methyl
- prepns
- ethyl
- oxyquinolate
- fenpiclonil
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title abstract 2
- -1 (1-(4-methyl phenyl)ethyl)amino-carbonyl Chemical group 0.000 abstract 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 abstract 2
- FKLFBQCQQYDUAM-UHFFFAOYSA-N fenpiclonil Chemical compound ClC1=CC=CC(C=2C(=CNC=2)C#N)=C1Cl FKLFBQCQQYDUAM-UHFFFAOYSA-N 0.000 abstract 2
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 abstract 1
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 abstract 1
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 abstract 1
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 abstract 1
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 abstract 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 abstract 1
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 abstract 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 abstract 1
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 abstract 1
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005757 Cyproconazole Substances 0.000 abstract 1
- 239000005766 Dodine Substances 0.000 abstract 1
- 239000005767 Epoxiconazole Substances 0.000 abstract 1
- 239000005775 Fenbuconazole Substances 0.000 abstract 1
- 239000005777 Fenpropidin Substances 0.000 abstract 1
- 239000005785 Fluquinconazole Substances 0.000 abstract 1
- 239000005814 Pencycuron Substances 0.000 abstract 1
- 229930182764 Polyoxin Natural products 0.000 abstract 1
- 239000005821 Propamocarb Substances 0.000 abstract 1
- 239000005822 Propiconazole Substances 0.000 abstract 1
- 239000005840 Tetraconazole Substances 0.000 abstract 1
- 239000005847 Triazoxide Substances 0.000 abstract 1
- 239000005858 Triflumizole Substances 0.000 abstract 1
- 239000005859 Triticonazole Substances 0.000 abstract 1
- 239000005870 Ziram Substances 0.000 abstract 1
- 239000011717 all-trans-retinol Substances 0.000 abstract 1
- 235000019169 all-trans-retinol Nutrition 0.000 abstract 1
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 abstract 1
- DSKJPMWIHSOYEA-UHFFFAOYSA-N bupirimate Chemical compound CCCCC1=C(C)N=C(NCC)N=C1OS(=O)(=O)N(C)C DSKJPMWIHSOYEA-UHFFFAOYSA-N 0.000 abstract 1
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 abstract 1
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 abstract 1
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 abstract 1
- BBXXLROWFHWFQY-UHFFFAOYSA-N ethirimol Chemical compound CCCCC1=C(C)NC(NCC)=NC1=O BBXXLROWFHWFQY-UHFFFAOYSA-N 0.000 abstract 1
- IGUYEXXAGBDLLX-UHFFFAOYSA-N ethyl 3-(3,5-dichlorophenyl)-5-methyl-2,4-dioxo-1,3-oxazolidine-5-carboxylate Chemical compound O=C1C(C(=O)OCC)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 IGUYEXXAGBDLLX-UHFFFAOYSA-N 0.000 abstract 1
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 abstract 1
- WDQNIWFZKXZFAY-UHFFFAOYSA-M fentin acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 WDQNIWFZKXZFAY-UHFFFAOYSA-M 0.000 abstract 1
- IPENDKRRWFURRE-UHFFFAOYSA-N fluoroimide Chemical compound C1=CC(F)=CC=C1N1C(=O)C(Cl)=C(Cl)C1=O IPENDKRRWFURRE-UHFFFAOYSA-N 0.000 abstract 1
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 1
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 abstract 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 abstract 1
- 229920000940 maneb Polymers 0.000 abstract 1
- JPLCQHHISLYGRA-UHFFFAOYSA-N n-(6-methoxypyridin-3-yl)cyclopropanecarboxamide Chemical compound C1=NC(OC)=CC=C1NC(=O)C1CC1 JPLCQHHISLYGRA-UHFFFAOYSA-N 0.000 abstract 1
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 abstract 1
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 abstract 1
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 abstract 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 abstract 1
- OVPLZYJGTGDFNB-UHFFFAOYSA-N propan-2-yl carbamate Chemical compound CC(C)OC(N)=O OVPLZYJGTGDFNB-UHFFFAOYSA-N 0.000 abstract 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 abstract 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 abstract 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000004308 thiabendazole Substances 0.000 abstract 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 abstract 1
