AR097314A1 - SYNERGIC COMPOSITIONS FOR THE CONTROL OF DISEASES IN PLANTS, WHICH INCLUDE DERIVATIVES OF PICOLINIC ACID - Google Patents
SYNERGIC COMPOSITIONS FOR THE CONTROL OF DISEASES IN PLANTS, WHICH INCLUDE DERIVATIVES OF PICOLINIC ACIDInfo
- Publication number
- AR097314A1 AR097314A1 ARP140102535A ARP140102535A AR097314A1 AR 097314 A1 AR097314 A1 AR 097314A1 AR P140102535 A ARP140102535 A AR P140102535A AR P140102535 A ARP140102535 A AR P140102535A AR 097314 A1 AR097314 A1 AR 097314A1
- Authority
- AR
- Argentina
- Prior art keywords
- inhibitors
- group
- plants
- disease control
- diseases
- Prior art date
Links
- 201000010099 disease Diseases 0.000 title abstract 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 9
- 239000000203 mixture Substances 0.000 title abstract 5
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 title 1
- 230000002195 synergetic effect Effects 0.000 title 1
- 239000003112 inhibitor Substances 0.000 abstract 12
- 239000003795 chemical substances by application Substances 0.000 abstract 6
- 230000015572 biosynthetic process Effects 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 isopropylcarbonyloxymethyl group Chemical group 0.000 abstract 3
- 238000003898 horticulture Methods 0.000 abstract 2
- 230000010627 oxidative phosphorylation Effects 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 238000003786 synthesis reaction Methods 0.000 abstract 2
- LWLJEQHTPVPKSJ-UHFFFAOYSA-N tebufloquin Chemical compound C1=C(C(C)(C)C)C=C2C(OC(=O)C)=C(C)C(C)=NC2=C1F LWLJEQHTPVPKSJ-UHFFFAOYSA-N 0.000 abstract 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 abstract 1
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 abstract 1
- IAQLCKZJGNTRDO-UHFFFAOYSA-N 1-(4-{4-[5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-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=2F)F)CC1 IAQLCKZJGNTRDO-UHFFFAOYSA-N 0.000 abstract 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 abstract 1
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 abstract 1
- YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 abstract 1
- PDPWCKVFIFAQIQ-UHFFFAOYSA-N 2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide Chemical compound CNC(=O)C(OC)C1=CC=CC=C1COC1=CC(C)=CC=C1C PDPWCKVFIFAQIQ-UHFFFAOYSA-N 0.000 abstract 1
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 abstract 1
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 abstract 1
- NRTLIYOWLVMQBO-UHFFFAOYSA-N 5-chloro-1,3-dimethyl-N-(1,1,3-trimethyl-1,3-dihydro-2-benzofuran-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)OC(C)(C)C2=CC=CC=1NC(=O)C=1C(C)=NN(C)C=1Cl NRTLIYOWLVMQBO-UHFFFAOYSA-N 0.000 abstract 1
- NEKULYKCZPJMMJ-UHFFFAOYSA-N 5-chloro-N-{1-[4-(difluoromethoxy)phenyl]propyl}-6-methylpyrimidin-4-amine Chemical compound C=1C=C(OC(F)F)C=CC=1C(CC)NC1=NC=NC(C)=C1Cl NEKULYKCZPJMMJ-UHFFFAOYSA-N 0.000 abstract 1
- GOFJDXZZHFNFLV-UHFFFAOYSA-N 5-fluoro-1,3-dimethyl-N-[2-(4-methylpentan-2-yl)phenyl]pyrazole-4-carboxamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=C(F)N(C)N=C1C GOFJDXZZHFNFLV-UHFFFAOYSA-N 0.000 abstract 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 abstract 1
- 230000002407 ATP formation Effects 0.000 abstract 1
- 239000005726 Ametoctradin Substances 0.000 abstract 1
- 239000005727 Amisulbrom Substances 0.000 abstract 1
- 239000005730 Azoxystrobin Substances 0.000 abstract 1
- 239000005737 Benzovindiflupyr Substances 0.000 abstract 1
- 239000005738 Bixafen Substances 0.000 abstract 1
