JP2015523971A5 - - Google Patents
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- Publication number
- JP2015523971A5 JP2015523971A5 JP2015514477A JP2015514477A JP2015523971A5 JP 2015523971 A5 JP2015523971 A5 JP 2015523971A5 JP 2015514477 A JP2015514477 A JP 2015514477A JP 2015514477 A JP2015514477 A JP 2015514477A JP 2015523971 A5 JP2015523971 A5 JP 2015523971A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- carboxamide
- pyrazole
- biphenyl
- trifluoromethyl
- 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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- -1 simoxanyl Chemical compound 0.000 claims 16
- 125000006269 biphenyl-2-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C(*)C([H])=C([H])C([H])=C1[H] 0.000 claims 13
- 239000003112 inhibitor Substances 0.000 claims 11
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 10
- 244000063299 Bacillus subtilis Species 0.000 claims 7
- 235000014469 Bacillus subtilis Nutrition 0.000 claims 7
- 241000196324 Embryophyta Species 0.000 claims 7
- 102000001424 Ryanodine receptors Human genes 0.000 claims 6
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 6
- 108091052345 ryanodine receptor (TC 1.A.3.1) family Proteins 0.000 claims 6
- 230000000855 fungicidal effect Effects 0.000 claims 5
- 239000000417 fungicide Substances 0.000 claims 5
- 239000002917 insecticide Substances 0.000 claims 5
- 235000005152 nicotinamide Nutrition 0.000 claims 5
- 239000011570 nicotinamide Substances 0.000 claims 5
- 230000000853 biopesticidal effect Effects 0.000 claims 4
- 229940075993 receptor modulator Drugs 0.000 claims 4
- 241000194103 Bacillus pumilus Species 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 235000013399 edible fruits Nutrition 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 235000013311 vegetables Nutrition 0.000 claims 3
- 241000238876 Acari Species 0.000 claims 2
- 239000005889 Cyantraniliprole Substances 0.000 claims 2
- 108700042658 GAP-43 Proteins 0.000 claims 2
- 241000238631 Hexapoda Species 0.000 claims 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 claims 2
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 claims 2
- 241000244206 Nematoda Species 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- 239000002671 adjuvant Substances 0.000 claims 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 claims 2
- DVBUIBGJRQBEDP-UHFFFAOYSA-N cyantraniliprole Chemical compound CNC(=O)C1=CC(C#N)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl DVBUIBGJRQBEDP-UHFFFAOYSA-N 0.000 claims 2
- 150000001470 diamides Chemical group 0.000 claims 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 claims 2
- 239000000575 pesticide Substances 0.000 claims 2
- JGCSKOVQDXEQHI-UHFFFAOYSA-N phenazine-1-carboxylic acid Chemical compound C1=CC=C2N=C3C(C(=O)O)=CC=CC3=NC2=C1 JGCSKOVQDXEQHI-UHFFFAOYSA-N 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- QJBZDBLBQWFTPZ-UHFFFAOYSA-N pyrrolnitrin Chemical compound [O-][N+](=O)C1=C(Cl)C=CC=C1C1=CNC=C1Cl QJBZDBLBQWFTPZ-UHFFFAOYSA-N 0.000 claims 2
- 230000035806 respiratory chain Effects 0.000 claims 2
- SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 claims 1
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical compound CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 claims 1