- 229960004546 thiabendazole Drugs 0.000 abstract 1
- 235000010296 thiabendazole Nutrition 0.000 abstract 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 abstract 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 abstract 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 abstract 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 abstract 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- A01N37/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides containing at least one oxygen or sulfur atom being directly attached to the same aromatic ring system
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4437048A DE4437048A1 (de) | 1994-10-17 | 1994-10-17 | Fungizide Wirkstoffkombinationen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE175839T1 true ATE175839T1 (de) | 1999-02-15 |
Family
ID=6530969
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT95115677T ATE175839T1 (de) | 1994-10-17 | 1995-10-05 | Fungizide wirkstoffkombinationen |
Country Status (16)
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU664392B2 (en) * | 1991-10-18 | 1995-11-16 | Monsanto Technology Llc | Fungicides for the control of take-all disease of plants |
| DE4313867A1 (de) * | 1993-04-28 | 1994-11-03 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| DE19543746A1 (de) * | 1995-11-24 | 1997-05-28 | Basf Ag | Fungizide Mittel |
| DE19615977A1 (de) * | 1996-04-22 | 1997-10-23 | Basf Ag | Mittel und Verfahren zur Bekämpfung von Schadpilzen |
| FR2751173B1 (fr) * | 1996-07-16 | 1998-08-28 | Rhone Poulenc Agrochimie | Composition fongicide a base de 2 composes de type triazole |
| AP1119A (en) | 1996-12-13 | 2002-11-29 | Bayer Ag | A microbicide composition for plant protection. |
| PL194328B1 (pl) * | 1997-12-18 | 2007-05-31 | Basf Ag | Mieszanina grzybobójcza |
| TW431861B (en) * | 1997-12-18 | 2001-05-01 | Basf Ag | Fungicidal mixtures based on amide compounds and azoles |
| GB2336539B (en) * | 1998-04-25 | 2003-11-19 | Agrevo Uk Ltd | Wood treatment |
| UA70327C2 (uk) * | 1998-06-08 | 2004-10-15 | Баєр Акціенгезельшафт | Спосіб боротьби з фітопатогенними хворобами сільськогосподарських рослин та фунгіцидна композиція |
| IL136798A0 (en) * | 1998-11-02 | 2001-06-14 | Bayer Ag | Agricultural, fungicidal compositions containing a diguanidine derivative and a carboxamide derivative |
| US6696497B2 (en) | 2000-02-23 | 2004-02-24 | Basf Aktiengesellschaft | Fungicidal mixtures |
| ES2199199T3 (es) * | 2000-12-14 | 2004-02-16 | Basf Aktiengesellschaft | Mezclas fungicidas a base de amidocompuestos. |
| DE10141618A1 (de) * | 2001-08-24 | 2003-03-06 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| TW200531632A (en) * | 2004-01-15 | 2005-10-01 | Basf Ag | Fungicidal mixtures for controlling harmful fungi |
| TWI379635B (en) * | 2004-10-14 | 2012-12-21 | Dow Agrosciences Llc | Isomeric mixtures of dinitro-octylphenyl esters and synergistic fungicidal mixtures therefrom |
| CN100376156C (zh) * | 2005-09-15 | 2008-03-26 | 南京第一农药有限公司 | 一种含嘧菌酯和春雷霉素的杀菌组合物及其应用 |
| CN101926342A (zh) * | 2010-03-02 | 2010-12-29 | 陕西美邦农资贸易有限公司 | 一种含丙环唑与代森锌的杀菌组合物 |
| EP2499911A1 (en) * | 2011-03-11 | 2012-09-19 | Bayer Cropscience AG | Active compound combinations comprising fenhexamid |
| CN102302028A (zh) * | 2011-04-23 | 2012-01-04 | 陕西韦尔奇作物保护有限公司 | 一种含螺环菌胺与苯并咪唑类的杀菌组合物 |
| CN103300004B (zh) * | 2012-03-16 | 2016-02-17 | 陕西韦尔奇作物保护有限公司 | 一种含有环酰菌胺与甲氧基丙烯酸酯类的杀菌组合物 |
| CN105685032A (zh) * | 2012-03-17 | 2016-06-22 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺的增效杀菌组合物 |
| CN103300027A (zh) * | 2012-03-17 | 2013-09-18 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺的杀菌组合物 |
| CN103300041B (zh) * | 2012-03-17 | 2016-04-06 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺的增效杀菌组合物 |
| CN103314967B (zh) * | 2012-03-21 | 2016-02-17 | 陕西韦尔奇作物保护有限公司 | 一种含有环酰菌胺的杀菌组合物 |
