RU2542767C2 - Композиция и способ регулирования оомицетных грибковых патогенов - Google Patents
Композиция и способ регулирования оомицетных грибковых патогенов Download PDFInfo
- Publication number
- RU2542767C2 RU2542767C2 RU2012119530/13A RU2012119530A RU2542767C2 RU 2542767 C2 RU2542767 C2 RU 2542767C2 RU 2012119530/13 A RU2012119530/13 A RU 2012119530/13A RU 2012119530 A RU2012119530 A RU 2012119530A RU 2542767 C2 RU2542767 C2 RU 2542767C2
- Authority
- RU
- Russia
- Prior art keywords
- aldehyde
- hydrazone
- zoospores
- attractant
- mancozeb
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract 25
- 241000233654 Oomycetes Species 0.000 title claims abstract 5
- 238000000034 method Methods 0.000 title claims 5
- 244000053095 fungal pathogen Species 0.000 title claims 4
- 230000001105 regulatory effect Effects 0.000 title 1
- 239000005667 attractant Substances 0.000 claims abstract 21
- 230000031902 chemoattractant activity Effects 0.000 claims abstract 21
- 239000002245 particle Substances 0.000 claims abstract 17
- 239000011230 binding agent Substances 0.000 claims abstract 12
- 230000000855 fungicidal effect Effects 0.000 claims abstract 11
- 239000000417 fungicide Substances 0.000 claims abstract 11
- 201000010099 disease Diseases 0.000 claims abstract 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract 6
- 239000004816 latex Substances 0.000 claims abstract 5
- 229920000126 latex Polymers 0.000 claims abstract 5
- 241000233866 Fungi Species 0.000 claims abstract 3
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims abstract 3
- 230000015572 biosynthetic process Effects 0.000 claims abstract 2
- 150000001299 aldehydes Chemical class 0.000 claims 32
- -1 kineb Substances 0.000 claims 21
- 241000196324 Embryophyta Species 0.000 claims 19
- 150000007857 hydrazones Chemical class 0.000 claims 10
- YGHRJJRRZDOVPD-UHFFFAOYSA-N 3-methylbutanal Chemical compound CC(C)CC=O YGHRJJRRZDOVPD-UHFFFAOYSA-N 0.000 claims 8
- 238000002360 preparation method Methods 0.000 claims 8
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 5
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims 5
- BYGQBDHUGHBGMD-UHFFFAOYSA-N 2-methylbutanal Chemical compound CCC(C)C=O BYGQBDHUGHBGMD-UHFFFAOYSA-N 0.000 claims 4
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 claims 4
- 239000005802 Mancozeb Substances 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 229940079593 drug Drugs 0.000 claims 4
- 235000013399 edible fruits Nutrition 0.000 claims 4
- 239000001963 growth medium Substances 0.000 claims 4
- 239000004615 ingredient Substances 0.000 claims 4
- 239000007788 liquid Substances 0.000 claims 4
- 239000007787 solid Substances 0.000 claims 4
- 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 claims 3
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 claims 3
- OQNKZWDYYSHLPO-UHFFFAOYSA-N 3-methylbutanehydrazide Chemical compound CC(C)CC(=O)NN OQNKZWDYYSHLPO-UHFFFAOYSA-N 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 239000005756 Cymoxanil Substances 0.000 claims 3
- 239000005780 Fluazinam Substances 0.000 claims 3
- 239000005807 Metalaxyl Substances 0.000 claims 3
- 239000005809 Metiram Substances 0.000 claims 3
- 239000005821 Propamocarb Substances 0.000 claims 3
- 239000005823 Propineb Substances 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 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 3
- ZQEIXNIJLIKNTD-GFCCVEGCSA-N metalaxyl-M Chemical compound COCC(=O)N([C@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-GFCCVEGCSA-N 0.000 claims 3
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 claims 3
