The biotic pesticide and the composition which includes the insecticide 机翻标题: 暂无翻译,请尝试点击翻译按钮。

源语言标题
(JP6117347) 生物​農薬​および​殺虫​剤​を​含む​組成​物
公开号/公开日
JP2015523971 A 2015-08-20 [JP2015523971]JP6117347 B2 2017-04-19 [JP6117347] / 2015-08-202017-04-19
申请号/申请日
2015JP-0514477 / 2013-05-29
发明人
Anderushiyu Borufuramu;Shiyutentsueru Klaus;Shiyupuringa Bernd;
申请人
BAYER CROPSCIENCE;
主分类号
IPC分类号
A01C-001/00A01N-041/10A01N-043/56A01N-063/00A01P-007/04
摘要
(JP6117347) The present invention relates to a composition comprising at least one biological control agent.  Furthermore, the present invention relates to the use of this composition as well as a method for reducing overall damage of plants and plant parts.  (From US2015141244 A1)
机翻摘要
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地址
代理人
代理机构
;
优先权号
2012EP-0169936 2012-05-30 2012EP-0197137 2012-12-14 2013WO-EP61036 2013-05-29
主权利要求
(JP6117347)  1. Bacillus [pumirusu] (Bacillus pumilus) (NRRL trust number B-30087), the Bacillus subtilis (Bacillus subtilis) AQ713 (NRRL trust number B-21661), and the Bacillus subtilis (Bacillus subtilis) AQ30002 (NRRL trust number B-50421) at least one which is selected from the group which consists of biotic pesticide, And at least one which is selected from the group which consists of [kurorantoraniripuroru], [shiantoraniripuroru] and [hurubenjiamido] insecticide Implication, the composition where the biotic pesticide and weight ratio of the insecticide are the 10000:1 from the 1:10.  2. At least, one bactericide furthermore is included, however in the claim 1 where the aforementioned biotic pesticide and the aforementioned bactericide are not identical the composition of statement.  3. The aforementioned bactericide, the inhibiter of ergosterol biosynthesis, mixture with the inhibiter of I or II respiratory chain and the inhibiter of the respiratory chain with of mixture III, the inhibiter of indirect division and cell division, the claim which is selected from the group which consists of the chemical compound which can operate the chemical compound which can induce landlord defense, amino acid and/or the inhibiter of protein biosynthesis, the inhibiter of ATP production and the inhibiter of cell wall synthesis, as a inhibiter of the lipid and membrane synthesis, a inhibiter of melanin biosynthesis, a inhibiter of nuclear acid synthesis, a inhibiter and a uncoupler of signal transmissionIn 2 composition of statement.  4. The chemical compound which can operate as the aforementioned uncoupler, in the claim 3 which is selected from the group which consists of [binapakuriru], [jinokatsupu], [huerimuzon], [huruajinamu] and [mepuchirujinokatsupu] the composition of statement.  