- 239000005740 Boscalid Substances 0.000 abstract 1
- 239000005746 Carboxin Substances 0.000 abstract 1
- 239000005754 Cyazofamid Substances 0.000 abstract 1
- 239000005755 Cyflufenamid Substances 0.000 abstract 1
- 239000005756 Cymoxanil Substances 0.000 abstract 1
- 239000005762 Dimoxystrobin Substances 0.000 abstract 1
- 239000005766 Dodine Substances 0.000 abstract 1
- 102000015782 Electron Transport Complex III Human genes 0.000 abstract 1
- 108010024882 Electron Transport Complex III Proteins 0.000 abstract 1
- 239000005767 Epoxiconazole Substances 0.000 abstract 1
- 239000005772 Famoxadone Substances 0.000 abstract 1
- 239000005774 Fenamidone Substances 0.000 abstract 1
- 239000005775 Fenbuconazole Substances 0.000 abstract 1
- 239000005781 Fludioxonil Substances 0.000 abstract 1
- 239000005783 Fluopyram Substances 0.000 abstract 1
- 239000005784 Fluoxastrobin Substances 0.000 abstract 1
- 239000005786 Flutolanil Substances 0.000 abstract 1
- 239000005788 Fluxapyroxad Substances 0.000 abstract 1
- 239000005790 Fosetyl Substances 0.000 abstract 1
- 239000005798 Isofetamid Substances 0.000 abstract 1
- 239000005799 Isopyrazam Substances 0.000 abstract 1
- 239000005800 Kresoxim-methyl Substances 0.000 abstract 1
- 239000005803 Mandestrobin Substances 0.000 abstract 1
- 229940127408 Melanin Synthesis Inhibitors Drugs 0.000 abstract 1
- 239000005868 Metconazole Substances 0.000 abstract 1
- 239000005810 Metrafenone Substances 0.000 abstract 1
- CCCGEKHKTPTUHJ-UHFFFAOYSA-N N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC2=C1C1CCC2C1=C(Cl)Cl CCCGEKHKTPTUHJ-UHFFFAOYSA-N 0.000 abstract 1
- XQJQCBDIXRIYRP-UHFFFAOYSA-N N-{2-[1,1'-bi(cyclopropyl)-2-yl]phenyl}-3-(difluoromethyl)-1-methyl-1pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1C(C2CC2)C1 XQJQCBDIXRIYRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005812 Oxathiapiprolin Substances 0.000 abstract 1
- 239000005815 Penflufen Substances 0.000 abstract 1
- 239000005816 Penthiopyrad Substances 0.000 abstract 1
- 239000005818 Picoxystrobin Substances 0.000 abstract 1
- 239000005869 Pyraclostrobin Substances 0.000 abstract 1
- 239000005829 Pyriofenone Substances 0.000 abstract 1
- 239000005834 Sedaxane Substances 0.000 abstract 1
- 239000005847 Triazoxide Substances 0.000 abstract 1
- 239000005857 Trifloxystrobin Substances 0.000 abstract 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- GGKQIOFASHYUJZ-UHFFFAOYSA-N ametoctradin Chemical compound NC1=C(CCCCCCCC)C(CC)=NC2=NC=NN21 GGKQIOFASHYUJZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000001413 amino acids Chemical class 0.000 abstract 1
- BREATYVWRHIPIY-UHFFFAOYSA-N amisulbrom Chemical compound CN(C)S(=O)(=O)N1C=NC(S(=O)(=O)N2C3=CC(F)=CC=C3C(Br)=C2C)=N1 BREATYVWRHIPIY-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- LJOZMWRYMKECFF-UHFFFAOYSA-N benodanil Chemical compound IC1=CC=CC=C1C(=O)NC1=CC=CC=C1 LJOZMWRYMKECFF-UHFFFAOYSA-N 0.000 abstract 1
- 125000005605 benzo group Chemical group 0.000 abstract 1
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 abstract 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 abstract 1
- 229940118790 boscalid Drugs 0.000 abstract 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 abstract 1
- 230000032823 cell division Effects 0.000 abstract 1
- 210000000170 cell membrane Anatomy 0.000 abstract 1
- 210000002421 cell wall Anatomy 0.000 abstract 1
- 230000001413 cellular effect Effects 0.000 abstract 1