- 229920000257 metiram Polymers 0.000 claims 3
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 claims 3
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims 3
- 239000002689 soil Substances 0.000 claims 3
- ZNGSVRYVWHOWLX-KHFUBBAMSA-N (1r,2s)-2-(methylamino)-1-phenylpropan-1-ol;hydrate Chemical compound O.CN[C@@H](C)[C@H](O)C1=CC=CC=C1.CN[C@@H](C)[C@H](O)C1=CC=CC=C1 ZNGSVRYVWHOWLX-KHFUBBAMSA-N 0.000 claims 2
- 239000001893 (2R)-2-methylbutanal Substances 0.000 claims 2
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 claims 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims 2
- 239000005761 Dimethomorph Substances 0.000 claims 2
- 239000005782 Fluopicolide Substances 0.000 claims 2
- 241000238631 Hexapoda Species 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- IBVAQQYNSHJXBV-UHFFFAOYSA-N adipic acid dihydrazide Chemical compound NNC(=O)CCCCC(=O)NN IBVAQQYNSHJXBV-UHFFFAOYSA-N 0.000 claims 2
- UTTHLMXOSUFZCQ-UHFFFAOYSA-N benzene-1,3-dicarbohydrazide Chemical compound NNC(=O)C1=CC=CC(C(=O)NN)=C1 UTTHLMXOSUFZCQ-UHFFFAOYSA-N 0.000 claims 2
- ALHNLFMSAXZKRC-UHFFFAOYSA-N benzene-1,4-dicarbohydrazide Chemical compound NNC(=O)C1=CC=C(C(=O)NN)C=C1 ALHNLFMSAXZKRC-UHFFFAOYSA-N 0.000 claims 2
- FCCCRBDJBTVFSJ-UHFFFAOYSA-N butanehydrazide Chemical compound CCCC(=O)NN FCCCRBDJBTVFSJ-UHFFFAOYSA-N 0.000 claims 2
- 238000007865 diluting Methods 0.000 claims 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
- YTQHSQQSLTYMSL-UHFFFAOYSA-N dodecanohydrazide Chemical compound CCCCCCCCCCCC(=O)NN YTQHSQQSLTYMSL-UHFFFAOYSA-N 0.000 claims 2
- SWRGUMCEJHQWEE-UHFFFAOYSA-N ethanedihydrazide Chemical compound NNC(=O)C(=O)NN SWRGUMCEJHQWEE-UHFFFAOYSA-N 0.000 claims 2
- GBOYJIHYACSLGN-UHFFFAOYSA-N fluopicolide Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CNC(=O)C1=C(Cl)C=CC=C1Cl GBOYJIHYACSLGN-UHFFFAOYSA-N 0.000 claims 2
- FAWGDZUNQZJISX-UHFFFAOYSA-N heptanehydrazide Chemical compound CCCCCCC(=O)NN FAWGDZUNQZJISX-UHFFFAOYSA-N 0.000 claims 2
- SSVSELJXJJCANX-UHFFFAOYSA-N hexadecanehydrazide Chemical compound CCCCCCCCCCCCCCCC(=O)NN SSVSELJXJJCANX-UHFFFAOYSA-N 0.000 claims 2
- QKWRNBNHSRYCOE-UHFFFAOYSA-N hexanehydrazide Chemical compound CCCCCC(=O)NN QKWRNBNHSRYCOE-UHFFFAOYSA-N 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 235000015097 nutrients Nutrition 0.000 claims 2
- BYTFESSQUGDMQQ-UHFFFAOYSA-N octadecanehydrazide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NN BYTFESSQUGDMQQ-UHFFFAOYSA-N 0.000 claims 2
- LGYJSPMYALQHBL-UHFFFAOYSA-N pentanedihydrazide Chemical compound NNC(=O)CCCC(=O)NN LGYJSPMYALQHBL-UHFFFAOYSA-N 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
- 229920002554 vinyl polymer Polymers 0.000 claims 2
- IQGZCSXWIRBTRW-ZZXKWVIFSA-N (2E)-2-ethyl-2-butenal Chemical compound CC\C(=C/C)C=O IQGZCSXWIRBTRW-ZZXKWVIFSA-N 0.000 claims 1
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 claims 1
- ROFVGYAMRSGUSQ-UHFFFAOYSA-N 1-(2-bromoethyl)piperazine;hydrobromide Chemical compound Br.BrCCN1CCNCC1 ROFVGYAMRSGUSQ-UHFFFAOYSA-N 0.000 claims 1
- FTZILAQGHINQQR-UHFFFAOYSA-N 2-Methylpentanal Chemical compound CCCC(C)C=O FTZILAQGHINQQR-UHFFFAOYSA-N 0.000 claims 1
- YZZDEYSCSPZMIG-UHFFFAOYSA-N 2-fluoro-1-methoxy-3-(trifluoromethyl)benzene Chemical compound COC1=CC=CC(C(F)(F)F)=C1F YZZDEYSCSPZMIG-UHFFFAOYSA-N 0.000 claims 1
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 claims 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims 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 claims 1
- 239000005727 Amisulbrom Substances 0.000 claims 1
- 239000005730 Azoxystrobin Substances 0.000 claims 1
- 239000005734 Benalaxyl Substances 0.000 claims 1