5. At least, furthermore to include one bactericide, the particular further bactericide, Venn thiazole, [betokisajin] and [kapushimaishin] (capsimycin), carbon, [kinomechioneto] and [piriohuenon] (pyriofenone) ([kurazahuenon] (chlazafenone))[kuhuranebu], [shihuruhuenamido], [shimokisaniru], [shipurosuruhuamido], [dazometsuto], [debakarubu], [jikurorohuen], [jikuromejin], [jihuenzokoto] and [jihuenzokotomechiru] sulfate, diphenylamine, [ekomeito] and [huenpirazamin] (fenpyrazamine), [hurumetoberu] and [huruoruimido], full sulfamide, [huruchianiru] and Jose chill - aluminum and Jose chill - calcium and Jose chill - sodium, hexa- chlorobenzene, [irumamaishin] and [metasuruhokarubu], [isochioshian] acid methyl, [metorahuenon], [mirudeiomaishin], [natamaishin] and [jimechirujichiokarubamin] nitsukeru, nitro barrel - isopropyl, [okuchirinon] and [okisamokarubu] (oxamocarb), [okishihuenchiin] (oxyfenthiin), pentachlorophenol and salt and [huenotorin], phosphoric acid and that salt, [puropamokarubu] - [hosechireto] (propamocarb-fosetylate), [puropanoshin] - sodium (propanosine-sodium), [purokinajido],[pirimoruhu], (2E) - 3- (*** -tert-buchiru phenyl) - 3- (2 - [kuroropirijin] - 4 - [iru]) - 1- (morpholine - 4 - [iru]) prop - 2 - [en] - 1 - on, (2Z) - 3- (*** -tert-buchiru phenyl) - 3- (2 - [kuroropirijin] - 4 - [iru]) - 1- (morpholine - 4 - [iru]) prop - 2 - [en] - 1 - on and pyrrole nit phosphorus, [tebuhurokin], [tekurohutaramu], [torunihuanido], [toriazokishido], [torikuramido] and [zariramido], 2 - isobutane acid (3S, 6S, 7R and 8R) - 8 - benzyl - 3- [({3-[([isobuchiriruokishi]) methoxy] - 4 - methoxy pyridine - 2 - [iru]} carbonyl) amino] - 6 - methyl - 4,9 - [jiokiso] - 1,5 - [jiokisonan] - 7 - [iru], 1- (4- {4- [(5R) - 5- (2,6 - [jihuruorohueniru]) - 4,5 - [jihidoro] - 1,2 - [okisazoru] - 3 - [iru]] - 1,3 - thiazole - 2 - [iru]} piperidine - 1 - [iru]) - 2- [5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] eta non, 1- (4- {4- [(5S) - 5- (2,6 - [jihuruorohueniru]) - 4,5- [jihidoro] - 1,2 - [okisazoru] - 3 - [iru]] - 1,3 - thiazole - 2 - [iru]} piperidine - 1 - [iru]) - 2- [5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] eta non, 1- (4- {4- [5- (2,6 - [jihuruorohueniru]) - 4,5 - [jihidoro] - 1,2 - [okisazoru] - 3 - [iru]] - 1,3 - thiazole - 2 - [iru]} piperidine - 1 - [iru]) - 2- [5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] eta non, 1- (4 - methoxy phenoxy) - 3,3 - dimethyl butane- 2 - [iru] - *** H-imidazoru - 1 - [karubokishireto], 2,3,5,6 - [tetorakuroro] - 4- (methyl sulfonyl) pyridine, 2,3 - dibutyl - 6 - [kurorochieno] [2,3-d] pyrimidine - 4 (3H) - on, 2,6 - dimethyl - 1H and 5H- [1,4] [jichiino] [2,3-c: 5,6-c '] [jipiroru] - 1,3,5,7 (2H and 6H) - tetron, 2- [5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] - 1- (4- {4- [(5R) - 5 - phenyl - 4,5 - [jihidoro] - 1,2 - [okisazoru] - 3 - [iru]] - 1,3 - thiazole - 2 - [iru]} piperidine - 1 - [iru]) eta non, 2- [5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] - 1- (4- {4- [(5S) - 5 - phenyl - 4,5 - [jihidoro] - 1,2 - [okisazoru] - 3 - [iru]]- 1,3 - Thiazole - 2 - [iru]} piperidine - 1 - [iru]) eta non, 2- [5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] - 1- {4- [4- (5 - phenyl - 4,5 - [jihidoro] - 1,2 - [okisazoru] - 3 - [iru]) - 1,3 - thiazole - 2 - [iru]] piperidine - 1 - [iru]} eta non, 2 - [butokishi] - 6 - iodine - 3 - propyl - *** H-kuromen - 4 - on, 2 - [kuroro] - 5- [2 - [kuroro] - 1- (2,6 - [jihuruoro] - 4 - methoxy phenyl) - 4 - methyl -*** H-imidazoru - 5 - [iru]] pyridine, 2 - phenyl phenol and salt, 3- (4,4,5 - [torihuruoro] - 3,3 - dimethyl - 3,4 - [jihidoroisokinorin] - 1 - [iru]) [kinoron], 3,4,5 - trichlororo pyridine - 2,6 - [jikarubonitoriru], 3- [5- (4 - [kurorohueniru]) - 2,3 - dimethyl - 1,2 - [okisazorijin] - 3 - [iru]] pyridine, 3 - [kuroro] - 5- (4 - [kurorohueniru]) - 4- (2,6 - [jihuruorohueniru]) - 6 - methyl pyridazine, 4- (4 - [kurorohueniru]) - 5- (2,6 - [jihuruorohueniru]) - 3,6 - dimethyl pyridazine, 5 - amino - 1,3,4 - cheer diazole - 2 -Thiol, 5 - [kuroro] - N ' - phenyl - N ' - ([puropa] - 2 - in - 1 - [iru]) thiophene - 2 - [suruhonohidorajido], 5 - fluoro - 2- [(4 - fluoro benzyl) oxy] pyrimidine - 4 - amine, 5 - fluoro - 2- [(4 - methyl benzyl) oxy] pyrimidine - 4 - amine, 5 - methyl - 6 - octyl [1,2,4] [toriazoro] [1,5-a] pyrimidine - 7 - amine, (2Z) - 3 - amino - 2 - cyano - 3 - [huenirupuropa] - 2 - [en] acid ethyl, N ' - (4- {[3- (4 - [kurorobenjiru]) - 1,2,4 - cheer diazole - 5 - [iru]] oxy} - 2,5 - dimethyl phenyl) - [N]-ECHIRU-N-MECHIRU imido formamide, N- (4 - [kurorobenjiru]) - 3- [3 - methoxy - 4- ([puropa] - 2 - in - 1 - [iruokishi]) phenyl] propane amide, N- [(4 - [kurorohueniru]) (cyano) methyl] - 3- [3 - methoxy - 4- ([puropa] - 2 - in - 1 - [iruokishi]) phenyl] propane amide, N- [(5 - [buromo] - 3 - [kuroropirijin] - 2 - [iru]) methyl] - 2,4 - [jikuroropirijin] - 3 - [karubokisamidoN]- [1- (5 - [buromo] - 3 - [kuroropirijin]  - 2 - [iru]) ethyl] - 2,4 - [jikuroropirijin] - 3 - [karubokisamido] and N- [1- (5 - [buromo] - 3 - [kuroropirijin] - 2 - [iru]) ethyl] - 2 - fluoro - 4 - iodine pyridine - 3 - [karubokisamido] and N- {(E)- [([shikuropuropirumetokishi]) imino] [6- ([jihuruorometokishi]) - 2,3 - [jihuruorohueniru]] methyl} - 2 - phenyl acetamide, N- {(Z) - [([shikuropuropirumetokishi]) imino] [6- ([jihuruorometokishi]) - 2,3 - [jihuruorohueniru]] methyl} - 2 - phenyl acetamide, N ' -{4- [(*** -tert-buchiru - 4 - cyano - 1,2 - thiazole - 5 - [iru]) oxy] - 2 - [kuroro] - 5 - methylphenyl} - [N]-ECHIRU-N-MECHIRU imido formamide, [N]-mechiru - 2- (1- {[5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] acetyl} piperidine - 4 - [iru]) - N- (1,2,3,4 - tetrahydronaphthalene - 1 - [iru]) - 1,3 - thiazole - 4 - [karubokisamido] and [N]-mechiru - 2- (1- {[5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] acetyl} piperidine - 4 - [iru]) - N- [(1R)- 1,2,3,4 - Tetrahydronaphthalene - 1 - [iru]] - 1,3 - thiazole - 4 - [karubokisamido] and [N]-mechiru - 2- (1- {[5 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 1 - [iru]] acetyl} piperidine - 4 - [iru]) - N- [(1S) - 1,2,3,4 - tetrahydronaphthalene - 1 - [iru]] - 1,3 - thiazole - 4 - [karubokisamido] and pentyl {6- [({[(1 - methyl - *** H-tetorazoru - 5 - [iru]) (phenyl) [mechiriden]] amino} oxy) methyl] pyridine - 2 - [iru]} the Kaaba mate, phenazine - 1 - carboxylic acid and quinoline - 8 -All and quinoline - 8 - all sulfate (2:1), [tert]-buchiru {6- [({[(1 - methyl - *** H-tetorazoru - 5 - [iru]) (phenyl) methylene] amino} oxy) methyl] pyridine - 2 - [iru]} the Kaaba mate, 1 - methyl - 3- (trifluoromethyl) - N- [2 ' - (trifluoromethyl) biphenyl - 2 - [iru]] - *** H-pirazoru - 4 - [karubokisamido] and