- CWVRPJSBNHNJSI-XQNSMLJCSA-N coumoxystrobin Chemical compound C1=C2OC(=O)C(CCCC)=C(C)C2=CC=C1OCC1=CC=CC=C1\C(=C/OC)C(=O)OC CWVRPJSBNHNJSI-XQNSMLJCSA-N 0.000 abstract 1
- YXKMMRDKEKCERS-UHFFFAOYSA-N cyazofamid Chemical compound CN(C)S(=O)(=O)N1C(C#N)=NC(Cl)=C1C1=CC=C(C)C=C1 YXKMMRDKEKCERS-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- 230000007123 defense Effects 0.000 abstract 1
- UWQMKVBQKFHLCE-UHFFFAOYSA-N diclomezine Chemical compound C1=C(Cl)C(C)=C(Cl)C=C1C1=NNC(=O)C=C1 UWQMKVBQKFHLCE-UHFFFAOYSA-N 0.000 abstract 1
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 abstract 1
- VMNULHCTRPXWFJ-UJSVPXBISA-N enoxastrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)\C=C\C1=CC=C(Cl)C=C1 VMNULHCTRPXWFJ-UJSVPXBISA-N 0.000 abstract 1
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 abstract 1
- RBWGTZRSEOIHFD-UHUFKFKFSA-N fenaminstrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C=C\C1=C(Cl)C=CC=C1Cl RBWGTZRSEOIHFD-UHUFKFKFSA-N 0.000 abstract 1
- JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 abstract 1
- GOWLARCWZRESHU-AQTBWJFISA-N ferimzone Chemical compound C=1C=CC=C(C)C=1C(/C)=N\NC1=NC(C)=CC(C)=N1 GOWLARCWZRESHU-AQTBWJFISA-N 0.000 abstract 1
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 abstract 1
- MBHXIQDIVCJZTD-RVDMUPIBSA-N flufenoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=C(C(F)(F)F)C=C1Cl MBHXIQDIVCJZTD-RVDMUPIBSA-N 0.000 abstract 1
- KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 abstract 1
- UFEODZBUAFNAEU-NLRVBDNBSA-N fluoxastrobin Chemical compound C=1C=CC=C(OC=2C(=C(OC=3C(=CC=CC=3)Cl)N=CN=2)F)C=1C(=N/OC)\C1=NOCCO1 UFEODZBUAFNAEU-NLRVBDNBSA-N 0.000 abstract 1
- GNVDAZSPJWCIQZ-UHFFFAOYSA-N flusulfamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 GNVDAZSPJWCIQZ-UHFFFAOYSA-N 0.000 abstract 1
- KGXUEPOHGFWQKF-ZCXUNETKSA-N flutianil Chemical compound COC1=CC=CC=C1N(CCS\1)C/1=C(C#N)/SC1=CC(C(F)(F)F)=CC=C1F KGXUEPOHGFWQKF-ZCXUNETKSA-N 0.000 abstract 1
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 abstract 1
- SXSGXWCSHSVPGB-UHFFFAOYSA-N fluxapyroxad Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 SXSGXWCSHSVPGB-UHFFFAOYSA-N 0.000 abstract 1
- VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical compound CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 abstract 1
- 239000000411 inducer Substances 0.000 abstract 1
- 125000005929 isobutyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])OC(*)=O 0.000 abstract 1
- WMKZDPFZIZQROT-UHFFFAOYSA-N isofetamid Chemical compound CC1=CC(OC(C)C)=CC=C1C(=O)C(C)(C)NC(=O)C1=C(C)C=CS1 WMKZDPFZIZQROT-UHFFFAOYSA-N 0.000 abstract 1
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- 239000012528 membrane Substances 0.000 abstract 1
- BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 abstract 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 abstract 1
- IXJOSTZEBSTPAG-UHFFFAOYSA-N methasulfocarb Chemical compound CNC(=O)SC1=CC=C(OS(C)(=O)=O)C=C1 IXJOSTZEBSTPAG-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 abstract 1
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 abstract 1
- 230000011278 mitosis Effects 0.000 abstract 1
- 238000001668 nucleic acid synthesis Methods 0.000 abstract 1
- JHIPUJPTQJYEQK-ZLHHXESBSA-N orysastrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C(=N\OC)\C(\C)=N\OC JHIPUJPTQJYEQK-ZLHHXESBSA-N 0.000 abstract 1
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 abstract 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 abstract 1