- 239000005739 Bordeaux mixture Substances 0.000 claims 1
- 239000005745 Captan Substances 0.000 claims 1
- 239000005747 Chlorothalonil Substances 0.000 claims 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 claims 1
- 239000005750 Copper hydroxide Substances 0.000 claims 1
- 239000005752 Copper oxychloride Substances 0.000 claims 1
- 239000005772 Famoxadone Substances 0.000 claims 1
- 239000005789 Folpet Substances 0.000 claims 1
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 1
- 239000002174 Styrene-butadiene Substances 0.000 claims 1
- 239000005843 Thiram Substances 0.000 claims 1
- 239000005857 Trifloxystrobin Substances 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 239000005860 Valifenalate Substances 0.000 claims 1
- 239000005863 Zoxamide Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 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 claims 1
- 150000008064 anhydrides Chemical class 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
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims 1
- HCOMFAYPHBFMKU-UHFFFAOYSA-N butanedihydrazide Chemical compound NNC(=O)CCC(=O)NN HCOMFAYPHBFMKU-UHFFFAOYSA-N 0.000 claims 1
- 229940117949 captan Drugs 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 claims 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000007859 condensation product Substances 0.000 claims 1
- 229910001956 copper hydroxide Inorganic materials 0.000 claims 1
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 claims 1
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 claims 1
- VELDYOPRLMJFIK-UHFFFAOYSA-N cyclopentanecarbaldehyde Chemical compound O=CC1CCCC1 VELDYOPRLMJFIK-UHFFFAOYSA-N 0.000 claims 1
- JMYVMOUINOAAPA-UHFFFAOYSA-N cyclopropanecarbaldehyde Chemical compound O=CC1CC1 JMYVMOUINOAAPA-UHFFFAOYSA-N 0.000 claims 1
- 239000006185 dispersion Substances 0.000 claims 1
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims 1
- OXAGUPFRAIIDLT-UHFFFAOYSA-N heptanedihydrazide Chemical compound NNC(=O)CCCCCC(=O)NN OXAGUPFRAIIDLT-UHFFFAOYSA-N 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 claims 1
- 229920000940 maneb Polymers 0.000 claims 1
- 125000005395 methacrylic acid group Chemical group 0.000 claims 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 1
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 claims 1
- YNTOKMNHRPSGFU-UHFFFAOYSA-N n-Propyl carbamate Chemical compound CCCOC(N)=O YNTOKMNHRPSGFU-UHFFFAOYSA-N 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- GSUBXIVOZXWGKF-UHFFFAOYSA-N oxolane-3-carbaldehyde Chemical compound O=CC1CCOC1 GSUBXIVOZXWGKF-UHFFFAOYSA-N 0.000 claims 1
- 230000037361 pathway Effects 0.000 claims 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N pentanal Chemical compound CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims 1
- 150000007659 semicarbazones Chemical class 0.000 claims 1
- 239000011115 styrene butadiene Substances 0.000 claims 1
- 229920003048 styrene butadiene rubber Polymers 0.000 claims 1
- 239000001384 succinic acid Substances 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- KXTZPAQXYKUVLD-UHFFFAOYSA-N tetradecanehydrazide Chemical class CCCCCCCCCCCCCC(=O)NN KXTZPAQXYKUVLD-UHFFFAOYSA-N 0.000 claims 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims 1
- 229960002447 thiram Drugs 0.000 claims 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 claims 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 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- BKOOMYPCSUNDGP-UHFFFAOYSA-N trimethyl-ethylene Natural products CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 claims 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 244000052769 pathogen Species 0.000 abstract 1
