CN117794908A - (3-喹啉基)-喹唑啉 - Google Patents
(3-喹啉基)-喹唑啉 Download PDFInfo
- Publication number
- CN117794908A CN117794908A CN202280053834.1A CN202280053834A CN117794908A CN 117794908 A CN117794908 A CN 117794908A CN 202280053834 A CN202280053834 A CN 202280053834A CN 117794908 A CN117794908 A CN 117794908A
- Authority
- CN
- China
- Prior art keywords
- alkyl
- group
- phenyl
- haloalkyl
- halogen
- 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.)
- Pending
Links
- SPXVFIFLLSWZET-UHFFFAOYSA-N C1=CC=CC2=CC(C3=NC4=CC=CC=C4C=N3)=CN=C21 Chemical class C1=CC=CC2=CC(C3=NC4=CC=CC=C4C=N3)=CN=C21 SPXVFIFLLSWZET-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 168
- 239000000203 mixture Substances 0.000 claims abstract description 106
- -1 C 1 -C 4 -alkoxy Chemical group 0.000 claims description 220
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 58
- 229910052736 halogen Inorganic materials 0.000 claims description 47
- 150000002367 halogens Chemical class 0.000 claims description 45
- 229910052799 carbon Inorganic materials 0.000 claims description 34
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 29
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 25
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 24
- 241000233866 Fungi Species 0.000 claims description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 239000002689 soil Substances 0.000 claims description 20
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 19
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 17
- 125000000623 heterocyclic group Chemical group 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- 239000000417 fungicide Substances 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 15
- 125000001424 substituent group Chemical group 0.000 claims description 14
- 238000006467 substitution reaction Methods 0.000 claims description 14
- 229910052717 sulfur Inorganic materials 0.000 claims description 14
- 125000005842 heteroatom Chemical group 0.000 claims description 13
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 150000001204 N-oxides Chemical class 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 125000001072 heteroaryl group Chemical group 0.000 claims description 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- 230000002538 fungal effect Effects 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 230000003032 phytopathogenic effect Effects 0.000 claims description 5
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 3
- 241000196324 Embryophyta Species 0.000 description 131
- 240000008042 Zea mays Species 0.000 description 68
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 64
- 235000010469 Glycine max Nutrition 0.000 description 55
- 244000068988 Glycine max Species 0.000 description 54
- 241000894007 species Species 0.000 description 43
- 239000003112 inhibitor Substances 0.000 description 39
- 235000021307 Triticum Nutrition 0.000 description 36
- 241000209140 Triticum Species 0.000 description 36
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 36
- 235000013339 cereals Nutrition 0.000 description 36
- 235000005822 corn Nutrition 0.000 description 36
- 239000000575 pesticide Substances 0.000 description 33
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 27
- 235000013399 edible fruits Nutrition 0.000 description 26
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 24
- 230000000694 effects Effects 0.000 description 24
- 235000009973 maize Nutrition 0.000 description 24
- 241000589180 Rhizobium Species 0.000 description 22
- 239000013543 active substance Substances 0.000 description 22
- 108090000623 proteins and genes Proteins 0.000 description 22
- 238000012360 testing method Methods 0.000 description 22
- 235000013311 vegetables Nutrition 0.000 description 22
- 239000000047 product Substances 0.000 description 21
- 240000007594 Oryza sativa Species 0.000 description 20
- 235000007164 Oryza sativa Nutrition 0.000 description 20
- 235000009566 rice Nutrition 0.000 description 20
- 235000007340 Hordeum vulgare Nutrition 0.000 description 19
- 240000005979 Hordeum vulgare Species 0.000 description 19
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 19
- 239000004009 herbicide Substances 0.000 description 19
- 239000000243 solution Substances 0.000 description 19
- 241000193744 Bacillus amyloliquefaciens Species 0.000 description 18
- 201000010099 disease Diseases 0.000 description 18
- 230000000813 microbial effect Effects 0.000 description 18
- 241000223600 Alternaria Species 0.000 description 16
- 241000193830 Bacillus <bacterium> Species 0.000 description 16
- 235000002595 Solanum tuberosum Nutrition 0.000 description 16
- 244000061456 Solanum tuberosum Species 0.000 description 16
- 235000014113 dietary fatty acids Nutrition 0.000 description 16
- 239000000194 fatty acid Substances 0.000 description 16
- 229930195729 fatty acid Natural products 0.000 description 16
- 230000000855 fungicidal effect Effects 0.000 description 16
- 239000000725 suspension Substances 0.000 description 16
- 241000221785 Erysiphales Species 0.000 description 15
- 230000015572 biosynthetic process Effects 0.000 description 15
- 230000012010 growth Effects 0.000 description 15
- 230000002363 herbicidal effect Effects 0.000 description 15
- 230000001717 pathogenic effect Effects 0.000 description 15
- 241000193388 Bacillus thuringiensis Species 0.000 description 14
- 229920000742 Cotton Polymers 0.000 description 14
- 241000219146 Gossypium Species 0.000 description 14
- 241001533598 Septoria Species 0.000 description 14
- 229940097012 bacillus thuringiensis Drugs 0.000 description 14
- 244000052769 pathogen Species 0.000 description 14
- 241000123650 Botrytis cinerea Species 0.000 description 13
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 13
- 241000223218 Fusarium Species 0.000 description 13
- 230000001568 sexual effect Effects 0.000 description 13
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 12
- 235000006008 Brassica napus var napus Nutrition 0.000 description 12
- 241000371644 Curvularia ravenelii Species 0.000 description 12
- 235000021536 Sugar beet Nutrition 0.000 description 12
- 150000004665 fatty acids Chemical class 0.000 description 12
- 230000000749 insecticidal effect Effects 0.000 description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 12
- 241001443610 Aschersonia Species 0.000 description 11
- 241001157813 Cercospora Species 0.000 description 11
- 241000222199 Colletotrichum Species 0.000 description 11
- 241000221300 Puccinia Species 0.000 description 11
- 108700019146 Transgenes Proteins 0.000 description 11
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 11
- 150000003254 radicals Chemical class 0.000 description 11
- 210000004215 spore Anatomy 0.000 description 11
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 10
- 241000228453 Pyrenophora Species 0.000 description 10
- 241000221662 Sclerotinia Species 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 10
- 239000000284 extract Substances 0.000 description 10
- 229910052740 iodine Inorganic materials 0.000 description 10
- 230000008635 plant growth Effects 0.000 description 10
- 235000012015 potatoes Nutrition 0.000 description 10
- 239000004094 surface-active agent Substances 0.000 description 10
- 230000009261 transgenic effect Effects 0.000 description 10
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 9
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 9
- 240000000385 Brassica napus var. napus Species 0.000 description 9
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 9
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 9
- 235000003222 Helianthus annuus Nutrition 0.000 description 9
- 241000238631 Hexapoda Species 0.000 description 9
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 9
- 241000244206 Nematoda Species 0.000 description 9
- 240000003768 Solanum lycopersicum Species 0.000 description 9
- 235000007244 Zea mays Nutrition 0.000 description 9
- 239000002671 adjuvant Substances 0.000 description 9
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 9
- 102000004169 proteins and genes Human genes 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 8
- 241001000605 Semia Species 0.000 description 8
- 241001360088 Zymoseptoria tritici Species 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 8
- 230000000844 anti-bacterial effect Effects 0.000 description 8
- 239000003139 biocide Substances 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 8
- 244000005700 microbiome Species 0.000 description 8
- 238000002703 mutagenesis Methods 0.000 description 8
- 231100000350 mutagenesis Toxicity 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 238000003786 synthesis reaction Methods 0.000 description 8
- 241000701366 unidentified nuclear polyhedrosis viruses Species 0.000 description 8
- 240000007124 Brassica oleracea Species 0.000 description 7
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 7
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 7
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 7
- 244000025254 Cannabis sativa Species 0.000 description 7
- 241001330975 Magnaporthe oryzae Species 0.000 description 7
- 241000736122 Parastagonospora nodorum Species 0.000 description 7
- 244000046052 Phaseolus vulgaris Species 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 241000700605 Viruses Species 0.000 description 7
- 240000006365 Vitis vinifera Species 0.000 description 7
- 235000014787 Vitis vinifera Nutrition 0.000 description 7
- 230000000895 acaricidal effect Effects 0.000 description 7
- 239000012872 agrochemical composition Substances 0.000 description 7
- JLQUFIHWVLZVTJ-UHFFFAOYSA-N carbosulfan Chemical compound CCCCN(CCCC)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 JLQUFIHWVLZVTJ-UHFFFAOYSA-N 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 238000003306 harvesting Methods 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 241000194103 Bacillus pumilus Species 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 244000020551 Helianthus annuus Species 0.000 description 6
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 6
- 241000233679 Peronosporaceae Species 0.000 description 6
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 6
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 6
- 241001361634 Rhizoctonia Species 0.000 description 6
- 240000000111 Saccharum officinarum Species 0.000 description 6
- 235000007201 Saccharum officinarum Nutrition 0.000 description 6
- 235000007238 Secale cereale Nutrition 0.000 description 6
- 244000082988 Secale cereale Species 0.000 description 6
- 241000722133 Tilletia Species 0.000 description 6
- 241000223259 Trichoderma Species 0.000 description 6
- 239000012190 activator Substances 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 6
- 230000007123 defense Effects 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 230000036541 health Effects 0.000 description 6
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 6
- 230000002013 molluscicidal effect Effects 0.000 description 6
- 230000001069 nematicidal effect Effects 0.000 description 6
- 229940031826 phenolate Drugs 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 239000000741 silica gel Substances 0.000 description 6
- 229910002027 silica gel Inorganic materials 0.000 description 6
- 239000001632 sodium acetate Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 150000003871 sulfonates Chemical class 0.000 description 6
- 230000003253 viricidal effect Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- BINQFWQYTCAARG-UHFFFAOYSA-N 1-(1-acetylindolizin-3-yl)ethanone Chemical compound C1=CC=CC2=C(C(=O)C)C=C(C(C)=O)N21 BINQFWQYTCAARG-UHFFFAOYSA-N 0.000 description 5
- 241000751139 Beauveria bassiana Species 0.000 description 5
- 235000016068 Berberis vulgaris Nutrition 0.000 description 5
- 241000335053 Beta vulgaris Species 0.000 description 5
- 239000005874 Bifenthrin Substances 0.000 description 5
- 241000219198 Brassica Species 0.000 description 5
- 240000002791 Brassica napus Species 0.000 description 5
- 240000007154 Coffea arabica Species 0.000 description 5
- 102000015782 Electron Transport Complex III Human genes 0.000 description 5
- 108010024882 Electron Transport Complex III Proteins 0.000 description 5
- 240000009088 Fragaria x ananassa Species 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 241000701443 Helicoverpa zea single nucleopolyhedrovirus Species 0.000 description 5
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 description 5
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 description 5
- 241000179039 Paenibacillus Species 0.000 description 5
- 241000194105 Paenibacillus polymyxa Species 0.000 description 5
- 241000228143 Penicillium Species 0.000 description 5
- 206010039509 Scab Diseases 0.000 description 5
- 239000005857 Trifloxystrobin Substances 0.000 description 5
- 235000009754 Vitis X bourquina Nutrition 0.000 description 5
- 235000012333 Vitis X labruscana Nutrition 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 235000016213 coffee Nutrition 0.000 description 5
- 235000013353 coffee beverage Nutrition 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 230000001276 controlling effect Effects 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 5
- 235000013312 flour Nutrition 0.000 description 5
- 239000003016 pheromone Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 5
- 235000021012 strawberries Nutrition 0.000 description 5
- 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 description 5
- 229910052727 yttrium Inorganic materials 0.000 description 5
- ZFHGXWPMULPQSE-UKSCLKOJSA-N (Z)-(1R)-cis-tefluthrin Chemical compound FC1=C(F)C(C)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@H]1\C=C(/Cl)C(F)(F)F ZFHGXWPMULPQSE-UKSCLKOJSA-N 0.000 description 4
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 4
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 4
- 108010000700 Acetolactate synthase Proteins 0.000 description 4
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 4
- 241001163841 Albugo ipomoeae-panduratae Species 0.000 description 4
- 244000105624 Arachis hypogaea Species 0.000 description 4
- 244000075850 Avena orientalis Species 0.000 description 4
- 235000007319 Avena orientalis Nutrition 0.000 description 4
- 244000063299 Bacillus subtilis Species 0.000 description 4
- 235000014469 Bacillus subtilis Nutrition 0.000 description 4
- 241001465178 Bipolaris Species 0.000 description 4
- 235000011331 Brassica Nutrition 0.000 description 4
- 235000008534 Capsicum annuum var annuum Nutrition 0.000 description 4
- 241000222290 Cladosporium Species 0.000 description 4
- 240000004792 Corchorus capsularis Species 0.000 description 4
- 241000219112 Cucumis Species 0.000 description 4
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 4
- 240000008067 Cucumis sativus Species 0.000 description 4
- 244000000626 Daucus carota Species 0.000 description 4
- 235000002767 Daucus carota Nutrition 0.000 description 4
- 241000125117 Elsinoe Species 0.000 description 4
- 241000223195 Fusarium graminearum Species 0.000 description 4
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 4
- 241001480224 Heterodera Species 0.000 description 4
- 206010020751 Hypersensitivity Diseases 0.000 description 4
- 241000228456 Leptosphaeria Species 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 244000070406 Malus silvestris Species 0.000 description 4
- 240000005561 Musa balbisiana Species 0.000 description 4
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 4
- 244000061176 Nicotiana tabacum Species 0.000 description 4
- 241000256259 Noctuidae Species 0.000 description 4
- 241000235400 Phycomyces Species 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000005869 Pyraclostrobin Substances 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 241000220324 Pyrus Species 0.000 description 4
- 241000233639 Pythium Species 0.000 description 4
- 241000256251 Spodoptera frugiperda Species 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 241000223260 Trichoderma harzianum Species 0.000 description 4
- 241000223261 Trichoderma viride Species 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 241000221566 Ustilago Species 0.000 description 4
- 241000607479 Yersinia pestis Species 0.000 description 4
- 230000009471 action Effects 0.000 description 4
- 238000003556 assay Methods 0.000 description 4
- 235000021015 bananas Nutrition 0.000 description 4
- 230000000443 biocontrol Effects 0.000 description 4
- 230000000853 biopesticidal effect Effects 0.000 description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 4
- 239000004495 emulsifiable concentrate Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 230000002708 enhancing effect Effects 0.000 description 4
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 4
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 4
- 239000002207 metabolite Substances 0.000 description 4
- 230000002438 mitochondrial effect Effects 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 125000006239 protecting group Chemical group 0.000 description 4
- 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 description 4
- 239000004575 stone Substances 0.000 description 4
- 230000035882 stress Effects 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 230000009466 transformation Effects 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 description 3
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 description 3
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 3
- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-methylbutan-1-ol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 description 3
- 108010068327 4-hydroxyphenylpyruvate dioxygenase Proteins 0.000 description 3
- 102100028626 4-hydroxyphenylpyruvate dioxygenase Human genes 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 241001019659 Acremonium <Plectosphaerellaceae> Species 0.000 description 3
- 241000234282 Allium Species 0.000 description 3
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 3
- 241001530056 Athelia rolfsii Species 0.000 description 3
- 241000193400 Bacillus simplex Species 0.000 description 3
- 241001453380 Burkholderia Species 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 3
- 240000001980 Cucurbita pepo Species 0.000 description 3
- 241001635274 Cydia pomonella Species 0.000 description 3
- 239000005757 Cyproconazole Substances 0.000 description 3
- 241001508801 Diaporthe phaseolorum Species 0.000 description 3
- 239000005504 Dicamba Substances 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 239000005901 Flubendiamide Substances 0.000 description 3
- 239000005789 Folpet Substances 0.000 description 3
- 241000223221 Fusarium oxysporum Species 0.000 description 3
- 240000008669 Hedera helix Species 0.000 description 3
- 241000208818 Helianthus Species 0.000 description 3
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 3
- 241001248590 Isaria Species 0.000 description 3
- 235000003228 Lactuca sativa Nutrition 0.000 description 3
- 240000008415 Lactuca sativa Species 0.000 description 3
- 241000228457 Leptosphaeria maculans Species 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- 241001668536 Oculimacula yallundae Species 0.000 description 3
- 240000007817 Olea europaea Species 0.000 description 3
- 241000606856 Pasteurella multocida Species 0.000 description 3
- 241000123107 Phellinus Species 0.000 description 3
- 241001480007 Phomopsis Species 0.000 description 3
- 240000004713 Pisum sativum Species 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 244000078856 Prunus padus Species 0.000 description 3
- 235000006040 Prunus persica var persica Nutrition 0.000 description 3
- 241000589516 Pseudomonas Species 0.000 description 3
- 241000196686 Ramulariopsis gossypii Species 0.000 description 3
- 244000153955 Reynoutria sachalinensis Species 0.000 description 3
- 235000003202 Reynoutria sachalinensis Nutrition 0.000 description 3
- 241000235527 Rhizopus Species 0.000 description 3
- 239000005939 Tefluthrin Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 241000221577 Uromyces appendiculatus Species 0.000 description 3
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 3
- 241001123668 Verticillium dahliae Species 0.000 description 3
- 241000482268 Zea mays subsp. mays Species 0.000 description 3