- AESOVJYUXGEHCV-UHFFFAOYSA-N (5-bromo-2-methoxy-4-methylpyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Br)=CN=C1OC AESOVJYUXGEHCV-UHFFFAOYSA-N 0.000 claims 1
- IAQLCKZJGNTRDO-LJQANCHMSA-N (R)-oxathiapiprolin Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C=2C[C@@H](ON=2)C=2C(=CC=CC=2F)F)CC1 IAQLCKZJGNTRDO-LJQANCHMSA-N 0.000 claims 1
- IAQLCKZJGNTRDO-IBGZPJMESA-N (S)-oxathiapiprolin Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C=2C[C@H](ON=2)C=2C(=CC=CC=2F)F)CC1 IAQLCKZJGNTRDO-IBGZPJMESA-N 0.000 claims 1
- QEUOHPLVFSQWME-CYVLTUHYSA-N (z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-morpholin-4-ylprop-2-en-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1C(\C=1C=C(Cl)N=CC=1)=C\C(=O)N1CCOCC1 QEUOHPLVFSQWME-CYVLTUHYSA-N 0.000 claims 1
- DUWKZHIPEWZXNC-UHFFFAOYSA-N 1-methyl-3-(trifluoromethyl)-n-[2-[2-(trifluoromethyl)phenyl]phenyl]pyrazole-4-carboxamide Chemical compound FC(F)(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=CC=C1C(F)(F)F DUWKZHIPEWZXNC-UHFFFAOYSA-N 0.000 claims 1
- XODZOJBRMYSETR-UHFFFAOYSA-N 2,3-dibutyl-6-chlorothieno[2,3-d]pyrimidin-4-one Chemical compound O=C1N(CCCC)C(CCCC)=NC2=C1C=C(Cl)S2 XODZOJBRMYSETR-UHFFFAOYSA-N 0.000 claims 1
- DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 claims 1
- QKJJCZYFXJCKRX-HZHKWBLPSA-N 2-[(2s,3s,6r)-6-[4-amino-5-(hydroxymethyl)-2-oxopyrimidin-1-yl]-3-[[(2s)-2-amino-3-hydroxypropanoyl]amino]-3,6-dihydro-2h-pyran-2-yl]-5-(diaminomethylideneamino)-2,4-dihydroxypentanoic acid Chemical compound O1[C@H](C(O)(CC(O)CN=C(N)N)C(O)=O)[C@@H](NC(=O)[C@H](CO)N)C=C[C@@H]1N1C(=O)N=C(N)C(CO)=C1 QKJJCZYFXJCKRX-HZHKWBLPSA-N 0.000 claims 1
- GFTWHAGNSGTEGO-UHFFFAOYSA-N 2-[1-(4-methoxyphenoxy)-3,3-dimethylbutan-2-yl]imidazole-1-carboxylic acid Chemical compound C1=CC(OC)=CC=C1OCC(C(C)(C)C)C1=NC=CN1C(O)=O GFTWHAGNSGTEGO-UHFFFAOYSA-N 0.000 claims 1
- MQFJRLQNQOJQEI-UHFFFAOYSA-N 2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]-1-[4-[4-(5-phenyl-4,5-dihydro-1,2-oxazol-3-yl)-1,3-thiazol-2-yl]piperidin-1-yl]ethanone Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C=2CC(ON=2)C=2C=CC=CC=2)CC1 MQFJRLQNQOJQEI-UHFFFAOYSA-N 0.000 claims 1
- MQFJRLQNQOJQEI-HXUWFJFHSA-N 2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]-1-[4-[4-[(5r)-5-phenyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl]piperidin-1-yl]ethanone Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C=2C[C@@H](ON=2)C=2C=CC=CC=2)CC1 MQFJRLQNQOJQEI-HXUWFJFHSA-N 0.000 claims 1
- MQFJRLQNQOJQEI-FQEVSTJZSA-N 2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]-1-[4-[4-[(5s)-5-phenyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl]piperidin-1-yl]ethanone Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C=2C[C@H](ON=2)C=2C=CC=CC=2)CC1 MQFJRLQNQOJQEI-FQEVSTJZSA-N 0.000 claims 1
- ZQMRDENWZKMOTM-UHFFFAOYSA-N 2-butoxy-6-iodo-3-propylchromen-4-one Chemical compound C1=C(I)C=C2C(=O)C(CCC)=C(OCCCC)OC2=C1 ZQMRDENWZKMOTM-UHFFFAOYSA-N 0.000 claims 1
- URSDKQVCLKINOM-UHFFFAOYSA-N 2-chloro-5-[2-chloro-3-(2,6-difluoro-4-methoxyphenyl)-5-methylimidazol-4-yl]pyridine Chemical compound FC1=CC(OC)=CC(F)=C1N1C(C=2C=NC(Cl)=CC=2)=C(C)N=C1Cl URSDKQVCLKINOM-UHFFFAOYSA-N 0.000 claims 1
- 229940061334 2-phenylphenol Drugs 0.000 claims 1
- ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 claims 1
- ZVOWUYIDRJPVTD-UHFFFAOYSA-N 3,4,5-trichloropyridine-2,6-dicarbonitrile Chemical compound ClC1=C(Cl)C(C#N)=NC(C#N)=C1Cl ZVOWUYIDRJPVTD-UHFFFAOYSA-N 0.000 claims 1
- OSRHUTRVDLFDRE-UHFFFAOYSA-N 3-(4,4,5-trifluoro-3,3-dimethylisoquinolin-1-yl)-1h-quinolin-2-one Chemical compound C1=CC=C2NC(=O)C(C3=NC(C(C4=C(F)C=CC=C43)(F)F)(C)C)=CC2=C1 OSRHUTRVDLFDRE-UHFFFAOYSA-N 0.000 claims 1
- DHTJFQWHCVTNRY-UHFFFAOYSA-N 3-[5-(4-chlorophenyl)-2,3-dimethyl-1,2-oxazolidin-3-yl]pyridine Chemical compound CN1OC(C=2C=CC(Cl)=CC=2)CC1(C)C1=CC=CN=C1 DHTJFQWHCVTNRY-UHFFFAOYSA-N 0.000 claims 1
- DNDLJUVNJLTMIE-UHFFFAOYSA-N 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine Chemical compound C=1C=C(Cl)C=CC=1C=1C(C)=NN=C(Cl)C=1C1=C(F)C=CC=C1F DNDLJUVNJLTMIE-UHFFFAOYSA-N 0.000 claims 1
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 claims 1
- ZMYKITJYWFYRFJ-UHFFFAOYSA-N 4-oxo-4-(2-phenylethylamino)butanoic acid Chemical compound OC(=O)CCC(=O)NCCC1=CC=CC=C1 ZMYKITJYWFYRFJ-UHFFFAOYSA-N 0.000 claims 1
- ZALZMUXMSIVXKA-UHFFFAOYSA-N 5-fluoro-2-[(4-fluorophenyl)methoxy]pyrimidin-4-amine Chemical compound C1=C(F)C(N)=NC(OCC=2C=CC(F)=CC=2)=N1 ZALZMUXMSIVXKA-UHFFFAOYSA-N 0.000 claims 1
- CGRCPZUQMBYVPZ-UHFFFAOYSA-N 5-fluoro-2-[(4-methylphenyl)methoxy]pyrimidin-4-amine Chemical compound C1=CC(C)=CC=C1COC1=NC=C(F)C(N)=N1 CGRCPZUQMBYVPZ-UHFFFAOYSA-N 0.000 claims 1
- JMBYFCMNFXBELT-UHFFFAOYSA-N 5-methyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound NC1=C(CCCCCCCC)C(C)=NC2=NC=NN21 JMBYFCMNFXBELT-UHFFFAOYSA-N 0.000 claims 1
- 230000002407 ATP formation Effects 0.000 claims 1
- 239000005730 Azoxystrobin Substances 0.000 claims 1
- 239000005973 Carvone Substances 0.000 claims 1
- 239000005886 Chlorantraniliprole Substances 0.000 claims 1
- 239000005644 Dazomet Substances 0.000 claims 1
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 claims 1
- 102000015782 Electron Transport Complex III Human genes 0.000 claims 1
- 108010024882 Electron Transport Complex III Proteins 0.000 claims 1
- 239000005779 Fenpyrazamine Substances 0.000 claims 1
- 239000005780 Fluazinam Substances 0.000 claims 1
- 241000209094 Oryza Species 0.000 claims 1
- 239000005847 Triazoxide Substances 0.000 claims 1
- NHTFLYKPEGXOAN-UHFFFAOYSA-N Trichlamide Chemical compound CCCCOC(C(Cl)(Cl)Cl)NC(=O)C1=CC=CC=C1O NHTFLYKPEGXOAN-UHFFFAOYSA-N 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 125000003368 amide group Chemical group 0.000 claims 1
- 150000001413 amino acids Chemical class 0.000 claims 1
- 230000000844 anti-bacterial effect Effects 0.000 claims 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims 1
- 239000003899 bactericide agent Substances 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 claims 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 230000032823 cell division Effects 0.000 claims 1
- PSOVNZZNOMJUBI-UHFFFAOYSA-N chlorantraniliprole Chemical group CNC(=O)C1=CC(Cl)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl PSOVNZZNOMJUBI-UHFFFAOYSA-N 0.000 claims 1
- 239000002577 cryoprotective agent Substances 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- ACMXQHFNODYQAT-UHFFFAOYSA-N cyflufenamid Chemical compound FC1=CC=C(C(F)(F)F)C(C(NOCC2CC2)=NC(=O)CC=2C=CC=CC=2)=C1F ACMXQHFNODYQAT-UHFFFAOYSA-N 0.000 claims 1