- DWTVBEZBWMDXIY-UHFFFAOYSA-N pyrametostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=C(C)C(C=2C=CC=CC=2)=NN1C DWTVBEZBWMDXIY-UHFFFAOYSA-N 0.000 abstract 1
- URXNNPCNKVAQRA-XMHGGMMESA-N pyraoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC(C=2C=CC(Cl)=CC=2)=NN1C URXNNPCNKVAQRA-XMHGGMMESA-N 0.000 abstract 1
- CRFYLQMIDWBKRT-LPYMAVHISA-N pyribencarb Chemical compound C1=C(Cl)C(CNC(=O)OC)=CC(C(\C)=N\OCC=2N=C(C)C=CC=2)=C1 CRFYLQMIDWBKRT-LPYMAVHISA-N 0.000 abstract 1
- YYXSCUSVVALMNW-FOWTUZBSSA-N pyriminostrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC(C(F)(F)F)=NC(NC=2C(=CC(Cl)=CC=2)Cl)=N1 YYXSCUSVVALMNW-FOWTUZBSSA-N 0.000 abstract 1
- NMVCBWZLCXANER-UHFFFAOYSA-N pyriofenone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Cl)=CN=C1OC NMVCBWZLCXANER-UHFFFAOYSA-N 0.000 abstract 1
- 230000019491 signal transduction Effects 0.000 abstract 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 abstract 1
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 abstract 1
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- QFNFRZHOXWNWAQ-UHFFFAOYSA-N triclopyricarb Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NC(Cl)=C(Cl)C=C1Cl QFNFRZHOXWNWAQ-UHFFFAOYSA-N 0.000 abstract 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 abstract 1
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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Protection Of Plants (AREA)
Abstract
Reivindicación 1: Una composición o un producto combinado para el control de enfermedades en plantas, que comprenden al menos un compuesto representado por la fórmula (1), un enantiómero de este o una mezcla de este, o una sal de este aceptable en la agricultura y la horticultura, en donde R representa un grupo isopropilcarboniloximetilo, un grupo acetilo, un grupo acetiloximetilo, un grupo isobutiloxicarbonilo o un grupo benzo[d][1,3]dioxo-5-ilmetilo, y al menos un agente de control de enfermedades en plantas, seleccionado del grupo (II) que consiste en (i) a (xviii) siguientes: (i) inhibidores de la síntesis de ácidos nucleicos, (ii) inhibidores de la división celular y la mitosis, (iii) inhibidores del complejo I, (iv) inhibidores del complejo II, (v) inhibidores del complejo III, (vi) desacopladores de la fosforilación oxidativa, (vii) inhibidores de la fosforilación oxidativa, (viii) inhibidores de la producción de ATP, (ix) inhibidores de la síntesis de aminoácidos y proteínas, (x) inhibidores de la transducción de señal, (xi) inhibidores de la síntesis de lípidos y de la membrana celular, (xii) inhibidores de la biosíntesis de esteroles en la membrana, (xiii) inhibidores de la biosíntesis de la pared celular, (xiv) inhibidores de la síntesis de melanina en la pared celular, (xv) inductores de la defensa de la planta huésped, (xvi) agentes activos de contacto en múltiples sitios, (xvii) agentes de control de enfermedades en plantas, seleccionados de: cymoxanil, fosetyl, ácido fosforoso, teclofthalam, triazoxide, flusulfamide, diclomezine, methasulfocarb, cyflufenamid, metrafenone, pyriofenone, dodine, flutianil, ferimzone, tebufloquin, oxathiapiprolin, NNF-0721, MIF-1002 y NF-171, y (xviii) agentes del control de enfermedades en plantas, seleccionados de: los compuestos descritos en JP 2009-078991 A, JP 2009-073823 A, WO 2008/102678, JP 2010-083763 A, republicación nacional de la solicitud internacional PCT WO 2008/066148, republicación nacional de la solicitud internacional