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000000304 alkynyl group Chemical group 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 235000021016 apples Nutrition 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 description 3
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 description 3
- 229960000074 biopharmaceutical Drugs 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 235000020971 citrus fruits Nutrition 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 3
- 238000010410 dusting Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 235000019439 ethyl acetate Nutrition 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
- 244000037666 field crops Species 0.000 description 3
- ZGNITFSDLCMLGI-UHFFFAOYSA-N flubendiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(I)=C1C(=O)NC(C)(C)CS(C)(=O)=O ZGNITFSDLCMLGI-UHFFFAOYSA-N 0.000 description 3
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 3
- 238000010353 genetic engineering Methods 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000002054 inoculum Substances 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004811 liquid chromatography Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 235000005152 nicotinamide Nutrition 0.000 description 3
- 239000011570 nicotinamide Substances 0.000 description 3
- 229940079888 nitenpyram Drugs 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229940051027 pasteurella multocida Drugs 0.000 description 3
- 235000020232 peanut Nutrition 0.000 description 3
- 235000021017 pears Nutrition 0.000 description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
- 235000021039 pomes Nutrition 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 125000004289 pyrazol-3-yl group Chemical group [H]N1N=C(*)C([H])=C1[H] 0.000 description 3
- 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 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 230000000241 respiratory effect Effects 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000011550 stock solution Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 3
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 3
- 230000003612 virological effect Effects 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- ULDHMXUKGWMISQ-SECBINFHSA-N (-)-carvone Chemical compound CC(=C)[C@@H]1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-SECBINFHSA-N 0.000 description 2
- GEWDNTWNSAZUDX-WQMVXFAESA-N (-)-methyl jasmonate Chemical compound CC\C=C/C[C@@H]1[C@@H](CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-WQMVXFAESA-N 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
- 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 description 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 description 2
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 description 2
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 2
- 102000040650 (ribonucleotides)n+m Human genes 0.000 description 2
- 125000004515 1,2,4-thiadiazol-3-yl group Chemical group S1N=C(N=C1)* 0.000 description 2
- 125000004317 1,3,5-triazin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=N1 0.000 description 2
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 2
- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 description 2
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 2
- IUVLCCCHQJDWDT-UHFFFAOYSA-N 2-n-(1-methylsulfonylpropan-2-yl)benzene-1,2-dicarboxamide Chemical compound CS(=O)(=O)CC(C)NC(=O)C1=CC=CC=C1C(N)=O IUVLCCCHQJDWDT-UHFFFAOYSA-N 0.000 description 2
- CMWKITSNTDAEDT-UHFFFAOYSA-N 2-nitrobenzaldehyde Chemical class [O-][N+](=O)C1=CC=CC=C1C=O CMWKITSNTDAEDT-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 description 2
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 2
- 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 description 2
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 description 2
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 2
- 125000001397 3-pyrrolyl group Chemical group [H]N1C([H])=C([*])C([H])=C1[H] 0.000 description 2
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- SBUKOHLFHYSZNG-UHFFFAOYSA-N 4-dodecyl-2,6-dimethylmorpholine Chemical compound CCCCCCCCCCCCN1CC(C)OC(C)C1 SBUKOHLFHYSZNG-UHFFFAOYSA-N 0.000 description 2
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 2
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 125000006163 5-membered heteroaryl group Chemical group 0.000 description 2
- 125000006164 6-membered heteroaryl group Chemical group 0.000 description 2
- 239000001606 7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chroman-4-one Substances 0.000 description 2
- 239000005875 Acetamiprid Substances 0.000 description 2
- 102000012440 Acetylcholinesterase Human genes 0.000 description 2
- 108010022752 Acetylcholinesterase Proteins 0.000 description 2
- 241000223602 Alternaria alternata Species 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 241000187643 Amycolatopsis Species 0.000 description 2
- 244000144730 Amygdalus persica Species 0.000 description 2
- 241001530392 Aphos Species 0.000 description 2
- 244000003416 Asparagus officinalis Species 0.000 description 2
- 235000005340 Asparagus officinalis Nutrition 0.000 description 2
- 239000005724 Aureobasidium pullulans (strains DSM 14940 and DSM 14941) Substances 0.000 description 2
- 235000000832 Ayote Nutrition 0.000 description 2
- 241000193747 Bacillus firmus Species 0.000 description 2
- 239000005733 Bacillus pumilus QST 2808 Substances 0.000 description 2
- 239000005883 Beauveria bassiana strains ATCC 74040 and GHA Substances 0.000 description 2
- 239000005735 Benalaxyl-M Substances 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 2
- 241001450781 Bipolaris oryzae Species 0.000 description 2
- 241000190150 Bipolaris sorokiniana Species 0.000 description 2
- 241000228439 Bipolaris zeicola Species 0.000 description 2
- 239000005738 Bixafen Substances 0.000 description 2
- 241001480061 Blumeria graminis Species 0.000 description 2
- 241000589173 Bradyrhizobium Species 0.000 description 2
- 241000589174 Bradyrhizobium japonicum Species 0.000 description 2
- 235000011293 Brassica napus Nutrition 0.000 description 2
- 241000186146 Brevibacterium Species 0.000 description 2
- 238000009631 Broth culture Methods 0.000 description 2
- 240000001548 Camellia japonica Species 0.000 description 2
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 2
- 240000004160 Capsicum annuum Species 0.000 description 2
- 240000008384 Capsicum annuum var. annuum Species 0.000 description 2
- 235000007862 Capsicum baccatum Nutrition 0.000 description 2
- 239000005745 Captan Substances 0.000 description 2
- 239000005746 Carboxin Substances 0.000 description 2
- 241001290235 Ceratobasidium cereale Species 0.000 description 2
- 241000437818 Cercospora vignicola Species 0.000 description 2
- 108091006146 Channels Proteins 0.000 description 2
- 229920002101 Chitin Polymers 0.000 description 2
- 239000005654 Clofentezine Substances 0.000 description 2
- 241001149472 Clonostachys rosea Species 0.000 description 2
- DBPRUZCKPFOVDV-UHFFFAOYSA-N Clorprenaline hydrochloride Chemical compound O.Cl.CC(C)NCC(O)C1=CC=CC=C1Cl DBPRUZCKPFOVDV-UHFFFAOYSA-N 0.000 description 2
- 241001133184 Colletotrichum agaves Species 0.000 description 2
- 241000222201 Colletotrichum capsici Species 0.000 description 2
- 241001480650 Colletotrichum kahawae Species 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 241000223935 Cryptosporidium Species 0.000 description 2
- 235000009854 Cucurbita moschata Nutrition 0.000 description 2
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 2
- 241000223208 Curvularia Species 0.000 description 2
- 239000005889 Cyantraniliprole Substances 0.000 description 2
- 239000005758 Cyprodinil Substances 0.000 description 2
- 239000005892 Deltamethrin Substances 0.000 description 2
- 241000522190 Desmodium Species 0.000 description 2
- 239000005760 Difenoconazole Substances 0.000 description 2
- 235000001950 Elaeis guineensis Nutrition 0.000 description 2
- 244000127993 Elaeis melanococca Species 0.000 description 2
- 241001492222 Epicoccum Species 0.000 description 2
- 241000510928 Erysiphe necator Species 0.000 description 2
- 206010051814 Eschar Diseases 0.000 description 2
- 239000005657 Fenpyroximate Substances 0.000 description 2
- 239000005899 Fipronil Substances 0.000 description 2
- 239000005783 Fluopyram Substances 0.000 description 2
- 241000427940 Fusarium solani Species 0.000 description 2
- 239000005561 Glufosinate Substances 0.000 description 2
- 239000005562 Glyphosate Substances 0.000 description 2
- 244000286779 Hansenula anomala Species 0.000 description 2
- 239000005904 Helicoverpa armigera nucleopolyhedrovirus (HearNPV) Substances 0.000 description 2
- 241000255967 Helicoverpa zea Species 0.000 description 2
- 235000008694 Humulus lupulus Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 241000221931 Hypomyces rosellus Species 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- XMLSXPIVAXONDL-PLNGDYQASA-N Jasmone Chemical compound CC\C=C/CC1=C(C)CCC1=O XMLSXPIVAXONDL-PLNGDYQASA-N 0.000 description 2
- 241000193386 Lysinibacillus sphaericus Species 0.000 description 2
- 241001495426 Macrophomina phaseolina Species 0.000 description 2
- 241001344131 Magnaporthe grisea Species 0.000 description 2
- 235000011430 Malus pumila Nutrition 0.000 description 2
- 235000015103 Malus silvestris Nutrition 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 239000005802 Mancozeb Substances 0.000 description 2
- 241000223250 Metarhizium anisopliae Species 0.000 description 2
- 241001518729 Monilinia Species 0.000 description 2
- 241001459558 Monographella nivalis Species 0.000 description 2
- 241000235395 Mucor Species 0.000 description 2
- IUOKJNROJISWRO-UHFFFAOYSA-N N-(2-cyano-3-methylbutan-2-yl)-2-(2,4-dichlorophenoxy)propanamide Chemical compound CC(C)C(C)(C#N)NC(=O)C(C)OC1=CC=C(Cl)C=C1Cl IUOKJNROJISWRO-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 241001226034 Nectria <echinoderm> Species 0.000 description 2
- 241000221960 Neurospora Species 0.000 description 2
- ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 description 2
- 241000233654 Oomycetes Species 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000005813 Penconazole Substances 0.000 description 2
- 239000005815 Penflufen Substances 0.000 description 2
- 241001223281 Peronospora Species 0.000 description 2
- 241000047853 Phaeomoniella chlamydospora Species 0.000 description 2
- 241000440445 Phakopsora meibomiae Species 0.000 description 2
- 241000682645 Phakopsora pachyrhizi Species 0.000 description 2
- 241000222385 Phanerochaete Species 0.000 description 2
- 241000975369 Phoma betae Species 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000233614 Phytophthora Species 0.000 description 2
- 241000233616 Phytophthora capsici Species 0.000 description 2
- 241000233622 Phytophthora infestans Species 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 235000010582 Pisum sativum Nutrition 0.000 description 2
- 241000233626 Plasmopara Species 0.000 description 2
- 241001281803 Plasmopara viticola Species 0.000 description 2
- 241000317981 Podosphaera fuliginea Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 241000132152 Polymyxa Species 0.000 description 2
- 239000005820 Prochloraz Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- 241000087479 Pseudocercospora fijiensis Species 0.000 description 2
- 241000386899 Pseudocercospora vitis Species 0.000 description 2
- 241001281802 Pseudoperonospora Species 0.000 description 2
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 2
- 239000005828 Pyrimethanil Substances 0.000 description 2
- 241000918585 Pythium aphanidermatum Species 0.000 description 2
- 241001092473 Quillaja Species 0.000 description 2
- 235000009001 Quillaja saponaria Nutrition 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 241000813090 Rhizoctonia solani Species 0.000 description 2
- 241000220222 Rosaceae Species 0.000 description 2
- 241001299714 Rosellinia necatrix Species 0.000 description 2
- 241000332749 Setosphaeria turcica Species 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 235000002597 Solanum melongena Nutrition 0.000 description 2
- 244000061458 Solanum melongena Species 0.000 description 2
- 241001250070 Sporisorium reilianum Species 0.000 description 2
- 229930182558 Sterol Natural products 0.000 description 2
- 241000187395 Streptomyces microflavus Species 0.000 description 2
- 229940100389 Sulfonylurea Drugs 0.000 description 2
- 241000561282 Thielaviopsis basicola Species 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 241001460073 Trichoderma asperellum Species 0.000 description 2
- 239000005855 Trichoderma harzianum strains T-22 and ITEM 908 Substances 0.000 description 2
- 241001149558 Trichoderma virens Species 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 235000019714 Triticale Nutrition 0.000 description 2
- 241001106462 Ulmus Species 0.000 description 2
- 239000005863 Zoxamide Substances 0.000 description 2
- 230000036579 abiotic stress Effects 0.000 description 2
- 229940022698 acetylcholinesterase Drugs 0.000 description 2
- 125000004442 acylamino group Chemical group 0.000 description 2
- 230000010933 acylation Effects 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000007798 antifreeze agent Substances 0.000 description 2
- ONHBDDJJTDTLIR-UHFFFAOYSA-N azocyclotin Chemical compound C1CCCCC1[Sn](N1N=CN=C1)(C1CCCCC1)C1CCCCC1 ONHBDDJJTDTLIR-UHFFFAOYSA-N 0.000 description 2
- 229940005348 bacillus firmus Drugs 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- 235000021028 berry Nutrition 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 230000004790 biotic stress Effects 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 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 description 2
- 238000009395 breeding Methods 0.000 description 2
- 230000001488 breeding effect Effects 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- 229960003168 bronopol Drugs 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 229940117949 captan Drugs 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 125000004452 carbocyclyl group Chemical group 0.000 description 2
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 230000032823 cell division Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 description 2
- IVLCENBZDYVJPA-ARJAWSKDSA-N cis-Jasmone Natural products C\C=C/CC1=C(C)CCC1=O IVLCENBZDYVJPA-ARJAWSKDSA-N 0.000 description 2
- UXADOQPNKNTIHB-UHFFFAOYSA-N clofentezine Chemical compound ClC1=CC=CC=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 UXADOQPNKNTIHB-UHFFFAOYSA-N 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 235000018597 common camellia Nutrition 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 244000038559 crop plants Species 0.000 description 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 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 229960002483 decamethrin Drugs 0.000 description 2
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 2
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 description 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 2
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 2
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 2
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 235000013601 eggs Nutrition 0.000 description 2
- 239000003623 enhancer Substances 0.000 description 2
- 231100000333 eschar Toxicity 0.000 description 2
- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 2
- OPCRGEVPIBLWAY-QNRZBPGKSA-N ethyl (2E,4Z)-deca-2,4-dienoate Chemical compound CCCCC\C=C/C=C/C(=O)OCC OPCRGEVPIBLWAY-QNRZBPGKSA-N 0.000 description 2
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 229940013764 fipronil Drugs 0.000 description 2
- 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 description 2
- 239000000499 gel Substances 0.000 description 2
- 230000035784 germination Effects 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 229940097068 glyphosate Drugs 0.000 description 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000003906 humectant Substances 0.000 description 2
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 description 2
- 125000003037 imidazol-2-yl group Chemical group [H]N1C([*])=NC([H])=C1[H] 0.000 description 2
- 125000002140 imidazol-4-yl group Chemical group [H]N1C([H])=NC([*])=C1[H] 0.000 description 2
- 125000000336 imidazol-5-yl group Chemical group [H]N1C([H])=NC([H])=C1[*] 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- VRWKTAYJTKRVCU-UHFFFAOYSA-N iron(6+);hexacyanide Chemical compound [Fe+6].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] VRWKTAYJTKRVCU-UHFFFAOYSA-N 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- 125000004500 isothiazol-4-yl group Chemical group S1N=CC(=C1)* 0.000 description 2
- 125000004284 isoxazol-3-yl group Chemical group [H]C1=C([H])C(*)=NO1 0.000 description 2
- 125000004498 isoxazol-4-yl group Chemical group O1N=CC(=C1)* 0.000 description 2
- 125000004499 isoxazol-5-yl group Chemical group O1N=CC=C1* 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 230000001418 larval effect Effects 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 244000129185 maize Species 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 229950003442 methoprene Drugs 0.000 description 2
- GEWDNTWNSAZUDX-UHFFFAOYSA-N methyl 7-epi-jasmonate Natural products CCC=CCC1C(CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-UHFFFAOYSA-N 0.000 description 2
- 229960001952 metrifonate Drugs 0.000 description 2
- 108091088140 miR162 stem-loop Proteins 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- LWGJTAZLEJHCPA-UHFFFAOYSA-N n-(2-chloroethyl)-n-nitrosomorpholine-4-carboxamide Chemical compound ClCCN(N=O)C(=O)N1CCOCC1 LWGJTAZLEJHCPA-UHFFFAOYSA-N 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- DFPMSGMNTNDNHN-ZPHOTFPESA-N naringin Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]1[C@H](OC=2C=C3O[C@@H](CC(=O)C3=C(O)C=2)C=2C=CC(O)=CC=2)O[C@H](CO)[C@@H](O)[C@@H]1O DFPMSGMNTNDNHN-ZPHOTFPESA-N 0.000 description 2
- 229940052490 naringin Drugs 0.000 description 2
- 229930019673 naringin Natural products 0.000 description 2
- 239000005445 natural material Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000003865 nucleic acid synthesis inhibitor Substances 0.000 description 2
- 235000014571 nuts Nutrition 0.000 description 2
- 210000000056 organ Anatomy 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 125000004287 oxazol-2-yl group Chemical group [H]C1=C([H])N=C(*)O1 0.000 description 2
- 125000004304 oxazol-5-yl group Chemical group O1C=NC=C1* 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 2
- RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 229960000490 permethrin Drugs 0.000 description 2
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 2
- 230000000361 pesticidal effect Effects 0.000 description 2
- 239000004477 pesticide formulation type Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- 230000037039 plant physiology Effects 0.000 description 2
- 229920000867 polyelectrolyte Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 229940121649 protein inhibitor Drugs 0.000 description 2
- 239000012268 protein inhibitor Substances 0.000 description 2
- 235000015136 pumpkin Nutrition 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 description 2
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 description 2
- 125000004497 pyrazol-5-yl group Chemical group N1N=CC=C1* 0.000 description 2
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 2
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 2
- 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 description 2
- 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 2
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 2
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 description 2
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 description 2
- 229940044601 receptor agonist Drugs 0.000 description 2
- 239000000018 receptor agonist Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 201000005404 rubella Diseases 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 150000003432 sterols Chemical class 0.000 description 2
- 235000003702 sterols Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 description 2
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 2