- OAWUUPVZMNKZRY-UHFFFAOYSA-N cyprosulfamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC2CC2)C=C1 OAWUUPVZMNKZRY-UHFFFAOYSA-N 0.000 claims 1
- NMCCNOZOBBWFMN-UHFFFAOYSA-N davicil Chemical compound CS(=O)(=O)C1=C(Cl)C(Cl)=NC(Cl)=C1Cl NMCCNOZOBBWFMN-UHFFFAOYSA-N 0.000 claims 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 claims 1
- 230000007123 defense Effects 0.000 claims 1
- 229960003887 dichlorophen Drugs 0.000 claims 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- 230000008686 ergosterol biosynthesis Effects 0.000 claims 1
- YKRQBWKLHCEKQH-KHPPLWFESA-N ethyl (z)-3-amino-2-cyano-3-phenylprop-2-enoate Chemical compound CCOC(=O)C(\C#N)=C(/N)C1=CC=CC=C1 YKRQBWKLHCEKQH-KHPPLWFESA-N 0.000 claims 1
- UTOHZQYBSYOOGC-UHFFFAOYSA-N fenpyrazamine Chemical compound O=C1N(C(C)C)N(C(=O)SCC=C)C(N)=C1C1=CC=CC=C1C UTOHZQYBSYOOGC-UHFFFAOYSA-N 0.000 claims 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 claims 1
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 150000002632 lipids Chemical class 0.000 claims 1
- 230000008099 melanin synthesis Effects 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- KCIRYJNISRMYFI-UHFFFAOYSA-N mildiomycin Natural products NC(CO)C(=O)NC1C=CC(OC1C(O)(CC(O)CNC(=N)N)C(=O)O)N2CN=C(N)C(=C2)CO KCIRYJNISRMYFI-UHFFFAOYSA-N 0.000 claims 1
- 230000000394 mitotic effect Effects 0.000 claims 1
- CDXKAMHMYQAUSW-UHFFFAOYSA-N n'-[4-[(3-tert-butyl-4-cyano-1,2-thiazol-5-yl)oxy]-2-chloro-5-methylphenyl]-n-ethyl-n-methylmethanimidamide Chemical compound C1=C(Cl)C(N=CN(C)CC)=CC(C)=C1OC1=C(C#N)C(C(C)(C)C)=NS1 CDXKAMHMYQAUSW-UHFFFAOYSA-N 0.000 claims 1
- BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 claims 1
- GCIZLUZYQSYVSS-UHFFFAOYSA-N n-[(5-bromo-3-chloropyridin-2-yl)methyl]-2,4-dichloropyridine-3-carboxamide Chemical compound ClC1=CC=NC(Cl)=C1C(=O)NCC1=NC=C(Br)C=C1Cl GCIZLUZYQSYVSS-UHFFFAOYSA-N 0.000 claims 1
- HQUIFHINFGFWLJ-UHFFFAOYSA-N n-[(cyclopropylmethoxyamino)-[6-(difluoromethoxy)-2,3-difluorophenyl]methylidene]-2-phenylacetamide Chemical compound FC(F)OC1=CC=C(F)C(F)=C1C(NOCC1CC1)=NC(=O)CC1=CC=CC=C1 HQUIFHINFGFWLJ-UHFFFAOYSA-N 0.000 claims 1
- RRRNUBCOWJALGN-UHFFFAOYSA-N n-[1-(5-bromo-3-chloropyridin-2-yl)ethyl]-2,4-dichloropyridine-3-carboxamide Chemical compound N=1C=C(Br)C=C(Cl)C=1C(C)NC(=O)C1=C(Cl)C=CN=C1Cl RRRNUBCOWJALGN-UHFFFAOYSA-N 0.000 claims 1
- ZWWBRKGFSLERLP-UHFFFAOYSA-N n-[2-(2,4-dichlorophenyl)phenyl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=C(Cl)C=C1Cl ZWWBRKGFSLERLP-UHFFFAOYSA-N 0.000 claims 1
- FHJSOSUERYQSIZ-UHFFFAOYSA-N n-[2-(4-chlorophenyl)phenyl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=C(Cl)C=C1 FHJSOSUERYQSIZ-UHFFFAOYSA-N 0.000 claims 1
- AHJKPWGTBVOQFA-UHFFFAOYSA-N n-methyl-2-[1-[2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-n-(1,2,3,4-tetrahydronaphthalen-1-yl)-1,3-thiazole-4-carboxamide Chemical compound C1CCC2=CC=CC=C2C1N(C)C(=O)C(N=1)=CSC=1C(CC1)CCN1C(=O)CN1N=C(C(F)(F)F)C=C1C AHJKPWGTBVOQFA-UHFFFAOYSA-N 0.000 claims 1
- AHJKPWGTBVOQFA-JOCHJYFZSA-N n-methyl-2-[1-[2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-n-[(1r)-1,2,3,4-tetrahydronaphthalen-1-yl]-1,3-thiazole-4-carboxamide Chemical compound CN([C@H]1C2=CC=CC=C2CCC1)C(=O)C(N=1)=CSC=1C(CC1)CCN1C(=O)CN1N=C(C(F)(F)F)C=C1C AHJKPWGTBVOQFA-JOCHJYFZSA-N 0.000 claims 1