PCT WO 2009/028280, WO 2005/115994, JP 2006-290883 A, WO 2007/072999, WO 2007/108483, WO 2008/062878 y WO 2006/098128. Reivindicación 3: La composición o el producto combinado para el control de enfermedades en plantas de acuerdo con la reivindicación 1, en donde el agente de control de enfermedades en plantas seleccionado del grupo (II) se selecciona de diflumetorim, tolfenpyrad, benodanil, flutolanil, mepronil, isofetamid, fluopyram, fenfuram, carboxin, oxycarboxin, thifluzamide, benzovindiflupyr, bixafen, fluxapyroxad, furametpyr, isopyrazam, penflufen, penthiopyrad, sedaxane, boscalid, azoxystrobin, coumoxystrobin, enoxastrobin, flufenoxystrobin, picoxystrobin, pyraoxystrobin, pyraclostrobin, pyrametostrobin, triclopyricarb, kresoxim-metilo, trifloxystrobin, dimoxystrobin, fenaminstrobin, metominostrobin, orysastrobin, famoxadone, fluoxastrobin, mandestrobin, pyriminostrobin, fenamidone, pyribencarb, cyazofamid, amisulbrom, ametoctradin, fludioxonil, epoxiconazole, fenbuconazole, metconazole, simeconazole y tebufloquin. Reivindicación 5: Un método para controlar enfermedades en plantas, que comprende aplicar, como ingredientes activos, al menos un compuesto representado por la fórmula (1) definida en la reivindicación 1, un enantiómero de este o una mezcla de este, o una sal de este aceptable en la agricultura y la horticultura, y al menos un agente de control de enfermedades en plantas seleccionado del grupo (II) definido en la reivindicación 1, de manera simultánea o por separado, al área que se desea tratar.Claim 1: A composition or a combined product for the control of diseases in plants, comprising at least one compound represented by the formula (1), an enantiomer of this or a mixture thereof, or a salt thereof acceptable in agriculture and horticulture, where R represents an isopropylcarbonyloxymethyl group, an acetyl group, an acetyloxymethyl group, an isobutyloxycarbonyl group or a benzo [d] [1,3] dioxo-5-ylmethyl group, and at least one disease control agent in plants, selected from group (II) consisting of (i) to (xviii) the following: (i) inhibitors of nucleic acid synthesis, (ii) inhibitors of cell division and mitosis, (iii) complex inhibitors I, (iv) complex II inhibitors, (v) complex III inhibitors, (vi) oxidative phosphorylation decouplers, (vii) oxidative phosphorylation inhibitors, (viii) ATP production inhibitors, (ix) inhibitors of amino acid synthesis and proteins, (x) signal transduction inhibitors, (xi) lipid and cell membrane synthesis inhibitors, (xii) membrane sterile biosynthesis inhibitors, (xiii) wall biosynthesis inhibitors cellular, (xiv) melanin synthesis inhibitors in the cell wall, (xv) host plant defense inducers, (xvi) multi-site active contact agents, (xvii) plant disease control agents, Selected from: cymoxanil, fosetyl, phosphorous acid, teclofthalam, triazoxide, flusulfamide, diclomezine, methasulfocarb, cyflufenamid, metrafenone, pyriofenone, dodine, flutianil, ferimzone, tebufloquin, oxathiapiprolin, NNF-07, M-NF-171, NNF-100, NNF-171, NF-171 xviii) disease control agents in plants, selected from: the compounds described in JP 2009-078991 A, JP 2009-073823 A, WO 2008/102678, JP 2010-083763 A, national republication of the PCT international application WO 2008 / 066148, republished National application of the PCT international application WO 2009/028280, WO 2005/115994, JP 2006-290883 A, WO 2007/072999, WO 2007/108483, WO 2008/062878 and WO 