- 239000004308 thiabendazole Substances 0.000 description 2
- 235000010296 thiabendazole Nutrition 0.000 description 2
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 2
- 229960004546 thiabendazole Drugs 0.000 description 2
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 description 2
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 2
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 description 2
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 2
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 2
- 241000701451 unidentified granulovirus Species 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- 230000009105 vegetative growth Effects 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 241000228158 x Triticosecale Species 0.000 description 2
- VSMOENVRRABVKN-UHFFFAOYSA-N (+/-)-matsutakeol Natural products CCCCCC(O)C=C VSMOENVRRABVKN-UHFFFAOYSA-N 0.000 description 1
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 1
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 description 1
- 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 description 1
- ZXQYGBMAQZUVMI-RDDWSQKMSA-N (1S)-cis-(alphaR)-cyhalothrin Chemical compound CC1(C)[C@H](\C=C(/Cl)C(F)(F)F)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-RDDWSQKMSA-N 0.000 description 1
- 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 description 1
- AGMMRUPNXPWLGF-AATRIKPKSA-N (2,3,5,6-tetrafluoro-4-methylphenyl)methyl 2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound CC1(C)C(/C=C/C)C1C(=O)OCC1=C(F)C(F)=C(C)C(F)=C1F AGMMRUPNXPWLGF-AATRIKPKSA-N 0.000 description 1
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 1
- WXBHKHTWAPLUSQ-UHFFFAOYSA-N (2-methyl-5-prop-2-ynylfuran-3-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=C(C)OC(CC#C)=C1 WXBHKHTWAPLUSQ-UHFFFAOYSA-N 0.000 description 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 description 1
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 1
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 1
- YCOMGIOWVNOOBC-RAPDCGKPSA-N (2e,13z)-octadeca-2,13-dien-1-ol Chemical compound CCCC\C=C/CCCCCCCCC\C=C\CO YCOMGIOWVNOOBC-RAPDCGKPSA-N 0.000 description 1
- CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 description 1
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 description 1
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 description 1
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 description 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 description 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 description 1
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 description 1
- BKBSMMUEEAWFRX-NBVRZTHBSA-N (E)-flumorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(F)=CC=1)=C\C(=O)N1CCOCC1 BKBSMMUEEAWFRX-NBVRZTHBSA-N 0.000 description 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- JERZEQUMJNCPRJ-KRWDZBQOSA-N (R)-mefentrifluconazole Chemical compound C([C@@](O)(C)C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)C(F)(F)F)N1C=NC=N1 JERZEQUMJNCPRJ-KRWDZBQOSA-N 0.000 description 1
- VSMOENVRRABVKN-QMMMGPOBSA-N (R)-oct-1-en-3-ol Chemical compound CCCCC[C@@H](O)C=C VSMOENVRRABVKN-QMMMGPOBSA-N 0.000 description 1
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 description 1
- RMOGWMIKYWRTKW-UONOGXRCSA-N (S,S)-paclobutrazol Chemical compound C([C@@H]([C@@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1 RMOGWMIKYWRTKW-UONOGXRCSA-N 0.000 description 1
- 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 description 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 description 1
- QKTFNIWYLYTNIS-ALCCZGGFSA-N (z)-tetradec-3-ene Chemical compound CCCCCCCCCC\C=C/CC QKTFNIWYLYTNIS-ALCCZGGFSA-N 0.000 description 1
- XBCKTJDKWPZLJH-ZUPCBTBPSA-N (z,2e)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-n,3-dimethylpent-3-enamide Chemical compound N1=C(OC\C=C(\C)/C(=N\OC)/C(=O)NC)C=CN1C1=CC=C(Cl)C=C1 XBCKTJDKWPZLJH-ZUPCBTBPSA-N 0.000 description 1
- 125000001766 1,2,4-oxadiazol-3-yl group Chemical group [H]C1=NC(*)=NO1 0.000 description 1
- 125000004505 1,2,4-oxadiazol-5-yl group Chemical group O1N=CN=C1* 0.000 description 1
- 125000004516 1,2,4-thiadiazol-5-yl group Chemical group S1N=CN=C1* 0.000 description 1
- 125000001305 1,2,4-triazol-3-yl group Chemical group [H]N1N=C([*])N=C1[H] 0.000 description 1
- 125000001414 1,2,4-triazol-5-yl group Chemical group [H]N1N=C([H])N=C1[*] 0.000 description 1
- KANAPVJGZDNSCZ-UHFFFAOYSA-N 1,2-benzothiazole 1-oxide Chemical class C1=CC=C2S(=O)N=CC2=C1 KANAPVJGZDNSCZ-UHFFFAOYSA-N 0.000 description 1
- LRANPJDWHYRCER-UHFFFAOYSA-N 1,2-diazepine Chemical compound N1C=CC=CC=N1 LRANPJDWHYRCER-UHFFFAOYSA-N 0.000 description 1
- 125000005918 1,2-dimethylbutyl group Chemical group 0.000 description 1
- CXWGKAYMVASWDQ-UHFFFAOYSA-N 1,2-dithiane Chemical compound C1CCSSC1 CXWGKAYMVASWDQ-UHFFFAOYSA-N 0.000 description 1
- PZJHKKSBOGBKRL-UHFFFAOYSA-N 1,2-oxazolidine-2-carboxamide Chemical compound NC(=O)N1CCCO1 PZJHKKSBOGBKRL-UHFFFAOYSA-N 0.000 description 1
- VUWCWMOCWKCZTA-UHFFFAOYSA-N 1,2-thiazol-4-one Chemical class O=C1CSN=C1 VUWCWMOCWKCZTA-UHFFFAOYSA-N 0.000 description 1
- FXVNBZGTAWLLNE-UHFFFAOYSA-N 1,3-thiazole;zinc Chemical compound [Zn].C1=CSC=N1 FXVNBZGTAWLLNE-UHFFFAOYSA-N 0.000 description 1
- NOLHRFLIXVQPSZ-UHFFFAOYSA-N 1,3-thiazolidin-4-one Chemical compound O=C1CSCN1 NOLHRFLIXVQPSZ-UHFFFAOYSA-N 0.000 description 1
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 description 1
- SWLKEFRRPJMDIT-UHFFFAOYSA-N 1-(3-chloro-2-methylphenyl)-3-[[(4-chlorophenyl)-[4-[methyl(methylsulfonyl)amino]phenyl]methylidene]amino]urea Chemical compound CN(c1ccc(cc1)C(=NNC(=O)Nc1cccc(Cl)c1C)c1ccc(Cl)cc1)S(C)(=O)=O SWLKEFRRPJMDIT-UHFFFAOYSA-N 0.000 description 1
- GXVOAHIRFOAGLK-UHFFFAOYSA-N 1-(4,4-difluorocyclohexyl)-N,5-dimethyl-N-pyridazin-4-ylpyrazole-4-carboxamide Chemical compound FC1(CCC(CC1)N1N=CC(=C1C)C(=O)N(C1=CN=NC=C1)C)F GXVOAHIRFOAGLK-UHFFFAOYSA-N 0.000 description 1
- FMFZDPXBNCGGGI-UHFFFAOYSA-N 1-(4,4-difluorocyclohexyl)-N-ethyl-5-methyl-N-pyridazin-4-ylpyrazole-4-carboxamide Chemical compound FC1(CCC(CC1)N1N=CC(=C1C)C(=O)N(C1=CN=NC=C1)CC)F FMFZDPXBNCGGGI-UHFFFAOYSA-N 0.000 description 1
- IHGSAQHSAGRWNI-UHFFFAOYSA-N 1-(4-bromophenyl)-2,2,2-trifluoroethanone Chemical compound FC(F)(F)C(=O)C1=CC=C(Br)C=C1 IHGSAQHSAGRWNI-UHFFFAOYSA-N 0.000 description 1
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 1
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 description 1
- KEBVBTRIOHKRMU-UHFFFAOYSA-N 1-[(6-chloropyridin-3-yl)methyl]-5-methoxy-7-methyl-8-nitro-3,5,6,7-tetrahydro-2h-imidazo[1,2-a]pyridine Chemical compound C1CN2C(OC)CC(C)C([N+]([O-])=O)=C2N1CC1=CC=C(Cl)N=C1 KEBVBTRIOHKRMU-UHFFFAOYSA-N 0.000 description 1
- SJFPJGQQUXJYPK-UHFFFAOYSA-N 1-[(6-chloropyridin-3-yl)methyl]-7-methyl-8-nitro-3,5,6,7-tetrahydro-2h-imidazo[1,2-a]pyridin-5-ol Chemical compound C12=C([N+]([O-])=O)C(C)CC(O)N2CCN1CC1=CC=C(Cl)N=C1 SJFPJGQQUXJYPK-UHFFFAOYSA-N 0.000 description 1
- MOTGVPXRLDDMSK-UHFFFAOYSA-N 1-[(6-chloropyridin-3-yl)methyl]-7-methyl-8-nitro-5-propoxy-3,5,6,7-tetrahydro-2h-imidazo[1,2-a]pyridine Chemical compound C1CN2C(OCCC)CC(C)C([N+]([O-])=O)=C2N1CC1=CC=C(Cl)N=C1 MOTGVPXRLDDMSK-UHFFFAOYSA-N 0.000 description 1
- CVGWUIISHQTYPZ-UHFFFAOYSA-N 1-[1-(1-cyanocyclopropyl)ethyl]-N,5-dimethyl-N-pyridazin-4-ylpyrazole-4-carboxamide Chemical compound C(#N)C1(CC1)C(C)N1N=CC(=C1C)C(=O)N(C1=CN=NC=C1)C CVGWUIISHQTYPZ-UHFFFAOYSA-N 0.000 description 1
- QUHCCINTOSIBEB-UHFFFAOYSA-N 1-[1-(1-cyanocyclopropyl)ethyl]-n-ethyl-5-methyl-n-pyridazin-4-ylpyrazole-4-carboxamide Chemical compound C=1C=NN=CC=1N(CC)C(=O)C(=C1C)C=NN1C(C)C1(C#N)CC1 QUHCCINTOSIBEB-UHFFFAOYSA-N 0.000 description 1
- HVQHXBNMBZJPLK-UHFFFAOYSA-N 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-[(2-methylprop-2-en-1-yl)amino]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound CC(=C)CNC1=C([S+]([O-])C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl HVQHXBNMBZJPLK-UHFFFAOYSA-N 0.000 description 1
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 1
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 description 1
- 125000006083 1-bromoethyl group Chemical group 0.000 description 1
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000004972 1-butynyl group Chemical group [H]C([H])([H])C([H])([H])C#C* 0.000 description 1
- 125000001478 1-chloroethyl group Chemical group [H]C([H])([H])C([H])(Cl)* 0.000 description 1
- 125000006218 1-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004776 1-fluoroethyl group Chemical group [H]C([H])([H])C([H])(F)* 0.000 description 1
- 125000006019 1-methyl-1-propenyl group Chemical group 0.000 description 1
- 125000006021 1-methyl-2-propenyl group Chemical group 0.000 description 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 description 1
- 125000006018 1-methyl-ethenyl group Chemical group 0.000 description 1
- NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 1
- 125000006017 1-propenyl group Chemical group 0.000 description 1
- JVVRJMXHNUAPHW-UHFFFAOYSA-N 1h-pyrazol-5-amine Chemical compound NC=1C=CNN=1 JVVRJMXHNUAPHW-UHFFFAOYSA-N 0.000 description 1
- ZVXKYWHJBYIYNI-UHFFFAOYSA-N 1h-pyrazole-4-carboxamide Chemical compound NC(=O)C=1C=NNC=1 ZVXKYWHJBYIYNI-UHFFFAOYSA-N 0.000 description 1
- UMPSXRYVXUPCOS-UHFFFAOYSA-N 2,3-dichlorophenol Chemical compound OC1=CC=CC(Cl)=C1Cl UMPSXRYVXUPCOS-UHFFFAOYSA-N 0.000 description 1
- NFTOEHBFQROATQ-UHFFFAOYSA-N 2,3-dihydrofuran-5-carboxylic acid Chemical compound OC(=O)C1=CCCO1 NFTOEHBFQROATQ-UHFFFAOYSA-N 0.000 description 1
- SCLSKOXHUCZTEI-UHFFFAOYSA-N 2,3-dihydropyrazol-1-yl Chemical group C1C=[C]N=N1 SCLSKOXHUCZTEI-UHFFFAOYSA-N 0.000 description 1
- DFPIGVDNBRPLIL-UHFFFAOYSA-N 2,3-dimethyl-5-(4-methylphenyl)-3-pyridin-3-yl-1,2-oxazolidine Chemical compound CN1OC(C=2C=CC(C)=CC=2)CC1(C)C1=CC=CN=C1 DFPIGVDNBRPLIL-UHFFFAOYSA-N 0.000 description 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 description 1
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 description 1
- NCEHACHJIXJSPD-UHFFFAOYSA-N 2-(2,4-difluorophenyl)-1,1-difluoro-3-(tetrazol-1-yl)-1-[5-[4-(trifluoromethoxy)phenyl]pyridin-2-yl]propan-2-ol Chemical compound C=1C=C(F)C=C(F)C=1C(C(F)(F)C=1N=CC(=CC=1)C=1C=CC(OC(F)(F)F)=CC=1)(O)CN1C=NN=N1 NCEHACHJIXJSPD-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- AVOKNZWKPLQRGP-UHFFFAOYSA-N 2-(3-ethylsulfonylpyridin-2-yl)-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine Chemical compound CCS(=O)(=O)C1=CC=CN=C1C1=NC2=CC(C(F)(F)F)=CN=C2N1C AVOKNZWKPLQRGP-UHFFFAOYSA-N 0.000 description 1
- SCFZORZKZIEAIV-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-2-methoxy-n-propylacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(OC)C(=O)NCCC)=CC(C)=C21 SCFZORZKZIEAIV-UHFFFAOYSA-N 0.000 description 1
- ZZXLGPONYSOLKU-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-2-methylsulfanyl-n-propylacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(C(=O)NCCC)SC)=CC(C)=C21 ZZXLGPONYSOLKU-UHFFFAOYSA-N 0.000 description 1
- LQIVUKUXIHENQE-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-n-(2-fluoroethyl)-2-methoxyacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(OC)C(=O)NCCF)=CC(C)=C21 LQIVUKUXIHENQE-UHFFFAOYSA-N 0.000 description 1
- FTROJHYITVGKDZ-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-n-(2-fluoroethyl)-2-methylsulfanylacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(SC)C(=O)NCCF)=CC(C)=C21 FTROJHYITVGKDZ-UHFFFAOYSA-N 0.000 description 1
- OMKJEAMIPWDWAL-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-n-propylbutanamide Chemical compound N1=CC(C#C)=CC2=CC(OC(CC)C(=O)NCCC)=CC(C)=C21 OMKJEAMIPWDWAL-UHFFFAOYSA-N 0.000 description 1
- HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- IHASCEQSGGMLRB-UHFFFAOYSA-N 2-(4-chlorophenyl)-n-[4-(3,4-dimethoxyphenyl)-1,2-oxazol-5-yl]-2-prop-2-ynoxyacetamide Chemical compound C1=C(OC)C(OC)=CC=C1C1=C(NC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)ON=C1 IHASCEQSGGMLRB-UHFFFAOYSA-N 0.000 description 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 description 1
- NGLCOYIAJMJYQI-UHFFFAOYSA-N 2-(4-methoxyiminocyclohexyl)-2-(3,3,3-trifluoropropylsulfonyl)acetonitrile Chemical compound CON=C1CCC(C(C#N)S(=O)(=O)CCC(F)(F)F)CC1 NGLCOYIAJMJYQI-UHFFFAOYSA-N 0.000 description 1
- LMBOBAWFGUTZRU-UHFFFAOYSA-N 2-(5-fluoropyridin-3-yl)-5-(6-pyrimidin-2-ylpyridin-2-yl)-1,3-thiazole Chemical compound FC1=CN=CC(C=2SC(=CN=2)C=2N=C(C=CC=2)C=2N=CC=CN=2)=C1 LMBOBAWFGUTZRU-UHFFFAOYSA-N 0.000 description 1
- AGVACZYQCJRDQE-UHFFFAOYSA-N 2-(6-benzylpyridin-2-yl)quinazoline Chemical compound C=1C=CC(C=2N=C3C=CC=CC3=CN=2)=NC=1CC1=CC=CC=C1 AGVACZYQCJRDQE-UHFFFAOYSA-N 0.000 description 1
- WBNYTAFVEZEKBB-UHFFFAOYSA-N 2-(6-bromo-3-ethylsulfonylimidazo[1,2-a]pyridin-2-yl)-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine Chemical compound BrC=1C=CC=2N(C=1)C(=C(N=2)C1=NC=2C(=NC=C(C=2)C(F)(F)F)N1C)S(=O)(=O)CC WBNYTAFVEZEKBB-UHFFFAOYSA-N 0.000 description 1
- HIJCWWNABYNXOO-UHFFFAOYSA-N 2-(6-chloro-3-ethylsulfonylimidazo[1,2-a]pyridin-2-yl)-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine Chemical compound ClC=1C=CC=2N(C=1)C(=C(N=2)C1=NC=2C(=NC=C(C=2)C(F)(F)F)N1C)S(=O)(=O)CC HIJCWWNABYNXOO-UHFFFAOYSA-N 0.000 description 1
- KAQJMEHRXVENSF-UHFFFAOYSA-N 2-(trichloromethyl)pyridine Chemical compound ClC(Cl)(Cl)C1=CC=CC=N1 KAQJMEHRXVENSF-UHFFFAOYSA-N 0.000 description 1
- WOXFMYVTSLAQMO-UHFFFAOYSA-N 2-Pyridinemethanamine Chemical compound NCC1=CC=CC=N1 WOXFMYVTSLAQMO-UHFFFAOYSA-N 0.000 description 1
- UYJGFPYLYFSNSS-UHFFFAOYSA-N 2-[(4-chlorophenyl)methoxy]-5-fluoropyrimidin-4-amine Chemical compound C1=C(F)C(N)=NC(OCC=2C=CC(Cl)=CC=2)=N1 UYJGFPYLYFSNSS-UHFFFAOYSA-N 0.000 description 1
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 description 1
- LEVDFRLAITVRQI-UHFFFAOYSA-N 2-[3-ethylsulfonyl-5-(trifluoromethyl)pyridin-2-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine Chemical compound CCS(=O)(=O)C1=CC(C(F)(F)F)=CN=C1C1=NC2=CC(C(F)(F)F)=CN=C2N1C LEVDFRLAITVRQI-UHFFFAOYSA-N 0.000 description 1
- QWBPODPZJOVEID-UHFFFAOYSA-N 2-[3-ethylsulfonyl-6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine Chemical compound C(C)S(=O)(=O)C1=C(N=C2N1C=C(C=C2)C(F)(F)F)C1=NC=2C(=NC=C(C=2)C(F)(F)F)N1C QWBPODPZJOVEID-UHFFFAOYSA-N 0.000 description 1
- QOYIVLGICMMIGT-UHFFFAOYSA-N 2-[3-ethylsulfonyl-7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridine Chemical compound C(C)S(=O)(=O)C1=C(N=C2N1C=CC(=C2)C(F)(F)F)C1=NC2=C(C=NC(=C2)C(F)(F)F)N1C QOYIVLGICMMIGT-UHFFFAOYSA-N 0.000 description 1
- FCKSUIXOGYGAIB-UHFFFAOYSA-N 2-[3-ethylsulfonyl-7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]-3-methyl-6-(trifluoromethylsulfinyl)imidazo[4,5-b]pyridine Chemical compound C(C)S(=O)(=O)C1=C(N=C2N1C=CC(=C2)C(F)(F)F)C1=NC=2C(=NC=C(C=2)S(=O)C(F)(F)F)N1C FCKSUIXOGYGAIB-UHFFFAOYSA-N 0.000 description 1
- KMVXHZMDXIJJRW-UHFFFAOYSA-N 2-[3-ethylsulfonyl-8-fluoro-6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine Chemical compound C(C)S(=O)(=O)C1=C(N=C2N1C=C(C=C2F)C(F)(F)F)C1=NC=2C(=NC=C(C=2)C(F)(F)F)N1C KMVXHZMDXIJJRW-UHFFFAOYSA-N 0.000 description 1
- BOTNFCTYKJBUMU-UHFFFAOYSA-N 2-[4-(2-methylpropyl)piperazin-4-ium-1-yl]-2-oxoacetate Chemical compound CC(C)C[NH+]1CCN(C(=O)C([O-])=O)CC1 BOTNFCTYKJBUMU-UHFFFAOYSA-N 0.000 description 1
- YANWOMFJWXJQEF-UHFFFAOYSA-N 2-[6-(3-fluoro-4-methoxyphenyl)-5-methylpyridin-2-yl]quinazoline Chemical compound C1=C(F)C(OC)=CC=C1C1=NC(C=2N=C3C=CC=CC3=CN=2)=CC=C1C YANWOMFJWXJQEF-UHFFFAOYSA-N 0.000 description 1
- QCBWUXVEKBGXGM-UHFFFAOYSA-N 2-[6-(4-bromophenoxy)-2-(trifluoromethyl)pyridin-3-yl]-1-(1,2,4-triazol-1-yl)propan-2-ol Chemical compound BrC1=CC=C(OC2=CC=C(C(=N2)C(F)(F)F)C(CN2N=CN=C2)(C)O)C=C1 QCBWUXVEKBGXGM-UHFFFAOYSA-N 0.000 description 1
- NGPCLTYABBZNEC-UHFFFAOYSA-N 2-[6-(4-chlorophenoxy)-2-(trifluoromethyl)pyridin-3-yl]-1-(1,2,4-triazol-1-yl)propan-2-ol Chemical compound ClC1=CC=C(OC2=CC=C(C(=N2)C(F)(F)F)C(CN2N=CN=C2)(C)O)C=C1 NGPCLTYABBZNEC-UHFFFAOYSA-N 0.000 description 1
- PVTHJAPFENJVNC-UHFFFAOYSA-N 2-amino-2-[5-amino-2-methyl-6-(2,3,4,5,6-pentahydroxycyclohexyl)oxyoxan-3-yl]iminoacetic acid Chemical compound NC1CC(N=C(N)C(O)=O)C(C)OC1OC1C(O)C(O)C(O)C(O)C1O PVTHJAPFENJVNC-UHFFFAOYSA-N 0.000 description 1
- DHVLDKHFGIVEIP-UHFFFAOYSA-N 2-bromo-2-(bromomethyl)pentanedinitrile Chemical compound BrCC(Br)(C#N)CCC#N DHVLDKHFGIVEIP-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000000069 2-butynyl group Chemical group [H]C([H])([H])C#CC([H])([H])* 0.000 description 1
- 125000004780 2-chloro-2,2-difluoroethyl group Chemical group [H]C([H])(*)C(F)(F)Cl 0.000 description 1
- 125000004779 2-chloro-2-fluoroethyl group Chemical group [H]C([H])(*)C([H])(F)Cl 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- AWSZRJQNBMEZOI-UHFFFAOYSA-N 2-methoxyethyl 2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-[2-(trifluoromethyl)phenyl]propanoate Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(C#N)(C(=O)OCCOC)C(=O)C1=CC=CC=C1C(F)(F)F AWSZRJQNBMEZOI-UHFFFAOYSA-N 0.000 description 1
- 125000006020 2-methyl-1-propenyl group Chemical group 0.000 description 1
- 125000006022 2-methyl-2-propenyl group Chemical group 0.000 description 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- NNWTYSZJLCDUDC-UHFFFAOYSA-N 2-propoxyquinoline Chemical compound C1=CC=CC2=NC(OCCC)=CC=C21 NNWTYSZJLCDUDC-UHFFFAOYSA-N 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- KRYQDBFHAFVBSW-UHFFFAOYSA-N 2-pyridin-3-yl-5-(6-pyrimidin-2-ylpyridin-2-yl)-1,3-thiazole Chemical compound C=1N=C(C=2C=NC=CC=2)SC=1C(N=1)=CC=CC=1C1=NC=CC=N1 KRYQDBFHAFVBSW-UHFFFAOYSA-N 0.000 description 1
- 125000004485 2-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])C1([H])* 0.000 description 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 description 1
- ABOOPXYCKNFDNJ-UHFFFAOYSA-N 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-UHFFFAOYSA-N 0.000 description 1
- AZSNMRSAGSSBNP-UHFFFAOYSA-N 22,23-dihydroavermectin B1a Natural products C1CC(C)C(C(C)CC)OC21OC(CC=C(C)C(OC1OC(C)C(OC3OC(C)C(O)C(OC)C3)C(OC)C1)C(C)C=CC=C1C3(C(C(=O)O4)C=C(C)C(O)C3OC1)O)CC4C2 AZSNMRSAGSSBNP-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- 125000004011 3 membered carbocyclic group Chemical group 0.000 description 1
- YPUFJIJQDMKJHE-UHFFFAOYSA-N 3,4,5-trifluoropyridin-2-amine Chemical compound NC1=NC=C(F)C(F)=C1F YPUFJIJQDMKJHE-UHFFFAOYSA-N 0.000 description 1
- GXORHMWHEXWRDU-UHFFFAOYSA-N 3,4-dihydrooxazol-5-yl Chemical group C1[N-]C[O+]=C1 GXORHMWHEXWRDU-UHFFFAOYSA-N 0.000 description 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 1
- SWBHWUYHHJCADA-UHFFFAOYSA-N 3-(2-chlorophenyl)-6-(2,6-difluorophenyl)-1,2,4,5-tetrazine Chemical compound FC1=CC=CC(F)=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 SWBHWUYHHJCADA-UHFFFAOYSA-N 0.000 description 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 description 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 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- 125000000474 3-butynyl group Chemical group [H]C#CC([H])([H])C([H])([H])* 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- HDKWFBCPLKNOCK-SFHVURJKSA-N 3-methyl-n-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-5-[(5s)-5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]thiophene-2-carboxamide Chemical compound S1C(C(=O)NCC(=O)NCC(F)(F)F)=C(C)C=C1C1=NO[C@](C(F)(F)F)(C=2C=C(Cl)C(Cl)=C(Cl)C=2)C1 HDKWFBCPLKNOCK-SFHVURJKSA-N 0.000 description 1
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- QBNCGBJHGBGHLS-IYUNJCAYSA-N 3E,13Z-Octadecadien-1-ol Chemical compound CCCC\C=C/CCCCCCCC\C=C\CCO QBNCGBJHGBGHLS-IYUNJCAYSA-N 0.000 description 1
- HWPJPNQEVWTZSJ-XBZOLNABSA-N 3E,8Z,11Z-Tetradecatrienyl acetate Chemical compound CC\C=C/C\C=C/CCC\C=C\CCOC(C)=O HWPJPNQEVWTZSJ-XBZOLNABSA-N 0.000 description 1
- 125000001845 4 membered carbocyclic group Chemical group 0.000 description 1
- NMWKWBPNKPGATC-UHFFFAOYSA-N 4,5,6,7-tetrachloro-2-benzofuran-1(3H)-one Chemical compound ClC1=C(Cl)C(Cl)=C2COC(=O)C2=C1Cl NMWKWBPNKPGATC-UHFFFAOYSA-N 0.000 description 1
- JPQMWVUHLNFHSH-UHFFFAOYSA-N 4,5,6-trifluoro-2-phenylpyrimidine Chemical compound FC1=C(C(=NC(=N1)C1=CC=CC=C1)F)F JPQMWVUHLNFHSH-UHFFFAOYSA-N 0.000 description 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- LBGMYUQCXJJLIR-UHFFFAOYSA-N 4-(2-bromo-4-fluorophenyl)-n-(2-chloro-6-fluorophenyl)-2,5-dimethylpyrazol-3-amine Chemical compound C=1C=C(F)C=C(Br)C=1C=1C(C)=NN(C)C=1NC1=C(F)C=CC=C1Cl LBGMYUQCXJJLIR-UHFFFAOYSA-N 0.000 description 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 description 1