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- 239000004311 natamycin Substances 0.000 claims 1
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- 235000010292 orthophenyl phenol Nutrition 0.000 claims 1
- 229960003536 phenothrin Drugs 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- 244000000003 plant pathogen Species 0.000 claims 1
- 230000004260 plant-type cell wall biogenesis Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 229960002132 pyrrolnitrin Drugs 0.000 claims 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 claims 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims 1
- 230000019491 signal transduction Effects 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- IYYIUOWKEMQYNV-UHFFFAOYSA-N sodium;ethoxy-oxido-oxophosphanium Chemical compound [Na+].CCO[P+]([O-])=O IYYIUOWKEMQYNV-UHFFFAOYSA-N 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 230000002269 spontaneous effect Effects 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- URHWNXDZOULUHC-UHFFFAOYSA-N tert-butyl n-[6-[[[(1-methyltetrazol-5-yl)-phenylmethylidene]amino]oxymethyl]pyridin-2-yl]carbamate Chemical compound CN1N=NN=C1C(C=1C=CC=CC=1)=NOCC1=CC=CC(NC(=O)OC(C)(C)C)=N1 URHWNXDZOULUHC-UHFFFAOYSA-N 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- YIBACQHAKISWLZ-UHFFFAOYSA-N thiophene-2-sulfonohydrazide Chemical compound NNS(=O)(=O)C1=CC=CS1 YIBACQHAKISWLZ-UHFFFAOYSA-N 0.000 claims 1
- 230000009261 transgenic effect Effects 0.000 claims 1
- 230000014616 translation Effects 0.000 claims 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 claims 1
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| NZ725994A (en) | 2012-05-30 | 2018-07-27 | Bayer Cropscience Ag | Composition comprising a biological control agent and a fungicide selected from inhibitors of the ergosterol biosynthesis |
| AU2013269662B2 (en) | 2012-05-30 | 2016-12-15 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| WO2013178658A1 (en) | 2012-05-30 | 2013-12-05 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| EP3281526A1 (en) | 2012-05-30 | 2018-02-14 | Bayer CropScience Aktiengesellschaft | Composition comprising a biological control agent and a fungicide |
| PT2854552T (pt) | 2012-05-30 | 2019-07-25 | Bayer Cropscience Ag | Composição compreendendo um agente de controlo biológico e um fungicida selecionado a partir de inibidores da biossíntese de aminoácidos ou proteínas, inibidores da produção de atp e inibidores da síntese da parede celular |
| KR20150023475A (ko) | 2012-05-30 | 2015-03-05 | 바이엘 크롭사이언스 아게 | 생물학적 방제제, 및 지질막 합성, 멜라닌 생합성, 핵산 합성 또는 신호 전달의 억제제로부터 선택된 살진균제를 포함하는 조성물 |
| HRP20181752T1 (hr) | 2012-05-30 | 2018-12-28 | Bayer Cropscience Ag | Pripravak koji sadrži biološko kontrolno sredstvo i fluopikolid |
| CA2921846C (en) | 2013-08-19 | 2022-07-05 | The Mosaic Company | System and methods for addition of beneficial agricultural, biological, and/or dedusting additives to granular fertilizers |
| US9485994B2 (en) | 2013-11-08 | 2016-11-08 | The Regents Of The University Of California | Synergy-based biocontrol of plant pathogens |