2006/098128. Claim 3: The composition or the combined product for the control of plant diseases according to claim 1, wherein the plant disease control agent selected from group (II) is selected from diflumetorim, tolfenpyrad, benodanil, flutolanil, mepronil, isofetamid, fluopyram, fenfuram, carboxin, oxycarboxin, thifluzamide, benzovindiflupyr, bixafen, fluxapyroxad, Furametpyr, isopyrazam, penflufen, penthiopyrad, sedaxane, boscalid, azoxystrobin, coumoxystrobin, enoxastrobin, flufenoxystrobin, picoxystrobin, pyraoxystrobin, pyraclostrobin, pyrametostrobin, triclopyricarb, kresoxim-methyl, trifloxystrobin, dimoxystrobin, fenaminstrobin, metominostrobin, orysastrobin, famoxadone, fluoxastrobin, mandestrobin, pyriminostrobin, fenamidone, pyribencarb, cyazofamid, amisulbrom, ametoctradin, fludioxonil, epoxiconazole, fenbuconazole, metconazole, simeconazole and tebufloquin. Claim 5: A method for controlling diseases in plants, which comprises applying, as active ingredients, at least one compound represented by the formula (1) defined in claim 1, an enantiomer of this or a mixture thereof, or a salt of it is acceptable in agriculture and horticulture, and at least one plant disease control agent selected from group (II) defined in claim 1, simultaneously or separately, to the area to be treated.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013144633 | 2013-07-10 |
Publications (1)
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| AR097314A1 true AR097314A1 (en) | 2016-03-09 |
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| ARP140102535A AR097314A1 (en) | 2013-07-10 | 2014-07-08 | SYNERGIC COMPOSITIONS FOR THE CONTROL OF DISEASES IN PLANTS, WHICH INCLUDE DERIVATIVES OF PICOLINIC ACID |
Country Status (4)
| Country | Link |
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| JP (1) | JP6539205B2 (en) |
| AR (1) | AR097314A1 (en) |
| TW (1) | TW201542089A (en) |
| WO (1) | WO2015005355A1 (en) |
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| US20160037774A1 (en) * | 2014-08-08 | 2016-02-11 | Dow Agrosciences Llc | Synergistic fungicidal mixtures for fungal control in cereals |
| EP3240419B1 (en) | 2014-12-30 | 2020-05-06 | Dow Agrosciences LLC | Picolinamide compounds with fungicidal activity |
| RU2708392C2 (en) | 2014-12-30 | 2019-12-06 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Picolinamide compounds with fungicidal activity |
| JP2018500362A (en) | 2014-12-30 | 2018-01-11 | ダウ アグロサイエンシィズ エルエルシー | Use of picolinamide compounds having fungicidal activity |
| CA2972034A1 (en) | 2014-12-30 | 2016-07-07 | Dow Agrosciences Llc | Picolinamides with fungicidal activity |
| CN107105652A (en) * | 2014-12-30 | 2017-08-29 | 美国陶氏益农公司 | fungicidal composition |
| MX2017008442A (en) | 2014-12-30 | 2017-10-02 | Dow Agrosciences Llc | Use of picolinamides as fungicides. |
| WO2016174042A1 (en) | 2015-04-27 | 2016-11-03 | BASF Agro B.V. | Pesticidal compositions |
| JP2018123056A (en) * | 2015-04-27 | 2018-08-09 | 日本農薬株式会社 | Disinfectant composition and method of using the same |
| BR102017018267A2 (en) * | 2016-08-26 | 2018-03-13 | Dow Agrosciences Llc | Use of UK-2A PROFUNGICIDES FOR CONTROL OF MURDER DISEASES IN POMOID FRUITS AND DRUGS |
| KR102659552B1 (en) | 2017-05-02 | 2024-04-23 | 코르테바 애그리사이언스 엘엘씨 | Use of acyclic picolinamide compounds as fungicides against fungal diseases on turf grasses |
| TW201842851A (en) | 2017-05-02 | 2018-12-16 | 美商陶氏農業科學公司 | Synergistic mixture for fungal control in cereals |