- KZOZKFJGERLOJN-UHFFFAOYSA-N 4-({6-[2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(5-sulfanyl-1H-1,2,4-triazol-1-yl)propyl]pyridin-3-yl}oxy)benzonitrile Chemical compound FC1=C(C=CC(=C1)F)C(C(F)(F)C1=CC=C(C=N1)OC1=CC=C(C#N)C=C1)(CN1N=CNC1=S)O KZOZKFJGERLOJN-UHFFFAOYSA-N 0.000 description 1
- CUSXUSVGOOSADT-UHFFFAOYSA-N 4-[1-[2-[3,5-bis(difluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)pyridine-2-carboxamide Chemical compound FC(C1=NN(C(=C1)C(F)F)CC(=O)N1CCC(CC1)C1=CC(=NC=C1)C(=O)NC1CCCC2=CC=CC=C12)F CUSXUSVGOOSADT-UHFFFAOYSA-N 0.000 description 1
- PNICFNRAKHFRHN-UHFFFAOYSA-N 4-[1-[2-[3,5-bis(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)pyridine-2-carboxamide Chemical compound FC(C1=NN(C(=C1)C(F)(F)F)CC(=O)N1CCC(CC1)C1=CC(=NC=C1)C(=O)NC1CCCC2=CC=CC=C12)(F)F PNICFNRAKHFRHN-UHFFFAOYSA-N 0.000 description 1
- NSLNLNXAEPBGRV-UHFFFAOYSA-N 4-[1-[2-[3-(difluoromethyl)-5-(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)pyridine-2-carboxamide Chemical compound FC(C1=NN(C(=C1)C(F)(F)F)CC(=O)N1CCC(CC1)C1=CC(=NC=C1)C(=O)NC1CCCC2=CC=CC=C12)F NSLNLNXAEPBGRV-UHFFFAOYSA-N 0.000 description 1
- OEZNWKGNYIKMOI-UHFFFAOYSA-N 4-[1-[2-[3-(difluoromethyl)-5-methylpyrazol-1-yl]acetyl]piperidin-4-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)pyridine-2-carboxamide Chemical compound FC(C1=NN(C(=C1)C)CC(=O)N1CCC(CC1)C1=CC(=NC=C1)C(=O)NC1CCCC2=CC=CC=C12)F OEZNWKGNYIKMOI-UHFFFAOYSA-N 0.000 description 1
- SUDKTHLYEGJVKF-UHFFFAOYSA-N 4-[1-[2-[5-(difluoromethyl)-3-(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)pyridine-2-carboxamide Chemical compound FC(C1=CC(=NN1CC(=O)N1CCC(CC1)C1=CC(=NC=C1)C(=O)NC1CCCC2=CC=CC=C12)C(F)(F)F)F SUDKTHLYEGJVKF-UHFFFAOYSA-N 0.000 description 1
- MLUYQAXGWMNECN-UHFFFAOYSA-N 4-[1-[2-[5-cyclopropyl-3-(difluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)pyridine-2-carboxamide Chemical compound C1(CC1)C1=CC(=NN1CC(=O)N1CCC(CC1)C1=CC(=NC=C1)C(=O)NC1CCCC2=CC=CC=C12)C(F)F MLUYQAXGWMNECN-UHFFFAOYSA-N 0.000 description 1
- SYTNGALGRYRILA-UHFFFAOYSA-N 4-[1-[2-[5-cyclopropyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)pyridine-2-carboxamide Chemical compound C1(CC1)C1=CC(=NN1CC(=O)N1CCC(CC1)C1=CC(=NC=C1)C(=O)NC1CCCC2=CC=CC=C12)C(F)(F)F SYTNGALGRYRILA-UHFFFAOYSA-N 0.000 description 1
- GGCKILCJTFONPS-UHFFFAOYSA-N 4-[1-[2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-n-(1,2,3,4-tetrahydronaphthalen-1-yl)pyridine-2-carboxamide Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2C=C(N=CC=2)C(=O)NC2C3=CC=CC=C3CCC2)CC1 GGCKILCJTFONPS-UHFFFAOYSA-N 0.000 description 1
- JTCSEWBIRWUSAV-UHFFFAOYSA-N 4-[6-[2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(1,2,4-triazol-1-yl)propyl]pyridin-3-yl]oxybenzonitrile Chemical compound FC1=C(C=CC(=C1)F)C(C(F)(F)C1=CC=C(C=N1)OC1=CC=C(C#N)C=C1)(CN1N=CN=C1)O JTCSEWBIRWUSAV-UHFFFAOYSA-N 0.000 description 1
- VFYIDGHLULLRBH-UHFFFAOYSA-N 4-cyano-3-[(4-cyano-2-methylbenzoyl)amino]-n-[2,6-dichloro-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]-2-fluorobenzamide Chemical compound CC1=CC(C#N)=CC=C1C(=O)NC1=C(F)C(C(=O)NC=2C(=CC(=CC=2Cl)C(F)(C(F)(F)F)C(F)(F)C(F)(F)F)Cl)=CC=C1C#N VFYIDGHLULLRBH-UHFFFAOYSA-N 0.000 description 1
- CSJFAXFICOCFLH-UHFFFAOYSA-N 4-cyano-n-[2-cyano-5-[[2,6-dibromo-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]carbamoyl]phenyl]-2-methylbenzamide Chemical compound CC1=CC(C#N)=CC=C1C(=O)NC1=CC(C(=O)NC=2C(=CC(=CC=2Br)C(F)(C(F)(F)F)C(F)(F)C(F)(F)F)Br)=CC=C1C#N CSJFAXFICOCFLH-UHFFFAOYSA-N 0.000 description 1
- REQCFOSCPFWLHT-UHFFFAOYSA-N 4-cyano-n-[2-cyano-5-[[2,6-dichloro-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]carbamoyl]phenyl]-2-methylbenzamide Chemical compound CC1=CC(C#N)=CC=C1C(=O)NC1=CC(C(=O)NC=2C(=CC(=CC=2Cl)C(F)(C(F)(F)F)C(F)(F)C(F)(F)F)Cl)=CC=C1C#N REQCFOSCPFWLHT-UHFFFAOYSA-N 0.000 description 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 description 1
- HQAMEPONHQKVKQ-UHFFFAOYSA-N 4-cyclopropyl-n-(2,4-dimethoxyphenyl)thiadiazole-5-carboxamide Chemical compound COC1=CC(OC)=CC=C1NC(=O)C1=C(C2CC2)N=NS1 HQAMEPONHQKVKQ-UHFFFAOYSA-N 0.000 description 1
- PGYDGBCATBINCB-UHFFFAOYSA-N 4-diethoxyphosphoryl-n,n-dimethylaniline Chemical compound CCOP(=O)(OCC)C1=CC=C(N(C)C)C=C1 PGYDGBCATBINCB-UHFFFAOYSA-N 0.000 description 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 125000004487 4-tetrahydropyranyl group Chemical group [H]C1([H])OC([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001054 5 membered carbocyclic group Chemical group 0.000 description 1
- AWQSAIIDOMEEOD-UHFFFAOYSA-N 5,5-Dimethyl-4-(3-oxobutyl)dihydro-2(3H)-furanone Chemical compound CC(=O)CCC1CC(=O)OC1(C)C AWQSAIIDOMEEOD-UHFFFAOYSA-N 0.000 description 1
- HQJIHVZTLDUUBP-UHFFFAOYSA-N 5-[6-(1,3-dioxan-2-yl)pyridin-2-yl]-2-pyridin-3-yl-1,3-thiazole Chemical compound O1CCCOC1C1=CC=CC(C=2SC(=NC=2)C=2C=NC=CC=2)=N1 HQJIHVZTLDUUBP-UHFFFAOYSA-N 0.000 description 1
- ONILAONOGQYBHW-UHFFFAOYSA-N 5-bromo-n-[2,4-dichloro-6-(methylcarbamoyl)phenyl]-2-(3,5-dichloropyridin-2-yl)pyrazole-3-carboxamide Chemical compound CNC(=O)C1=CC(Cl)=CC(Cl)=C1NC(=O)C1=CC(Br)=NN1C1=NC=C(Cl)C=C1Cl ONILAONOGQYBHW-UHFFFAOYSA-N 0.000 description 1
- XJFIKRXIJXAJGH-UHFFFAOYSA-N 5-chloro-1,3-dihydroimidazo[4,5-b]pyridin-2-one Chemical group ClC1=CC=C2NC(=O)NC2=N1 XJFIKRXIJXAJGH-UHFFFAOYSA-N 0.000 description 1
- ZGBKIRCRHOIXAN-UHFFFAOYSA-N 5-chloro-1-(4,6-dimethoxypyrimidin-2-yl)-2-methylbenzimidazole Chemical compound COC1=CC(OC)=NC(N2C3=CC=C(Cl)C=C3N=C2C)=N1 ZGBKIRCRHOIXAN-UHFFFAOYSA-N 0.000 description 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 description 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 description 1
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 description 1
- 125000004008 6 membered carbocyclic group Chemical group 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- SXCDAEFYAJTNJF-YURISSCBSA-N 7Z,11Z,13E-Hexadecatrienal Chemical compound CC\C=C\C=C/CC\C=C/CCCCCC=O SXCDAEFYAJTNJF-YURISSCBSA-N 0.000 description 1
- ZFQMGOCRWDJUCX-HJWRWDBZSA-N 7Z-Tetradecen-2-one Chemical compound CCCCCC\C=C/CCCCC(C)=O ZFQMGOCRWDJUCX-HJWRWDBZSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- PFDRCQPNBZLTJQ-UHFFFAOYSA-N 8-fluoro-3-iodoquinoline Chemical compound IC1=CN=C2C(F)=CC=CC2=C1 PFDRCQPNBZLTJQ-UHFFFAOYSA-N 0.000 description 1
- SPBDXSGPUHCETR-JFUDTMANSA-N 8883yp2r6d Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O[C@@H]([C@@H](C)CC4)C(C)C)O3)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1C[C@H](C)[C@@H]([C@@H](C)CC)O[C@@]21O[C@H](C\C=C(C)\[C@@H](O[C@@H]1O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 SPBDXSGPUHCETR-JFUDTMANSA-N 0.000 description 1
- ZZGJZGSVLNSDPG-FDTUMDBZSA-N 9Z,12E-Tetradecadienyl acetate Chemical compound C\C=C\C\C=C/CCCCCCCCOC(C)=O ZZGJZGSVLNSDPG-FDTUMDBZSA-N 0.000 description 1
- XXPBOEBNDHAAQH-SREVYHEPSA-N 9Z-Tetradecenyl acetate Chemical compound CCCC\C=C/CCCCCCCCOC(C)=O XXPBOEBNDHAAQH-SREVYHEPSA-N 0.000 description 1
- 239000005660 Abamectin Substances 0.000 description 1
- 241000427159 Achyranthes Species 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000253994 Acyrthosiphon pisum Species 0.000 description 1
- 241000589155 Agrobacterium tumefaciens Species 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 235000008553 Allium fistulosum Nutrition 0.000 description 1
- 244000257727 Allium fistulosum Species 0.000 description 1
- 241000212251 Alternaria dauci Species 0.000 description 1
- 241000212254 Alternaria porri Species 0.000 description 1
- 241001608435 Alternaria triticina Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000005726 Ametoctradin Substances 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 229920000856 Amylose Polymers 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical class NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 241001661349 Anthracocystis flocculosa Species 0.000 description 1
- 241001444083 Aphanomyces Species 0.000 description 1
- 235000003276 Apios tuberosa Nutrition 0.000 description 1
- 240000007087 Apium graveolens Species 0.000 description 1
- 235000015849 Apium graveolens Dulce Group Nutrition 0.000 description 1
- 235000010591 Appio Nutrition 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000010744 Arachis villosulicarpa Nutrition 0.000 description 1
- 241000186063 Arthrobacter Species 0.000 description 1
- 241000222195 Ascochyta Species 0.000 description 1
- 241000887188 Ascochyta hordei Species 0.000 description 1
- 244000309473 Ascochyta tritici Species 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 241000223678 Aureobasidium pullulans Species 0.000 description 1
- 241000050634 Aureobasidium zeae Species 0.000 description 1
- 235000007558 Avena sp Nutrition 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- 239000005878 Azadirachtin Substances 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 241000589941 Azospirillum Species 0.000 description 1
- 241000589938 Azospirillum brasilense Species 0.000 description 1
- 241000420792 Azospirillum brasilense Sp245 Species 0.000 description 1
- 239000005730 Azoxystrobin Substances 0.000 description 1
- 241000193755 Bacillus cereus Species 0.000 description 1
- 239000005957 Bacillus firmus I-1582 Substances 0.000 description 1
- 241000194107 Bacillus megaterium Species 0.000 description 1
- 241001249117 Bacillus mojavensis Species 0.000 description 1
- 241001104862 Bacillus pumilus INR7 Species 0.000 description 1
- 101100114760 Bacillus thuringiensis cry3Bb gene Proteins 0.000 description 1
- 241001147758 Bacillus thuringiensis serovar kurstaki Species 0.000 description 1
- 101100007609 Bacillus thuringiensis subsp. aizawai cry1Fa gene Proteins 0.000 description 1
- 101100497235 Bacillus thuringiensis subsp. kenyae cry1Ea gene Proteins 0.000 description 1
- 101100497219 Bacillus thuringiensis subsp. kurstaki cry1Ac gene Proteins 0.000 description 1
- 101100275683 Bacillus thuringiensis subsp. kurstaki cry2Ab gene Proteins 0.000 description 1
- 241000563903 Bacillus velezensis Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 241001302652 Bassiana Species 0.000 description 1
- 235000021537 Beetroot Nutrition 0.000 description 1
- 239000005734 Benalaxyl Substances 0.000 description 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
- 239000005737 Benzovindiflupyr Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 239000005653 Bifenazate Substances 0.000 description 1
- 241000228438 Bipolaris maydis Species 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- 239000005740 Boscalid Substances 0.000 description 1
- 241000499339 Botrytis allii Species 0.000 description 1
- 241000493670 Botrytis elliptica Species 0.000 description 1
- 241000167854 Bourreria succulenta Species 0.000 description 1
- RTONBWTZPZBIAC-UHFFFAOYSA-N Br[P]Br Chemical compound Br[P]Br RTONBWTZPZBIAC-UHFFFAOYSA-N 0.000 description 1
- 241000310268 Brachycaudus tragopogonis Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- 241000219193 Brassicaceae Species 0.000 description 1
- 241000233685 Bremia lactucae Species 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 239000005489 Bromoxynil Substances 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- 239000005742 Bupirimate Substances 0.000 description 1
- 239000005885 Buprofezin Substances 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- LSGCKAKHASGTSY-QGOAFFKASA-N C(#N)C=1C=CC(=C(OCC2=C(C=CC=C2)/C(/C(=O)OC)=C\OC)C=1)C Chemical compound C(#N)C=1C=CC(=C(OCC2=C(C=CC=C2)/C(/C(=O)OC)=C\OC)C=1)C LSGCKAKHASGTSY-QGOAFFKASA-N 0.000 description 1
- DDRYKVCZGOCYSW-UHFFFAOYSA-N C(C)S(=O)(=O)C1=C(N=C2N1C=C(C=C2)I)C1=NC=2C(=NC=C(C=2)C(F)(F)F)N1C Chemical compound C(C)S(=O)(=O)C1=C(N=C2N1C=C(C=C2)I)C1=NC=2C(=NC=C(C=2)C(F)(F)F)N1C DDRYKVCZGOCYSW-UHFFFAOYSA-N 0.000 description 1
- PNHBNCDHRJQZOP-HQVKBPLPSA-N C(\C=C\CCCCCCCCC\C=C/CCCC)O.C(C)(=O)O Chemical compound C(\C=C\CCCCCCCCC\C=C/CCCC)O.C(C)(=O)O PNHBNCDHRJQZOP-HQVKBPLPSA-N 0.000 description 1
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 description 1
- GXWSIHPKMYYHLH-UHFFFAOYSA-N CC(C)[Mg]C1=CC=CC=C1 Chemical compound CC(C)[Mg]C1=CC=CC=C1 GXWSIHPKMYYHLH-UHFFFAOYSA-N 0.000 description 1
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 description 1
- 238000010453 CRISPR/Cas method Methods 0.000 description 1
- 241000498608 Cadophora gregata Species 0.000 description 1
- 101100442689 Caenorhabditis elegans hdl-1 gene Proteins 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000006009 Calcium phosphide Substances 0.000 description 1
- 208000003643 Callosities Diseases 0.000 description 1
- 241000572575 Candidatus Pasteuria usgae Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 208000001573 Cataplexy Diseases 0.000 description 1
- 229940123982 Cell wall synthesis inhibitor Drugs 0.000 description 1
- 241000530549 Cercospora beticola Species 0.000 description 1
- 241000113401 Cercospora sojina Species 0.000 description 1
- 241000221955 Chaetomium Species 0.000 description 1
- 239000005886 Chlorantraniliprole Substances 0.000 description 1
- 229940127437 Chloride Channel Antagonists Drugs 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000005747 Chlorothalonil Substances 0.000 description 1
- 239000005945 Chlorpyrifos-methyl Substances 0.000 description 1
- 239000005887 Chromafenozide Substances 0.000 description 1
- 241001332334 Chromobacterium subtsugae Species 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 241000675108 Citrus tangerina Species 0.000 description 1
- 240000000560 Citrus x paradisi Species 0.000 description 1
- BZSZIAPWBMBDHX-UHFFFAOYSA-N ClC1=C(C=CC(=C1)Cl)N1N=C(C=C1)OCC=C(/C(/C(=O)NC)=NOC)C Chemical compound ClC1=C(C=CC(=C1)Cl)N1N=C(C=C1)OCC=C(/C(/C(=O)NC)=NOC)C BZSZIAPWBMBDHX-UHFFFAOYSA-N 0.000 description 1
- 241001264160 Cladobotryum Species 0.000 description 1
- 241001136168 Clavibacter michiganensis Species 0.000 description 1
- 241000221751 Claviceps purpurea Species 0.000 description 1
- 241000896542 Clonostachys rosea f. catenulata Species 0.000 description 1
- 239000005888 Clothianidin Substances 0.000 description 1
- 241001465977 Coccoidea Species 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 241000222235 Colletotrichum orbiculare Species 0.000 description 1
- 241000218631 Coniferophyta Species 0.000 description 1
- 239000005748 Coniothyrium minitans Strain CON/M/91-08 (DSM 9660) Substances 0.000 description 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 1
- 239000005750 Copper hydroxide Substances 0.000 description 1
- 239000005752 Copper oxychloride Substances 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 241001529717 Corticium <basidiomycota> Species 0.000 description 1
- 241000609458 Corynespora Species 0.000 description 1
- 235000009852 Cucurbita pepo Nutrition 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- 239000005754 Cyazofamid Substances 0.000 description 1
- 241001135545 Cydia pomonella granulovirus Species 0.000 description 1
- 239000005755 Cyflufenamid Substances 0.000 description 1
- 239000005655 Cyflumetofen Substances 0.000 description 1
- 241000723247 Cylindrocarpon Species 0.000 description 1
- 239000005756 Cymoxanil Substances 0.000 description 1
- 239000005946 Cypermethrin Substances 0.000 description 1
- 239000005891 Cyromazine Substances 0.000 description 1
- 241000235819 Cytospora Species 0.000 description 1
- 241001255637 Dactylium Species 0.000 description 1
- 239000005644 Dazomet Substances 0.000 description 1
- GCPYCNBGGPHOBD-UHFFFAOYSA-N Delphinidin Natural products OC1=Cc2c(O)cc(O)cc2OC1=C3C=C(O)C(=O)C(=C3)O GCPYCNBGGPHOBD-UHFFFAOYSA-N 0.000 description 1
- 229940122680 Demethylase inhibitor Drugs 0.000 description 1
- 241001508802 Diaporthe Species 0.000 description 1
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 description 1
- 239000005759 Diethofencarb Substances 0.000 description 1
- 239000005947 Dimethoate Substances 0.000 description 1
- 239000005761 Dimethomorph Substances 0.000 description 1
- 239000005762 Dimoxystrobin Substances 0.000 description 1
- BVTJGGGYKAMDBN-UHFFFAOYSA-N Dioxetane Chemical compound C1COO1 BVTJGGGYKAMDBN-UHFFFAOYSA-N 0.000 description 1
- 239000005764 Dithianon Substances 0.000 description 1
- AIGRXSNSLVJMEA-UHFFFAOYSA-N EPN Chemical compound C=1C=CC=CC=1P(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 AIGRXSNSLVJMEA-UHFFFAOYSA-N 0.000 description 1
- 241000353522 Earias insulana Species 0.000 description 1
- 241000901048 Elsinoe ampelina Species 0.000 description 1
- 241001568743 Elsinoe piri Species 0.000 description 1
- 241000191410 Elsinoe veneta Species 0.000 description 1
- 241000508725 Elymus repens Species 0.000 description 1
- 239000005767 Epoxiconazole Substances 0.000 description 1
- 241000588698 Erwinia Species 0.000 description 1
- 241000922683 Erwinia tracheiphila Species 0.000 description 1
- 241000221787 Erysiphe Species 0.000 description 1
- 241000896250 Erysiphe betae Species 0.000 description 1
- 241001337814 Erysiphe glycines Species 0.000 description 1
- 241001489205 Erysiphe pisi Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 239000005976 Ethephon Substances 0.000 description 1
- FNELVJVBIYMIMC-UHFFFAOYSA-N Ethiprole Chemical compound N1=C(C#N)C(S(=O)CC)=C(N)N1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl FNELVJVBIYMIMC-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000005897 Etoxazole Substances 0.000 description 1
- 244000004281 Eucalyptus maculata Species 0.000 description 1
- 241000318140 Exidia saccharina Species 0.000 description 1
- 241000306559 Exserohilum Species 0.000 description 1
- 239000005774 Fenamidone Substances 0.000 description 1
- 239000005656 Fenazaquin Substances 0.000 description 1
- 239000005775 Fenbuconazole Substances 0.000 description 1
- 239000005776 Fenhexamid Substances 0.000 description 1
- 239000005898 Fenoxycarb Substances 0.000 description 1
- 239000005777 Fenpropidin Substances 0.000 description 1
- 239000005778 Fenpropimorph Substances 0.000 description 1
- 235000016622 Filipendula ulmaria Nutrition 0.000 description 1
- 235000009009 Filipendula vulgaris Nutrition 0.000 description 1
- 244000061544 Filipendula vulgaris Species 0.000 description 1
- 241000589565 Flavobacterium Species 0.000 description 1
- 239000005900 Flonicamid Substances 0.000 description 1
- 239000005780 Fluazinam Substances 0.000 description 1
- 239000005781 Fludioxonil Substances 0.000 description 1
- 239000005782 Fluopicolide Substances 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 239000005784 Fluoxastrobin Substances 0.000 description 1
- 239000005785 Fluquinconazole Substances 0.000 description 1
- 239000005787 Flutriafol Substances 0.000 description 1
- 239000005788 Fluxapyroxad Substances 0.000 description 1
- 208000014770 Foot disease Diseases 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 239000005959 Fosthiazate Substances 0.000 description 1
- 241001610411 Fourraea alpina Species 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 241000223194 Fusarium culmorum Species 0.000 description 1
- 241000577846 Fusarium dimerum Species 0.000 description 1
- 241000221778 Fusarium fujikuroi Species 0.000 description 1
- 108091006027 G proteins Proteins 0.000 description 1
- 102000030782 GTP binding Human genes 0.000 description 1
- 108091000058 GTP-Binding Proteins 0.000 description 1
- 241001149475 Gaeumannomyces graminis Species 0.000 description 1
- 239000005903 Gamma-cyhalothrin Substances 0.000 description 1
- 241000222336 Ganoderma Species 0.000 description 1
- 208000018779 Globus Sensation Diseases 0.000 description 1
- 229920001503 Glucan Polymers 0.000 description 1
- 235000014683 Hansenula anomala Nutrition 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005661 Hexythiazox Substances 0.000 description 1
- 229940124136 Histidine kinase inhibitor Drugs 0.000 description 1
- 101000615488 Homo sapiens Methyl-CpG-binding domain protein 2 Proteins 0.000 description 1
- 241000218228 Humulus Species 0.000 description 1
- 241000549404 Hyaloperonospora parasitica Species 0.000 description 1
- 239000005794 Hymexazol Substances 0.000 description 1
- 206010020649 Hyperkeratosis Diseases 0.000 description 1
- 241001291865 Hypomyces odoratus Species 0.000 description 1
- 241000803621 Ilyonectria liriodendri Species 0.000 description 1
- 239000005795 Imazalil Substances 0.000 description 1
- 239000005906 Imidacloprid Substances 0.000 description 1
