JP2005529936A5 - - Google Patents
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- Publication number
- JP2005529936A5 JP2005529936A5 JP2004510532A JP2004510532A JP2005529936A5 JP 2005529936 A5 JP2005529936 A5 JP 2005529936A5 JP 2004510532 A JP2004510532 A JP 2004510532A JP 2004510532 A JP2004510532 A JP 2004510532A JP 2005529936 A5 JP2005529936 A5 JP 2005529936A5
- Authority
- JP
- Japan
- Prior art keywords
- fungicidal
- compound
- composition according
- plant
- alkyl
- 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
Links
- 239000000203 mixture Substances 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 14
- 230000000855 fungicidal effect Effects 0.000 claims description 13
- 241000221785 Erysiphales Species 0.000 claims description 8
- 241000233866 Fungi Species 0.000 claims description 6
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 6
- 229930182558 Sterol Natural products 0.000 claims description 6
- 230000006696 biosynthetic metabolic pathway Effects 0.000 claims description 6
- 150000003432 sterols Chemical class 0.000 claims description 6
- 235000003702 sterols Nutrition 0.000 claims description 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000000417 fungicide Substances 0.000 claims description 5
- 201000010099 disease Diseases 0.000 claims description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 4
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 claims description 4
- 102000004190 Enzymes Human genes 0.000 claims description 3
- 108090000790 Enzymes Proteins 0.000 claims description 3
- 101000615488 Homo sapiens Methyl-CpG-binding domain protein 2 Proteins 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 102100021299 Methyl-CpG-binding domain protein 2 Human genes 0.000 claims description 3
- -1 dinitrophenol compound Chemical class 0.000 claims description 3
- 230000002538 fungal effect Effects 0.000 claims description 3
- 244000053095 fungal pathogen Species 0.000 claims description 3
- 244000000004 fungal plant pathogen Species 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 210000003470 mitochondria Anatomy 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 150000003053 piperidines Chemical class 0.000 claims description 3
- 230000035806 respiratory chain Effects 0.000 claims description 3
- 230000027756 respiratory electron transport chain Effects 0.000 claims description 3
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 230000000844 anti-bacterial effect Effects 0.000 claims description 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 2
- 230000010534 mechanism of action Effects 0.000 claims description 2
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical class OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 229930192474 thiophene Natural products 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 6
- 238000000034 method Methods 0.000 description 4
- 0 **(Oc(c(*)cc([N+]([O-])=O)c1)c1[N+]([O-])=O)=O Chemical compound **(Oc(c(*)cc([N+]([O-])=O)c1)c1[N+]([O-])=O)=O 0.000 description 2
- IXRUZEMDNAMNFO-UHFFFAOYSA-N 6-chloro-2-propoxy-3-propylthieno[2,3-d]pyrimidin-4-one Chemical compound O=C1N(CCC)C(OCCC)=NC2=C1C=C(Cl)S2 IXRUZEMDNAMNFO-UHFFFAOYSA-N 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- BKSAMSZTYMCNEK-UHFFFAOYSA-N 3-(cyclopropylmethyl)-6-iodo-2-propylsulfanylpyrido[2,3-d]pyrimidin-4-one Chemical compound CCCSC1=NC2=NC=C(I)C=C2C(=O)N1CC1CC1 BKSAMSZTYMCNEK-UHFFFAOYSA-N 0.000 description 1
- YLOOFEXWGHVZRU-UHFFFAOYSA-N 6,7-dibromo-2-propoxy-3-propylthieno[3,2-d]pyrimidin-4-one Chemical compound O=C1N(CCC)C(OCCC)=NC2=C1SC(Br)=C2Br YLOOFEXWGHVZRU-UHFFFAOYSA-N 0.000 description 1
- QQLGQHGKSPJXTO-UHFFFAOYSA-N 6,8-diiodo-2-propoxy-3-propylquinazolin-4-one Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1I QQLGQHGKSPJXTO-UHFFFAOYSA-N 0.000 description 1
- GFALABICUSQHNW-UHFFFAOYSA-N 6-bromo-2-propoxy-3-propylpyrido[2,3-d]pyrimidin-4-one Chemical compound C1=C(Br)C=C2C(=O)N(CCC)C(OCCC)=NC2=N1 GFALABICUSQHNW-UHFFFAOYSA-N 0.000 description 1