N- (4 ' - [kurorobihueniru] - 2 - [iru]) - 3- ([jihuruoromechiru]) - 1 - methyl - *** H-pirazoru - 4 - [karubokisamido] and N- (2 ', 4 ' - [jikurorobihueniru] - 2 - [iru]) - 3- ([jihuruoromechiru]) - 1 - methyl - *** H-pirazoru - 4 - [karubokisamido], 3- ([jihuruoromechiru]) - 1 - methyl - N- [4 ' - (trifluoromethyl) biphenyl - 2 - [iru]] - *** H-pirazoru - 4 - [karubokisamido] and N- (2 ', 5 ' - [jihuruorobihueniru] - 2 - [iru]) - 1 - methyl - 3- (trifluoromethyl) - *** H-pirazoru - 4 - [karubokisamido], 3- ([jihuruoromechiru]) - 1 - methyl - N- [4 ' - (prop - 1 - in - 1 - [iru]) biphenyl - 2 - [iru]] - *** H-pirazoru - 4 - [karubokisamido], 5 - fluoro - 1,3- Dimethyl - N- [4 ' - (prop - 1 - in - 1 - [iru]) biphenyl - 2 - [iru]] - *** H-pirazoru - 4 - [karubokisamido], 2 - [kuroro] - N- [4 ' - (prop - 1 - in - 1 - [iru]) biphenyl - 2 - [iru]] pyridine - 3 - [karubokisamido], 3- ([jihuruoromechiru]) - N- [4 ' - (3,3 - [jimechirubuto] - 1 - in - 1 - [iru]) biphenyl - 2 - [iru]] - 1 - methyl - *** H-pirazoru - 4 - [karubokisamido] and N- [4 ' - (3,3 - [jimechirubuto] - 1 - in - 1 -[iru]) biphenyl - 2 - [iru]] - 5 - fluoro - 1,3 - dimethyl - *** H-pirazoru - 4 - [karubokisamido], 3- ([jihuruoromechiru]) - N- (4 ' - [echinirubihueniru] - 2 - [iru]) - 1 - methyl - *** H-pirazoru - 4 - [karubokisamido] and N- (4 ' - [echinirubihueniru] - 2 - [iru]) - 5 - fluoro - 1 ,3 - dimethyl - *** H-pirazoru - 4 - [karubokisamido], 2 - [kuroro] - N- (4 ' - [echinirubihueniru] - 2 - [iru]) pyridine - 3 - [karubokisamido], 2 - [kuroro] - N- [4 ' - (3,3 - [jimechirubuto] - 1 - in - 1 - [iru]) biphenyl- 2 - [iru]] pyridine - 3 - [karubokisamido], 4- ([jihuruoromechiru]) - 2 - methyl - N- [4 ' - (trifluoromethyl) biphenyl - 2 - [iru]] - 1,3 - thiazole - 5 - [karubokisamido], 5 - fluoro - N- [4 ' - (3 - hydroxy - 3 - [mechirubuto] - 1 - in - 1 - [iru]) biphenyl - 2 - [iru]] - 1,3 - dimethyl - *** H-pirazoru - 4 - [karubokisamido], 2 - [kuroro] - N- [4 ' - (3 - hydroxy - 3 - [mechirubuto] - 1 - in - 1 - [iru]) biphenyl - 2 - [iru]] pyridine -3 - [karubokisamido], 3- ([jihuruoromechiru]) - N- [4 ' - (3 - methoxy - 3 - [mechirubuto] - 1 - in - 1 - [iru]) biphenyl - 2 - [iru]] - 1 - methyl - *** H-pirazoru - 4 - [karubokisamido], 5 - fluoro - N- [4 ' - (3 - methoxy - 3 - [mechirubuto] - 1 - in - 1 - [iru]) biphenyl - 2 - [iru]] - 1,3 - dimethyl - *** H-pirazoru - 4 - [karubokisamido], 2 - [kuroro] - N- [4 ' - (3 - methoxy - 3 - [mechirubuto] - 1 - in - 1 - [iru]) biphenyl - 2- [iru]] pyridine - 3 - [karubokisamido], (5 - [buromo] - 2 - methoxy - 4 - methyl pyridine - 3 - [iru]) (2,3,4 - [torimetokishi] - 6 - methylphenyl) meta non, N- [2- (4- {[3- (4 - [kurorohueniru]) prop - 2 - in - 1 - [iru]] oxy} - 3 - methoxy phenyl) ethyl] - N2- (methyl sulfonyl) valine amide, 4 - oxo - 4- [(2 - phenyl ethyl) amino] butane acid, [buto] - 3 - in - 1 - [iru] {6- [({[(Z) - (1 -Methyl - *** H-tetorazoru - 5 - [iru]) (phenyl) methylene] amino} oxy) methyl] pyridine - 2 - [iru]} the Kaaba mate, 4 - amino - 5 - fluoro pyrimidine - 2 - all, 3,4,5 - [torihidorokishi] benzoic acid In the claim 1 which is selected from the group which consists of propyl and [orizasutorobin] the composition of statement.  