- FKWDSATZSMJRLC-UHFFFAOYSA-N Iminoctadine acetate Chemical compound CC([O-])=O.CC([O-])=O.CC([O-])=O.NC([NH3+])=NCCCCCCCC[NH2+]CCCCCCCCN=C(N)[NH3+] FKWDSATZSMJRLC-UHFFFAOYSA-N 0.000 description 1
- 241000692870 Inachis io Species 0.000 description 1
- 239000005907 Indoxacarb Substances 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 239000005796 Ipconazole Substances 0.000 description 1
- 240000002867 Ipomoea alba Species 0.000 description 1
- 239000005867 Iprodione Substances 0.000 description 1
- 239000005797 Iprovalicarb Substances 0.000 description 1
- 241000188153 Isaria fumosorosea Species 0.000 description 1
- 239000005908 Isaria fumosorosea Apopka strain 97 (formely Paecilomyces fumosoroseus) Substances 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 241000256602 Isoptera Species 0.000 description 1
- 239000005799 Isopyrazam Substances 0.000 description 1
- 239000005571 Isoxaflutole Substances 0.000 description 1
- 241000721662 Juniperus Species 0.000 description 1
- 241000274177 Juniperus sabina Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 241000218195 Lauraceae Species 0.000 description 1
- 244000165082 Lavanda vera Species 0.000 description 1
- 235000010663 Lavandula angustifolia Nutrition 0.000 description 1
- 241001121967 Lecanicillium Species 0.000 description 1
- 241000906090 Lecanicillium longisporum Species 0.000 description 1
- 240000004322 Lens culinaris Species 0.000 description 1
- 235000014647 Lens culinaris subsp culinaris Nutrition 0.000 description 1
- 241000222978 Leptosphaeria biglobosa Species 0.000 description 1
- 241000251953 Leucotrichia Species 0.000 description 1
- 241000757048 Libertella blepharis Species 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 239000005912 Lufenuron Substances 0.000 description 1
- 241001660189 Lysobacter antibioticus Species 0.000 description 1
- 229940122696 MAP kinase inhibitor Drugs 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000005949 Malathion Substances 0.000 description 1
- 244000081841 Malus domestica Species 0.000 description 1
- 239000005803 Mandestrobin Substances 0.000 description 1
- 240000007679 Mandevilla laxa Species 0.000 description 1
- 239000005804 Mandipropamid Substances 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 244000217433 Melampodium divaricatum Species 0.000 description 1
- 229940127408 Melanin Synthesis Inhibitors Drugs 0.000 description 1
- 241001599018 Melanogaster Species 0.000 description 1
- 208000003351 Melanosis Diseases 0.000 description 1
- 241001646834 Mesona Species 0.000 description 1
- 239000005578 Mesotrione Substances 0.000 description 1
- 239000005914 Metaflumizone Substances 0.000 description 1
- MIFOMMKAVSCNKQ-HWIUFGAZSA-N Metaflumizone Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)N\N=C(C=1C=C(C=CC=1)C(F)(F)F)\CC1=CC=C(C#N)C=C1 MIFOMMKAVSCNKQ-HWIUFGAZSA-N 0.000 description 1
- 239000005807 Metalaxyl Substances 0.000 description 1
- 239000005808 Metalaxyl-M Substances 0.000 description 1
- 241000223201 Metarhizium Species 0.000 description 1
- 239000005868 Metconazole Substances 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- 239000005916 Methomyl Substances 0.000 description 1
- 239000005917 Methoxyfenozide Substances 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- 102100021299 Methyl-CpG-binding domain protein 2 Human genes 0.000 description 1
- 239000005810 Metrafenone Substances 0.000 description 1
- 239000005918 Milbemectin Substances 0.000 description 1
- 102000013379 Mitochondrial Proton-Translocating ATPases Human genes 0.000 description 1
- 108010026155 Mitochondrial Proton-Translocating ATPases Proteins 0.000 description 1
- 241001661277 Moelleriella libera Species 0.000 description 1
- 241000237852 Mollusca Species 0.000 description 1
- 241001518731 Monilinia fructicola Species 0.000 description 1
- 241001518836 Monilinia fructigena Species 0.000 description 1
- 241000143639 Monocystis Species 0.000 description 1
- 241001645777 Muscodor albus Species 0.000 description 1
- 241000226677 Myceliophthora Species 0.000 description 1
- 239000005811 Myclobutanil Substances 0.000 description 1
- 241000204031 Mycoplasma Species 0.000 description 1
- 239000005041 Mylar™ Substances 0.000 description 1
- 241001477931 Mythimna unipuncta Species 0.000 description 1
- XSYIIGPTLDKNNH-UHFFFAOYSA-N N'-[5-bromo-2-methyl-6-(1-phenylethoxy)pyridin-3-yl]-N-ethyl-N-methylmethanimidamide Chemical compound BrC=1C=C(C(=NC=1OC(C)C1=CC=CC=C1)C)N=CN(C)CC XSYIIGPTLDKNNH-UHFFFAOYSA-N 0.000 description 1
- XMDNVMZGIIOPPG-UHFFFAOYSA-N N,5-dimethyl-1-(3-methylbutan-2-yl)-N-pyridazin-4-ylpyrazole-4-carboxamide Chemical compound CC(C(C)C)N1N=CC(=C1C)C(=O)N(C1=CN=NC=C1)C XMDNVMZGIIOPPG-UHFFFAOYSA-N 0.000 description 1
- IEKSGOPPBDNFFP-UHFFFAOYSA-N N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide Chemical compound FC1=C(C=CC=C1)NC(C1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F)=O IEKSGOPPBDNFFP-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- IJUBXIZEMAPEDB-UHFFFAOYSA-N N-[1-(oxiran-2-ylmethyl)-4,5-dihydroimidazol-2-yl]nitramide Chemical compound C(C1CO1)N1C(NCC1)=N[N+](=O)[O-] IJUBXIZEMAPEDB-UHFFFAOYSA-N 0.000 description 1
- QDGAKFOEVQTUGQ-UHFFFAOYSA-N N-[2-[2-chloro-4-(trifluoromethyl)phenoxy]phenyl]-3-(difluoromethyl)-5-fluoro-1-methylpyrazole-4-carboxamide Chemical compound ClC1=C(OC2=C(C=CC=C2)NC(=O)C=2C(=NN(C=2F)C)C(F)F)C=CC(=C1)C(F)(F)F QDGAKFOEVQTUGQ-UHFFFAOYSA-N 0.000 description 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 description 1
- NQRFDNJEBWAUBL-UHFFFAOYSA-N N-[cyano(2-thienyl)methyl]-4-ethyl-2-(ethylamino)-1,3-thiazole-5-carboxamide Chemical compound S1C(NCC)=NC(CC)=C1C(=O)NC(C#N)C1=CC=CS1 NQRFDNJEBWAUBL-UHFFFAOYSA-N 0.000 description 1
- ZQPIADKUNVJRFW-UHFFFAOYSA-N N-ethyl-1-(3-fluorobutan-2-yl)-5-methyl-N-pyridazin-4-ylpyrazole-4-carboxamide Chemical compound C(C)N(C(=O)C=1C=NN(C=1C)C(C(C)F)C)C1=CN=NC=C1 ZQPIADKUNVJRFW-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 240000007695 Nandina domestica Species 0.000 description 1
- 101100172173 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) hcr-1 gene Proteins 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 241001329956 Nothopassalora personata Species 0.000 description 1
- BOCQVBGTUSMQRV-UHFFFAOYSA-N O=C(C1=C(C=CC=C2)C2=NN1C1=CC=CN=C1)NC1CCCCC1 Chemical compound O=C(C1=C(C=CC=C2)C2=NN1C1=CC=CN=C1)NC1CCCCC1 BOCQVBGTUSMQRV-UHFFFAOYSA-N 0.000 description 1
- DWWJBKSSHBITBL-UHFFFAOYSA-N O=C(NC1CC1)c1cccc2nn(cc12)-c1cccnc1 Chemical compound O=C(NC1CC1)c1cccc2nn(cc12)-c1cccnc1 DWWJBKSSHBITBL-UHFFFAOYSA-N 0.000 description 1
- DGGNOYAGSYOVOG-UHFFFAOYSA-N O=C(NC1CCCCC1)c1cccc2nn(cc12)-c1cccnc1 Chemical compound O=C(NC1CCCCC1)c1cccc2nn(cc12)-c1cccnc1 DGGNOYAGSYOVOG-UHFFFAOYSA-N 0.000 description 1
- FQZYJHRPNOHECR-UHFFFAOYSA-N O=C(NCc1ncccn1)c1ccc2nn(cc2c1)-c1cccnc1 Chemical compound O=C(NCc1ncccn1)c1ccc2nn(cc2c1)-c1cccnc1 FQZYJHRPNOHECR-UHFFFAOYSA-N 0.000 description 1
- 241000144610 Oculimacula acuformis Species 0.000 description 1
- 241000207836 Olea <angiosperm> Species 0.000 description 1
- 235000002725 Olea europaea Nutrition 0.000 description 1
- 108091034117 Oligonucleotide Proteins 0.000 description 1
- 241000221671 Ophiostoma ulmi Species 0.000 description 1
- 241000266501 Ormosia ormondii Species 0.000 description 1
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 description 1
- 239000004100 Oxytetracycline Substances 0.000 description 1
- 241001560086 Pachyrhizus Species 0.000 description 1
- 241001479578 Packera contermina Species 0.000 description 1
- 239000005985 Paclobutrazol Substances 0.000 description 1
- 241001236817 Paecilomyces <Clavicipitaceae> Species 0.000 description 1
- 239000005960 Paecilomyces lilacinus strain 251 Substances 0.000 description 1
- 241000588912 Pantoea agglomerans Species 0.000 description 1
- 241000315044 Passalora arachidicola Species 0.000 description 1
- 241000222291 Passalora fulva Species 0.000 description 1
- 241000606860 Pasteurella Species 0.000 description 1
- 241000291055 Pasteuria ramosa Species 0.000 description 1
- 241000220289 Pedunculata Species 0.000 description 1
- 239000005814 Pencycuron Substances 0.000 description 1
- 235000002245 Penicillium camembertii Nutrition 0.000 description 1
- 239000005816 Penthiopyrad Substances 0.000 description 1
- 229920001774 Perfluoroether Polymers 0.000 description 1
- 241001670203 Peronospora manshurica Species 0.000 description 1
- 241000582441 Peronospora tabacina Species 0.000 description 1
- 244000025272 Persea americana Species 0.000 description 1
- 235000008673 Persea americana Nutrition 0.000 description 1
- 241000263269 Phaeoacremonium minimum Species 0.000 description 1
- 244000089933 Phoebe grandis Species 0.000 description 1
- 241001503951 Phoma Species 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241001147478 Phyllophora <Rhodophyta> Species 0.000 description 1
- 244000302661 Phyllostachys pubescens Species 0.000 description 1
- 235000003570 Phyllostachys pubescens Nutrition 0.000 description 1
- 241000210649 Phyllosticta ampelicida Species 0.000 description 1
- 241000932914 Physalospora obtusa Species 0.000 description 1
- 241000471406 Physoderma maydis Species 0.000 description 1
- 241000233624 Phytophthora megasperma Species 0.000 description 1
- 241000233647 Phytophthora nicotianae var. parasitica Species 0.000 description 1
- 241000370518 Phytophthora ramorum Species 0.000 description 1
- 239000005818 Picoxystrobin Substances 0.000 description 1
- 241001503436 Plasmodiophora brassicae Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 241000896242 Podosphaera Species 0.000 description 1
- 241000951259 Podosphaera xanthii Species 0.000 description 1
- 241000768494 Polymorphum Species 0.000 description 1
- 229930182764 Polyoxin Natural products 0.000 description 1
- 241000222640 Polyporus Species 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000005819 Potassium phosphonate Substances 0.000 description 1
- 239000005821 Propamocarb Substances 0.000 description 1
- 239000005822 Propiconazole Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229940123573 Protein synthesis inhibitor Drugs 0.000 description 1
- 241000192142 Proteobacteria Species 0.000 description 1
- 239000005825 Prothioconazole Substances 0.000 description 1
- 240000008519 Prunus americana Species 0.000 description 1
- 240000005809 Prunus persica Species 0.000 description 1
- 241000113418 Pseudocercospora humuli Species 0.000 description 1
- 241000184297 Pseudocercospora musae Species 0.000 description 1
- 241000589540 Pseudomonas fluorescens Species 0.000 description 1
- 241001281805 Pseudoperonospora cubensis Species 0.000 description 1
- 241001008025 Pseudopezicula Species 0.000 description 1
- 241001008026 Pseudopezicula tetraspora Species 0.000 description 1
- 241001038563 Pseudostellaria Species 0.000 description 1
- 241000601159 Puccinia asparagi Species 0.000 description 1
- 241000221301 Puccinia graminis Species 0.000 description 1
- 241001123559 Puccinia hordei Species 0.000 description 1
- 241000928333 Puccinia kuehnii Species 0.000 description 1
- 241001123569 Puccinia recondita Species 0.000 description 1
- 241001123583 Puccinia striiformis Species 0.000 description 1
- 241001465752 Purpureocillium lilacinum Species 0.000 description 1
- 239000005925 Pymetrozine Substances 0.000 description 1
- 241000520648 Pyrenophora teres Species 0.000 description 1
- 241000231139 Pyricularia Species 0.000 description 1
- 239000005663 Pyridaben Substances 0.000 description 1
- 239000005926 Pyridalyl Substances 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 239000005927 Pyriproxyfen Substances 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- 244000184734 Pyrus japonica Species 0.000 description 1
- 241000131360 Pythium oligandrum Species 0.000 description 1
- 240000003085 Quassia amara Species 0.000 description 1
- 235000009694 Quassia amara Nutrition 0.000 description 1
- 241000959624 Ramaria Species 0.000 description 1
- 241000173767 Ramularia Species 0.000 description 1
- 241000771943 Ramularia beticola Species 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 241000235546 Rhizopus stolonifer Species 0.000 description 1
- 241001515790 Rhynchosporium secalis Species 0.000 description 1
- 235000001537 Ribes X gardonianum Nutrition 0.000 description 1
- 235000001535 Ribes X utile Nutrition 0.000 description 1
- 235000016919 Ribes petraeum Nutrition 0.000 description 1
- 244000281247 Ribes rubrum Species 0.000 description 1
- 235000002355 Ribes spicatum Nutrition 0.000 description 1
- 240000000528 Ricinus communis Species 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 235000004789 Rosa xanthina Nutrition 0.000 description 1
- 241001500041 Rossella Species 0.000 description 1
- 240000007651 Rubus glaucus Species 0.000 description 1
- 241000698291 Rugosa Species 0.000 description 1
- 240000000296 Sabal minor Species 0.000 description 1
- 241001134661 Saccharopolyspora rectivirgula Species 0.000 description 1
- 241000800294 Sarocladium oryzae Species 0.000 description 1
- 241000767840 Semiaquilegia Species 0.000 description 1
- 241000589196 Sinorhizobium meliloti Species 0.000 description 1
- 241000254152 Sitophilus oryzae Species 0.000 description 1
- 108010052164 Sodium Channels Proteins 0.000 description 1
- 102000018674 Sodium Channels Human genes 0.000 description 1
- 241000862632 Soja Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 240000003829 Sorghum propinquum Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 241000626935 Sphaerodes mycoparasitica Species 0.000 description 1
- 235000009337 Spinacia oleracea Nutrition 0.000 description 1
- 244000300264 Spinacia oleracea Species 0.000 description 1
- 239000005930 Spinosad Substances 0.000 description 1
- 239000005664 Spirodiclofen Substances 0.000 description 1
- 239000005665 Spiromesifen Substances 0.000 description 1
- 239000005931 Spirotetramat Substances 0.000 description 1
- 239000005837 Spiroxamine Substances 0.000 description 1
- 241000256248 Spodoptera Species 0.000 description 1
- 241000256247 Spodoptera exigua Species 0.000 description 1
- 241000397423 Spongospora subterranea f. sp. subterranea Species 0.000 description 1
- 241000533281 Stagonospora Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241000509371 Steinernema feltiae Species 0.000 description 1
- 244000228451 Stevia rebaudiana Species 0.000 description 1
- 241000187747 Streptomyces Species 0.000 description 1
- 241000187392 Streptomyces griseus Species 0.000 description 1
- 241000218483 Streptomyces lydicus Species 0.000 description 1
- 241000187095 Streptomyces purpureus Species 0.000 description 1
- 241000790699 Strumigenys glycon Species 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 206010042434 Sudden death Diseases 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000005934 Sulfoxaflor Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241000827175 Synchytrium endobioticum Species 0.000 description 1
- 238000010459 TALEN Methods 0.000 description 1
- 102000003563 TRPV Human genes 0.000 description 1
- 108060008564 TRPV Proteins 0.000 description 1
- 240000004460 Tanacetum coccineum Species 0.000 description 1
- 241000228446 Taphrina Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000005839 Tebuconazole Substances 0.000 description 1
- 239000005937 Tebufenozide Substances 0.000 description 1
- 239000005658 Tebufenpyrad Substances 0.000 description 1
- 241000254109 Tenebrio molitor Species 0.000 description 1
- 241000270708 Testudinidae Species 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 241000223258 Thermomyces lanuginosus Species 0.000 description 1
- 239000005940 Thiacloprid Substances 0.000 description 1
- 239000005941 Thiamethoxam Substances 0.000 description 1
- 241000865903 Thielaviopsis Species 0.000 description 1
- 239000005842 Thiophanate-methyl Substances 0.000 description 1
- 239000005843 Thiram Substances 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000005845 Tolclofos-methyl Substances 0.000 description 1
- 241000223997 Toxoplasma gondii Species 0.000 description 1
- 108010043645 Transcription Activator-Like Effector Nucleases Proteins 0.000 description 1
- 241001390947 Trichoderma asperelloides Species 0.000 description 1
- 241000894120 Trichoderma atroviride Species 0.000 description 1
- 241000499912 Trichoderma reesei Species 0.000 description 1
- 239000005858 Triflumizole Substances 0.000 description 1
- 239000005942 Triflumuron Substances 0.000 description 1
- 241000219793 Trifolium Species 0.000 description 1
- 239000005859 Triticonazole Substances 0.000 description 1
- 241000001727 Tropicoporus linteus Species 0.000 description 1
- 241000722921 Tulipa gesneriana Species 0.000 description 1
- 241000959260 Typhula Species 0.000 description 1
- 241000959214 Typhula phacorrhiza Species 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 241001286670 Ulmus x hollandica Species 0.000 description 1
- 241000083901 Urocystis agropyri Species 0.000 description 1
- 241000221576 Uromyces Species 0.000 description 1
- 241001091387 Uromyces beticola Species 0.000 description 1
- 241000965666 Uromyces pisi Species 0.000 description 1
- 241000544594 Uromyces viciae-fabae Species 0.000 description 1
- 241000981775 Urospora <green alga> Species 0.000 description 1
- 241001474928 Ustilaginoidea virens Species 0.000 description 1
- 241000007070 Ustilago nuda Species 0.000 description 1
- 244000078534 Vaccinium myrtillus Species 0.000 description 1
- 229930195482 Validamycin Natural products 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 241001447693 Verticillium longisporum Species 0.000 description 1
- 241000607598 Vibrio Species 0.000 description 1
- 241000219977 Vigna Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- CVQODEWAPZVVBU-UHFFFAOYSA-N XMC Chemical compound CNC(=O)OC1=CC(C)=CC(C)=C1 CVQODEWAPZVVBU-UHFFFAOYSA-N 0.000 description 1
- 235000011902 Zea mays var everta Nutrition 0.000 description 1
- 244000171502 Zea mays var. everta Species 0.000 description 1
- 244000015069 Zephyranthes candida Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 108010017070 Zinc Finger Nucleases Proteins 0.000 description 1
- 239000006011 Zinc phosphide Substances 0.000 description 1
- 239000005870 Ziram Substances 0.000 description 1
- YGCODSQDUUUKIV-UHFFFAOYSA-N Zoxazolamine Chemical compound ClC1=CC=C2OC(N)=NC2=C1 YGCODSQDUUUKIV-UHFFFAOYSA-N 0.000 description 1
- 241001520823 Zoysia Species 0.000 description 1
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 1
- YDHZUCLRCLIJRL-UHFFFAOYSA-N [3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-pyridin-3-ylmethanol Chemical compound C=1C=CN=CC=1C(O)C=1C(C=2C(=CC(Cl)=CC=2)F)=NOC=1C1=CC=C(F)C=C1F YDHZUCLRCLIJRL-UHFFFAOYSA-N 0.000 description 1
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 description 1
- DSVGQVZAZSZEEX-UHFFFAOYSA-N [C].[Pt] Chemical compound [C].[Pt] DSVGQVZAZSZEEX-UHFFFAOYSA-N 0.000 description 1
- KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical group [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 description 1
- 241000192248 [Candida] saitoana Species 0.000 description 1
- FZDSRQVIUUCVMI-UHFFFAOYSA-N [ClH]1N=CCC1 Chemical compound [ClH]1N=CCC1 FZDSRQVIUUCVMI-UHFFFAOYSA-N 0.000 description 1
- HNSXCKBVOZPUIE-UHFFFAOYSA-N [Mg][I]I Chemical group [Mg][I]I HNSXCKBVOZPUIE-UHFFFAOYSA-N 0.000 description 1
- KENSTCMZRGKACJ-UHFFFAOYSA-N [P].C(CCC)C1=NC=CC=N1 Chemical compound [P].C(CCC)C1=NC=CC=N1 KENSTCMZRGKACJ-UHFFFAOYSA-N 0.000 description 1
- ZXQYGBMAQZUVMI-UHFFFAOYSA-N [cyano-(3-phenoxyphenyl)methyl] 3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UHFFFAOYSA-N 0.000 description 1
- YXWCBRDRVXHABN-JCMHNJIXSA-N [cyano-(4-fluoro-3-phenoxyphenyl)methyl] 3-[(z)-2-chloro-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound C=1C=C(F)C(OC=2C=CC=CC=2)=CC=1C(C#N)OC(=O)C1C(C)(C)C1\C=C(/Cl)C1=CC=C(Cl)C=C1 YXWCBRDRVXHABN-JCMHNJIXSA-N 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 229950008167 abamectin Drugs 0.000 description 1
- YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-N 0.000 description 1
- 229940121373 acetyl-coa carboxylase inhibitor Drugs 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- QGLZXHRNAYXIBU-WEVVVXLNSA-N aldicarb Chemical compound CNC(=O)O\N=C\C(C)(C)SC QGLZXHRNAYXIBU-WEVVVXLNSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 239000011717 all-trans-retinol Substances 0.000 description 1
