UA71569C2 - Method of controlling weeds and a herbicidal agent - Google Patents
Method of controlling weeds and a herbicidal agent Download PDFInfo
- Publication number
- UA71569C2 UA71569C2 UA2001031685A UA2001031685A UA71569C2 UA 71569 C2 UA71569 C2 UA 71569C2 UA 2001031685 A UA2001031685 A UA 2001031685A UA 2001031685 A UA2001031685 A UA 2001031685A UA 71569 C2 UA71569 C2 UA 71569C2
- Authority
- UA
- Ukraine
- Prior art keywords
- herbicides
- group
- plants
- compounds
- inhibitors
- Prior art date
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- 241000196324 Embryophyta Species 0.000 title claims abstract description 142
- 239000004009 herbicide Substances 0.000 title claims abstract description 133
- 238000000034 method Methods 0.000 title claims description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 56
- 235000013339 cereals Nutrition 0.000 claims abstract description 50
- 150000003839 salts Chemical class 0.000 claims abstract description 41
- 230000000694 effects Effects 0.000 claims abstract description 31
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 31
- 239000003112 inhibitor Substances 0.000 claims abstract description 28
- 239000002689 soil Substances 0.000 claims abstract description 21
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- 229940097068 glyphosate Drugs 0.000 claims abstract description 12
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- YWICANUUQPYHOW-UHFFFAOYSA-M sodium;2-(phosphonomethylamino)acetate Chemical compound [Na+].OP(O)(=O)CNCC([O-])=O YWICANUUQPYHOW-UHFFFAOYSA-M 0.000 description 1
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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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19836700A DE19836700A1 (de) | 1998-08-13 | 1998-08-13 | Herbizide Mittel für tolerante oder resistente Getreidekulturen |
PCT/EP1999/005801 WO2000008940A1 (de) | 1998-08-13 | 1999-08-10 | Herbizide mittel für tolerante oder resistente getreidekulturen |
Publications (1)
Publication Number | Publication Date |
---|---|
UA71569C2 true UA71569C2 (en) | 2004-12-15 |
Family
ID=7877416
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA2001031685A UA71569C2 (en) | 1998-08-13 | 1999-10-08 | Method of controlling weeds and a herbicidal agent |
Country Status (24)
Country | Link |
---|---|
US (1) | US6723681B2 (hu) |
EP (1) | EP1104992B2 (hu) |
JP (1) | JP2002522460A (hu) |
KR (2) | KR20010087182A (hu) |
CN (1) | CN1220437C (hu) |
AR (2) | AR020162A1 (hu) |
AT (1) | ATE290317T1 (hu) |
AU (1) | AU767032B2 (hu) |
BR (1) | BR9913006A (hu) |
CA (4) | CA2936388C (hu) |
CZ (1) | CZ304256B6 (hu) |
DE (2) | DE19836700A1 (hu) |
ES (1) | ES2239850T5 (hu) |
HU (1) | HU230431B1 (hu) |
IL (1) | IL141144A (hu) |
NZ (1) | NZ509845A (hu) |
PL (24) | PL217911B1 (hu) |
PT (1) | PT1104992E (hu) |
RU (1) | RU2250614C2 (hu) |
SK (1) | SK288448B6 (hu) |
TR (1) | TR200100479T2 (hu) |
UA (1) | UA71569C2 (hu) |
WO (1) | WO2000008940A1 (hu) |
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Families Citing this family (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19836700A1 (de) † | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Getreidekulturen |
DE19836684A1 (de) * | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Reiskulturen |
JP2003528117A (ja) | 2000-03-27 | 2003-09-24 | ビーエーエスエフ アクチェンゲゼルシャフト | 相乗作用による除草方法及び除草剤組成物 |
PL204904B1 (pl) * | 2000-04-04 | 2010-02-26 | Basf Ag | Kompozycja chwastobójcza, sposób zwalczania niepożądanych roślin i zastosowanie kompozycji chwastobójczej |