- 230000001717 pathogenic effect Effects 0.000 abstract 1
- 239000000126 substance Substances 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/002—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing a foodstuff as carrier or diluent, i.e. baits
- A01N25/006—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing a foodstuff as carrier or diluent, i.e. baits insecticidal
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- A01N47/14—Di-thio analogues thereof
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
- A01N47/44—Guanidine; Derivatives thereof
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Insects & Arthropods (AREA)
- Food Science & Technology (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
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| US25103709P | 2009-10-13 | 2009-10-13 | |
| US61/251,037 | 2009-10-13 | ||
| PCT/US2010/052477 WO2011047025A1 (en) | 2009-10-13 | 2010-10-13 | Compositions and methods to control oomycete fungal pathogens |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2012119530A RU2012119530A (ru) | 2013-11-20 |
| RU2542767C2 true RU2542767C2 (ru) | 2015-02-27 |
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| RU2012119530/13A RU2542767C2 (ru) | 2009-10-13 | 2010-10-13 | Композиция и способ регулирования оомицетных грибковых патогенов |
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| EP (1) | EP2488021A4 (enExample) |
| JP (1) | JP2013507450A (enExample) |
| KR (1) | KR20120097499A (enExample) |
| CN (1) | CN102655744A (enExample) |
| AR (1) | AR079415A1 (enExample) |
| BR (1) | BR112012008786A2 (enExample) |
| CA (1) | CA2776716A1 (enExample) |
| IN (1) | IN2012DN03096A (enExample) |
| MX (1) | MX2012004418A (enExample) |
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| UA (1) | UA108212C2 (enExample) |
| WO (1) | WO2011047025A1 (enExample) |
| ZA (1) | ZA201202426B (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2781839C1 (ru) * | 2022-03-02 | 2022-10-18 | Общество с ограниченной ответственностью "Агро Эксперт Груп" | Фунгицидная композиция в виде масляной дисперсии |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2938195A4 (en) | 2012-12-31 | 2016-06-29 | Dow Agrosciences Llc | COMPOSITIONS AND METHODS FOR MODULATING THE RATE OF PRODUCTION OF EBIS FROM DITHIOCARBAMATE FUNGICIDES |
| CN103651431B (zh) * | 2013-12-13 | 2015-12-02 | 广西田园生化股份有限公司 | 含辛唑嘧菌胺与甲氧基丙烯酸酯类杀菌剂组合物的超低容量液剂及其制备方法和应用 |
| CN104068032A (zh) * | 2014-07-03 | 2014-10-01 | 深圳诺普信农化股份有限公司 | 一种杀菌组合物 |
| CN105638698A (zh) * | 2016-03-02 | 2016-06-08 | 陕西上格之路生物科学有限公司 | 一种含氟吡菌胺和缬菌胺的杀菌组合物 |
| CN108835712B (zh) * | 2018-03-21 | 2021-02-02 | 云南中烟工业有限责任公司 | 一种降低烟气中巴豆醛释放量的复配添加剂及其制备方法和应用 |
| EP4611544A2 (en) * | 2022-11-02 | 2025-09-10 | Syngenta Crop Protection AG | Method of controlling, limiting or preventing oomycetes |
| CN116869003B (zh) * | 2023-06-25 | 2025-07-04 | 海南大学 | 大豆苷在防治辣椒疫病中的应用 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US6436421B1 (en) * | 1997-03-03 | 2002-08-20 | ?Rohm And Haas Company | Pesticide compositions |
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| JPH0699244B2 (ja) * | 1985-04-10 | 1994-12-07 | 日本ペイント株式会社 | 抗有害生物性を有する微小樹脂粒子 |
| DE69119752T2 (de) * | 1990-03-06 | 1997-01-23 | Tate | Fungizide zusammensetzungen zur anwendung bei pflanzen |
| DE69331580T2 (de) * | 1992-09-25 | 2002-08-14 | The Australian National University, Acton | Nachweis von beweglichen zellen in einer probe |
| US6004570A (en) * | 1998-04-17 | 1999-12-21 | Rohm And Haas Company | Dithiocarbamate fungicide compositions with improved properties |