- 235000019169 all-trans-retinol Nutrition 0.000 description 1
- 230000003281 allosteric effect Effects 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- GGKQIOFASHYUJZ-UHFFFAOYSA-N ametoctradin Chemical compound NC1=C(CCCCCCCC)C(CC)=NC2=NC=NN21 GGKQIOFASHYUJZ-UHFFFAOYSA-N 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 229960002587 amitraz Drugs 0.000 description 1
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000005667 attractant Substances 0.000 description 1
- VEHPJKVTJQSSKL-UHFFFAOYSA-N azadirachtin Natural products O1C2(C)C(C3(C=COC3O3)O)CC3C21C1(C)C(O)C(OCC2(OC(C)=O)C(CC3OC(=O)C(C)=CC)OC(C)=O)C2C32COC(C(=O)OC)(O)C12 VEHPJKVTJQSSKL-UHFFFAOYSA-N 0.000 description 1
- FTNJWQUOZFUQQJ-NDAWSKJSSA-N azadirachtin A Chemical compound C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C\C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-NDAWSKJSSA-N 0.000 description 1
- FTNJWQUOZFUQQJ-IRYYUVNJSA-N azadirachtin A Natural products C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C/C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-IRYYUVNJSA-N 0.000 description 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 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 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 1
- USRKFGIXLGKMKU-ABAIWWIYSA-N benthiavalicarb-isopropyl Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@H](C(C)C)NC(=O)OC(C)C)=NC2=C1 USRKFGIXLGKMKU-ABAIWWIYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- ZYXYTGQFPZEUFX-UHFFFAOYSA-N benzpyrimoxan Chemical compound O1C(OCCC1)C=1C(=NC=NC=1)OCC1=CC=C(C=C1)C(F)(F)F ZYXYTGQFPZEUFX-UHFFFAOYSA-N 0.000 description 1
- YOUGRGFIHBUKRS-UHFFFAOYSA-N benzyl(trimethyl)azanium Chemical compound C[N+](C)(C)CC1=CC=CC=C1 YOUGRGFIHBUKRS-UHFFFAOYSA-N 0.000 description 1
- VHLKTXFWDRXILV-UHFFFAOYSA-N bifenazate Chemical compound C1=C(NNC(=O)OC(C)C)C(OC)=CC=C1C1=CC=CC=C1 VHLKTXFWDRXILV-UHFFFAOYSA-N 0.000 description 1
- 239000003124 biologic agent Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 235000021029 blackberry Nutrition 0.000 description 1
- CXNPLSGKWMLZPZ-UHFFFAOYSA-N blasticidin-S Natural products O1C(C(O)=O)C(NC(=O)CC(N)CCN(C)C(N)=N)C=CC1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229940118790 boscalid Drugs 0.000 description 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 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 125000005997 bromomethyl group Chemical group 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- DSKJPMWIHSOYEA-UHFFFAOYSA-N bupirimate Chemical compound CCCCC1=C(C)N=C(NCC)N=C1OS(=O)(=O)N(C)C DSKJPMWIHSOYEA-UHFFFAOYSA-N 0.000 description 1
- PRLVTUNWOQKEAI-VKAVYKQESA-N buprofezin Chemical compound O=C1N(C(C)C)\C(=N\C(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-VKAVYKQESA-N 0.000 description 1
- RCXKBXKSCSBVKZ-MOHJPFBDSA-N but-3-ynyl n-[6-[[(z)-[(1-methyltetrazol-5-yl)-phenylmethylidene]amino]oxymethyl]pyridin-2-yl]carbamate Chemical compound CN1N=NN=C1\C(C=1C=CC=CC=1)=N/OCC1=CC=CC(NC(=O)OCCC#C)=N1 RCXKBXKSCSBVKZ-MOHJPFBDSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- OMAAXMJMHFXYFY-UHFFFAOYSA-L calcium trioxidophosphanium Chemical compound [Ca+2].[O-]P([O-])=O OMAAXMJMHFXYFY-UHFFFAOYSA-L 0.000 description 1
- NLKUPINTOLSSLD-UHFFFAOYSA-L calcium;4-(1-oxidopropylidene)-3,5-dioxocyclohexane-1-carboxylate Chemical compound [Ca+2].CCC([O-])=C1C(=O)CC(C([O-])=O)CC1=O NLKUPINTOLSSLD-UHFFFAOYSA-L 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229960005286 carbaryl Drugs 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- 239000006013 carbendazim Substances 0.000 description 1
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- IRUJZVNXZWPBMU-UHFFFAOYSA-N cartap Chemical compound NC(=O)SCC(N(C)C)CSC(N)=O IRUJZVNXZWPBMU-UHFFFAOYSA-N 0.000 description 1
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Natural products CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- NDHXMRFNYMNBKO-PWSUYJOCSA-N chembl2227757 Chemical compound [O-][N+](=O)C([C@H]1CC[C@H](O1)N1CC2)=C1N2CC1=CC=C(Cl)N=C1 NDHXMRFNYMNBKO-PWSUYJOCSA-N 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
- PSOVNZZNOMJUBI-UHFFFAOYSA-N chlorantraniliprole Chemical compound CNC(=O)C1=CC(Cl)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl PSOVNZZNOMJUBI-UHFFFAOYSA-N 0.000 description 1
- UISUNVFOGSJSKD-UHFFFAOYSA-N chlorfluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1Cl)=CC(Cl)=C1OC1=NC=C(C(F)(F)F)C=C1Cl UISUNVFOGSJSKD-UHFFFAOYSA-N 0.000 description 1
- 239000003467 chloride channel stimulating agent Substances 0.000 description 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 description 1
- 125000004775 chlorodifluoromethyl group Chemical group FC(F)(Cl)* 0.000 description 1
- 125000004773 chlorofluoromethyl group Chemical group [H]C(F)(Cl)* 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- LFHISGNCFUNFFM-UHFFFAOYSA-N chloropicrin Chemical compound [O-][N+](=O)C(Cl)(Cl)Cl LFHISGNCFUNFFM-UHFFFAOYSA-N 0.000 description 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
- HPNSNYBUADCFDR-UHFFFAOYSA-N chromafenozide Chemical compound CC1=CC(C)=CC(C(=O)N(NC(=O)C=2C(=C3CCCOC3=CC=2)C)C(C)(C)C)=C1 HPNSNYBUADCFDR-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 235000017803 cinnamon Nutrition 0.000 description 1
- 229940043350 citral Drugs 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000001332 colony forming effect Effects 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 229940125773 compound 10 Drugs 0.000 description 1
- 229940125797 compound 12 Drugs 0.000 description 1
- 239000007891 compressed tablet Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 208000012839 conversion disease Diseases 0.000 description 1
- 239000005068 cooling lubricant Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910001956 copper hydroxide Inorganic materials 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- BXNANOICGRISHX-UHFFFAOYSA-N coumaphos Chemical compound CC1=C(Cl)C(=O)OC2=CC(OP(=S)(OCC)OCC)=CC=C21 BXNANOICGRISHX-UHFFFAOYSA-N 0.000 description 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 description 1
- QPNKYNYIKKVVQB-UHFFFAOYSA-N crotaleschenine Natural products O1C(=O)C(C)C(C)C(C)(O)C(=O)OCC2=CCN3C2C1CC3 QPNKYNYIKKVVQB-UHFFFAOYSA-N 0.000 description 1
- 101150065438 cry1Ab gene Proteins 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 101150049887 cspB gene Proteins 0.000 description 1
- 101150041068 cspJ gene Proteins 0.000 description 1
- 101150010904 cspLB gene Proteins 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 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 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- APJLTUBHYCOZJI-VZCXRCSSSA-N cyenopyrafen Chemical compound CC1=NN(C)C(\C(OC(=O)C(C)(C)C)=C(/C#N)C=2C=CC(=CC=2)C(C)(C)C)=C1C APJLTUBHYCOZJI-VZCXRCSSSA-N 0.000 description 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 description 1
- NNRSYETYEADPBW-UHFFFAOYSA-N cyhalodiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(Cl)=C1C(=O)NC(C)(C)C#N NNRSYETYEADPBW-UHFFFAOYSA-N 0.000 description 1
- 229960005424 cypermethrin Drugs 0.000 description 1
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 1
- WULALRGFFYJWOL-UHFFFAOYSA-N cyproflanilide Chemical compound BrC1=C(C(=CC(=C1)C(C(F)(F)F)(C(F)(F)F)F)C(F)(F)F)NC(C1=C(C(=CC=C1)N(C(C1=CC=C(C=C1)F)=O)CC1CC1)F)=O WULALRGFFYJWOL-UHFFFAOYSA-N 0.000 description 1
- LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 description 1
- 229950000775 cyromazine Drugs 0.000 description 1
- 210000004292 cytoskeleton Anatomy 0.000 description 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 235000007242 delphinidin Nutrition 0.000 description 1
- FFNDMZIBVDSQFI-UHFFFAOYSA-N delphinidin chloride Chemical compound [Cl-].[O+]=1C2=CC(O)=CC(O)=C2C=C(O)C=1C1=CC(O)=C(O)C(O)=C1 FFNDMZIBVDSQFI-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- 125000004774 dichlorofluoromethyl group Chemical group FC(Cl)(Cl)* 0.000 description 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
- 229950001327 dichlorvos Drugs 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- LNJNFVJKDJYTEU-UHFFFAOYSA-N diethofencarb Chemical compound CCOC1=CC=C(NC(=O)OC(C)C)C=C1OCC LNJNFVJKDJYTEU-UHFFFAOYSA-N 0.000 description 1
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 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 description 1
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 description 1
- YXXXKCDYKKSZHL-UHFFFAOYSA-M dipotassium;dioxido(oxo)phosphanium Chemical compound [K+].[K+].[O-][P+]([O-])=O YXXXKCDYKKSZHL-UHFFFAOYSA-M 0.000 description 1
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 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 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- GCKZANITAMOIAR-XWVCPFKXSA-N dsstox_cid_14566 Chemical compound [O-]C(=O)C1=CC=CC=C1.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H]([NH2+]C)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 GCKZANITAMOIAR-XWVCPFKXSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 108010057988 ecdysone receptor Proteins 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 239000002895 emetic Substances 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 description 1
- 229960002125 enilconazole Drugs 0.000 description 1
- 230000000967 entomopathogenic effect Effects 0.000 description 1
- 231100000290 environmental risk assessment Toxicity 0.000 description 1
- VJYFKVYYMZPMAB-UHFFFAOYSA-N ethoprophos Chemical compound CCCSP(=O)(OCC)SCCC VJYFKVYYMZPMAB-UHFFFAOYSA-N 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 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 description 1
- GATNOFPXSDHULC-UHFFFAOYSA-N ethylphosphonic acid Chemical compound CCP(O)(O)=O GATNOFPXSDHULC-UHFFFAOYSA-N 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 description 1
- VJJPUSNTGOMMGY-MRVIYFEKSA-N etoposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@H](C)OC[C@H]4O3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 VJJPUSNTGOMMGY-MRVIYFEKSA-N 0.000 description 1
- 229960005420 etoposide Drugs 0.000 description 1
- IXSZQYVWNJNRAL-UHFFFAOYSA-N etoxazole Chemical compound CCOC1=CC(C(C)(C)C)=CC=C1C1N=C(C=2C(=CC=CC=2F)F)OC1 IXSZQYVWNJNRAL-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 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 description 1
- DMYHGDXADUDKCQ-UHFFFAOYSA-N fenazaquin Chemical compound C1=CC(C(C)(C)C)=CC=C1CCOC1=NC=NC2=CC=CC=C12 DMYHGDXADUDKCQ-UHFFFAOYSA-N 0.000 description 1
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 description 1
- DIRFUJHNVNOBMY-UHFFFAOYSA-N fenobucarb Chemical compound CCC(C)C1=CC=CC=C1OC(=O)NC DIRFUJHNVNOBMY-UHFFFAOYSA-N 0.000 description 1
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 description 1
- XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 description 1
- WDQNIWFZKXZFAY-UHFFFAOYSA-M fentin acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 WDQNIWFZKXZFAY-UHFFFAOYSA-M 0.000 description 1
- NJVOZLGKTAPUTQ-UHFFFAOYSA-M fentin chloride Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 NJVOZLGKTAPUTQ-UHFFFAOYSA-M 0.000 description 1
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 230000035558 fertility Effects 0.000 description 1
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 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 description 1
- XRECTZIEBJDKEO-UHFFFAOYSA-N flucytosine Chemical compound NC1=NC(=O)NC=C1F XRECTZIEBJDKEO-UHFFFAOYSA-N 0.000 description 1
- 229960004413 flucytosine Drugs 0.000 description 1
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 description 1
- LPEPZBJOKDYZAD-UHFFFAOYSA-M flufenamate Chemical compound [O-]C(=O)C1=CC=CC=C1NC1=CC=CC(C(F)(F)F)=C1 LPEPZBJOKDYZAD-UHFFFAOYSA-M 0.000 description 1
- 229940067594 flufenamate Drugs 0.000 description 1
- RYLHNOVXKPXDIP-UHFFFAOYSA-N flufenoxuron Chemical compound C=1C=C(NC(=O)NC(=O)C=2C(=CC=CC=2F)F)C(F)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl RYLHNOVXKPXDIP-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 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 description 1
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 description 1
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 description 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 description 1
- 239000004459 forage Substances 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- DUFVKSUJRWYZQP-UHFFFAOYSA-N fosthiazate Chemical compound CCC(C)SP(=O)(OCC)N1CCSC1=O DUFVKSUJRWYZQP-UHFFFAOYSA-N 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 208000024386 fungal infectious disease Diseases 0.000 description 1
- ZXQYGBMAQZUVMI-GCMPRSNUSA-N gamma-cyhalothrin Chemical compound CC1(C)[C@@H](\C=C(/Cl)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-GCMPRSNUSA-N 0.000 description 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
- 150000002303 glucose derivatives Chemical class 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 235000019674 grape juice Nutrition 0.000 description 1
- 239000003966 growth inhibitor Substances 0.000 description 1
- 239000007952 growth promoter Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- SCCLFGAYCGKMEI-UHFFFAOYSA-N heptylphosphane Chemical compound CCCCCCCP SCCLFGAYCGKMEI-UHFFFAOYSA-N 0.000 description 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
- RGNPBRKPHBKNKX-UHFFFAOYSA-N hexaflumuron Chemical compound C1=C(Cl)C(OC(F)(F)C(F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F RGNPBRKPHBKNKX-UHFFFAOYSA-N 0.000 description 1
- 150000004761 hexafluorosilicates Chemical class 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 238000009396 hybridization Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 description 1
- HICUREFSAIZXFQ-JOWPUVSESA-N i9z29i000j Chemical compound C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\[C@H](OC(=O)C(=N/OC)\C=1C=CC=CC=1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 HICUREFSAIZXFQ-JOWPUVSESA-N 0.000 description 1
- 229940056881 imidacloprid Drugs 0.000 description 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- VBCVPMMZEGZULK-NRFANRHFSA-N indoxacarb Chemical compound C([C@@]1(OC2)C(=O)OC)C3=CC(Cl)=CC=C3C1=NN2C(=O)N(C(=O)OC)C1=CC=C(OC(F)(F)F)C=C1 VBCVPMMZEGZULK-NRFANRHFSA-N 0.000 description 1
- 239000000411 inducer Substances 0.000 description 1
- YTCIYOXHHQLDEI-SNVBAGLBSA-N inpyrfluxam Chemical compound C([C@H](C=12)C)C(C)(C)C2=CC=CC=1NC(=O)C1=CN(C)N=C1C(F)F YTCIYOXHHQLDEI-SNVBAGLBSA-N 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 description 1
- OEXHQOGQTVQTAT-JRNQLAHRSA-N ipratropium Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)[N@@+]2(C)C(C)C)C(=O)C(CO)C1=CC=CC=C1 OEXHQOGQTVQTAT-JRNQLAHRSA-N 0.000 description 1
- 229960001888 ipratropium Drugs 0.000 description 1
- FCOAHACKGGIURQ-UHFFFAOYSA-N iprobenfos Chemical compound CC(C)OP(=O)(OC(C)C)SCC1=CC=CC=C1 FCOAHACKGGIURQ-UHFFFAOYSA-N 0.000 description 1
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- QBSJMKIUCUGGNG-UHFFFAOYSA-N isoprocarb Chemical compound CNC(=O)OC1=CC=CC=C1C(C)C QBSJMKIUCUGGNG-UHFFFAOYSA-N 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 description 1
- 125000001793 isothiazol-3-yl group Chemical group [H]C1=C([H])C(*)=NS1 0.000 description 1
- 125000004501 isothiazol-5-yl group Chemical group S1N=CC=C1* 0.000 description 1
- OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 description 1
- 229940088649 isoxaflutole Drugs 0.000 description 1
- 229960002418 ivermectin Drugs 0.000 description 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
- 229930014550 juvenile hormone Natural products 0.000 description 1
- 239000002949 juvenile hormone Substances 0.000 description 1
- 150000003633 juvenile hormone derivatives Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000005910 lambda-Cyhalothrin Substances 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 0.000 description 1
- 235000021374 legumes Nutrition 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 230000003859 lipid peroxidation Effects 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229950002303 lotilaner Drugs 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 229960000521 lufenuron Drugs 0.000 description 1
- PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910001623 magnesium bromide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- IUYHWZFSGMZEOG-UHFFFAOYSA-M magnesium;propane;chloride Chemical compound [Mg+2].[Cl-].C[CH-]C IUYHWZFSGMZEOG-UHFFFAOYSA-M 0.000 description 1
- 229960000453 malathion Drugs 0.000 description 1
- 230000036244 malformation Effects 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000035800 maturation Effects 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 description 1
- 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 description 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 description 1
- NNKVPIKMPCQWCG-UHFFFAOYSA-N methamidophos Chemical compound COP(N)(=O)SC NNKVPIKMPCQWCG-UHFFFAOYSA-N 0.000 description 1
- MEBQXILRKZHVCX-UHFFFAOYSA-N methidathion Chemical compound COC1=NN(CSP(=S)(OC)OC)C(=O)S1 MEBQXILRKZHVCX-UHFFFAOYSA-N 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 1
- 229930002897 methoprene Natural products 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-UHFFFAOYSA-N 0.000 description 1
- 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 description 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 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229940116837 methyleugenol Drugs 0.000 description 1
- PRHTXAOWJQTLBO-UHFFFAOYSA-N methyleugenol Natural products COC1=CC=C(C(C)=C)C=C1OC PRHTXAOWJQTLBO-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- PQIOSYKVBBWRRI-UHFFFAOYSA-N methylphosphonyl difluoride Chemical group CP(F)(F)=O PQIOSYKVBBWRRI-UHFFFAOYSA-N 0.000 description 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 description 1
- 108091040857 miR-604 stem-loop Proteins 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 239000011785 micronutrient Substances 0.000 description 1
- 235000013369 micronutrients Nutrition 0.000 description 1
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- QVCMHGGNRFRMAD-XFGHUUIASA-N monocrotaline Chemical compound C1OC(=O)[C@](C)(O)[C@@](O)(C)[C@@H](C)C(=O)O[C@@H]2CCN3[C@@H]2C1=CC3 QVCMHGGNRFRMAD-XFGHUUIASA-N 0.000 description 1
- QVCMHGGNRFRMAD-UHFFFAOYSA-N monocrotaline Natural products C1OC(=O)C(C)(O)C(O)(C)C(C)C(=O)OC2CCN3C2C1=CC3 QVCMHGGNRFRMAD-UHFFFAOYSA-N 0.000 description 1
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 231100000707 mutagenic chemical Toxicity 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- RXFQELGMJUSBGP-UHFFFAOYSA-N n'-[4-[4-chloro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-n-ethyl-n-methylmethanimidamide Chemical compound C1=C(C)C(N=CN(C)CC)=CC(C)=C1OC1=CC=C(Cl)C(C(F)(F)F)=C1 RXFQELGMJUSBGP-UHFFFAOYSA-N 0.000 description 1
- PAGDTTPJSICKIZ-UHFFFAOYSA-N n'-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-thiadiazol-5-yl]oxy]-2,5-dimethylphenyl]-n-ethyl-n-methylmethanimidamide Chemical compound C1=C(C)C(N=CN(C)CC)=CC(C)=C1OC1=NC(CC=2C=CC(Cl)=CC=2)=NS1 PAGDTTPJSICKIZ-UHFFFAOYSA-N 0.000 description 1
- SURYGMYUVAMSRO-UHFFFAOYSA-N n'-[5-(difluoromethyl)-2-methyl-4-(3-trimethylsilylpropoxy)phenyl]-n-ethyl-n-methylmethanimidamide Chemical compound CCN(C)C=NC1=CC(C(F)F)=C(OCCC[Si](C)(C)C)C=C1C SURYGMYUVAMSRO-UHFFFAOYSA-N 0.000 description 1
- XMSYZKCBUKZYIU-UHFFFAOYSA-N n'-[5-bromo-2-methyl-6-(4-propan-2-ylcyclohexyl)oxypyridin-3-yl]-n-ethyl-n-methylmethanimidamide Chemical compound N1=C(C)C(N=CN(C)CC)=CC(Br)=C1OC1CCC(C(C)C)CC1 XMSYZKCBUKZYIU-UHFFFAOYSA-N 0.000 description 1
- QPWDBFQQYNCENC-UHFFFAOYSA-N n'-[5-bromo-6-(2,3-dihydro-1h-inden-2-yloxy)-2-methylpyridin-3-yl]-n-ethyl-n-methylmethanimidamide Chemical compound N1=C(C)C(N=CN(C)CC)=CC(Br)=C1OC1CC2=CC=CC=C2C1 QPWDBFQQYNCENC-UHFFFAOYSA-N 0.000 description 1
- QUBHBTSVQMARKX-UHFFFAOYSA-N n'-[5-bromo-6-[1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl]-n-ethyl-n-methylmethanimidamide Chemical compound N1=C(C)C(N=CN(C)CC)=CC(Br)=C1OC(C)C1=CC(F)=CC(F)=C1 QUBHBTSVQMARKX-UHFFFAOYSA-N 0.000 description 1
- XDRDPGIDCNALCL-UHFFFAOYSA-N n,5-dimethyl-1-propan-2-yl-n-pyridazin-4-ylpyrazole-4-carboxamide Chemical compound CC(C)N1N=CC(C(=O)N(C)C=2C=NN=CC=2)=C1C XDRDPGIDCNALCL-UHFFFAOYSA-N 0.000 description 1