- FVQAEZOUDXAZGN-UHFFFAOYSA-N 6-bromo-2-propoxy-3-propylquinazolin-4-one Chemical compound C1=C(Br)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FVQAEZOUDXAZGN-UHFFFAOYSA-N 0.000 description 1
- SHIIIVHYHHZLFW-UHFFFAOYSA-N 6-bromo-2-propoxy-3-propylthieno[2,3-d]pyrimidin-4-one Chemical compound O=C1N(CCC)C(OCCC)=NC2=C1C=C(Br)S2 SHIIIVHYHHZLFW-UHFFFAOYSA-N 0.000 description 1
- OMTYROZFKUXLAQ-UHFFFAOYSA-N 7-bromo-2-propoxy-3-propylthieno[3,2-d]pyrimidin-4-one Chemical compound O=C1N(CCC)C(OCCC)=NC2=C1SC=C2Br OMTYROZFKUXLAQ-UHFFFAOYSA-N 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38763602P | 2002-06-11 | 2002-06-11 | |
| PCT/US2003/018608 WO2003103393A1 (en) | 2002-06-11 | 2003-06-10 | Mixtures of fused pyrimidinones and dinitrophenolic compounds useful for controlling powdery mildews |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005529936A JP2005529936A (ja) | 2005-10-06 |
| JP2005529936A5 true JP2005529936A5 (enExample) | 2006-08-03 |
| JP4414882B2 JP4414882B2 (ja) | 2010-02-10 |
Family
ID=29736342
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004510532A Expired - Lifetime JP4414882B2 (ja) | 2002-06-11 | 2003-06-10 | うどんこ病菌の防除に有用な縮合されたピリミジノン類およびジニトロフェノール化合物の混合物 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20050239805A1 (enExample) |
| EP (1) | EP1511380B1 (enExample) |
| JP (1) | JP4414882B2 (enExample) |
| AT (1) | ATE342660T1 (enExample) |
| AU (1) | AU2003239994A1 (enExample) |
| BR (2) | BRPI0311600B8 (enExample) |
| DE (1) | DE60309166T2 (enExample) |
| ES (1) | ES2274242T3 (enExample) |
| PT (1) | PT1511380E (enExample) |
| WO (1) | WO2003103393A1 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2005244420A1 (en) * | 2004-05-13 | 2005-11-24 | Basf Aktiengesellschaft | Triazolopyrimidine derivative-based fungicide mixtures |
| EP1830641B1 (en) | 2004-10-14 | 2011-05-25 | Dow AgroSciences LLC | Isomeric mixtures of dinitro-octylphenyl esters and synergistic fungicidal mixtures therefrom |
| CL2007003256A1 (es) * | 2006-11-15 | 2008-07-25 | Du Pont | Mezcla fungicida que comprende al menos tres compuestos diferentes; composicion fungicida que comprende dicha mezcla; y metodo para controlar una enfermedad en plantas causada por el patogeno fungico vegetal que comprende aplicar una cantidad de la m |
| US8557866B2 (en) | 2007-04-13 | 2013-10-15 | Dow Agrosciences, Llc. | Isomeric mixtures of dinitro-octylphenyl esters and synergistic fungicidal mixtures therefrom |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2810767A (en) * | 1957-10-22 | Denitration of o-alkylphenols | ||
| US2526660A (en) * | 1946-07-06 | 1950-10-24 | Rohm & Haas | Capryldintrophenyl crotonate |
| NL276256A (enExample) * | 1961-03-22 | |||
| ES2163445T3 (es) * | 1993-05-12 | 2002-02-01 | Du Pont | Pirimidinonas biciclicas fusionadas con actividad fungicida. |
| EP0836602B1 (en) * | 1995-07-05 | 2002-01-30 | E.I. Du Pont De Nemours And Company | Fungicidal pyrimidinones |
| DE69712331T2 (de) * | 1996-03-11 | 2002-11-28 | Syngenta Participations Ag, Basel | Pyrimidin-4-on derivate als pestizidesmittel |
| IL132474A (en) * | 1997-05-08 | 2003-05-29 | Agrevo Uk Ltd | 3,4-dihydrothienopyrimidine-4-(thi) ones for combating plant fungi and a novel such compound |
| GB9719411D0 (en) * | 1997-09-12 | 1997-11-12 | Ciba Geigy Ag | New Pesticides |
-
2003
- 2003-06-10 BR BRPI0311600A patent/BRPI0311600B8/pt not_active IP Right Cessation
- 2003-06-10 US US10/512,020 patent/US20050239805A1/en not_active Abandoned
- 2003-06-10 EP EP03734571A patent/EP1511380B1/en not_active Expired - Lifetime
- 2003-06-10 WO PCT/US2003/018608 patent/WO2003103393A1/en not_active Ceased
- 2003-06-10 PT PT03734571T patent/PT1511380E/pt unknown
- 2003-06-10 BR BRPI0311600-0A patent/BR0311600B1/pt active IP Right Grant
- 2003-06-10 JP JP2004510532A patent/JP4414882B2/ja not_active Expired - Lifetime
- 2003-06-10 AU AU2003239994A patent/AU2003239994A1/en not_active Abandoned
- 2003-06-10 DE DE60309166T patent/DE60309166T2/de not_active Expired - Lifetime
- 2003-06-10 AT AT03734571T patent/ATE342660T1/de not_active IP Right Cessation
- 2003-06-10 ES ES03734571T patent/ES2274242T3/es not_active Expired - Lifetime
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