JP2016523228A5 - - Google Patents
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- Publication number
- JP2016523228A5 JP2016523228A5 JP2016517255A JP2016517255A JP2016523228A5 JP 2016523228 A5 JP2016523228 A5 JP 2016523228A5 JP 2016517255 A JP2016517255 A JP 2016517255A JP 2016517255 A JP2016517255 A JP 2016517255A JP 2016523228 A5 JP2016523228 A5 JP 2016523228A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- group
- alkoxy
- substituted
- cycloalkyl
- 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.)
- Granted
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 65
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 35
- 125000001424 substituent group Chemical group 0.000 claims 35
- 150000001875 compounds Chemical class 0.000 claims 31
- 229910052736 halogen Inorganic materials 0.000 claims 31
- 150000002367 halogens Chemical class 0.000 claims 31
- -1 cyano, hydroxy Chemical group 0.000 claims 30
- 229910052717 sulfur Inorganic materials 0.000 claims 30
- 229910052760 oxygen Inorganic materials 0.000 claims 29
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 24
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 24
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 23
- 125000004432 carbon atom Chemical group C* 0.000 claims 22
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 19
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 17
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims 17
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 15
- 229910052757 nitrogen Inorganic materials 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 13
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 12
- 125000005842 heteroatom Chemical group 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 11
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 11
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 11
- 125000002947 alkylene group Chemical group 0.000 claims 11
- 229910052799 carbon Inorganic materials 0.000 claims 11
- 125000004093 cyano group Chemical group *C#N 0.000 claims 11
- 150000003254 radicals Chemical class 0.000 claims 11
- 150000003839 salts Chemical class 0.000 claims 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 10
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 10
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 10
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 10
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 9
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 9
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 9
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 8
- 125000001309 chloro group Chemical group Cl* 0.000 claims 7
- 125000004122 cyclic group Chemical group 0.000 claims 7
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 claims 6
- 125000004438 haloalkoxy group Chemical group 0.000 claims 6
- 150000002431 hydrogen Chemical class 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 5
- 239000000460 chlorine Substances 0.000 claims 5
- 125000004433 nitrogen atom Chemical class N* 0.000 claims 5
- 125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Substances 0.000 claims 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 4
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 125000002950 monocyclic group Chemical group 0.000 claims 4
- 125000004043 oxo group Chemical group O=* 0.000 claims 4
- 125000006413 ring segment Chemical group 0.000 claims 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 4
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 4
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 3