- JEFUQUGZXLEHLD-UHFFFAOYSA-N n-[(5-chloro-2-propan-2-ylphenyl)methyl]-n-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1=CC=C(Cl)C=C1CN(C(=O)C=1C(=NN(C)C=1F)C(F)F)C1CC1 JEFUQUGZXLEHLD-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- OPTZFFATLKEJAV-UHFFFAOYSA-N n-ethyl-2-(3-ethynyl-8-methylquinolin-6-yl)oxy-2-methylsulfanylacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(C(=O)NCC)SC)=CC(C)=C21 OPTZFFATLKEJAV-UHFFFAOYSA-N 0.000 description 1
- NQPGZXOPMRKAGJ-UHFFFAOYSA-N n-ethyl-5-methyl-1-(3-methylbutan-2-yl)-n-pyridazin-4-ylpyrazole-4-carboxamide Chemical compound C=1C=NN=CC=1N(CC)C(=O)C=1C=NN(C(C)C(C)C)C=1C NQPGZXOPMRKAGJ-UHFFFAOYSA-N 0.000 description 1
- OKQXFDSPKIACRT-UHFFFAOYSA-N n-ethyl-n'-[4-[4-fluoro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-n-methylmethanimidamide Chemical compound C1=C(C)C(N=CN(C)CC)=CC(C)=C1OC1=CC=C(F)C(C(F)(F)F)=C1 OKQXFDSPKIACRT-UHFFFAOYSA-N 0.000 description 1
- FCDOWQOIVVEOJB-UHFFFAOYSA-N n-propan-2-yl-2-pyridin-3-ylindazole-4-carboxamide Chemical compound C1=C2C(C(=O)NC(C)C)=CC=CC2=NN1C1=CC=CN=C1 FCDOWQOIVVEOJB-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000002018 neem oil Substances 0.000 description 1
- 125000005244 neohexyl group Chemical group [H]C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 108010003516 norsynephrine receptor Proteins 0.000 description 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000001668 nucleic acid synthesis Methods 0.000 description 1
- PZXOQEXFMJCDPG-UHFFFAOYSA-N omethoate Chemical compound CNC(=O)CSP(=O)(OC)OC PZXOQEXFMJCDPG-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 150000004045 organic chlorine compounds Chemical class 0.000 description 1
- 150000004967 organic peroxy acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
- 125000003145 oxazol-4-yl group Chemical group O1C=NC(=C1)* 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000010627 oxidative phosphorylation Effects 0.000 description 1
- 229960000321 oxolinic acid Drugs 0.000 description 1
- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 description 1
- 229960000625 oxytetracycline Drugs 0.000 description 1
- 235000019366 oxytetracycline Nutrition 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 description 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- WPIFGDDVIKNHOC-PLRJNAJWSA-N pentyl n-[6-[[(z)-[(1-methyltetrazol-5-yl)-phenylmethylidene]amino]oxymethyl]pyridin-2-yl]carbamate Chemical compound CCCCCOC(=O)NC1=CC=CC(CO\N=C(/C=2N(N=NN=2)C)C=2C=CC=CC=2)=N1 WPIFGDDVIKNHOC-PLRJNAJWSA-N 0.000 description 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- 229960003536 phenothrin Drugs 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- BULVZWIRKLYCBC-UHFFFAOYSA-N phorate Chemical compound CCOP(=S)(OCC)SCSCC BULVZWIRKLYCBC-UHFFFAOYSA-N 0.000 description 1
- HOKBIQDJCNTWST-UHFFFAOYSA-N phosphanylidenezinc;zinc Chemical compound [Zn].[Zn]=P.[Zn]=P HOKBIQDJCNTWST-UHFFFAOYSA-N 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 1
- 229950001664 phoxim Drugs 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 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 description 1
- 239000000049 pigment Substances 0.000 description 1
- 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 description 1
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 description 1
- 239000005962 plant activator Substances 0.000 description 1
- 244000000003 plant pathogen Species 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 description 1
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000001243 protein synthesis Methods 0.000 description 1
- 239000000007 protein synthesis inhibitor Substances 0.000 description 1
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 description 1
- AEHJMNVBLRLZKK-UHFFFAOYSA-N pyridalyl Chemical group N1=CC(C(F)(F)F)=CC=C1OCCCOC1=C(Cl)C=C(OCC=C(Cl)Cl)C=C1Cl AEHJMNVBLRLZKK-UHFFFAOYSA-N 0.000 description 1
- ZDYVRSLAEXCVBX-UHFFFAOYSA-N pyridinium p-toluenesulfonate Chemical compound C1=CC=[NH+]C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1 ZDYVRSLAEXCVBX-UHFFFAOYSA-N 0.000 description 1
- BAUQXSYUDSNRHL-UHFFFAOYSA-N pyrimorph Chemical compound C1=CC(C(C)(C)C)=CC=C1C(C=1C=NC(Cl)=CC=1)=CC(=O)N1CCOCC1 BAUQXSYUDSNRHL-UHFFFAOYSA-N 0.000 description 1
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
- 229940013788 quassia Drugs 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 150000003246 quinazolines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 238000002708 random mutagenesis Methods 0.000 description 1
- 235000021013 raspberries Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- HELXLJCILKEWJH-NCGAPWICSA-N rebaudioside A Chemical compound O([C@H]1[C@H](O)[C@@H](CO)O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HELXLJCILKEWJH-NCGAPWICSA-N 0.000 description 1
- 229940075993 receptor modulator Drugs 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 229940080817 rotenone Drugs 0.000 description 1
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 description 1
- GNHDVXLWBQYPJE-UHFFFAOYSA-N saflufenacil Chemical compound C1=C(Cl)C(C(=O)NS(=O)(=O)N(C)C(C)C)=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C1F GNHDVXLWBQYPJE-UHFFFAOYSA-N 0.000 description 1
- 201000000306 sarcoidosis Diseases 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- MXMXHPPIGKYTAR-UHFFFAOYSA-N silthiofam Chemical compound CC=1SC([Si](C)(C)C)=C(C(=O)NCC=C)C=1C MXMXHPPIGKYTAR-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- WRIKHQLVHPKCJU-UHFFFAOYSA-N sodium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([Na])[Si](C)(C)C WRIKHQLVHPKCJU-UHFFFAOYSA-N 0.000 description 1
- 229940125794 sodium channel blocker Drugs 0.000 description 1
- 239000003195 sodium channel blocking agent Substances 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 1
- GOLXNESZZPUPJE-UHFFFAOYSA-N spiromesifen Chemical compound CC1=CC(C)=CC(C)=C1C(C(O1)=O)=C(OC(=O)CC(C)(C)C)C11CCCC1 GOLXNESZZPUPJE-UHFFFAOYSA-N 0.000 description 1
- CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 210000003046 sporozoite Anatomy 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 102000026778 sterol binding proteins Human genes 0.000 description 1
- 108091008459 sterol binding proteins Proteins 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
- 125000005537 sulfoxonium group Chemical group 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 239000005936 tau-Fluvalinate Substances 0.000 description 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 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 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 description 1
- 229940095068 tetradecene Drugs 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 125000004523 tetrazol-1-yl group Chemical group N1(N=NN=C1)* 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- XSROQCDVUIHRSI-UHFFFAOYSA-N thietane Chemical compound C1CSC1 XSROQCDVUIHRSI-UHFFFAOYSA-N 0.000 description 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 description 1
- VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 description 1
- MBNMHBAJUNHZRE-UHFFFAOYSA-M thiosultap monosodium Chemical compound [Na+].OS(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O MBNMHBAJUNHZRE-UHFFFAOYSA-M 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- VJQYLJSMBWXGDV-UHFFFAOYSA-N tiadinil Chemical compound N1=NSC(C(=O)NC=2C=C(Cl)C(C)=CC=2)=C1C VJQYLJSMBWXGDV-UHFFFAOYSA-N 0.000 description 1
- IHNSIFFSNUQGQN-UHFFFAOYSA-N tioxazafen Chemical compound C1=CSC(C=2ON=C(N=2)C=2C=CC=CC=2)=C1 IHNSIFFSNUQGQN-UHFFFAOYSA-N 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 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 description 1
- RSOBJVBYZCMJOS-CYBMUJFWSA-N tolprocarb Chemical compound FC(F)(F)COC(=O)N[C@@H](C(C)C)CNC(=O)C1=CC=C(C)C=C1 RSOBJVBYZCMJOS-CYBMUJFWSA-N 0.000 description 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 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000723 toxicological property Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- GFNANZIMVAIWHM-OBYCQNJPSA-N triamcinolone Chemical compound O=C1C=C[C@]2(C)[C@@]3(F)[C@@H](O)C[C@](C)([C@@]([C@H](O)C4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 GFNANZIMVAIWHM-OBYCQNJPSA-N 0.000 description 1
- 229960005294 triamcinolone Drugs 0.000 description 1
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- KRTNITDCKAVIFI-UHFFFAOYSA-N tridecyl benzenesulfonate Chemical class CCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 KRTNITDCKAVIFI-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical class C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 1
- 239000003744 tubulin modulator Substances 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 210000004291 uterus Anatomy 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 244000052613 viral pathogen Species 0.000 description 1
- YEIGUXGHHKAURB-VAMGGRTRSA-N viridin Chemical compound O=C1C2=C3CCC(=O)C3=CC=C2[C@@]2(C)[C@H](O)[C@H](OC)C(=O)C3=COC1=C23 YEIGUXGHHKAURB-VAMGGRTRSA-N 0.000 description 1
- 108010086097 viridin Proteins 0.000 description 1
- YEIGUXGHHKAURB-UHFFFAOYSA-N viridine Natural products O=C1C2=C3CCC(=O)C3=CC=C2C2(C)C(O)C(OC)C(=O)C3=COC1=C23 YEIGUXGHHKAURB-UHFFFAOYSA-N 0.000 description 1
- 244000000187 viroid pathogen Species 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 208000005494 xerophthalmia Diseases 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229940048462 zinc phosphide Drugs 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
Abstract
本发明涉及具有式(I)的化合物,其中变量如在说明书和权利要求书中给出的定义。本发明进一步涉及它们的用途和组合物。
Description
本发明涉及作为杀真菌剂的新型喹唑啉化合物及其N-氧化物和盐,以及它们的用途。本发明还涉及包含至少一种化合物I的组合物、用于对抗植物病原性真菌的方法、以及涂覆有至少一种具有式I的化合物的种子。
JP 2011148714披露了一些类似的化合物。然而,在许多情况下,特别是在低施用率下,已知化合物的杀真菌活性并不令人满意。基于此,本发明的一个目的是提供对植物病原性真菌具有改善的活性和/或更宽的活性谱的化合物。本发明的另一个目的是提供具有改善的毒理学特性或具有改善的环境归宿特性的杀真菌剂。
这些和另外的目的由如以下定义的具有式(I)的喹啉化合物及其农业上适合的实现。
因此,本发明涉及作为杀真菌剂的具有式I的化合物及其N-氧化物和农业上可接受的盐
其中
R1是H、卤素、CN、C1-C4-烷基、C1-C4-卤代烷基;
R4是H、卤素、CN、C1-C4-烷基、C1-C4-卤代烷基;
R5在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、苯基、苄基,
其中R5的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R5a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
R6在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、苯基、苄基,
其中R6的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R6a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
或者
R5和R6与它们所键合的C原子一起形成C3-C6-环烷基、或含有1、2或3个来自由O和S组成的组的杂原子的3元至6元饱和杂环;
R7在每种情况下独立地选自氢、CN、CH2CN、CH(CH3)CN、CH(=O)、C(=O)C1-C6-烷基、C(=O)C2-C6-烯基、C(=O)C2-C6-炔基、C(=O)C3-C6-环烷基、C(=O)NH-C1-C4-烷基、C(=O)N-(C1-C4-烷基)2、C1-C6-烷基、O-C1-C6-烷基、C1-C4-卤代烷基、C3-C6-环烷基、C3-C6-卤代环烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、-S(=O)2-R7a、五元或六元杂芳基和芳基或苄基;其中该杂芳基含有一个、两个或三个选自N、O和S的杂原子;其中该芳基或苄基是未取代的或带有一个、两个、三个、四个或五个选自由以下组成的组的取代基:CN、卤素、OH、C1-C4-烷基、C1-C4-卤代烷基、C1-C4-烷氧基、和C1-C4-卤代烷氧基;其中
R7a选自C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、苯基、苄基,其中苯基和苄基可以是未取代的或被卤素、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基取代;
X在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基、O-C1-C6-卤代烷基;
n是0、1、2或3;
Y在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
m是1、2或3。
N-氧化物可以由本发明的化合物根据常规的氧化方法制备,例如通过用有机过酸如间氯过氧苯甲酸(参见WO 03/64572或J.Med.Chem.[药物化学杂志]38(11),1892-903,1995);或用无机氧化剂如过氧化氢(参见J.Heterocyc.Chem.[杂环化学杂志]18(7),1305-8,1981)或过硫酸氢钾制剂(参见J.Am.Chem.Soc.[美国化学会志]123(25),5962-5973,2001)处理化合物I。氧化可以产生纯的单-N-氧化物或不同N-氧化物的混合物,其可通过常规方法如色谱法分离。
具有式I的化合物的农业上可接受的盐尤其涵盖其阳离子和阴离子分别对化合物I的杀真菌作用没有不利影响的那些阳离子的盐或那些酸的酸加成盐。因此,合适的阳离子特别是碱金属(优选钠和钾)离子,碱土金属(优选钙、镁和钡)离子,过渡金属(优选锰、铜、锌和铁)离子,以及还有铵离子,如果需要,其可以被一至四个C1-C4-烷基取代基和/或一个苯基或苄基取代基取代,优选二异丙基铵、四甲基铵、四丁基铵、三甲基苄基铵,此外还有鏻离子,锍离子、优选三(C1-C4-烷基)锍,以及氧化锍离子、优选三(C1-C4-烷基)氧化锍。
可接受的酸加成盐的阴离子主要是氯离子,溴离子,氟离子,硫酸氢根,硫酸根,磷酸二氢根,磷酸氢根,磷酸根,硝酸根,碳酸氢根,碳酸根,六氟硅酸根,六氟磷酸根,苯甲酸根以及C1-C4-烷酸的阴离子,优选甲酸根、乙酸根、丙酸根和丁酸根。它们可以通过使化合物I与对应阴离子的酸,优选盐酸、氢溴酸、硫酸、磷酸或硝酸反应来形成。
具有式I的化合物可以作为一种或多种立体异构体存在。各种立体异构体包括对映异构体、非对映异构体、由围绕不对称基团的单键受限制旋转产生的阻转异构体和几何异构体。它们也形成本发明的主题的一部分。本领域的技术人员将理解,一种立体异构体当相对于一种或多种其他立体异构体富集时,或当与一种或多种其他立体异构体分离时,可能更有活性和/或可能表现出有益的效果。此外,技术人员知晓如何分离、富集和/或选择性地制备所述立体异构体。本发明的化合物可以作为立体异构体的混合物(例如外消旋物)、单独的立体异构体、或作为光学活性形式存在。
具有式I的化合物可以以其生物活性可能不同的不同的晶体变型存在。它们也形成本发明的主题的一部分。
就变量而言,化合物I制备期间获得的中间体的实施例对应于具有式I的化合物的实施例。术语“化合物I”是指具有式I的化合物。
在下文中,进一步描述中间体化合物。技术人员将容易理解,本文中结合化合物I给出的取代基的优选项、还特别是下表中对于相应取代基给出的优选项相应地适用于中间体。因此,每种情况下的取代基彼此独立地或更优选以组合的形式具有如本文所定义的含义。
如果合成产生异构体的混合物,则通常不一定要求分离,因为在一些情况下单独的异构体可能在为了使用而进行的后处理期间或在施用期间(例如在光、酸或碱的作用下)相互转化。此类转化也可以在使用后发生,例如在植物处理的情况下在被处理的植物中,或者在待控制的有害真菌中。
在以上给出的变量的定义中,使用了通常代表所讨论的取代基的集合性术语。术语“Cn-Cm”指示在每种情况下所讨论的取代基或取代基部分中可能的碳原子的数目。
术语“卤素”是指氟、氯、溴和碘。
术语“C1-C6-烷基”是指具有1至6个碳原子的直链或支链饱和烃基,例如甲基、乙基、丙基、1-甲基乙基、丁基、1-甲基丙基、2-甲基丙基、1,1-二甲基乙基、戊基、1-甲基丁基、2-甲基丁基、3-甲基丁基、2,2-二甲基丙基、1-乙基丙基、1,1-二甲基丙基、1,2-二甲基丙基、己基、1-甲基戊基、2-甲基戊基、3-甲基戊基、4-甲基戊基、1,1-二甲基丁基、1,2-二甲基丁基、1,3-二甲基丁基、2,2-二甲基丁基、2,3-二甲基丁基、3,3-二甲基丁基、1-乙基丁基、2-乙基丁基、1,1,2-三甲基丙基、1,2,2-三甲基丙基、1-乙基-1-甲基丙基和1-乙基-2-甲基丙基。类似地,术语“C2-C4-烷基”是指具有2至4个碳原子的直链或支链烷基,如乙基、丙基(正丙基)、1-甲基乙基(异丙基)、丁基、1-甲基丙基(仲丁基)、2-甲基丙基(异丁基)、1,1-二甲基乙基(叔丁基)。
术语“C1-C6-卤代烷基”是指如上文所定义的具有1或6个碳原子的烷基,其中这些基团中的一些或全部氢原子可以被如上所述的卤素原子替代。实例是“C1-C2-卤代烷基”基团,如氯甲基、溴甲基、二氯甲基、三氯甲基、氟甲基、二氟甲基、三氟甲基、氯氟甲基、二氯氟甲基、氯二氟甲基、1-氯乙基、1-溴乙基、1-氟乙基、2-氟乙基、2,2-二氟乙基、2,2,2-三氟乙基、2-氯-2-氟乙基、2-氯-2,2-二氟乙基、2,2-二氯-2-氟乙基、2,2,2-三氯乙基、或五氟乙基。
术语“C1-C6-烷氧基”是指经由氧在烷基中的任意位置上键合的具有1至6个碳原子的直链或支链烷基。实例是“C1-C4-烷氧基”基团,如甲氧基、乙氧基、正丙氧基、1-甲基乙氧基、丁氧基、1-甲基丙氧基、2-甲基丙氧基或1,1-二甲基乙氧基。
术语“C1-C6-卤代烷氧基”是指如上文所定义的C1-C6-烷氧基,其中这些基团中的一些或全部氢原子可以被如上所述的卤素原子替代。实例是“C1-C4-卤代烷氧基”基团,如OCH2F、OCHF2、OCF3、OCH2Cl、OCHCl2、OCCl3、氯氟甲氧基、二氯氟甲氧基、氯二氟甲氧基、2-氟乙氧基、2-氯乙氧基、2-溴乙氧基、2-碘乙氧基、2,2-二氟乙氧基、2,2,2-三氟乙氧基、2-氯-2-氟乙氧基、2-氯-2,2-二氟乙氧基、2,2-二氯-2-氟乙氧基、2,2,2-三氯乙氧基、OC2F5、2-氟丙氧基、3-氟丙氧基、2,2-二氟丙氧基、2,3-二氟丙氧基、2-氯丙氧基、3-氯丙氧基、2,3-二氯丙氧基、2-溴丙氧基、3-溴丙氧基、3,3,3-三氟丙氧基、3,3,3-三氯丙氧基、OCH2-C2F5、OCF2-C2F5、1-氟甲基-2-氟乙氧基、1-氯甲基-2-氯乙氧基、1-溴甲基-2-溴乙氧基、4-氟丁氧基、4-氯丁氧基、4-溴丁氧基或九氟丁氧基。
术语“C2-C6-烯基”是指具有2至6个碳原子且在任意位置具有双键的直链或支链不饱和烃基。实例是“C2-C4-烯基”基团,如乙烯基、1-丙烯基、2-丙烯基(烯丙基)、1-甲基乙烯基、1-丁烯基、2-丁烯基、3-丁烯基、1-甲基-1-丙烯基、2-甲基-1-丙烯基、1-甲基-2-丙烯基、2-甲基-2-丙烯基。
术语“C2-C6-卤代烯基”是指如上文所定义的具有2或6个碳原子的烷基,其中这些基团中的一些或全部氢原子可以被如上所述的卤素原子替代。
术语“C2-C6-烯氧基”是指经由氧在烯基中的任意位置上键合的具有2至6个碳原子的直链或支链烯基。实例是“C2-C4-烯氧基”基团。
术语“C2-C6-炔基”是指具有2至6个碳原子并且含有至少一个三键的直链或支链不饱和烃基。实例是“C2-C4-炔基”基团,例如乙炔基、丙-1-炔基、丙-2-炔基(炔丙基)、丁-1-炔基、丁-2-炔基、丁-3-炔基、1-甲基-丙-2-炔基。
术语“C2-C6-卤代炔基”是指如上文所定义的具有2或6个碳原子的烷基,其中这些基团中的一些或全部氢原子可以被如上所述的卤素原子替代。
术语“C2-C6-炔氧基”是指经由氧在炔基中的任意位置上键合的具有2至6个碳原子的直链或支链炔基。实例是“C2-C4-炔氧基”基团。
术语“C3-C6-环烷基”是指具有3至6个碳环成员的单环饱和烃基,如环丙基、环丁基、环戊基、环己基。因此,饱和三元、四元、五元、六元、七元、八元、九元或十元碳环基或碳环是“C3-C10-环烷基”。
术语“C3-C6-环烯基”是指具有3至6个碳环成员和至少一个双键的单环部分不饱和3元、4元、5元或6元碳环,如环戊烯基、环戊二烯基、环己二烯基。因此,部分不饱和三元、四元、五元、六元、七元、八元、九元或十元碳环基或碳环是“C3-C10-环烯基”。
术语“C3-C8-环烷基-C1-C4-烷基”是指具有1至4个碳原子的烷基(如上文所定义),其中烷基的一个氢原子被具有3至8个碳原子的环烷基(如上文所定义)替代。
术语“饱和或部分不饱和三元、四元、五元、六元、七元、八元、九元或十元杂环基或杂环,其中该杂环基或杂环含有1、2、3或4个选自N、O和S的杂原子”应理解为意指饱和杂环和部分不饱和的杂环两者,其中杂环的环成员原子除碳原子外还包括1、2、3或4个独立地选自O、N和S的组的杂原子。例如:
含有1或2个选自由O、N和S组成的组的杂原子作为环成员的3元或4元饱和杂环,如环氧乙烷、氮丙啶、硫杂环丙烷、氧杂环丁烷、氮杂环丁烷、硫杂环丁烷(thiethane)、[1,2]二氧杂环丁烷、[1,2]二硫杂环丁烷、[1,2]二氮杂环丁烷;以及
含有1、2或3个选自由O、N和S组成的组的杂原子作为环成员的5元或6元饱和或部分不饱和杂环,如2-四氢呋喃基、3-四氢呋喃基、2-四氢噻吩基、3-四氢噻吩基、2-吡咯烷基、3-吡咯烷基、3-异噁唑烷基、4-异噁唑烷基、5-异噁唑烷基、3-异噻唑烷基、4-异噻唑烷基、5-异噻唑烷基、3-吡唑烷基、4-吡唑烷基、5-吡唑烷基、2-噁唑烷基、4-噁唑烷基、5-噁唑烷基、2-噻唑烷基、4-噻唑烷基、5-噻唑烷基、2-咪唑烷基、4-咪唑烷基、1,2,4-噁二唑烷-3-基、1,2,4-噁二唑烷-5-基、1,2,4-噻二唑烷-3-基、1,2,4-噻二唑烷-5-基、1,2,4-三唑烷-3-基、1,3,4-噁二唑烷-2-基、1,3,4-噻二唑烷-2-基、1,3,4-三唑烷-2-基、2,3-二氢呋喃-2-基、2,3-二氢呋喃-3-基、2,4-二氢呋喃-2-基、2,4-二氢呋喃-3-基、2,3-二氢噻吩-2-基、2,3-二氢噻吩-3-基、2,4-二氢噻吩-2-基、2,4-二氢噻吩-3-基、2-吡咯啉-2-基、2-吡咯啉-3-基、3-吡咯啉-2-基、3-吡咯啉-3-基、2-异噁唑啉-3-基、3-异噁唑啉-3-基、4-异噁唑啉-3-基、2-异噁唑啉-4-基、3-异噁唑啉-4-基、4-异噁唑啉-4-基、2-异噁唑啉-5-基、3-异噁唑啉-5-基、4-异噁唑啉-5-基、2-异噻唑啉-3-基、3-异噻唑啉-3-基、4-异噻唑啉-3-基、2-异噻唑啉-4-基、3-异噻唑啉-4-基、4-异噻唑啉-4-基、2-异噻唑啉-5-基、3-异噻唑啉-5-基、4-异噻唑啉-5-基、2,3-二氢吡唑-1-基、2,3-二氢吡唑-2-基、2,3-二氢吡唑-3-基、2,3-二氢吡唑-4-基、2,3-二氢吡唑-5-基、3,4-二氢吡唑-1-基、3,4-二氢吡唑-3-基、3,4-二氢吡唑-4-基、3,4-二氢吡唑-5-基、4,5-二氢吡唑-1-基、4,5-二氢吡唑-3-基、4,5-二氢吡唑-4-基、4,5-二氢吡唑-5-基、2,3-二氢噁唑-2-基、2,3-二氢噁唑-3-基、2,3-二氢噁唑-4-基、2,3-二氢噁唑-5-基、3,4-二氢噁唑-2-基、3,4-二氢噁唑-3-基、3,4-二氢噁唑-4-基、3,4-二氢噁唑-5-基、3,4-二氢噁唑-2-基、3,4-二氢噁唑-3-基、3,4-二氢噁唑-4-基、2-哌啶基、3-哌啶基、4-哌啶基、1,3-二噁烷-5-基、2-四氢吡喃基、4-四氢吡喃基、2-四氢噻吩基、3-六氢哒嗪基、4-六氢哒嗪基、2-六氢嘧啶基、4-六氢嘧啶基、5-六氢嘧啶基、2-哌嗪基、1,3,5-六氢三嗪-2-基和1,2,4-六氢三嗪-3-基,以及还有对应的-亚基基团;以及
7元饱和或部分不饱和杂环如四-和六氢氮杂卓基,如2,3,4,5-四氢[1H]氮杂卓-1-、-2-、-3-、-4-、-5-、-6-或-7-基、3,4,5,6-四氢[2H]氮杂卓-2-、-3-、-4-、-5-、-6-或-7-基、2,3,4,7-四氢[1H]氮杂卓-1-、-2-、-3-、-4-、-5-、-6-或-7-基、2,3,6,7-四氢[1H]氮杂卓-1-、-2-、-3-、-4-、-5-、-6-或-7-基、六氢氮杂卓-1-、-2-、-3-或-4-基,四-和六氢氧杂卓基如2,3,4,5-四氢[1H]氧杂卓-2-、-3-、-4-、-5-、-6-或-7-基、2,3,4,7-四氢[1H]氧杂卓-2-、-3-、-4-、-5-、-6-或-7-基、2,3,6,7-四氢[1H]氧杂卓-2-、-3-、-4-、-5-、-6-或-7-基,六氢氮杂卓-1-、-2-、-3-或-4-基,四-和六氢-1,3-二氮杂卓基,四-和六氢-1,4-二氮杂卓基,四-和六氢-1,3-氧氮杂卓基,四-和六氢-1,4-氧氮杂卓基,四-和六氢-1,3-二氧杂卓基,四-和六氢-1,4-二氧杂卓基和对应的-亚基基团。
术语“取代的”是指被1、2、3个或最多达可能的最大数量的取代基取代。
术语“5元或6元杂芳基”或“5元或6元杂芳族基团(heteroaromatic)”是指除碳原子之外还包含1、2、3或4个独立地选自由N、O和S组成的组的杂原子的芳香族环体系,例如
5元杂芳基,如吡咯-1-基、吡咯-2-基、吡咯-3-基、噻吩-2-基、噻吩-3-基、呋喃-2-基、呋喃-3-基、吡唑-1-基、吡唑-3-基、吡唑-4-基、吡唑-5-基、咪唑-1-基、咪唑-2-基、咪唑-4-基、咪唑-5-基、噁唑-2-基、噁唑-4-基、噁唑-5-基、异噁唑-3-基、异噁唑-4-基、异噁唑-5-基、噻唑-2-基、噻唑-4-基、噻唑-5-基、异噻唑-3-基、异噻唑-4-基、异噻唑-5-基、1,2,4-三唑基-1-基、1,2,4-三唑-3-基、1,2,4-三唑-5-基、1,2,4-噁二唑-3-基、1,2,4-噁二唑-5-基和1,2,4-噻二唑-3-基、1,2,4-噻二唑-5-基;或者
6元杂芳基,如吡啶-2-基、吡啶-3-基、吡啶-4-基、哒嗪-3-基、哒嗪-4-基、嘧啶-2-基、嘧啶-4-基、嘧啶-5-基、吡嗪-2-基和1,3,5-三嗪-2-基和1,2,4-三嗪-3-基。
在下文中,描述了本发明化合物的特定实施例。其中,进一步详述了相应取代基的具体含义,其中这些含义在每种情况下其本身而且彼此任意组合是本发明特定实施例。
此外,就变量而言,总体上,化合物I的实施例同样适用于中间体。
根据具有式I的化合物的一个实施例,R1是H、卤素、CN、C1-C4-烷基、C1-C4-卤代烷基。
根据具有式I的化合物的一个实施例,R1是H。
根据具有式I的化合物的一个实施例,R1是CH3。
根据具有式I的化合物的一个实施例,R4是H、卤素、CN、C1-C4-烷基、C1-C4-卤代烷基。
根据具有式I的化合物的一个实施例,R4是H。
根据具有式I的化合物的一个实施例,R4是CH3。
R5在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、C1-C6-烷基-O-C1-C6-烷基、苯基、苄基,
其中R5的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R5a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基。
根据具有式I的化合物的一个实施例,R5在每种情况下独立地选自C1-C6-烷基(实施例5.1)、C1-C6-卤代烷基(实施例5.2)、C1-C6-烷基-O-C1-C6-烷基(实施例5.3)、苯基、CH2-苯基(实施例5.4)、卤素(实施例5.5),其中苯基和CH2-苯基是未取代的或被一个或两个卤素取代。
根据具有式I的化合物的一个另外的实施例,R5是CH3或CF3。
根据具有式I的化合物的一个另外的实施例,R5是CH2CH3、CH(CH3)2、CH(CH3)CH2CH3、C(CH3)3、CH2-CH(CH3)2、CH2-C(CH3)3、CH2-O-CH3。
根据具有式I的化合物的一个另外的实施例,R5是苯基、2-F-苯基、4-F-苯基、2,4-F2-苯基、2-Cl-苯基、4-Cl-苯基、CH2-苯基、CH2-2-F-苯基、CH2-4-F-苯基。
根据具有式I的化合物的一个实施例,R6在每种情况下独立地选自在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、C1-C6-烷基-O-C1-C6-烷基、苯基、苄基、C1-C6-烷基-O-苯基,
其中R6的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R6a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基。
根据具有式I的化合物的一个实施例,R6在每种情况下独立地选自C1-C6-烷基(实施例6.1)、C1-C6-烷基-O-苯基(实施例6.2)、C1-C6-烷基-O-C1-C6-烷基(实施例6.3)、卤素(实施例6.4)。
根据具有式I的化合物的一个另外的实施例,R6是CH3或CF3。
根据具有式I的化合物的一个另外的实施例,R6是CH2CH3、CH(CH3)2、CH(CH3)CH2CH3、C(CH3)3、CH2-CH(CH3)2、CH2-C(CH3)3、CH2-CH(CH3)-C(CH3)3、CH2-CH2-C(CH3)3、CH2-O-CH3、CH2-O-(CH3)3、CH2-O-苯基。
根据具有式I的化合物的一个另外的实施例,R5和R6与它们所键合的C原子一起形成C3-C6-环烷基、或含有1、2或3个来自由O和S组成的组的杂原子的3元至6元饱和杂环。
根据具有式I的化合物的一个另外的实施例,R5和R6形成C3-C6-环烷基(实施例6.5)。
根据具有式I的化合物的一个另外的实施例,R5和R6形成含有1、2或3个来自由O和S组成的组的杂原子的3元至6元饱和杂环。
根据具有式I的化合物的一个另外的实施例,R5和R6形成含有一个O的3元至6元饱和杂环(实施例6.6)。
根据本发明的R5、R6的优选实施例在下表P5中,其中行P5-1至P5-18的每一行对应于本发明的一个特定实施例,其中P5-1至P5-18还彼此任意组合是本发明的优选实施例。与R5和R6键合的碳原子的连接点在图中用“#”标记。
表P5,6:
R7在每种情况下独立地选自氢、CN、CH2CN、CH(CH3)CN、CH(=O)、C(=O)C1-C6-烷基、C(=O)C2-C6-烯基、C(=O)C2-C6-炔基、C(=O)C3-C6-环烷基、C(=O)NH-C1-C4-烷基、C(=O)N-(C1-C4-烷基)2、C1-C6-烷基、O-C1-C6-烷基、C1-C4-卤代烷基、C3-C6-环烷基、C3-C6-卤代环烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、CH2C(=O)C2-C6-烯基、CH2C(=O)C2-C6-炔基、CH2C(=O)C3-C6-环烷基、CH2C(=O)NH-C1-C4-烷基、CH2C(=O)N-(C1-C4-烷基)2、-S(=O)2-R7a、五元或六元杂芳基和芳基;其中该杂芳基含有一个、两个或三个选自N、O和S的杂原子;其中该芳基是未取代的或带有一个、两个、三个、四个或五个选自由以下组成的组的取代基:CN、卤素、OH、C1-C4-烷基、C1-C4-卤代烷基、C1-C4-烷氧基、和C1-C4-卤代烷氧基;其中
R7a选自C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、苯基、苄基,其中苯基和苄基可以是未取代的或被卤素、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基取代。
根据式I的一个实施例,R7是H。
根据式I的还另一个实施例,R7是Cl、F。
根据式I的还另一个实施例,R7是CN、CH2CN、或CH(CH3)CN。
根据式I的另一个具体实施例,R7是CH(=O)。
根据式I的另一个具体实施例,R7是OCH3。
根据式I的另一个具体实施例,R7是C(=O)C1-C6-烷基,其中烷基是CH3、C2H5、正丙基、异丙基、正丁基、异丁基、叔丁基、正戊基、或异戊基。
根据式I的另一个具体实施例,R7是C(=O)C2-C6-烯基,其中烯基是CH=CH2、CH2CH=CH2。
根据式I的另一个具体实施例,R7是C(=O)C2-C6-炔基,其中炔基是C≡CH、CH2C≡CH。
根据式I的另一个具体实施例,R7是C(=O)C3-C6-环烷基,其中环烷基是环丙基(C3H7)或环丁基(C4H9)。
根据式I的另一个具体实施例,R7是C(=O)NH-C1-C4-烷基或C(=O)N-(C1-C4-烷基)2,其中烷基是CH3、C2H5、正丙基、异丙基、正丁基、异丁基、叔丁基。
根据式I的还另一个实施例,R7是C1-C6-烷基,如CH3、C2H5、正丙基、异丙基、正丁基、异丁基、叔丁基、正戊基或异戊基。
根据式I的还另一个实施例,R7是C1-C6-烷基、特别是C1-C4-烷基,如CH3、C2H5、正丙基、异丙基。
根据式I的还另一个实施例,R7是C1-C6-卤代烷基,特别是C1-C4-卤代烷基,如CF3、CCl3、FCH2、ClCH2、F2CH、Cl2CH、CF3CH2、CCl3CH2或CF2CHF2。
根据式I的还另一个实施例,R7是C3-C6-环烷基、特别是环丙基。
根据式I的还另一个实施例,R7是C3-C6-卤代环烷基。在特殊实施例中,R5b是完全或部分卤代的环丙基,如1-F-环丙基、1-Cl-环丙基、1,1-F2-环丙基、1,1-Cl2-环丙基。
根据式I的还另一个实施例,R7是C2-C6-烯基,特别是C2-C4-烯基,如CH=CH2、C(CH3)=CH2、CH2CH=CH2。
根据式I的另一个具体实施例,R7是C2-C6-卤代烯基,特别是C2-C4-卤代烯基,更具体地C2-C3-卤代烯基,如CH=CHF、CH=CHCl、CH=CF2、CH=CCl2、CH2CH=CHF、CH2CH=CHCl、CH2CH=CF2、CH2CH=CCl2、CF2CH=CF2、CCl2CH=CCl2、CF2CF=CF2、CCl2CCl=CCl2。
根据式I的还另一个实施例,R7是C2-C6-炔基或C2-C6-卤代炔基,特别是C2-C4-炔基或C2-C4-卤代炔基,如C≡CH、CH2C≡CH。
根据式I的还另一个实施例,R7是-S(=O)2-R7a,其中R7a优选地是C1-C6-烷基,特别是C1-C4-烷基,如CH3、C2H5、正丙基、异丙基。