JP2003192511A (ja) * | 2001-12-27 | 2003-07-09 | Hodogaya Agros Kk | 気象変動に安定な雑草を防除する微粒剤 |
JP2003192510A (ja) * | 2001-12-27 | 2003-07-09 | Hodogaya Agros Kk | グリホサートを含む混合微粒剤 |
GB0215544D0 (en) * | 2002-07-04 | 2002-08-14 | Syngenta Ltd | Weed control process |
US20050026781A1 (en) | 2003-04-22 | 2005-02-03 | Monsanto Technology Llc | Herbicidal compositions containing glyphosate and a pyridine analog |
JP2005068011A (ja) * | 2003-06-24 | 2005-03-17 | Nihon Green & Garden Corp | 除草用混合微粒剤 |
WO2005087007A1 (en) | 2004-03-10 | 2005-09-22 | Monsanto Technology Llc | Herbicidal compositions containing n-phosphonomethyl glycine and an auxin herbicide |
JP4736480B2 (ja) * | 2004-05-17 | 2011-07-27 | 住友化学株式会社 | 雑草防除方法 |
US7903687B2 (en) | 2005-04-01 | 2011-03-08 | International Business Machines Corporation | Method for scheduling, writing, and reading data inside the partitioned buffer of a switch, router or packet processing device |
US7492771B2 (en) | 2005-04-01 | 2009-02-17 | International Business Machines Corporation | Method for performing a packet header lookup |
US7706409B2 (en) * | 2005-04-01 | 2010-04-27 | International Business Machines Corporation | System and method for parsing, filtering, and computing the checksum in a host Ethernet adapter (HEA) |
US7577151B2 (en) * | 2005-04-01 | 2009-08-18 | International Business Machines Corporation | Method and apparatus for providing a network connection table |
US7508771B2 (en) * | 2005-04-01 | 2009-03-24 | International Business Machines Corporation | Method for reducing latency in a host ethernet adapter (HEA) |
US7881332B2 (en) * | 2005-04-01 | 2011-02-01 | International Business Machines Corporation | Configurable ports for a host ethernet adapter |
EP2170079B1 (en) * | 2007-06-29 | 2013-05-29 | Dow AgroSciences LLC | Synergistic herbicidal composition containing a substituted phenoxy alkanoic acid derivative and a glyphosate derivative |
AU2009212525B2 (en) * | 2008-02-05 | 2012-06-21 | Arysta Lifescience North America, Llc | Solid formulation of low melting active compound |
US9253985B2 (en) | 2010-05-21 | 2016-02-09 | Bayer Intellectual Property Gmbh | Herbicidal composition for tolerant or resistant cereal crops |
US20110287934A1 (en) * | 2010-05-21 | 2011-11-24 | Bayer Cropscience Ag | Herbicidal composition for tolerant or resistant rice crops |
US20120100993A1 (en) * | 2010-10-20 | 2012-04-26 | Franklin Paul Silverman | Plant Growth Enhancement with Combinations of PESA and Herbicides |
CN102057915B (zh) * | 2011-01-07 | 2013-03-20 | 山东省农业科学院作物研究所 | 提高小麦抗逆性与籽粒产量的化控制剂及其应用 |
CN102239843B (zh) * | 2011-07-07 | 2013-11-06 | 永农生物科学有限公司 | 一种氯氟吡氧乙酸或其酯和乙羧氟草醚组合物及制备方法 |
BR122019001001B1 (pt) | 2011-10-26 | 2019-08-27 | Monsanto Technology Llc | sais herbicidas de auxina, mistura de aplicação herbicida compreendendo os mesmos para uso na eliminação e controle do crescimento de plantas indesejadas, bem como métodos de controle de plantas indesejadas e de plantas suscetíveis ao herbicida de auxina |
CN103371175A (zh) * | 2012-04-25 | 2013-10-30 | 陕西韦尔奇作物保护有限公司 | 一种含草铵膦的除草组合物 |
CN103371176A (zh) * | 2012-04-26 | 2013-10-30 | 陕西韦尔奇作物保护有限公司 | 一种含草铵膦的农药组合物 |
WO2013184622A2 (en) | 2012-06-04 | 2013-12-12 | Monsanto Technology Llc | Aqueous concentrated herbicidal compositions containing glyphosate salts and dicamba salts |
CN102763675B (zh) * | 2012-07-12 | 2014-03-26 | 美丰农化有限公司 | 一种除草剂 |