- 125000005862 (C1-C6)alkanoyl group Chemical group 0.000 claims 3
- 125000002015 acyclic group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 125000003367 polycyclic group Chemical group 0.000 claims 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 2
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 2
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims 2
- 125000006763 (C3-C9) cycloalkyl group Chemical group 0.000 claims 2
- YKYIFUROKBDHCY-ONEGZZNKSA-N (e)-4-ethoxy-1,1,1-trifluorobut-3-en-2-one Chemical group CCO\C=C\C(=O)C(F)(F)F YKYIFUROKBDHCY-ONEGZZNKSA-N 0.000 claims 2
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 claims 2
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 239000004009 herbicide Substances 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 2
- 239000005648 plant growth regulator Substances 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 1
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 230000000895 acaricidal effect Effects 0.000 claims 1
- 239000000642 acaricide Substances 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 239000003905 agrochemical Substances 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 244000038559 crop plants Species 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000003337 fertilizer Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 239000005645 nematicide Substances 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13171035.2 | 2013-06-07 | ||
| EP13171035 | 2013-06-07 | ||
| PCT/EP2014/061328 WO2014195253A1 (en) | 2013-06-07 | 2014-06-02 | Substituted 5-hydroxy-2,3-diphenylpentanonitrile derivatives, processes for their preparation and their use as herbicides and/or plant growth regulators |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016523228A JP2016523228A (ja) | 2016-08-08 |
| JP2016523228A5 true JP2016523228A5 (enExample) | 2017-07-20 |
| JP6466923B2 JP6466923B2 (ja) | 2019-02-06 |
Family
ID=48570008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016517255A Expired - Fee Related JP6466923B2 (ja) | 2013-06-07 | 2014-06-02 | 置換された５−ヒドロキシ−２，３−ジフェニルペンタノニトリル誘導体、それの製造方法、ならびにそれの除草剤および／または植物成長調節剤としての使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10021877B2 (enExample) |
| EP (1) | EP3003036B1 (enExample) |
| JP (1) | JP6466923B2 (enExample) |
| CN (1) | CN105451553A (enExample) |
| AR (1) | AR096517A1 (enExample) |
| BR (1) | BR112015030196A2 (enExample) |
| WO (1) | WO2014195253A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10172350B2 (en) | 2014-10-08 | 2019-01-08 | Bayer Cropscience Aktiengesellschaft | Substituted 5-hydroxy-2-phenyl-3-heteroaryl pentanenitrile derivatives, method for the production thereof and use thereof as herbicides and/or plant growth regulators |
| CN110672753B (zh) * | 2019-11-04 | 2022-05-20 | 青海省农林科学院 | 一种氟咯草酮异构体的拆分和检测方法 |
| CN111990400B (zh) * | 2020-07-29 | 2021-07-23 | 浙江工业大学 | 一种二芳基戊烷类化合物在除草剂中的应用 |
Family Cites Families (58)
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| US4224052A (en) * | 1978-05-05 | 1980-09-23 | American Cyanamid Company | Polysubstituted butanoic acids, esters and derivatives thereof utilizing the same as herbicides |
| JPS57209274A (en) * | 1981-06-16 | 1982-12-22 | Takeda Chem Ind Ltd | Urea derivative, its preparation and its use |
| MA19709A1 (fr) | 1982-02-17 | 1983-10-01 | Ciba Geigy Ag | Application de derives de quinoleine a la protection des plantes cultivees . |
| ATE103902T1 (de) | 1982-05-07 | 1994-04-15 | Ciba Geigy Ag | Verwendung von chinolinderivaten zum schuetzen von kulturpflanzen. |
