NO331464B1 - Antistoff for immunoanalyse for neonicotinyl-insekticider, proteinkonjugat, fremgangsmate for bestemmelse av konsentrasjon, samt et sett. - Google Patents
Antistoff for immunoanalyse for neonicotinyl-insekticider, proteinkonjugat, fremgangsmate for bestemmelse av konsentrasjon, samt et sett. Download PDFInfo
- Publication number
- NO331464B1 NO331464B1 NO20022684A NO20022684A NO331464B1 NO 331464 B1 NO331464 B1 NO 331464B1 NO 20022684 A NO20022684 A NO 20022684A NO 20022684 A NO20022684 A NO 20022684A NO 331464 B1 NO331464 B1 NO 331464B1
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- Prior art keywords
- antibody
- neonicotinoid
- sample
- hapten
- insecticide
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- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000001030 gas--liquid chromatography Methods 0.000 description 1
- 230000007274 generation of a signal involved in cell-cell signaling Effects 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
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- 238000004020 luminiscence type Methods 0.000 description 1
- HWYHZTIRURJOHG-UHFFFAOYSA-N luminol Chemical compound O=C1NNC(=O)C2=C1C(N)=CC=C2 HWYHZTIRURJOHG-UHFFFAOYSA-N 0.000 description 1
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
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- 238000001819 mass spectrum Methods 0.000 description 1
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- 239000012528 membrane Substances 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 1
- GLIKYKRDYKKEBJ-UHFFFAOYSA-N methyl n'-nitrocarbamimidate Chemical compound CO\C(N)=N/[N+]([O-])=O GLIKYKRDYKKEBJ-UHFFFAOYSA-N 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 230000036963 noncompetitive effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
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- 229920000573 polyethylene Polymers 0.000 description 1
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- BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 1
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- 238000010992 reflux Methods 0.000 description 1
- 238000000611 regression analysis Methods 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 210000004989 spleen cell Anatomy 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 125000002730 succinyl group Chemical group C(CCC(=O)*)(=O)* 0.000 description 1
- GZCRRIHWUXGPOV-UHFFFAOYSA-N terbium atom Chemical compound [Tb] GZCRRIHWUXGPOV-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
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- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/44—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material not provided for elsewhere, e.g. haptens, metals, DNA, RNA, amino acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Immunology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Peptides Or Proteins (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