| CN103314989B (zh) * | 2012-03-23 | 2016-08-03 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺与三唑类化合物的杀菌组合物 |
| CN103355298B (zh) * | 2012-03-29 | 2016-04-06 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺与抗生素类的杀菌组合物 |
| CN102763667A (zh) * | 2012-07-13 | 2012-11-07 | 王学权 | 一种含有环酰菌胺的杀菌剂 |
| US9000105B2 (en) * | 2013-03-15 | 2015-04-07 | John L. Lombardi | Antipathogenic guanidinium copolymer |
| CN105324645A (zh) * | 2013-04-29 | 2016-02-10 | 高准公司 | 砂分离器界面检测 |
| US9631052B2 (en) * | 2014-06-26 | 2017-04-25 | John L. Lombardi | Borate esters |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2099302B (en) * | 1981-05-22 | 1985-03-27 | Pan Britannica Ind Ltd | Fungicide preparation |
| DE3814505A1 (de) * | 1988-04-29 | 1989-11-09 | Bayer Ag | Substituierte cycloalkyl- bzw. heterocyclyl-carbonsaeureanilide |
| DE4313867A1 (de) * | 1993-04-28 | 1994-11-03 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| DE4318285A1 (de) * | 1993-06-02 | 1994-12-08 | Bayer Ag | Fungizide Wirkstoffkombinationen |
-
1994
- 1994-10-17 DE DE4437048A patent/DE4437048A1/de not_active Withdrawn
-
1995
- 1995-09-29 TW TW084110151A patent/TW322411B/zh not_active IP Right Cessation
- 1995-10-05 AT AT95115677T patent/ATE175839T1/de active
- 1995-10-05 EP EP95115677A patent/EP0707792B1/de not_active Expired - Lifetime
- 1995-10-05 ES ES95115677T patent/ES2129168T3/es not_active Expired - Lifetime
- 1995-10-05 DE DE59504892T patent/DE59504892D1/de not_active Expired - Lifetime
- 1995-10-06 CO CO95046715A patent/CO4600726A1/es unknown
- 1995-10-10 AU AU33173/95A patent/AU699963B2/en not_active Ceased
- 1995-10-11 KR KR1019950034973A patent/KR100414385B1/ko not_active Expired - Fee Related
- 1995-10-12 JP JP28921395A patent/JP3683015B2/ja not_active Expired - Fee Related
- 1995-10-13 PL PL95310937A patent/PL182712B1/pl not_active IP Right Cessation
- 1995-10-16 ZA ZA958711A patent/ZA958711B/xx unknown
- 1995-10-16 BR BR9504413A patent/BR9504413A/pt not_active IP Right Cessation
- 1995-10-16 HU HU9502984A patent/HU220370B/hu not_active IP Right Cessation
- 1995-10-17 CN CN95118107A patent/CN1102337C/zh not_active Expired - Fee Related
-
1997
- 1997-10-01 US US08/943,349 patent/US5962518A/en not_active Expired - Lifetime
-
1999
- 1999-02-12 GR GR990400484T patent/GR3029400T3/el unknown
- 1999-04-20 US US09/294,480 patent/US6207691B1/en not_active Expired - Fee Related
-
2001
- 2001-02-01 US US09/775,331 patent/US6448291B2/en not_active Expired - Fee Related
- 2001-02-09 CN CNB011034548A patent/CN1212762C/zh not_active Expired - Fee Related
-
2002
- 2002-06-17 US US10/173,409 patent/US6500836B1/en not_active Expired - Fee Related
- 2002-11-06 US US10/288,824 patent/US6767911B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| PL182712B1 (pl) | 2002-02-28 |
| CN1132591A (zh) | 1996-10-09 |
| JP3683015B2 (ja) | 2005-08-17 |
| CN1313032A (zh) | 2001-09-19 |
| HUT73550A (en) | 1996-08-28 |
| HU9502984D0 (en) | 1995-12-28 |
| HU220370B (hu) | 2002-01-28 |
| AU3317395A (en) | 1996-05-02 |
| BR9504413A (pt) | 1997-05-27 |
| KR960013200A (ko) | 1996-05-22 |
| US20030139454A1 (en) | 2003-07-24 |
| CO4600726A1 (es) | 1998-05-08 |
| US6207691B1 (en) | 2001-03-27 |
| US6500836B1 (en) | 2002-12-31 |
| EP0707792B1 (de) | 1999-01-20 |
| CN1102337C (zh) | 2003-03-05 |
| AU699963B2 (en) | 1998-12-17 |
| US5962518A (en) | 1999-10-05 |
| ZA958711B (en) | 1996-05-22 |
| US20010016591A1 (en) | 2001-08-23 |
| ES2129168T3 (es) | 1999-06-01 |
| CN1212762C (zh) | 2005-08-03 |
| KR100414385B1 (ko) | 2004-03-18 |
| US6448291B2 (en) | 2002-09-10 |
| EP0707792A1 (de) | 1996-04-24 |
| DE4437048A1 (de) | 1996-04-18 |
| US6767911B2 (en) | 2004-07-27 |
| JPH08208406A (ja) | 1996-08-13 |
| TW322411B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1997-12-11 |
| PL310937A1 (en) | 1996-04-29 |
| GR3029400T3 (en) | 1999-05-28 |
| DE59504892D1 (de) | 1999-03-04 |
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