| JPS60500438A (ja) | 1983-01-17 | 1985-04-04 | モンサント カンパニ− | 植物細胞を形質転換するためのプラスミド |
| BR8404834A (pt) | 1983-09-26 | 1985-08-13 | Agrigenetics Res Ass | Metodo para modificar geneticamente uma celula vegetal |
| JPS6087254A (ja) | 1983-10-19 | 1985-05-16 | Japan Carlit Co Ltd:The | 新規尿素化合物及びそれを含有する除草剤 |
| FR2561918A1 (fr) * | 1984-03-30 | 1985-10-04 | Hoechst Lab | Nouveaux medicaments appartenant a la famille des tetrahydropyrones-2 a action psychostimulante et leur procede de preparation |
| DE3525205A1 (de) | 1984-09-11 | 1986-03-20 | Hoechst Ag, 6230 Frankfurt | Pflanzenschuetzende mittel auf basis von 1,2,4-triazolderivaten sowie neue derivate des 1,2,4-triazols |
| BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
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| US4631211A (en) | 1985-03-25 | 1986-12-23 | Scripps Clinic & Research Foundation | Means for sequential solid phase organic synthesis and methods using the same |
| EP0221044B1 (en) | 1985-10-25 | 1992-09-02 | Monsanto Company | Novel plant vectors |
| ES2018274T5 (es) | 1986-03-11 | 1996-12-16 | Plant Genetic Systems Nv | Celulas vegetales resistentes a los inhibidores de glutamina sintetasa, preparadas por ingenieria genetica. |
| JPH01503663A (ja) | 1986-05-01 | 1989-12-07 | ハネウエル・インコーポレーテツド | 多重集積回路相互接続装置 |
| IL83348A (en) | 1986-08-26 | 1995-12-08 | Du Pont | Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase |
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| EP0266725A1 (en) * | 1986-11-06 | 1988-05-11 | American Cyanamid Company | 4-cyano-4-(fluorophenyl)-3-(substituted phenyl) butyric acids, esters and derivatives thereof, and a method of selectively controlling undesirable vegetation in rice therewith |
| DE3733017A1 (de) | 1987-09-30 | 1989-04-13 | Bayer Ag | Stilbensynthase-gen |
| DE3808896A1 (de) | 1988-03-17 | 1989-09-28 | Hoechst Ag | Pflanzenschuetzende mittel auf basis von pyrazolcarbonsaeurederivaten |
| DE3817192A1 (de) | 1988-05-20 | 1989-11-30 | Hoechst Ag | 1,2,4-triazolderivate enthaltende pflanzenschuetzende mittel sowie neue derivate des 1,2,4-triazols |
| ATE84302T1 (de) | 1988-10-20 | 1993-01-15 | Ciba Geigy Ag | Sulfamoylphenylharnstoffe. |
| DE3939010A1 (de) | 1989-11-25 | 1991-05-29 | Hoechst Ag | Isoxazoline, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschuetzende mittel |
| DE3939503A1 (de) | 1989-11-30 | 1991-06-06 | Hoechst Ag | Neue pyrazoline zum schutz von kulturpflanzen gegenueber herbiziden |
| ATE241007T1 (de) | 1990-03-16 | 2003-06-15 | Calgene Llc | Dnas, die für pflanzliche desaturasen kodieren und deren anwendungen |
| FI925228A7 (fi) | 1990-06-18 | 1992-11-18 | Monsanto Co | Lisääntynyt tärkkelyspitoisuus kasveissa |
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| DE4107396A1 (de) | 1990-06-29 | 1992-01-02 | Bayer Ag | Stilbensynthase-gene aus weinrebe |
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| SE467358B (sv) | 1990-12-21 | 1992-07-06 | Amylogene Hb | Genteknisk foeraendring av potatis foer bildning av staerkelse av amylopektintyp |
| DE4104782B4 (de) | 1991-02-13 | 2006-05-11 | Bayer Cropscience Gmbh | Neue Plasmide, enthaltend DNA-Sequenzen, die Veränderungen der Karbohydratkonzentration und Karbohydratzusammensetzung in Pflanzen hervorrufen, sowie Pflanzen und Pflanzenzellen enthaltend dieses Plasmide |
| TW259690B (enExample) | 1992-08-01 | 1995-10-11 | Hoechst Ag | |
| DE4331448A1 (de) | 1993-09-16 | 1995-03-23 | Hoechst Schering Agrevo Gmbh | Substituierte Isoxazoline, Verfahren zu deren Herstellung, diese enthaltende Mittel und deren Verwendung als Safener |