WO2014013998A1 (ja) * | 2012-07-18 | 2014-01-23 | 日本農薬株式会社 | 薬害が軽減された除草剤組成物及びその使用方法 |
MX2015007995A (es) * | 2012-12-20 | 2015-10-22 | Dow Agrosciences Llc | Composiciones herbicidas que contienen fluroxipir y flumetsulam. |
CN103053609B (zh) * | 2012-12-29 | 2014-12-31 | 广东中迅农科股份有限公司 | 草铵膦和吡啶羧酸类除草剂的除草组合物 |
WO2014134235A1 (en) | 2013-02-27 | 2014-09-04 | Monsanto Technology Llc | Glyphosate composition for dicamba tank mixtures with improved volatility |
CN103329929A (zh) * | 2013-06-04 | 2013-10-02 | 广东中迅农科股份有限公司 | 一种含有草铵膦和2,4-滴丁酯的除草组合物 |
CN103392733A (zh) * | 2013-06-30 | 2013-11-20 | 广东中迅农科股份有限公司 | 含有草铵膦和唑草酮的除草组合物 |
WO2015153281A1 (en) * | 2014-03-31 | 2015-10-08 | Fmc Corporation | Methods for selectively controlling plants using compositions containing photosystem ii inhibitors and protoporphyrinogen oxidase inhibitors |
CN104068051A (zh) * | 2014-05-27 | 2014-10-01 | 安徽省益农化工有限公司 | 一种杀虫除草复合制剂 |
CN104381296A (zh) * | 2014-11-25 | 2015-03-04 | 广东中迅农科股份有限公司 | 一种含有氨氯吡啶酸和草甘膦的除草组合物 |
US9834802B2 (en) | 2016-03-02 | 2017-12-05 | Agrimetis, Llc | Methods for making L-glufosinate |
CN105941468A (zh) * | 2016-05-11 | 2016-09-21 | 安徽省益农化工有限公司 | 一种含草甘膦、唑嘧磺草胺和双草醚的混合除草剂 |
CN106070305A (zh) * | 2016-06-08 | 2016-11-09 | 济南绿霸农药有限公司 | 一种含草铵膦和乙羧氟草醚的除草组合物及其制备方法 |
CN105935060A (zh) * | 2016-06-22 | 2016-09-14 | 南京华洲药业有限公司 | 一种含草铵膦与三氟丙磺隆的除草组合物及其应用 |
CA3069815A1 (en) | 2017-07-27 | 2019-01-31 | Basf Se | Use of herbicidal compositions based on l-glufosinate in tolerant field crops |
WO2019030091A2 (en) * | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE AND THEIR USE IN COTTON CULTURES |
CA3070177A1 (en) * | 2017-08-09 | 2019-02-14 | Basf Se | Herbicidal mixtures comprising l-glufosinate and their use in canola cultures |
EP3664606A1 (en) * | 2017-08-09 | 2020-06-17 | Basf Se | Herbicidal mixtures comprising l-glufosinate or its salt and at least one protoporphyrinogen-ix oxidase inhibitor |
EP3440939A1 (en) | 2017-08-09 | 2019-02-13 | Basf Se | Herbicidal mixtures comprising l-glufosinate |
CN107439586A (zh) * | 2017-09-25 | 2017-12-08 | 山东中新科农生物科技有限公司 | 一种含精草铵膦的三元除草组合物 |
CN107711878A (zh) * | 2017-10-06 | 2018-02-23 | 湖南泽丰农化有限公司 | 含2,4‑滴二甲胺盐和草铵膦的灭生性除草组合物 |
MX2020007564A (es) * | 2018-01-17 | 2020-09-03 | Upl Ltd | Combinaciones herbicidas. |
BR112021010436A2 (pt) * | 2018-12-26 | 2021-08-24 | Sumitomo Chemical Company, Limited | Método para o controle de erva daninha |
CN109588418A (zh) * | 2019-01-02 | 2019-04-09 | 南宁市德丰富化工有限责任公司 | 一种含草铵膦和灭草松的农药组合物 |
CN109645025A (zh) * | 2019-02-12 | 2019-04-19 | 苏农(广德)生物科技有限公司 | 一种草甘膦和异噁草松的除草剂组合物 |
US10555528B1 (en) * | 2019-03-20 | 2020-02-11 | Sumitomo Chemical Company, Limited | Herbicidal composition and method for controlling weeds |
WO2021151739A1 (en) | 2020-01-31 | 2021-08-05 | Basf Se | Herbicide combinations comprising glufosinate and pyraflufen-ethyl |
WO2021240489A2 (en) * | 2020-05-29 | 2021-12-02 | Best Agrolife Limited | A synergistic herbicidal composition |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4265654A (en) | 1977-12-28 | 1981-05-05 | Meiji Seika Kaisha Ltd. | Herbicidal compositions |
DE3122691A1 (de) * | 1981-06-06 | 1982-12-23 | Hoechst Ag, 6000 Frankfurt | Herbizide mittel |
US4535060A (en) | 1983-01-05 | 1985-08-13 | Calgene, Inc. | Inhibition resistant 5-enolpyruvyl-3-phosphoshikimate synthetase, production and use |
DE3765449D1 (de) | 1986-03-11 | 1990-11-15 | Plant Genetic Systems Nv | Durch gentechnologie erhaltene und gegen glutaminsynthetase-inhibitoren resistente pflanzenzellen. |