| WO2015092549A2 (en) * | 2013-12-18 | 2015-06-25 | Dupont Nutrition Biosciences Aps | Biologicals for plants |
| BR112017000358A2 (en) | 2014-07-07 | 2018-06-26 | The Mosaic Company | incorporation of biological agents in fertilizers |
| UY36478A (es) | 2014-12-29 | 2017-07-31 | Fmc Corp | Composiciones microbianas y metodos para usar para beneficiar el crecimiento de las plantas y tratar la enfermedad de las plantas |
| US10136647B2 (en) * | 2015-01-16 | 2018-11-27 | Valent Biosciences Llc | Synergistic Bacillus thuringiensis subsp. kurstaki and chlorantraniliprole mixtures for diamondback moth, beet armyworm, sugarcane borer, soybean looper and corn earworm control |
| AU2016206537B2 (en) | 2015-01-16 | 2019-04-04 | Valent Biosciences Llc | Synergistic Bacillus thuringiensis subsp. aizawai and chlorantraniliprole mixtures for plant pest control |
| WO2016115470A1 (en) | 2015-01-16 | 2016-07-21 | Valent Biosciences Corporation | Synergistic bacillus thuringiensis subsp. aizawai, bacillus thuringiensis subsp. kurstaki and chlorantraniliprole mixtures |
| US10487016B2 (en) | 2015-08-12 | 2019-11-26 | The Mosaic Company | Acid treatment for fertilizers to increase zinc solubility and availability |
| EP4234724A3 (en) | 2016-10-05 | 2023-11-01 | FMC Agricultural Solutions A/S | Bacillus thuringiensis rti545 compositions and methods of use for benefitting plant growth and controlling plant pests |
| BR122023022721A2 (pt) * | 2017-03-24 | 2023-12-26 | Novozymes Bioag A/S | Composição que compreende quantidades sinergicamente eficazes de yersinia entomophaga, ou um filtrado isento de células da mesma, e um inseticida químico; e método |
| CN107494453B (zh) * | 2017-09-21 | 2020-06-12 | 怀化学院 | 一种短小芽孢杆菌作为鳞翅目类昆虫的生长调节剂的用途 |
| EP3542630A1 (en) | 2018-03-20 | 2019-09-25 | University of Graz | Pesticidal compositions for pest control |
| WO2020065025A1 (en) | 2018-09-28 | 2020-04-02 | Bayer Aktiengesellschaft | Combination of bacterial biological control agent and fatty acids |
| CN114521571B (zh) * | 2022-02-24 | 2023-04-18 | 河北省农林科学院植物保护研究所 | 一种防治根螨的菌药组合物及应用 |
| CN115152794B (zh) * | 2022-08-17 | 2023-07-21 | 江苏省农业科学院 | 一种贝莱斯芽孢杆菌水稻生物种衣剂及其制备方法和用途 |
| CN116790406A (zh) * | 2022-11-18 | 2023-09-22 | 贵州省烟草科学研究院 | 一种具有兼防多种烟草真菌病害的贝莱斯芽孢杆菌菌剂及其制备方法和应用 |
| CN120036342B (zh) * | 2025-02-24 | 2025-12-23 | 江苏省血吸虫病防治研究所 | 枯草芽孢杆菌的诱变菌株在杀灭钉螺中的应用及诱变方法 |
Family Cites Families (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06291234A (ja) | 1993-04-01 | 1994-10-18 | Mitsubishi Electric Corp | 半導体装置用リードフレームおよびこれを使用した半導体装置の製造方法 |
| US5645831A (en) | 1996-03-22 | 1997-07-08 | Biodiscovery New Zealand Ltd. | Bacillus thuringiensis strain and metabolite which are active against corn rootworm |
| US5919447A (en) | 1996-11-18 | 1999-07-06 | Agraquest, Inc. | Strain of bacillus for controlling plant disease |
| US5733544A (en) | 1996-11-18 | 1998-03-31 | University Of Saskatchewan | Nematicidal bacillus strain and metabolite and methods of use thereof |
| JP2001503642A (ja) | 1996-11-18 | 2001-03-21 | アグリトープ，インコーポレイテッド | 植物の真菌感染の生物学的コントロール |
| US5869042A (en) | 1996-11-22 | 1999-02-09 | Agraquest, Inc. | Methods for controlling above-ground plant diseases using antibiotic-producing bacillus sp. ATCC 55608 or 55609 |