- Enzymes And Modification Thereof (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US45678299A | 1999-12-08 | 1999-12-08 | |
PCT/EP2000/012310 WO2001042787A2 (fr) | 1999-12-08 | 2000-12-06 | Dosage immunologique pour insecticides neonicotiniques |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20022684D0 NO20022684D0 (no) | 2002-06-06 |
NO20022684L NO20022684L (no) | 2002-06-25 |
NO331464B1 true NO331464B1 (no) | 2012-01-09 |
Family
ID=23814141
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20022684A NO331464B1 (no) | 1999-12-08 | 2002-06-06 | Antistoff for immunoanalyse for neonicotinyl-insekticider, proteinkonjugat, fremgangsmate for bestemmelse av konsentrasjon, samt et sett. |
Country Status (26)
Country | Link |
---|---|
US (1) | US7148029B2 (fr) |
EP (1) | EP1235805B1 (fr) |
JP (1) | JP4980536B2 (fr) |
KR (1) | KR100752536B1 (fr) |
CN (1) | CN100379725C (fr) |
AR (2) | AR026735A1 (fr) |
AT (1) | ATE343564T1 (fr) |
AU (1) | AU778677B2 (fr) |
BR (1) | BR0016265B1 (fr) |
CA (1) | CA2393084C (fr) |
CZ (1) | CZ303174B6 (fr) |
DE (1) | DE60031570T2 (fr) |
DK (1) | DK1235805T3 (fr) |
EA (1) | EA005380B1 (fr) |
ES (1) | ES2272357T3 (fr) |
HU (1) | HU229490B1 (fr) |
IL (2) | IL150009A0 (fr) |
MA (1) | MA25635A1 (fr) |
MX (1) | MXPA02005514A (fr) |
NO (1) | NO331464B1 (fr) |
NZ (1) | NZ519152A (fr) |
PL (1) | PL205061B1 (fr) |
PT (1) | PT1235805E (fr) |
UA (1) | UA76708C2 (fr) |
WO (1) | WO2001042787A2 (fr) |
ZA (1) | ZA200204582B (fr) |
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GB2433989B (en) | 2004-07-01 | 2009-04-08 | Central Science Lab | Analyte detection system |
JP2006282547A (ja) * | 2005-03-31 | 2006-10-19 | Horiba Ltd | ニテンピラムのハプテン化合物、抗体、ハイブリドーマ、およびその測定手段、測定用キットまたは測定方法 |
JP4841856B2 (ja) * | 2005-03-31 | 2011-12-21 | 株式会社堀場製作所 | クロチアニジンおよびジノテフランのハプテン化合物、抗体、ハイブリドーマおよびその測定手段、測定キットまたは測定方法 |
SI1888641T1 (sl) * | 2005-05-18 | 2012-05-31 | Ablynx Nv | Proteini ki vežejo serum albumin |
KR100696615B1 (ko) | 2005-10-06 | 2007-03-19 | 충북대학교 산학협력단 | 이미다크로플리드 분석 방법 및 이의 분석 시스템 |
JP2007187650A (ja) * | 2005-12-16 | 2007-07-26 | Horiba Ltd | 免疫測定法を用いたフィプロニルの測定キット |
US8323904B2 (en) | 2005-12-16 | 2012-12-04 | Bayer Cropscience Ag | Kit for measurement of termite insecticide active ingredient by immunoassay method |
CA2641544C (fr) * | 2006-02-10 | 2011-01-11 | Mitsui Chemicals, Inc. | Procede de fabrication de o-methyl-n-nitroisouree |
CN100402522C (zh) * | 2006-02-13 | 2008-07-16 | 中国农业大学 | 一种净化常山酮的方法及其专用免疫亲和色谱柱 |
KR100879222B1 (ko) | 2006-05-09 | 2009-01-15 | 재단법인서울대학교산학협력재단 | 제초제 메타미포프 잔류물 검출용 효소면역학적 분석법 |
KR100876435B1 (ko) | 2007-05-22 | 2008-12-31 | 재단법인서울대학교산학협력재단 | 살충제 비스트리플루론 잔류물의 효소면역학적 분석에이용되는 합텐-단백질 복합체 및 항체 |
KR100879223B1 (ko) | 2007-05-22 | 2009-01-15 | 재단법인서울대학교산학협력재단 | 살충제 비스트리플루론 잔류물 검출용 효소면역학적 분석법 |
US9207240B2 (en) * | 2007-11-14 | 2015-12-08 | Arbor Vita Corporation | Method of efficient extraction of protein from cells |