US5273894A (en) | 1986-08-23 | 1993-12-28 | Hoechst Aktiengesellschaft | Phosphinothricin-resistance gene, and its use |
ES2038631T3 (es) | 1986-08-23 | 1993-08-01 | Hoechst Aktiengesellschaft | Procedimiento para la obtencion de un gen de resistencia frente a fosfinotricina (ptc). |
US5276268A (en) | 1986-08-23 | 1994-01-04 | Hoechst Aktiengesellschaft | Phosphinothricin-resistance gene, and its use |
CN87100603A (zh) | 1987-01-21 | 1988-08-10 | 昂科公司 | 抗黑素瘤疫苗 |
US5310667A (en) | 1989-07-17 | 1994-05-10 | Monsanto Company | Glyphosate-tolerant 5-enolpyruvyl-3-phosphoshikimate synthases |
DE4327056A1 (de) * | 1993-08-12 | 1995-02-16 | Hoechst Schering Agrevo Gmbh | Verfahren zur Ertragssteigerung von herbizidresistenten Nutzpflanzen |
DE4003045A1 (de) | 1990-02-02 | 1991-08-08 | Hoechst Ag | Virus/herbizidresistenz-gene, verfahren zu ihrer herstellung und ihre verwendung |
US5633434A (en) | 1990-02-02 | 1997-05-27 | Hoechst Aktiengesellschaft | Transgenic plants displaying virus and phosphinothricin resistance |
CA2083948C (en) | 1990-06-25 | 2001-05-15 | Ganesh M. Kishore | Glyphosate tolerant plants |
WO1992008353A1 (de) * | 1990-11-13 | 1992-05-29 | Hoechst Aktiengesellschaft | Synergistische herbizide mittel |
US5599769A (en) | 1990-11-13 | 1997-02-04 | Hoechst Aktiengesellschaft | Synergistic herbicidal compositions comprising glyphosate or glufosinate in combination with a sulfonylurea herbicide |
DE4038430A1 (de) † | 1990-12-01 | 1992-06-04 | Basf Ag | Herbizide n-((1,3,5-triazin-2-yl)-aminocarbonyl) benzolsulfonamide |
EP0492367B1 (de) * | 1990-12-21 | 2000-09-27 | Aventis CropScience GmbH | Mischungen aus Herbiziden und Antidots |
US5238904A (en) † | 1991-01-22 | 1993-08-24 | Hoechst Aktiengesellschaft | Liquid preparations of herbicide mixture based on glufosinate |
DE19501986A1 (de) * | 1995-01-24 | 1996-07-25 | Hoechst Schering Agrevo Gmbh | Synergistische herbizide Mittel aus Basis Glufosinate und Nitrodiphenylethern sowie deren Formulierungen |
DE19520839A1 (de) † | 1995-06-08 | 1996-12-12 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit 4-Iodo-2-[3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) ureidosulfonyl] -benzoesäureestern |
DE19534910A1 (de) † | 1995-09-20 | 1997-03-27 | Basf Ag | Herbizide Mischungen mit synergistischer Wirkung |
CA2249332C (en) * | 1996-03-29 | 2006-10-10 | Monsanto Europe S.A. | New use of n-(phosphonomethyl)glycine and derivatives thereof |
DE19633271A1 (de) * | 1996-08-19 | 1998-02-26 | Basf Ag | Flüssige Formulierung von Ethyl-(Z)-2-chlor-3-[2-chlor-5-(4,5,6,7-tetrahydro-1,3-dioxoisoindoldion-2-yl)phenyl]acrylat |
AR008158A1 (es) | 1996-09-05 | 1999-12-09 | Syngenta Participations Ag | Proceso para el control de malas hierbas en cultivos de plantas utiles que son resistentes a un fosfo-herbicida y una composicion herbicida para dicho uso. |
EP0946737A2 (en) | 1996-11-07 | 1999-10-06 | Zeneca Limited | Herbicide resistant plants |
DE19650955A1 (de) | 1996-12-07 | 1998-06-10 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit N- [(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl] -5-methylsulfonamidomethyl-2-alkoxycarbonylbenzolsulfonamiden |
JPH11279009A (ja) * | 1998-03-26 | 1999-10-12 | Sumitomo Chem Co Ltd | 除草剤組成物 |
DE19836700A1 (de) † | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Getreidekulturen |
-
1998
- 1998-08-13 DE DE19836700A patent/DE19836700A1/de not_active Withdrawn
-
1999
- 1999-08-10 PL PL401504A patent/PL217911B1/pl unknown