| PL198772B1 (pl) | 1997-05-09 | 2008-07-31 | Agraquest | Biologicznie czysta kultura Bacillus subtilis, jej metabolit i supernatant z hodowli szczepu, kompozycje do ochrony roślin i owoców przed szkodnikami, sposób ochrony lub leczenia roślin i owoców, agrastatyny, sposób izolowania supernatantu o aktywności owadobójczej |
| US6027723A (en) | 1997-08-22 | 2000-02-22 | Agraquest, Inc. | Rhodococcus globerulus strain for controlling corn rootworm |
| US6001637A (en) | 1997-08-22 | 1999-12-14 | Agraquest, Inc. | Bacillus pumilus strain for controlling corn rootworm, nematode and armyworm infestations |
| US6015553A (en) | 1997-08-22 | 2000-01-18 | Agraquest, Inc. | Bacillus subtilis strain for controlling insect and nematode pests |
| US5906818A (en) | 1997-08-22 | 1999-05-25 | Agraquest, Inc. | Bacillus mycoides strain for controlling corn rootworm |
| HUP0200562A2 (en) | 1999-03-30 | 2002-06-29 | Agraquest Inc | A strain of baccilus pumilus for controlling plant diseases |
| EP2213743A1 (en) | 2000-04-12 | 2010-08-04 | Human Genome Sciences, Inc. | Albumin fusion proteins |
| US6524577B1 (en) | 2000-09-27 | 2003-02-25 | Agraquest, Inc. | Strain of Streptomyces for controlling plant diseases |
| NZ529086A (en) | 2001-04-16 | 2005-07-29 | Gary A Strobel | Method for obtaining Muscodor fungi comprising screening the fungi with volatiles of Muscodor albus or Muscodor roseus under culturing conditions |
| EA020203B1 (ru) | 2007-09-20 | 2014-09-30 | Басф Се | Композиции и агенты, содержащие фунгицидный штамм и активное соединение |
| WO2009060012A2 (en) * | 2007-11-06 | 2009-05-14 | Basf Se | Plant health compositions comprising a beneficial microorganism and a pesticide |
| AP2010005399A0 (en) * | 2008-04-07 | 2010-10-31 | Bayer Cropscience Ag | Combinations of biological control agents and insecticides or fungicides. |
| BRPI0918148A2 (pt) * | 2008-09-10 | 2015-10-06 | Bayer Cropscience Lp | semente geneticamente modificada, combinada com bactérias formadoras de esporos e opcionais agentes de controles de insetos |
| PE20120536A1 (es) | 2009-03-26 | 2012-05-05 | Basf Se | Combinacion de un agente fungicida sintetico y bacillus subtilis qst 173 para el control de hongos fitopatogenos |
| EP2427062B1 (en) * | 2009-05-06 | 2019-01-16 | Bayer CropScience LP | A method for increasing the crop yield of agricultural plants under essentially non-existent pathogen pressure |
| CN102480946A (zh) * | 2009-06-03 | 2012-05-30 | 拜尔农作物科学股份公司 | 氟虫双酰胺和有益生物的结合物 |
| BRPI1008143A2 (pt) * | 2009-06-05 | 2015-08-25 | Basf Se | Mistura composição agroquimica metodo para o combatre de fungos novicios fitopatogenicos e material de propagação de planta |
| WO2011128843A1 (en) | 2010-04-15 | 2011-10-20 | Basf Se | Fungicidal mixtures i comprising quinazolines |
| GB2481118A (en) * | 2010-06-09 | 2011-12-14 | Syngenta Participations Ag | Pesticidal mixtures comprising enantiomerically enriched isoxazoline derivatives |
| WO2011154494A2 (en) * | 2010-06-09 | 2011-12-15 | Syngenta Participations Ag | Pesticidal mixtures comprising isoxazoline derivatives |
| CN101940212A (zh) * | 2010-08-31 | 2011-01-12 | 山东农业大学 | 一种含氯虫苯甲酰胺和阿维菌素防治斑潜蝇的农药组合物 |
| EP2651220A1 (en) * | 2010-12-15 | 2013-10-23 | Syngenta Participations AG | Pesticidal mixtures |