6. The aforementioned biotic pesticide, the Bacillus subtilis (Bacillus subtilis) AQ713 (NRRL trust number B-21661) from the claim 1 which is either among 5 in 1 sections the composition of statement.  7. The dust diluent, the solvent, the carrier, the emulsifier, the dispersant and the freezing protective agent, from the claim 1 which at least furthermore includes one which is selected from the group which consists of the thickener and the adjuvant auxiliary substance either among 6 in 1 sections the composition of statement.  8. From claim 1 either among 7 the seed which was processed with the composition of statement to 1 sections.  9. In the claim 8 where the aforementioned insecticide in the aforementioned composition is [shiantoraniripuroru] the seed of statement.  10. From claim the insecticide and/or as a bactericide 1 either among 7 in 1 sections use of the composition of statement.  11. In claim 10 in order to make the loss decrease in the fruit or the vegetable which entire it is damaged and are harvested and of the plant and the plant part which are pulled up the insect, the tick and the nematode and/or by the plant pathogenic agent use of statement.  12. In claim 10 in order to process the former plant or the [toransujienitsuku] plant or that seed or 11 use of statement.  13. Bacillus [pumirusu] (Bacillus pumilus) (NRRL trust number B-30087), the Bacillus subtilis (Bacillus subtilis) AQ713 (NRRL trust number B-21661), and the Bacillus subtilis (Bacillus subtilis) AQ30002 (NRRL trust number B-50421) at least one which is selected from the group which consists of biotic pesticide, And at least one which is selected from the group which consists of [kurorantoraniripuroru], [shiantoraniripuroru] and [hurubenjiamido] insecticide Or as needed at least one bactericide (however, the aforementioned biotic pesticide and the appropriate bactericide are not identical.)The plant, the plant part, the fruit which is harvested, the vegetable and/or in the growth place of the plant, simultaneously or being the stage which is consecutively applied, it includes the stage where the biotic pesticide and weight ratio of the insecticide are the 10000:1 from the 1:10, the method of decreasing the loss in the fruit or the vegetable which entire it is damaged and are harvested and of the plant and the plant part which are pulled up the insect, the tick and the nematode and/or by the plant pathogenic agent.  14. With the arrangement which is separated spatially, Bacillus [pumirusu] (Bacillus pumilus) (NRRL trust number B-30087), the Bacillus subtilis (Bacillus subtilis) AQ713 (NRRL trust number B-21661), and the Bacillus subtilis (Bacillus subtilis) AQ30002 (NRRL trust number B-50421) at least one which is selected from the group which consists of biotic pesticide, And one which is selected from the group which consists of [kurorantoraniripuroru], [shiantoraniripuroru] and [hurubenjiamido] insecticide is included at least, the kit of the part where the biotic pesticide and weight ratio of the insecticide are the 10000:1 from the 1:10.