| DE19833061A1 (de) * | 1998-07-22 | 2000-02-03 | Elotex Ag Sempach Station | Verfahren zur Herstellung wäßriger Dispersionen von Latexteilchen mit heterogener Morphologie, die mit dem Verfahren erhältlichen Latexteilchen, die Dispersionen und redispergierbaren Pulver sowie deren Verwendung |
| DE60008925T2 (de) * | 1999-12-21 | 2005-01-20 | Dsm Ip Assets B.V. | Verfahren zur erhaltung der wirksamkeit eines fungizids in wässriger lösung |
| EP1293125B1 (en) * | 2000-05-15 | 2011-10-05 | Yosuke Oda | Synthetic hydrated organosulfur agent, production process and bactericidal method by using the same |
| IN2001MU01216A (enExample) * | 2001-01-19 | 2005-03-04 | Bayer Cropscience Ag | |
| WO2004014136A1 (ja) * | 2002-08-07 | 2004-02-19 | Nippon Soda Co., Ltd. | 顆粒状農薬組成物 |
| WO2006016248A1 (en) * | 2004-08-05 | 2006-02-16 | Firmenich Sa | Use of dynamic mixtures for a controlled release of fragrances |
| WO2008086948A1 (en) * | 2007-01-16 | 2008-07-24 | Syngenta Participations Ag | Pesticidal combinations |
| EP2124557B1 (en) * | 2007-02-02 | 2014-12-31 | Plant Health Care, Inc. | Synergistic fungicidal combinations comprising formononetin |
| US9049814B2 (en) * | 2007-02-23 | 2015-06-09 | Vamtech, Llc | Coated seeds and methods of making coated seeds |
| NZ585664A (en) * | 2007-12-03 | 2012-06-29 | Valent Usa Corp | Seed treatment formulations comprisiing a pesticide, a polyvinyl alcohol, a graft copolymer and a plasticizer |
| US20090246293A1 (en) * | 2008-04-01 | 2009-10-01 | Dow Agrosciences Llc | Compositions and methods to control oomycete fungal pathogens |
| US20090253612A1 (en) * | 2008-04-02 | 2009-10-08 | Symrise Gmbh & Co Kg | Particles having a high load of fragrance or flavor oil |
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- 2010-10-13 UA UAA201205787A patent/UA108212C2/uk unknown
- 2010-10-13 RU RU2012119530/13A patent/RU2542767C2/ru not_active IP Right Cessation
- 2010-10-13 US US12/903,708 patent/US20110086761A1/en not_active Abandoned
- 2010-10-13 IN IN3096DEN2012 patent/IN2012DN03096A/en unknown
- 2010-10-13 KR KR1020127012156A patent/KR20120097499A/ko not_active Withdrawn
- 2010-10-13 MX MX2012004418A patent/MX2012004418A/es not_active Application Discontinuation
- 2010-10-13 BR BR112012008786A patent/BR112012008786A2/pt not_active Application Discontinuation
- 2010-10-13 EP EP10824006.0A patent/EP2488021A4/en not_active Withdrawn
- 2010-10-13 WO PCT/US2010/052477 patent/WO2011047025A1/en not_active Ceased
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- 2010-10-14 AR ARP100103747A patent/AR079415A1/es unknown
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6436421B1 (en) * | 1997-03-03 | 2002-08-20 | ?Rohm And Haas Company | Pesticide compositions |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2781839C1 (ru) * | 2022-03-02 | 2022-10-18 | Общество с ограниченной ответственностью "Агро Эксперт Груп" | Фунгицидная композиция в виде масляной дисперсии |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2013507450A (ja) | 2013-03-04 |
| KR20120097499A (ko) | 2012-09-04 |
| EP2488021A4 (en) | 2013-07-31 |
| CA2776716A1 (en) | 2011-04-21 |
| EP2488021A1 (en) | 2012-08-22 |
| AR079415A1 (es) | 2012-01-25 |
| UA108212C2 (uk) | 2015-04-10 |
| MX2012004418A (es) | 2012-05-08 |
| BR112012008786A2 (pt) | 2015-09-22 |
| RU2012119530A (ru) | 2013-11-20 |
| ZA201202426B (en) | 2013-06-26 |
| IN2012DN03096A (enExample) | 2015-09-18 |
| US20110086761A1 (en) | 2011-04-14 |
| WO2011047025A1 (en) | 2011-04-21 |
| CN102655744A (zh) | 2012-09-05 |
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