- 1999-08-10 PL PL397705A patent/PL217213B1/pl unknown
- 1999-08-10 DE DE59911735T patent/DE59911735D1/de not_active Expired - Lifetime
- 1999-08-10 PL PL397713A patent/PL217230B1/pl unknown
- 1999-08-10 PL PL401516A patent/PL218880B1/pl unknown
- 1999-08-10 CA CA2936388A patent/CA2936388C/en not_active Expired - Lifetime
- 1999-08-10 PL PL387554A patent/PL218886B1/pl unknown
- 1999-08-10 PL PL401510A patent/PL218213B1/pl unknown
- 1999-08-10 PL PL397714A patent/PL217241B1/pl unknown
- 1999-08-10 CA CA2793821A patent/CA2793821C/en not_active Expired - Lifetime
- 1999-08-10 PL PL401506A patent/PL218242B1/pl unknown
- 1999-08-10 PL PL397711A patent/PL217247B1/pl unknown
- 1999-08-10 BR BR9913006-8A patent/BR9913006A/pt not_active IP Right Cessation
- 1999-08-10 PL PL401515A patent/PL218895B1/pl unknown
- 1999-08-10 CA CA2340193A patent/CA2340193C/en not_active Expired - Lifetime
- 1999-08-10 CZ CZ2001-555A patent/CZ304256B6/cs not_active IP Right Cessation
- 1999-08-10 PL PL397709A patent/PL217214B1/pl unknown
- 1999-08-10 US US09/371,770 patent/US6723681B2/en not_active Expired - Lifetime
- 1999-08-10 PL PL401513A patent/PL218894B1/pl unknown
- 1999-08-10 CN CNB998096164A patent/CN1220437C/zh not_active Expired - Lifetime
- 1999-08-10 CA CA2794516A patent/CA2794516C/en not_active Expired - Lifetime
- 1999-08-10 HU HU0103462A patent/HU230431B1/hu unknown
- 1999-08-10 PL PL401514A patent/PL219930B1/pl unknown
- 1999-08-10 ES ES99941559T patent/ES2239850T5/es not_active Expired - Lifetime
- 1999-08-10 PT PT99941559T patent/PT1104992E/pt unknown
- 1999-08-10 PL PL401512A patent/PL218250B1/pl unknown
- 1999-08-10 TR TR2001/00479T patent/TR200100479T2/xx unknown
- 1999-08-10 PL PL401509A patent/PL219915B1/pl unknown
- 1999-08-10 WO PCT/EP1999/005801 patent/WO2000008940A1/de active IP Right Grant
- 1999-08-10 KR KR1020017001848A patent/KR20010087182A/ko not_active Application Discontinuation
- 1999-08-10 AU AU55128/99A patent/AU767032B2/en not_active Expired
- 1999-08-10 KR KR1020087014141A patent/KR20080059342A/ko not_active Application Discontinuation
- 1999-08-10 PL PL393881A patent/PL215351B1/pl unknown
- 1999-08-10 PL PL397710A patent/PL217250B1/pl unknown
- 1999-08-10 PL PL346124A patent/PL212668B1/pl unknown
- 1999-08-10 PL PL401511A patent/PL218251B1/pl unknown
- 1999-08-10 PL PL397712A patent/PL217235B1/pl unknown
- 1999-08-10 SK SK213-2001A patent/SK288448B6/sk not_active IP Right Cessation
- 1999-08-10 AT AT99941559T patent/ATE290317T1/de not_active IP Right Cessation
- 1999-08-10 NZ NZ509845A patent/NZ509845A/xx unknown
- 1999-08-10 RU RU2001107014/04A patent/RU2250614C2/ru active
- 1999-08-10 PL PL397706A patent/PL217209B1/pl unknown
- 1999-08-10 IL IL14114499A patent/IL141144A/xx not_active IP Right Cessation
- 1999-08-10 PL PL401517A patent/PL217917B1/pl unknown
- 1999-08-10 PL PL401518A patent/PL218249B1/pl unknown
- 1999-08-10 PL PL401505A patent/PL217912B1/pl unknown
- 1999-08-10 EP EP99941559A patent/EP1104992B2/de not_active Expired - Lifetime
- 1999-08-10 JP JP2000564454A patent/JP2002522460A/ja not_active Abandoned
- 1999-08-11 AR ARP990104016A patent/AR020162A1/es active IP Right Grant
- 1999-10-08 UA UA2001031685A patent/UA71569C2/uk unknown
-
2001
- 2001-02-09 ZA ZA200101142A patent/ZA200101142B/en unknown
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2013
- 2013-02-07 AR ARP130100384A patent/AR089930A2/es not_active Application Discontinuation
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