| TWI774761B (en) | 2017-05-02 | 2022-08-21 | 美商科迪華農業科技有限責任公司 | Synergistic mixtures for fungal control in cereals |
| CN109380240B (en) * | 2017-08-03 | 2020-12-08 | 沈阳中化农药化工研发有限公司 | Pesticide composition containing oxathiapiprolin and application thereof |
| JP2021004176A (en) | 2017-09-06 | 2021-01-14 | 石原産業株式会社 | Bactericidal agent composition and method for controlling crop disease |
| CN107616040A (en) * | 2017-10-13 | 2018-01-23 | 北京博艺远景园林养护服务中心 | The early prevention and treatment method of ornamental plant droop and the treatment method of middle and later periods |
| BR102019004480B1 (en) | 2018-03-08 | 2023-03-28 | Dow Agrosciences Llc | PICOLINAMIDES AS FUNGICIDES |
| EP3866597A4 (en) | 2018-10-15 | 2022-06-29 | Corteva Agriscience LLC | Methods for sythesis of oxypicolinamides |
| CN110301436A (en) * | 2019-08-13 | 2019-10-08 | 福建拓烯新材料科技有限公司 | A kind of microcapsule formulations composition and preparation method thereof |
| BR112022007354A2 (en) | 2019-10-18 | 2022-08-23 | Corteva Agriscience Llc | PROCESS FOR SYNTHESIS OF PICOLINAMIDES |
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| MX2012002579A (en) * | 2009-09-01 | 2012-07-23 | Dow Agrosciences Llc | Synergistic fungicidal compositions containing a 5-fluoropyrimidine derivative for fungal control in cereals. |
| US8883811B2 (en) * | 2009-10-07 | 2014-11-11 | Dow Agrosciences, Llc. | Synergistic fungicidal mixtures for fungal control in cereals |
| IN2012DN03094A (en) * | 2009-10-07 | 2015-09-18 | Dow Agrosciences Llc | |
| ES2460716T3 (en) * | 2010-02-19 | 2014-05-14 | Dow Agrosciences Llc | Synergistic herbicide / fungicide composition containing 4-amino-3-chloro-6- (4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid and a fungicide |
| JP2011201853A (en) * | 2010-03-03 | 2011-10-13 | Sumitomo Chemical Co Ltd | Plant disease controlling composition and method for controlling plant disease |
| JP5997931B2 (en) * | 2011-05-25 | 2016-09-28 | 石原産業株式会社 | Agricultural / horticultural fungicide composition and method for controlling plant diseases |
| JP6063393B2 (en) * | 2011-11-30 | 2017-01-18 | クミアイ化学工業株式会社 | Glyoxime derivatives and pest control agents |
| WO2013092224A1 (en) * | 2011-12-21 | 2013-06-27 | Basf Se | Use of strobilurin type compounds for combating phytopathogenic fungi resistant to qo inhibitors |
| TWI568721B (en) * | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | Fungicide pyrazole mixture |
| EP2938191B1 (en) * | 2012-12-28 | 2018-01-31 | Dow AgroSciences LLC | Synergistic fungicidal mixtures for fungal control in cereals |
| US9247742B2 (en) * | 2012-12-31 | 2016-02-02 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
| US9750248B2 (en) * | 2012-12-31 | 2017-09-05 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
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- 2014-07-08 WO PCT/JP2014/068212 patent/WO2015005355A1/en not_active Ceased
- 2014-07-08 JP JP2015526358A patent/JP6539205B2/en not_active Expired - Fee Related
- 2014-07-08 AR ARP140102535A patent/AR097314A1/en unknown
- 2014-07-08 TW TW103123484A patent/TW201542089A/en unknown
Also Published As
| Publication number | Publication date |
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| JP6539205B2 (en) | 2019-07-03 |
| TW201542089A (en) | 2015-11-16 |
| JPWO2015005355A1 (en) | 2017-03-02 |
| WO2015005355A1 (en) | 2015-01-15 |
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