| WO1998013361A1 (en) | 1996-09-26 | 1998-04-02 | Novartis Ag | Herbicidal composition |
| DE19652961A1 (de) | 1996-12-19 | 1998-06-25 | Hoechst Schering Agrevo Gmbh | Neue 2-Fluoracrylsäurederivate, neue Mischungen aus Herbiziden und Antidots und deren Verwendung |
| US6071856A (en) | 1997-03-04 | 2000-06-06 | Zeneca Limited | Herbicidal compositions for acetochlor in rice |
| DE19727410A1 (de) | 1997-06-27 | 1999-01-07 | Hoechst Schering Agrevo Gmbh | 3-(5-Tetrazolylcarbonyl)-2-chinolone und diese enthaltende nutzpflanzenschützende Mittel |
| DE19742951A1 (de) | 1997-09-29 | 1999-04-15 | Hoechst Schering Agrevo Gmbh | Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung |
| JPH11335212A (ja) * | 1998-05-21 | 1999-12-07 | Nippon Bayer Agrochem Co Ltd | 水田用除草剤組成物 |
| AR031027A1 (es) | 2000-10-23 | 2003-09-03 | Syngenta Participations Ag | Composiciones agroquimicas |
| WO2004084631A1 (de) | 2003-03-26 | 2004-10-07 | Bayer Cropscience Gmbh | Verwendung von hydroxyaromaten als safener |
| DE10335726A1 (de) | 2003-08-05 | 2005-03-03 | Bayer Cropscience Gmbh | Verwendung von Hydroxyaromaten als Safener |
| DE10335725A1 (de) | 2003-08-05 | 2005-03-03 | Bayer Cropscience Gmbh | Safener auf Basis aromatisch-aliphatischer Carbonsäuredarivate |
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| DE102004035137A1 (de) | 2004-07-20 | 2006-02-16 | Bayer Cropscience Gmbh | Wirkstoffe zur Steigerung der Pathogenabwehr in Pflanzen und Methoden zu ihrer Auffindung |
| WO2007023719A1 (ja) | 2005-08-22 | 2007-03-01 | Kumiai Chemical Industry Co., Ltd. | 薬害軽減剤及び薬害が軽減された除草剤組成物 |
| JPWO2007023764A1 (ja) | 2005-08-26 | 2009-02-26 | クミアイ化学工業株式会社 | 薬害軽減剤及び薬害が軽減された除草剤組成物 |
| WO2011003776A2 (de) | 2009-07-09 | 2011-01-13 | Basf Se | Substituierte cyanobutyrate mit herbizider wirkung |
| WO2011003775A2 (de) | 2009-07-09 | 2011-01-13 | Basf Se | Substituierte cyanobutyrate mit herbizider wirkung |
| WO2011014383A1 (en) | 2009-07-27 | 2011-02-03 | Merck Sharp & Dohme Corp. | Radiolabeled cgrp antagonists |
| WO2011042378A1 (de) | 2009-10-09 | 2011-04-14 | Basf Se | Substituierte cyanobutyrate mit herbizider wirkung |
| WO2011073143A1 (en) | 2009-12-18 | 2011-06-23 | Basf Se | Substituted cyanobutyrates having herbicidal action |
| WO2012076513A1 (en) | 2010-12-09 | 2012-06-14 | F. Hoffmann-La Roche Ag | 3-cyano-1-hydroxymethyl-2-phenylpyrrolidine derivatives as inhibitors of mdm2-p53 interactions useful for the treatment of cancer |
| JP2014516919A (ja) * | 2011-03-18 | 2014-07-17 | バイエル・インテレクチユアル・プロパテイー・ゲー・エム・ベー・ハー | 置換された４−シアノ−３−（２，６−ジフルオロフェニル）−４−フェニルブタン酸化合物、それの製造方法ならびに除草剤および植物成長調節剤としてのそれらの使用 |
| BR112013023921A2 (pt) | 2011-03-18 | 2016-08-09 | Bayer Ip Gmbh | (3r,4r) -4-ciano-3, 4-difenilbutanoatos substituídos, processos para a sua preparação e sua utilização como herbecidas e reguladores de crescimento de plantas |
| CN103748075B (zh) * | 2011-07-15 | 2016-09-07 | 拜耳知识产权有限责任公司 | 2,3-二苯基戊腈衍生物、其制备方法及其作为除草剂和植物生长调节剂的用途 |
-
2014
- 2014-05-30 AR ARP140102149A patent/AR096517A1/es unknown
- 2014-06-02 WO PCT/EP2014/061328 patent/WO2014195253A1/en not_active Ceased
- 2014-06-02 EP EP14727513.5A patent/EP3003036B1/en not_active Not-in-force
- 2014-06-02 CN CN201480043764.7A patent/CN105451553A/zh active Pending
- 2014-06-02 JP JP2016517255A patent/JP6466923B2/ja not_active Expired - Fee Related
- 2014-06-02 US US14/895,343 patent/US10021877B2/en not_active Expired - Fee Related
- 2014-06-02 BR BR112015030196A patent/BR112015030196A2/pt not_active Application Discontinuation
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