| PE20141468A1 (es) | 2010-12-21 | 2014-11-05 | Bayer Cropscience Lp | Mutantes tipo papel de lija de bacillus y metodos de uso de los mismo para mejorar el crecimiento vegetal, promover la salud de plantas y controlar enfermedades y plagas |
| US20140017216A1 (en) | 2011-03-31 | 2014-01-16 | Bayer Cropscience Lp | Pesticidal mixtures |
| US20130045968A1 (en) * | 2011-08-15 | 2013-02-21 | Norman Helie | Plant treatment |
| WO2013178658A1 (en) | 2012-05-30 | 2013-12-05 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| KR20150023475A (ko) | 2012-05-30 | 2015-03-05 | 바이엘 크롭사이언스 아게 | 생물학적 방제제, 및 지질막 합성, 멜라닌 생합성, 핵산 합성 또는 신호 전달의 억제제로부터 선택된 살진균제를 포함하는 조성물 |
| TR201816257T4 (tr) | 2012-05-30 | 2018-11-21 | Bayer Cropscience Ag | Bir biyolojik kontrol ajanı ve trifloksistrobin içeren bileşim. |
| EP3281526A1 (en) | 2012-05-30 | 2018-02-14 | Bayer CropScience Aktiengesellschaft | Composition comprising a biological control agent and a fungicide |
| EP2854535A1 (en) | 2012-05-30 | 2015-04-08 | Bayer Cropscience AG | Compositions comprising a biological control agent and an insecticide |
| WO2013178661A1 (en) | 2012-05-30 | 2013-12-05 | Bayer Cropscience Ag | Compositiions comprising a biological control agent and an insecticide |
| WO2013178660A1 (en) | 2012-05-30 | 2013-12-05 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| AU2013269662B2 (en) | 2012-05-30 | 2016-12-15 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| PT2854552T (pt) | 2012-05-30 | 2019-07-25 | Bayer Cropscience Ag | Composição compreendendo um agente de controlo biológico e um fungicida selecionado a partir de inibidores da biossíntese de aminoácidos ou proteínas, inibidores da produção de atp e inibidores da síntese da parede celular |
| HRP20181752T1 (hr) | 2012-05-30 | 2018-12-28 | Bayer Cropscience Ag | Pripravak koji sadrži biološko kontrolno sredstvo i fluopikolid |
| NZ725994A (en) | 2012-05-30 | 2018-07-27 | Bayer Cropscience Ag | Composition comprising a biological control agent and a fungicide selected from inhibitors of the ergosterol biosynthesis |
| EP2854536A1 (en) | 2012-05-30 | 2015-04-08 | Bayer Cropscience AG | Compositions comprising a biological control agent and an insecticide |
| CN107027809A (zh) | 2012-05-30 | 2017-08-11 | 拜耳作物科学股份公司 | 包含生物防治剂和选自呼吸链复合物i或ii抑制剂的杀真菌剂的组合物 |
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2013
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- 2013-05-29 WO PCT/EP2013/061036 patent/WO2013178664A1/en not_active Ceased
- 2013-05-29 BR BR112014029122A patent/BR112014029122A8/pt not_active Application Discontinuation
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- 2013-05-29 IN IN9381DEN2014 patent/IN2014DN09381A/en unknown
- 2013-05-29 AU AU2013269663A patent/AU2013269663B2/en active Active
- 2013-05-29 JP JP2015514477A patent/JP6117347B2/ja active Active
- 2013-05-29 KR KR1020147033192A patent/KR102043083B1/ko active Active
- 2013-05-29 US US14/404,017 patent/US10306889B2/en active Active
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- 2014-11-19 CO CO14254026A patent/CO7270455A2/es unknown
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2019
- 2019-04-16 US US16/385,282 patent/US10542757B2/en active Active
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