CN101880325A (zh) * | 2010-06-22 | 2010-11-10 | 南京农业大学 | 一种应用于吡虫啉农药残留检测的单克隆抗体 |
WO2012151465A1 (fr) | 2011-05-04 | 2012-11-08 | Pop Test, Llc | Dispositif de diagnostic |
CN102636643A (zh) * | 2012-04-06 | 2012-08-15 | 上海交通大学 | 用于检测噻虫啉的免疫传感器及其制备方法 |
ES2666000T3 (es) | 2012-08-21 | 2018-04-30 | Janssen Pharmaceutica, N.V. | Anticuerpos para aripiprazol y uso de los mismos |
WO2014031587A1 (fr) * | 2012-08-21 | 2014-02-27 | Janssen Pharmaceutica Nv | Haptènes de l'olanzipine |
US20140057303A1 (en) | 2012-08-21 | 2014-02-27 | Janssen Pharmaceutica Nv | Antibodies to Olanzapine Haptens and Use Thereof |
EP2888234B1 (fr) * | 2012-08-21 | 2017-12-06 | Janssen Pharmaceutica NV | Haptènes d'aripiprazole et leur utilisation dans des dosages immunologiques |
CN107253993B (zh) | 2012-08-21 | 2021-10-22 | 詹森药业有限公司 | 奥氮平的抗体及其用途 |
CN104736567B (zh) | 2012-08-21 | 2019-09-03 | 詹森药业有限公司 | 阿立哌唑半抗原的抗体及其用途 |
CN102942519B (zh) * | 2012-10-31 | 2014-08-13 | 天津科技大学 | 烯啶虫胺半抗原、人工抗原和抗体及其制备方法与应用 |
CN104974256B (zh) * | 2015-04-10 | 2018-06-05 | 南京农业大学 | 一种抗噻虫啉单克隆抗体及其用途 |
CN105037344A (zh) * | 2015-06-16 | 2015-11-11 | 环境保护部南京环境科学研究所 | 一种噻虫啉半抗原的合成方法 |
CN105087498B (zh) * | 2015-09-07 | 2018-01-09 | 江南大学 | 一株苯噻氰单克隆抗体杂交瘤细胞株及其应用 |
CN105572376B (zh) * | 2016-03-07 | 2017-07-11 | 中国烟草总公司贵州省公司 | 一种检测农作物中甲基硫菌灵残留的试纸及其应用、制备方法 |
KR102225307B1 (ko) | 2017-10-19 | 2021-03-11 | 경북대학교 산학협력단 | 왁스 에스테르를 유효성분으로 포함하는 엔도설판 잔류 여부 판단용 또는 엔도설판 독성 확인용 바이오마커 조성물 및 이의 용도 |
CN109813894A (zh) * | 2017-11-18 | 2019-05-28 | 镇江亿特生物科技发展有限公司 | 一种检测大米中乙虫腈的化学发光免疫检测试剂盒 |
CN108998422A (zh) * | 2018-08-14 | 2018-12-14 | 江南大学 | 一种分泌噻虫嗪单克隆抗体的杂交瘤细胞株及其应用 |
CN109061158B (zh) * | 2018-09-21 | 2021-09-03 | 中国烟草总公司郑州烟草研究院 | 一种检测啶虫脒的时间分辨荧光免疫层析试纸条及其制备方法和应用 |
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CN109917126A (zh) * | 2019-02-27 | 2019-06-21 | 成都市房屋安全事务中心((成都市白蚁防治研究中心)) | 一种检测吡虫啉的试纸条、吡虫啉半抗原的制备方法及检测吡虫啉残留的方法 |
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CN112111011B (zh) * | 2020-07-28 | 2022-04-19 | 浙江大学 | 一种特异性抗噻虫嗪抗体的可变区序列及其重组全长抗体 |
CN113009057B (zh) * | 2020-10-22 | 2023-11-07 | 重庆医科大学 | 固相萃取-超高效液相色谱-串联质谱法检测尿液中新烟碱类杀虫剂及代谢产物的方法 |
CN112595850A (zh) * | 2020-11-18 | 2021-04-02 | 北京勤邦生物技术有限公司 | 一种噻虫胺人工抗原在酶联免疫试剂盒中的应用 |
CN113281501B (zh) * | 2021-05-12 | 2023-07-07 | 北京勤邦科技股份有限公司 | 一种五氯硝基苯人工抗原在酶联免疫试剂盒中的应用 |
CN113979994A (zh) * | 2021-12-28 | 2022-01-28 | 信达安检测技术(天津)有限公司 | 一种吡虫啉半抗原、完全抗原及其合成与应用 |
CN114397441A (zh) * | 2022-01-25 | 2022-04-26 | 中国农业科学院蔬菜花卉研究所 | 一种啶虫脒化学发光免疫分析试剂盒及其制备方法和应用 |
CN114636768B (zh) * | 2022-03-23 | 2023-11-07 | 广西-东盟食品检验检测中心 | 一种茉莉花中噻虫嗪残留的检测方法 |
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US5334528A (en) * | 1989-10-30 | 1994-08-02 | The Regents Of The University Of California | Monoclonal antibodies to cyclodiene insecticides and method for detecting the same |
JPH0580553A (ja) | 1991-09-24 | 1993-04-02 | Mita Ind Co Ltd | 電子写真感光体 |