法律状态
(JP6117347) LEGAL DETAILS FOR JP2015523971  Actual or expected expiration date=2033-05-29    Legal state=ALIVE    Status=GRANTED     Event publication date=2013-05-29  Event code=JP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=JP JP2015514477  Application date=2013-05-29  Standardized application number=2015JP-0514477     Event publication date=2015-08-20  Event code=JP/A  Event indicator=Pos  Event type=Examination events  Published application  Publication country=JP  Publication number=JP2015523971  Publication stage Code=A  Publication date=2015-08-20  Standardized publication number=JP2015523971     Event publication date=2016-05-25  Event code=JP/A521  Event type=Restitution or restoration  Written amendment  Effective date of the event=2016-05-25  JAPANESE INTERMEDIATE CODE: A523     Event publication date=2016-05-25  Event code=JP/A621  Event indicator=Pos  Event type=Examination events  Written request for application examination  Effective date of the event=2016-05-25  JAPANESE INTERMEDIATE CODE: A621     Event publication date=2016-09-30  Event code=JP/A977  Event type=Examination events  Report on retrieval  Effective date of the event=2016-09-30  JAPANESE INTERMEDIATE CODE: A971007     Event publication date=2016-10-11  Event code=JP/A131  Event indicator=Neg  Event type=Examination events  Notification of reasons for refusal  Effective date of the event=2016-10-11  JAPANESE INTERMEDIATE CODE: A131     Event publication date=2016-12-28  Event code=JP/A521  Event type=Restitution or restoration  Written amendment  Effective date of the event=2016-12-28  JAPANESE INTERMEDIATE CODE: A523     Event publication date=2017-01-31  Event code=JP/A131  Event indicator=Neg  Event type=Examination events  Notification of reasons for refusal  Effective date of the event=2017-01-31  JAPANESE INTERMEDIATE CODE: A131     Event publication date=2017-02-17  Event code=JP/A521  Event type=Restitution or restoration  Written amendment  Effective date of the event=2017-02-17  JAPANESE INTERMEDIATE CODE: A523     Event publication date=2017-02-27  Event code=JP/TRDD  Event indicator=Pos  Event type=Administrative notifications  Trial decision date    Event publication date=2017-03-07  Event code=JP/A01  Event indicator=Pos  Event type=Event indicating In Force  Written decision to grant a patent or to grant a registration (utility model)  Effective date of the event=2017-03-07  JAPANESE INTERMEDIATE CODE: A01     Event publication date=2017-03-30  Event code=JP/A61  Event indicator=Pos  Event type=Event indicating In Force  First payment of annual fees (during grant procedure)  Effective date of the event=2017-03-22  JAPANESE INTERMEDIATE CODE: A61     Event publication date=2017-03-31  Event code=JP/R150  Event indicator=Pos  Event type=Event indicating In Force   Certificate of patent (=grant) or registration of utility model JAPANESE INTERMEDIATE CODE: R150     Event publication date=2017-04-19  Event code=JP/B2  Event indicator=Pos  Event type=Event indicating In Force  Published granted patent (Second level)  from 01-03-1996 onwards (Published examined patent application (Second level) 1971-1996)  Publication country=JP  Publication number=JP6117347  Publication stage Code=B2  Publication date=2017-04-19  Standardized publication number=JP6117347
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