TW240163B (en) * | 1992-07-22 | 1995-02-11 | Syngenta Participations Ag | Oxadiazine derivatives |
GB9304191D0 (en) * | 1993-03-02 | 1993-04-21 | Ciba Geigy Ag | Process for the preparation of aqueous nicotinaldehyde |
DE4329952C1 (de) * | 1993-09-04 | 1994-08-04 | Draegerwerk Ag | Monoklonale Antikörper zum Nachweis von Pyrethroiden sowie Verfahren zu deren Herstellung |
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EP0854721B1 (fr) * | 1995-08-02 | 2001-10-24 | Smithkline Beecham Corporation | Antagonistes des recepteurs a l'endotheline |
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IL130298A (en) * | 1996-12-19 | 2004-03-28 | Syngenta Participations Ag | Process for preparing thiazole derivatives |
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-
2000
- 2000-06-12 UA UA2002075564A patent/UA76708C2/uk unknown
- 2000-12-06 KR KR1020027007294A patent/KR100752536B1/ko active IP Right Grant
- 2000-12-06 JP JP2001544026A patent/JP4980536B2/ja not_active Expired - Fee Related
- 2000-12-06 BR BRPI0016265-5A patent/BR0016265B1/pt not_active IP Right Cessation
- 2000-12-06 CZ CZ20021969A patent/CZ303174B6/cs not_active IP Right Cessation
- 2000-12-06 HU HU0203499A patent/HU229490B1/hu not_active IP Right Cessation
- 2000-12-06 NZ NZ519152A patent/NZ519152A/en not_active IP Right Cessation
- 2000-12-06 EA EA200200620A patent/EA005380B1/ru not_active IP Right Cessation
- 2000-12-06 PL PL355630A patent/PL205061B1/pl unknown
- 2000-12-06 EP EP00989956A patent/EP1235805B1/fr not_active Expired - Lifetime
- 2000-12-06 AR ARP000106458A patent/AR026735A1/es not_active Application Discontinuation
- 2000-12-06 CA CA2393084A patent/CA2393084C/fr not_active Expired - Lifetime
- 2000-12-06 AU AU26721/01A patent/AU778677B2/en not_active Ceased
- 2000-12-06 AT AT00989956T patent/ATE343564T1/de active
- 2000-12-06 CN CNB008177716A patent/CN100379725C/zh not_active Expired - Fee Related
- 2000-12-06 ES ES00989956T patent/ES2272357T3/es not_active Expired - Lifetime
- 2000-12-06 IL IL15000900A patent/IL150009A0/xx active IP Right Grant
- 2000-12-06 PT PT00989956T patent/PT1235805E/pt unknown
- 2000-12-06 US US10/149,512 patent/US7148029B2/en not_active Expired - Lifetime
- 2000-12-06 WO PCT/EP2000/012310 patent/WO2001042787A2/fr active IP Right Grant
- 2000-12-06 DE DE60031570T patent/DE60031570T2/de not_active Expired - Lifetime
- 2000-12-06 MX MXPA02005514A patent/MXPA02005514A/es active IP Right Grant
- 2000-12-06 DK DK00989956T patent/DK1235805T3/da active
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2002
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- 2002-06-06 NO NO20022684A patent/NO331464B1/no not_active IP Right Cessation
- 2002-06-07 MA MA26676A patent/MA25635A1/fr unknown
- 2002-06-07 ZA ZA200204582A patent/ZA200204582B/xx unknown
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2008
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