根据式I的还另一个实施例,R7是芳基,特别是苯基,其中该芳基或苯基部分在每种情况下是未取代的或被相同或不同的彼此独立地选自以下的基团R5b取代:卤素、C1-C2-烷基、C1-C2-烷氧基、C1-C2-卤代烷基和C1-C2-卤代烷氧基,特别是F、Cl、Br、CH3、OCH3、CF3、和OCF3。根据一个实施例,R5是未取代的苯基。根据另一个实施例,R5是被一个、两个、三个(特别是一个)特别是选自F、Cl和Br、更具体地选自F和Cl的卤素取代的苯基。
根据式I的还另一个实施例,R7是5元杂芳基,如吡咯-1-基、吡咯-2-基、吡咯-3-基、噻吩-2-基、噻吩-3-基、呋喃-2-基、呋喃-3-基、吡唑-1-基、吡唑-3-基、吡唑-4-基、吡唑-5-基、咪唑-1-基、咪唑-2-基、咪唑-4-基、咪唑-5-基、噁唑-2-基、噁唑-4-基、噁唑-5-基、异噁唑-3-基、异噁唑-4-基、异噁唑-5-基、噻唑-2-基、噻唑-4-基、噻唑-5-基、异噻唑-3-基、异噻唑-4-基、异噻唑-5-基、1,2,4-三唑基-1-基、1,2,4-三唑-3-基、1,2,4-三唑-5-基、1,2,4-噁二唑-3-基、1,2,4-噁二唑-5-基和1,2,4-噻二唑-3-基、1,2,4-噻二唑-5-基。
根据式I的还另一个实施例,R7是6元杂芳基,如吡啶-2-基、吡啶-3-基、吡啶-4-基、哒嗪-3-基、哒嗪-4-基、嘧啶-2-基、嘧啶-4-基、嘧啶-5-基、吡嗪-2-基和1,3,5-三嗪-2-基和1,2,4-三嗪-3-基。
根据式I的还另一个实施例,R7在每种情况下独立地选自H、卤素、OH、CN、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-炔基、C1-C6-烷氧基、C1-C6-卤代烷氧基、C3-C6-烯氧基、C3-C6-炔氧基和C3-C6-环烷基,其中R5的非环状部分是未取代的或被相同或不同的如所定义的并且优选如本文所定义的基团R5a取代,并且其中R5的碳环、苯基和杂芳基部分是未取代的或被相同或不同的如所定义的并且优选如本文所定义的基团R5b取代。
根据本发明的R7的特别优选的实施例在下表P7中,其中行P7-1至P7-33的每一行对应于本发明的一个特定实施例,其中P7-1至P7-33还彼此任意组合是本发明的优选实施例。与R7键合的碳原子的连接点在图中用“#”标记。
表P5:
根据具有式I的化合物的一个实施例,X在每种情况下独立地选自卤素(实施例X.1)、CN、C1-C6-烷基(实施例X.2)、C1-C6-卤代烷基(实施例X.3)、O-C1-C6-烷基(实施例X.4)、O-C1-C6-卤代烷基(实施例X.5)。
根据具有式I的化合物的一个实施例,X在每种情况下独立地选自卤素、O-C1-C6-烷基。
根据具有式I的化合物的一个实施例,X在每种情况下独立地选自F或Cl。
根据具有式I的化合物的一个实施例,n是0。
根据具有式I的化合物的一个实施例,n是1。
根据具有式I的化合物的一个实施例,n是2。
根据具有式I的化合物的一个实施例,Y是H。
根据具有式I的化合物的一个实施例(实施例Y.1),Y在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基。
根据具有式I的化合物的一个实施例(实施例Y.2),Y在每种情况下独立地选自卤素。
根据具有式I的化合物的一个实施例(实施例Y.3),Y在每种情况下独立地选自Fl和Cl。
根据具有式I的化合物的一个实施例(实施例Y.4),Y在子式(y.1至y.10)中定义
根据具有式I的化合物的一个实施例,m是1。
根据具有式I的化合物的一个实施例,m是2。
在一个实施例中,本发明涉及具有式I的化合物、或其N-氧化物或农业上可接受的盐,其中
R1是H;
R4是H;
R5在每种情况下独立地选自卤素、CN、C2-C6-烷基、C2-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、C1-C6-烷基-O-C1-C6-烷基、苯基、苄基,
其中R5的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R5a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
R6在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、C1-C6-烷基-O-C1-C6-烷基、苯基、苄基、C1-C6-烷基-O-苯基,
其中R6的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R6a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
或者
R5和R6与它们所键合的C原子一起形成C3-C6-环烷基、或含有1、2或3个来自由O和S组成的组的杂原子的3元至6元饱和杂环;
X在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基、O-C1-C6-卤代烷基;
n是0、1、2或3;
Y在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
m是1、2或3。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其表示上文针对变量Y(由实施例Y.1至Y.4和y.1至y.10表示)和X(由实施例X.1至X.6表示)中的每一个所定义的实施例的优选组合,具有式I的化合物中的n如下所定义。
表E:
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.1表示,并且R6由实施例6.1表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.2表示,并且R6由实施例6.1表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.3表示,并且R6由实施例6.1表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.4表示,并且R6由实施例6.1表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.5表示,并且R6由实施例6.1表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.1表示,并且R6由实施例6.2表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.2表示,并且R6由实施例6.2表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.3表示,并且R6由实施例6.2表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.4表示,并且R6由实施例6.2表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.5表示,并且R6由实施例6.2表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.1表示,并且R6由实施例6.3表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.2表示,并且R6由实施例6.3表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.3表示,并且R6由实施例6.3表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.4表示,并且R6由实施例6.3表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.5表示,并且R6由实施例6.3表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.1表示,并且R6由实施例6.4表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.2表示,并且R6由实施例6.4表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.3表示,并且R6由实施例6.4表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.4表示,并且R6由实施例6.4表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5由实施例5.5表示,并且R6由实施例6.4表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5和R6由实施例6.5表示。
在另外的方面,本发明涉及表E中列出的实施例E.1至E.280,其中R5和R6由实施例6.6表示。
本发明的优选实施例是以下化合物I.A-1、I.A-2、I.A-3、I.A-4。在这些式中,取代基R5、R6和Xn独立地如上文所定义或优选地如本文所定义:
特别地,考虑到它们的用途,根据一个实施例,优选的是化合物I.A-1、I.A-2、I.A-3、I.A-4中的化合物;其汇编于表1a至7a中。此外,在表中对于取代基提及的每个基团本身(独立于提及的组合)是所述取代基的特别优选的方面。
表1a具有式I.A-1、I.A-2、I.A-3、I.A-4的化合物,其中Xn是H,并且每种单独的化合物的R5、R6和R7的组合的含义在每种情况下对应于表B中的一行(化合物I.A-1.1a.B-1至I.A-1.1a.B-100、I.A-2.1a.B-1至I.A-2.1a.B-100、I.A-3.1a.B-1至I.A-3.1a.B-100、I.A-4.1a.B-1至I.A-4.1a.B-100)。
表2a具有式I.A-1、I.A-2、I.A-3、I.A-4的化合物;其中Xn是8-F,并且每种单独的化合物的R5、R6和R7的组合的含义在每种情况下对应于表B中的一行(化合物I.A-1.2a.B-1至I.A-1.2a.B-100、I.A-2.2a.B-1至I.A-2.2a.B-100、I.A-3.2a.B-1至I.A-3.2a.B-100、I.A-4.2a.B-1至I.A-4.2a.B-100)。
表3a具有式I.A-1、I.A-2、I.A-3、I.A-4的化合物;其中Xn是8-Cl,并且每种单独的化合物的R5、R6和R7的组合的含义在每种情况下对应于表B中的一行(化合物I.A-1.3a.B-1至I.A-1.3a.B-100、I.A-2.3a.B-1至I.A-2.3a.B-100、I.A-3.3a.B-1至I.A-3.3a.B-100、I.A-4.3a.B-1至I.A-4.3a.B-100)。
表4a具有式I.A-1、I.A-2、I.A-3、I.A-4的化合物;其中Xn是8-CH3,并且每种单独的化合物的R5、R6和R7的组合的含义在每种情况下对应于表B中的一行(化合物I.A-1.4a.B-1至I.A-1.4a.B-100、I.A-2.4a.B-1至I.A-2.4a.B-100、I.A-3.4a.B-1至I.A-3.4a.B-100、I.A-4.4a.B-1至I.A-4.4a.B-100)。
表5a具有式I.A-1、I.A-2、I.A-3、I.A-4的化合物;其中Xn是7,8-F2,并且每种单独的化合物的R5、R6和R7的组合的含义在每种情况下对应于表B中的一行(化合物I.A-1.5a.B-1至I.A-1.5a.B-100、I.A-2.5a.B-1至I.A-2.5a.B-100、I.A-3.5a.B-1至I.A-3.5a.B-100、I.A-4.5a.B-1至I.A-4.5a.B-100)。
表6a具有式I.A-1、I.A-2、I.A-3、I.A-4的化合物;其中Xn是8-OCH3,并且每种单独的化合物的R5、R6和R7的组合的含义在每种情况下对应于表B中的一行(化合物I.A-1.6a.B-1至I.A-1.6a.B-100、I.A-2.6a.B-1至I.A-2.6a.B-100、I.A-3.6a.B-1至I.A-3.6a.B-100、I.A-4.6a.B-1至I.A-45.6a.B-100)。
表7a具有式I.A-1、I.A-2、I.A-3、I.A-4的化合物;其中Xn是7-F-8-OCH3,并且每种单独的化合物的R5、R6和R7的组合的含义在每种情况下对应于表B中的一行(化合物I.A-1.7a.B-1至I.A-1.7a.B-100、I.A-2.7a.B-1至I.A-2.7a.B-100、I.A-3.7a.B-1至I.A-3.7a.B-100、I.A-4.7a.B-1至I.A-4.7a.B-100)。
表B
/>
/>
/>
本发明的化合物可以如在以下方案中所示来制造,其中除非另外说明,否则每一变量的定义是如上文针对具有式I的化合物所定义的。具有式I的化合物可以根据现有技术中描述的方法或类似于现有技术中描述的方法来制备。合成利用了可商购或者可以根据常规程序从容易获得的化合物开始制备的起始材料。
例如,由具有式2的化合物形成化合物I适合在碱如钾或钠的低级醇盐或氢化物存在下通过烷基化或酰化进行。二低级烷基硫酸酯也可用于实现所述烷基化或酰化,如US 3,625,959中所述。
具有式2的环状化合物可以由酮胺化合物1通过与具有式1a的酮或醛在乙酸铵存在下反应来制备。在一些情况下,酸如对甲苯磺酸(p-TsOH)、对甲苯磺酸吡啶鎓、硫酸或乙酸的存在提高了产率(对于先例,参见例如Chemistry Select[化学选择](2018),3(32),9388-9392和Organic&Biomolecular Chemistry[有机与生物分子化学](2003),1(2),367-372)。
化合物1是可商购的或者可以按照以下方案1中概述的一般途径通过使用例如二氧化锰氧化氨基醇7来获得,如Inorganica Chimica Acta[无机化学学报](2012),382,72-78,WO 2000038618,CN107879989 A,Chinese Science Bulletin[科学通报](2010),55(25),2817-2819中所述。
具有式7的化合物可以通过使用-镍催化氢化相应的硝基醇6来获得,如WO 2000038618,Inorganica Chimica Acta[无机化学学报](2012),382,72-78中所述。
2-硝基醇6可以如Knochel和同事所述(Angew.Chem.,Int.Ed.[德国应用化学国际版],2002,41,1610)由4通过异丙基苯基溴化镁介导的碘-镁交换并且随后与可商购的硝基苯甲醛衍生物5加成来制备。
方案1
具有式I的化合物(其中R7是烷氧基)可以由6通过以下合成路线制备,该合成路线的特征在于如RSC Advances[英国皇家化学会研究进展](2020),28585-28594中所述使用通过氨水和DMSO的组合液处理后的钝化的-镍或如IN1996CH00112中所述使用铂碳(类型F 103RS/W,来自德固赛公司(Degussa))将硝基醇6选择性催化氢化成对应的N-芳基羟胺8。
具有式9的化合物可以通过使用例如二氧化锰氧化羟基-胺醇8来制备,如Inorganica Chimica Acta[无机化学学报](2012),382,72-78和WO 2000038618中所述。
受保护的羟胺10可以通过文献中众所周知的用于氨基保护基团的方法来制备,这些氨基保护基团如Theodora W.Greene的书“Protective Groups in Organic Synthesis[有机合成中的保护基团]”中所论述的,如在适当溶剂(如DMSO)中使用二碳酸二叔丁酯的N-Boc。
可以使用标准碱如LDA、NaH或NaHMDS将化合物10烷基化以使羟胺去质子化,然后在适当溶剂中加成具有适当离去基团(如卤化物、甲磺酸酯或三氟甲磺酸酯)的烷基化剂以提供化合物11(对于先例,参见例如CN 207973751)。
可以通过许多文献中众所周知的方法,如在二氯甲烷中的TFA,除去N-Boc保护基团得到化合物12(对于先例,参见例如WO 2000038618)。
最后,可以由12通过用NH4OAc处理来制备其中R7是烷氧基的化合物I,如ChemistrySelect[化学选择](2018),3(32),9388-9392和Organic&Biomolecular Chemistry[有机与生物分子化学](2003),1(2),367-372中所述。
化合物I及其组合物分别适合作为杀真菌剂,有效对抗广谱植物病原性真菌,包括土壤传播的真菌,特别是来自根肿菌纲、卵菌纲(Peronosporomycetes)(同义词Oomycetes)、壶菌纲、接合菌纲、子囊菌纲、担子菌纲和半知菌纲(同义词不完全菌纲(Fungiimperfecti))的真菌。它们在作物保护中可以用作叶面杀真菌剂、拌种用杀真菌剂和土壤杀真菌剂。
化合物I及其组合物优选地可用于控制以下上的植物病原性真菌:各种栽培植物,如谷物,例如小麦、黑麦、大麦、黑小麦、燕麦或稻;甜菜,如糖用甜菜或饲用甜菜;水果,例如梨果(苹果、梨等)、核果(例如李子、桃、杏仁、樱桃)或软果,也称为浆果(草莓、覆盆子、黑莓、醋栗等);豆科植物,如扁豆、豌豆、苜蓿或大豆;油料植物,如油菜、芥菜、橄榄、向日葵、椰子、可可豆、蓖麻油植物、油棕榈、落花生或大豆;瓜类,例如南瓜、黄瓜或甜瓜;纤维植物,例如棉花、亚麻、大麻、或黄麻;柑橘类水果,如橙子、柠檬、葡萄柚或橘子;蔬菜,例如菠菜、莴苣、芦笋、卷心菜、胡萝卜、洋葱、番茄、马铃薯、葫芦或红辣椒;月桂科植物,如鳄梨、肉桂或樟脑;能源和原料植物,例如玉米、大豆、油菜、甘蔗或油棕榈;玉米;烟草;坚果;咖啡;茶;香蕉;葡萄藤(食用葡萄和葡萄汁葡萄藤);啤酒花;草皮;甜叶(也称为甜叶菊);天然橡胶植物;或观赏植物和森林植物,如花卉、灌木、阔叶树或常绿树(针叶树、桉树等);植物繁殖材料如种子;以及这些植物的作物材料。
更优选地,化合物I及其组合物分别用于控制以下上的真菌:大田作物如马铃薯、糖用甜菜、烟草、小麦、黑麦、大麦、燕麦、稻、玉米、棉花、大豆、油菜、豆类、向日葵、咖啡或甘蔗;水果;藤本植物;观赏植物;或蔬菜,如黄瓜、番茄、菜豆或南瓜。
术语“植物繁殖材料”应理解为表示植物的所有有生殖能力的部分,例如种子;以及可用于植物繁殖的营养植物材料,如插条和块茎(如马铃薯)。这包括植物的种子、根、果实、块茎、鳞茎、根茎、嫩枝、芽和其他部分;包括发芽后或出土后进行移植的籽苗和幼苗。
优选地,分别用化合物I及其组合物处理植物繁殖材料用于控制以下上的真菌:谷物如小麦、黑麦、大麦和燕麦;稻、玉米、棉花和大豆。
根据本发明,所有以上栽培植物应理解为包括所有属于相应栽培植物的物种、亚种、变种、品种和/或杂种,包括但不限于冬季和春季品种,特别是谷类如小麦和大麦,以及油菜,例如冬小麦、春小麦、冬大麦等。
玉米也称为印度玉米或玉蜀黍(maize/Zea mays),其包括所有种类的玉米如饲料玉米和甜玉米。根据本发明,包括所有玉蜀黍或玉米亚种和/或变种,特别是粉质玉米(玉蜀黍粉质型变种(Zea mays var.amylacea))、爆粒玉米(玉蜀黍爆粒型变种(Zea maysvar.everta))、马齿玉米(玉蜀黍马齿型变种(Zea mays var.indentata))、硬粒玉米(玉蜀黍硬粒型变种(Zea mays var.indurata))、甜玉米(玉蜀黍saccharata和rugosa变种(Zeamays var.saccharata和var.rugosa))、糯玉米(玉蜀黍ceratina变种(Zea maysvar.ceratina))、高直链淀粉玉米(amylomaize)(高直链淀粉玉蜀黍品种)、荚玉米或野生玉蜀黍(玉蜀黍tunicata变种(Zea mays var.tunicata))和条纹玉蜀黍(玉蜀黍japonica变种(Zea mays var.japonica))。
大多数大豆栽培品种可分为无限和有限生长习性,而野大豆(Glycine soja)(大豆的野生祖先)是无限的(PNAS2010,107(19)8563-856)。无限生长习性(成熟组,MG 00至MG4.9)的特征在于在开花开始后营养生长的持续,而有限大豆品种(MG 5至MG 8)特征性地在开花开始时已经完成了大部分其营养生长。根据本发明包括所有大豆栽培品种或品种,特别是无限和有限栽培品种或品种。
术语“栽培植物”应理解为包括已经通过诱变或基因工程修饰以便对植物提供新性状或者修饰已经存在的性状的植物。诱变包括使用X射线或致突变化学品的随机诱变,而且包括靶向诱变,以在植物基因组的特定基因座产生突变。靶向诱变经常使用寡核苷酸或蛋白质如CRISPR/Cas、锌指核酸酶、TALEN或大范围核酸酶。基因工程通常使用重组DNA技术在植物基因组中产生修饰,这种修饰在自然环境下不能通过杂交、诱变或自然重组轻易得到。典型地,将一个或多个基因整合到植物的基因组中以便增加性状或改善或修饰性状。这些整合的基因也称为转基因,而包含此类转基因的植物被称为转基因植物。植物转化过程通常产生若干个转化事件,它们在其中已经整合了转基因的基因组基因座上不同。在特定基因组基因座上包含特定转基因的植物通常被描述为包含特定“事件”,其由特定事件名称来指代。已经引入植物中或已经修饰的性状包括除草剂耐受性、昆虫抗性、提高的产量、以及对非生物条件如干旱的耐受性。
除草剂耐受性已经通过使用诱变和基因工程产生。已经通过诱变和育种致使对乙酰乳酸合酶(ALS)抑制剂除草剂耐受的植物是例如以名称可获得。已经通过使用转基因产生了对草甘膦、草铵膦、2,4-D、麦草畏、苯腈(oxynil)除草剂(如溴苯腈和碘苯腈)、磺酰脲除草剂、ALS抑制剂以及4-羟基苯基丙酮酸双加氧酶(HPPD)抑制剂(像异噁唑草酮和硝磺草酮)的除草剂耐受性。
提供除草剂耐受性性状的转基因包括:对于草甘膦耐受性:cp4epsps、epspsgrg23ace5、mepsps、2mepsps、gat4601、gat4621、goxv247;对于草铵膦耐受性:pat和bar,对于2,4-D耐受性:aad-1、aad-12;对于麦草畏耐受性:dmo;对于苯腈除草剂耐受性:bxn;对于磺酰脲除草剂耐受性:zm-hra、csr1-2、gm-hra、S4-HrA;对于ALS抑制剂耐受性:csr1-2;以及对于HPPD抑制剂耐受性:hppdPF、W336、avhppd-03。
包含除草剂耐受性基因的转基因玉米事件包括但不限于DAS40278、MON801、MON802、MON809、MON810、MON832、MON87411、MON87419、MON87427、MON88017、MON89034、NK603、GA21、MZHG0JG、HCEM485、VCO-1981-5、676、678、680、33121、4114、59122、98140、Bt10、Bt176、CBH-351、DBT418、DLL25、MS3、MS6、MZIR098、T25、TC1507和TC6275。包含除草剂耐受性基因的转基因大豆事件包括但不限于GTS 40-3-2、MON87705、MON87708、MON87712、MON87769、MON89788、A2704-12、A2704-21、A5547-127、A5547-35、DP356043、DAS44406-6、DAS68416-4、DAS-81419-2、GU262、/>W62、W98、FG72和CV127。包含除草剂耐受性基因的转基因棉花事件包括但不限于19-51a、31707、42317、81910、281-24-236、3006-210-23、BXN10211、BXN10215、BXN10222、BXN10224、MON1445、MON1698、MON88701、MON88913、GHB119、GHB614、LLCotton25、T303-3和T304-40。包含除草剂耐受性基因的转基因卡诺拉事件是例如,但不排除其他,MON88302、HCR-1、HCN10、HCN28、HCN92、MS1、MS8、PHY14、PHY23、PHY35、PHY36、RF1、RF2和RF3。
提供昆虫抗性的转基因优选是芽孢杆菌属(Bacillus)物种的毒素基因及其合成变体,如cry1A、cry1Ab、cry1Ab-Ac、cry1Ac、cry1A.105、cry1F、cry1Fa2、cry2Ab2、cry2Ae、mcry3A、ecry3.1Ab、cry3Bb1、cry34Ab1、cry35Ab1、cry9C、vip3A(a)、vip3Aa20。此外,可以使用植物来源的转基因,如编码蛋白酶抑制剂的基因,如CpTI和pinII。另一种途径使用转基因如dvsnf7在植物中产生双链RNA。
包含杀昆虫蛋白基因或双链RNA的转基因玉米事件包括但不限于Bt10、Bt11、Bt176、MON801、MON802、MON809、MON810、MON863、MON87411、MON88017、MON89034、33121、4114、5307、59122、TC1507、TC6275、CBH-351、MIR162、DBT418和MZIR098。包含杀昆虫蛋白基因的转基因大豆事件包括但不限于MON87701、MON87751和DAS-81419。包含杀昆虫蛋白基因的转基因棉花事件包括但不限于SGK321、MON531、MON757、MON1076、MON15985、31707、31803、31807、31808、42317、BNLA-601、Event1、COT67B、COT102、T303-3、T304-40、GFMCry1A、GK12、MLS 9124、281-24-236、3006-210-23、GHB119和SGK321。
已经通过使用转基因athb17(例如玉米事件MON87403)或bbx32(例如大豆事件MON87712)产生了具有提高的产量的栽培植物。
包含改良的油含量的栽培植物已经通过使用以下转基因产生:gm-fad2-1、Pj.D6D、Nc.Fad3、fad2-1A和fatb1-A(例如大豆事件260-05、MON87705和MON87769)。
对非生物条件(如干旱)的耐受性已经通过使用转基因cspB(玉米事件MON87460)和Hahb-4(大豆事件IND--5)产生。
通常通过在转化事件中将基因组合或者通过在育种过程期间将不同事件组合而将性状组合,从而产生具有叠加性状的栽培植物。性状的优选组合是对不同组的除草剂的除草剂耐受性性状的组合,对不同种类的昆虫的昆虫耐受性、特别是对鳞翅目和鞘翅目昆虫的耐受性的组合,除草剂耐受性与一种或若干种类型的昆虫抗性的组合,除草剂耐受性与提高的产量的组合,以及除草剂耐受性和对非生物条件的耐受性的组合。
包含单一或叠加性状的植物以及提供这些性状的基因和事件在本领域是众所周知的。例如,有关诱变或整合基因和相应事件的详细信息从机构“国际农业生物技术应用服务组织(ISAAA)”(http://www.isaaa.org/gmapprovaldatabase)和“环境风险评估中心(CERA)”(http://cera-gmc.org/GMCropDatabase)的网站可获得。有关特定事件和检测这些事件的方法的另外的信息,对于卡诺拉(canola)事件MS1、MS8、RF3、GT73、MON88302、KK179,可见于WO 01/031042、WO 01/041558、WO 01/041558、WO 02/036831、WO 11/153186、WO 13/003558;对于棉花事件MON1445、MON15985、MON531(MON15985)、LLCotton25、MON88913、COT102、281-24-236、3006-210-23、COT67B、GHB614、T304-40、GHB119、MON88701、81910,可见于WO 02/034946、WO 02/100163、WO 02/100163、WO 03/013224、WO 04/072235、WO 04/039986、WO 05/103266、WO 05/103266、WO 06/128573、WO 07/017186、WO 08/122406、WO 08/151000、WO 12/134808、WO 13/112527;对于玉米事件GA21、MON810、DLL25、TC1507、MON863、MIR604、LY038、MON88017、3272、59122、NK603、MIR162、MON89034、98140、32138、MON87460、5307、4114、MON87427、DAS40278、MON87411、33121、MON87403、MON87419,可见于WO 98/044140、US 02/102582、US 03/126634、WO 04/099447、WO 04/011601、WO 05/103301、WO 05/061720、WO 05/059103、WO 06/098952、WO 06/039376、US2007/292854、WO07/142840、WO 07/140256、WO 08/112019、WO 09/103049、WO 09/111263、WO 10/077816、WO11/084621、WO 11/062904、WO 11/022469、WO 13/169923、WO 14/116854、WO 15/053998、WO15/142571;对于马铃薯事件E12、F10、J3、J55、V11、X17、Y9,可见于WO 14/100910、WO 14/100913、WO 14/100941、WO 14/179276、WO 16/183445、WO 17/062831、WO 17/062825;对于稻事件LLRICE06、LLRICE601、LLRICE62,可见于WO 00/026345、WO 00/026356、WO 00/026345;并且对于大豆事件H7-1、MON89788、A2704-12、A5547-127、DP305423、DP356043、MON87701、MON87769、CV127、MON87705、DAS68416-4、MON87708、MON87712、SYHT0H2、DAS81419、DAS81419 x DAS44406-6、MON87751,可见于WO 04/074492、WO 06/130436、WO06/108674、WO 06/108675、WO 08/054747、WO 08/002872、WO 09/064652、WO 09/102873、WO10/080829、WO 10/037016、WO 11/066384、WO 11/034704、WO 12/051199、WO 12/082548、WO13/016527、WO 13/016516、WO 14/201235。
在栽培植物上分别使用化合物I及其组合物可以导致对包含某个转基因或事件的栽培植物具有特异性的效果。这些效果可能涉及生长行为的改变或改变的对生物或非生物胁迫因素的抗性。此类效果特别可能包括提高的产量,提高的对昆虫、线虫、真菌、细菌、支原体、病毒或类病毒病原体的抗性或耐受性以及早期生长势(early vigour)、早熟或延迟成熟、冷或热耐受性以及改变的氨基酸或脂肪酸谱或含量。
化合物I及其组合物分别特别适用于控制以下植物病害的致病病原:
观赏植物、蔬菜(例如,白锈菌(A.candida))和向日葵(例如婆罗门参白锈菌(A.tragopogonis))上的白锈菌属(Albugo)物种(白锈病);蔬菜(例如,胡萝卜链格孢(A.dauci)或葱链格孢(A.porri))、油菜(甘蓝链格孢(A.brassicola)或芸苔链格孢(A.brassicae))、糖用甜菜(细链格孢(A.tenuis))、水果(例如柚链格孢(A.grandis))、稻、大豆、马铃薯和番茄(例如茄链格孢、柚链格孢或互隔链格孢(A.alternata))、番茄(例如茄链格孢或互隔链格孢)、和小麦(例如小麦链格孢(A.triticina))上的链格孢属(Alternaria)物种(链格孢叶斑病);糖用甜菜和蔬菜上的丝囊霉属(Aphanomyces)物种;谷物和蔬菜上的壳二孢属(Ascochyta)物种,例如小麦上的小麦壳二孢(A.tritici)(炭疽病)和大麦上的大麦壳二孢(A.hordei);玉米上的玉米短柄霉(Aureobasidium zeae)(同义词Kapatiella zeae);平脐蠕孢属(Bipolaris)物种和内脐蠕孢属(Drechslera)物种(有性型:旋孢腔菌属(Cochliobolus)物种),例如玉米上的小斑病(玉蜀黍内脐蠕孢(D.maydis))或大斑病(玉米平脐蠕孢(B.zeicola)),例如谷物上的斑枯病(麦根腐平脐蠕孢(B.sorokiniana))以及例如稻和坪草上的稻平脐蠕孢(B.oryzae);谷物上(例如小麦或大麦上)的禾本科布氏白粉菌(Blumeria graminis)(之前称为禾生白粉菌(Erysiphegraminis))(白粉病);水果和浆果(例如草莓)、蔬菜(例如莴苣、胡萝卜、芹菜和卷心菜)上的灰葡萄孢(Botrytis cinerea)(有性型:富克葡萄孢盘菌(Botryotinia fuckeliana):灰霉);洋葱家族、油菜、观赏植物(例如椭圆葡萄孢(B eliptica))、藤本植物、森林植物和小麦上的葱鳞葡萄孢(B.squamosa)或葱腐葡萄孢(B.allii);莴苣上的莴苣盘梗霉(Bremialactucae)(霜霉病);阔叶树和常绿树上的长喙壳属(Ceratocystis)(同义词Ophiostoma)物种(腐病或萎蔫),例如榆树上的榆长喙壳(C.ulmi)(荷兰榆树病(Dutch elm disease));玉米(例如灰斑病:玉蜀黍尾孢(C.zeae-maydis))、稻、糖用甜菜(例如甜菜生尾孢(C.beticola))、甘蔗、蔬菜、咖啡、大豆(例如大豆尾孢(C.sojina)或菊池尾孢(C.kikuchii))和稻上的尾孢属(Cercospora)物种(尾孢菌叶斑(Cercospora leafspot));蘑菇上的指孢霉属(Cladobotryum)(同义词Dactylium)物种(例如嗜菌指孢霉(C.mycophilum)(之前称为树状指孢霉(Dactylium dendroides)),有性型:Nectriaalbertinii,粉红寄生菌(Nectria rosella)同义词Hypomyces rosellus);番茄(例如黄枝孢(C.fulvum):叶霉病)和谷物上的枝孢属(Cladosporium)物种,例如小麦上的多主枝孢(C.herbarum)(黑穗病(black ear));谷物上的麦角菌(Claviceps purpurea)(麦角病(ergot));玉米(炭色旋孢腔菌(C.carbonum))、谷物(例如禾旋孢腔菌(C.sativus),无性型:麦根腐平脐蠕孢(B.sorokiniana))和稻(例如宫部旋孢腔菌(C.miyabeanus),无性型:稻长蠕孢(H.oryzae))上的旋孢腔菌属(Cochliobolus)(无性型:平脐蠕孢属(Bipolaris)的长蠕孢属(Helminthosporium))物种(叶斑病);棉花(例如棉刺盘孢(C.gossypii))、玉米(例如禾生刺盘孢(C.graminicola):炭疽病茎腐)、软果、马铃薯(例如球炭疽菌(C.coccodes):黑点病)、菜豆(例如豆刺盘孢(C.lindemuthianum))、大豆(例如平头刺盘孢(C.truncatum)或盘长孢状刺盘孢(C.gloeosporioides))、蔬菜(例如葫芦刺盘孢(C.lagenarium)或辣椒刺盘孢(C.capsici))、水果(例如尖孢炭疽菌(C.acutatum))、咖啡(例如咖啡刺盘孢(C.coffeanum)或卡哈瓦刺盘孢(C.kahawae))以及多种作物(胶孢炭疽菌(C.gloeosporioides))上的刺盘孢属(Colletotrichum)(有性型:小丛壳属(Glomerella))物种(炭疽病);伏革菌属(Corticium)物种,例如稻上的笹木伏革菌(C.sasakii)(纹枯病(sheath blight));大豆、棉花和观赏植物上的山扁豆生棒孢菌(Corynesporacassiicola)(叶斑病);孔雀斑病菌属(Cycloconium)物种,例如橄榄树上的油橄榄孔雀斑病菌(C.oleaginum);果树、藤本植物(例如鹅掌楸柱孢(C.liriodendri),有性型:鹅掌楸新丛赤壳(Neonectria liriodendri):黑脚病(Black Foot Disease))和观赏植物上的柱孢属(Cylindrocarpon)物种(例如果树溃疡病或幼藤衰败,有性型:丛赤壳属(Nectria)或新丛赤壳属(Neonectria)物种);大豆上的白纹羽束丝菌(Dematophora necatrix)(有性型:褐座坚壳菌(Rosellinia necatrix))(根茎腐病);间座壳属(Diaporthe)物种,例如大豆上的菜豆间座壳(D.phaseolorum)(猝倒);玉米、谷物例如大麦(例如大麦网斑内脐蠕孢(D.teres),网斑病(net blotch))和小麦(例如偃麦草内脐蠕孢(D.tritici-repentis):褐斑病(tan spot))、稻和坪草上的内脐蠕孢属(Drechslera)(同义词长蠕孢属(Helminthosporium),有性型:核腔菌属(Pyrenophora))物种;藤本植物上的Esca(梢枯病(dieback)、干枯病(apoplexy)),由层卧孔菌(Formitiporia punctata)(同义词斑孔木层孔菌(Phellinus punctata))、地中海层卧孔菌(F.mediterranea)、厚孢小褐球壳(Phaeomoniella chlamydospora)(之前称为Phaeoacremonium chlamydosporum)、褐枝顶孢霉(Phaeoacremonium aleophilum)和/或树花地衣葡萄座腔菌(Botryosphaeriaobtusa)引起;梨果(梨痂囊腔菌(E.pyri))、软果(覆盆子痂囊腔菌(E.veneta):炭疽病)和藤本植物(痂囊腔菌(E.ampelina):炭疽病)上的痂囊腔菌属(Elsinoe)物种;稻上的稻叶黑粉菌(Entyloma oryzae)(叶黑粉病(leaf smut));小麦上的附球菌属(Epicoccum)物种(黑霉病(black mold));糖用甜菜(甜菜白粉菌(E.betae)),蔬菜(例如豌豆白粉菌(E.pisi))例如葫芦(例如二孢白粉菌(E.cichoracearum))、卷心菜、油菜(例如十字花科白粉菌(E.cruciferarum))上的白粉菌属(Erysiphe)物种(白粉病);果树、藤本植物和观赏木上的侧弯孢菌(Eutypa lata)(弯孢壳(Eutypa)溃疡病或梢枯病,无性型:Cytosporina lata,同义词Libertella blepharis);玉米(例如大斑凸脐蠕孢(E.turcicum))上的凸脐蠕孢属(Exserohilum)(同义词长蠕孢属(Helminthosporium))物种;多种植物上的镰孢菌属(Fusarium)(有性型:赤霉属(Gibberella))物种(萎蔫、根或茎腐病),如谷物(例如小麦或大麦)上的禾本科镰孢(F.graminearum)或黄色镰孢(F.culmorum)(根腐病、疮痂病(scab)或赤霉病(head blight))、番茄上的尖孢镰孢菌(F.oxysporum)、大豆上的腐皮镰孢(F.solani)(镰孢菌大豆专化型(f.sp.glycines),新的同义词大豆猝死综合症病原菌(F.virguliforme))和F.tucumaniae及F.brasiliense(均引起猝死综合征)和玉米上的轮枝镰孢(F.verticillioides);谷物(例如小麦或大麦)和玉米上的禾顶囊壳(Gaeumannomyces graminis)(全蚀病(take-all));谷物(例如玉蜀黍赤霉(G.zeae))和稻(例如藤仓赤霉(G.fujikuroi):恶苗病(Bakanae disease))上的赤霉属(Gibberella)物种;藤本植物、梨果和其他植物上的围小丛壳菌(Glomerella cingulata)和棉花上的棉小丛壳菌(G.gossypii);稻上的颗粒染色配合物(Grainstaining complex);藤本植物上的葡萄球座菌(Guignardia bidwellii)(黑腐病(black rot));蔷薇科植物和杜松上的胶锈菌属(Gymnosporangium)物种,例如梨上的褐色胶锈菌(G.sabinae)(锈病);玉米、谷物、马铃薯和稻上的长蠕孢属(Helminthosporium)物种(同义词内脐蠕孢属(Drechslera),有性型:旋孢腔菌属(Cochliobolus));驼孢锈菌属(Hemileia)物种,例如咖啡上的咖啡驼孢锈菌(H.vastatrix)(咖啡叶锈病);藤本植物上的褐斑拟棒束孢(Isariopsis clavispora)(同义词Cladosporium vitis);大豆和棉花上的菜豆壳球孢(Macrophomina phaseolina)(同义词Macrophomina phaseoli)(根茎腐病);谷物(例如小麦或大麦)上的雪腐微座孢(Microdochium nivale)(同义词雪腐镰孢(Fusarium nivale))(粉雪霉病(pink snowmold));大豆上的扩散叉丝壳(Microsphaera diffusa)(白粉病);核果和其他蔷薇科植物上的链核盘菌属(Monilinia)物种,例如松散链核盘菌(M.laxa)、果生链核盘菌(M.fructicola)和果产链核盘菌(M.fructigena)(同义词从梗孢属(Monilia)物种:花腐病和枝枯病、褐腐病);谷物、香蕉、软果和落花生上的球腔菌属(Mycosphaerella)物种,如小麦上的禾生球腔菌(M.graminicola)(无性型:小麦发酵壳针孢(Zymoseptoria tritici),之前称为小麦壳针孢(Septoria tritici):壳针孢斑枯病),或香蕉上的斐济球腔菌(M.fijiensis)(同义词Pseudocercospora fijiensis:黑叶斑病(black Sigatokadisease))和香蕉生球腔菌(M.musicola),花生上的花生球腔菌(M.arachidicola)(同义词M.arachidis或Cercospora arachidis)、伯克利球腔菌(M.berkeleyi),豌豆上的M.pisi以及芸苔属上的芸苔生球腔菌(M.brassiciola);卷心菜(例如芸苔霜霉(P.brassicae))、油菜(例如寄生霜霉(P.parasitica))、洋葱(例如葱霜霉(P.destructor))、烟草(烟草霜霉(P.tabacina))和大豆(例如东北霜霉(P.manshurica))上的霜霉属(Peronospora)物种(霜霉病);大豆上的豆薯层锈菌(Phakopsora pachyrhizi)和山马蝗层锈菌(P.meibomiae)(大豆锈病);瓶霉属(Phialophora)物种,例如藤本植物(例如嗜管瓶霉(P.tracheiphila)和四孢藻瓶霉(P.tetraspora))和大豆(例如大豆瓶霉(P.gregata):茎腐病)上;油菜和卷心菜上的黑胫茎点霉(Phoma lingam)(同义词黑胫病菌(Leptosphaeria biglobosa)和十字花科小球腔菌(L.maculans):根茎腐病)和糖用甜菜上的甜菜茎点霉(P.betae)(根腐病、叶斑病和猝倒),以及玉米上的P.zeae-maydis(同义词Phyllostica zeae);向日葵、藤本植物(例如葡萄生拟茎点霉(P.viticola):蔓和叶斑病)和大豆(例如茎腐病:菜豆拟茎点霉(P.phaseoli),有性型:菜豆间座壳(Diaporthe phaseolorum))上的拟茎点霉(Phomopsis)物种;玉米上的玉蜀黍节壶菌(Physoderma maydis)(褐斑病);多种植物上的疫霉属(Phytophthora)物种(萎蔫,根、叶、果实和茎腐病),如红辣椒和葫芦(例如辣椒疫霉(P.capsici))、大豆(例如大雄疫霉(P.megasperma),同义词大豆疫霉(P.sojae))、马铃薯和番茄(例如致病疫霉(P.infestans):晚疫病)和阔叶树(例如橡树疫霉(P.ramorum):橡树猝死);卷心菜、油菜、萝卜和其他植物上的芸苔根肿菌(Plasmodiophora brassicae)(根肿病(club root));单轴霉属(Plasmopara)物种,例如藤本植物上的葡萄生单轴霉(P.viticola)(葡萄霜霉病)和向日葵上的霍尔斯单轴霉(P.halstedii);蔷薇科植物、蛇麻、梨果和软果上的叉丝单囊壳属(Podosphaera)物种(白粉病),例如苹果上的白叉丝单囊壳(P.leucotricha)和葫芦上的瓜类单囊壳(P.xanthii);例如谷物如大麦和小麦(禾谷多粘霉(P.graminis))和糖用甜菜(甜菜多粘霉(P.betae))上的多粘霉属(Polymyxa)物种,和由此传播的病毒病;谷物例如小麦或大麦上的小麦基腐病菌(Pseudocercosporellaherpotrichoides)(同义词Oculimacula yallundae、O.acuformis:眼斑病,有性型:Tapesia yallundae);多种植物上的假霜霉属(Pseudoperonospora)(霜霉病),例如葫芦上的古巴假霜霉(P.cubensis)或蛇麻上的葎草假霜霉(P.humili);藤本植物上的八孢假无柄盘菌(Pseudopezicula tracheiphila)(红火病(red fire disease)或rotbrenner,无性型:瓶霉属(Phialophora));多种植物上的柄锈菌属(Puccinia)物种(锈病),例如谷物如小麦、大麦或黑麦上的小麦柄锈菌(P.triticina)(褐锈病或叶锈病)、条形柄锈菌(P.striiformis)(条锈病或黄锈病)、大麦柄锈菌(P.hordei)(矮锈病)、禾柄锈菌(P.graminis)(秆锈病或黑锈病)或隐匿柄锈菌(P.recondita)(棕锈病或叶锈病),甘蔗上的屈恩柄锈菌(P.kuehnii)(柑橘锈病)和芦笋上的天门冬属柄锈菌(P.asparagi);埋核盘菌属(Pyrenopeziza)物种,例如油菜上的芸苔埋核盘菌(P.brassicae);小麦上的偃麦草核腔菌(Pyrenophora tritici-repentis)(无性型:偃麦草内脐蠕孢(Drechslera tritici-repentis))(褐斑病)或大麦上的圆核腔菌(P.teres)(网斑病);梨孢属(Pyricularia)物种,例如稻上的稻梨孢(P.oryzae)(有性型:稻瘟病菌(Magnaporthe grisea):稻瘟病),以及坪草和谷物上的灰梨孢(P.grisea);坪草、稻、玉米、小麦、棉花、油菜、向日葵、大豆、糖用甜菜、蔬菜和多种其他植物上的腐霉属(Pythium)物种(猝倒)(例如终极腐霉(P.ultimum)或瓜果腐霉(P.aphanidermatum))以及蘑菇上的寡雄腐霉(P.oligandrum);柱隔孢属(Ramularia)物种,例如大麦上的R.Collo-cygni(柱隔孢叶斑病、生理叶斑病),棉花上的白斑柱隔孢(R.areola)(有性型:网孢球腔菌(Mycosphaerella areola))和糖用甜菜上的甜菜生柱隔孢(R.beticola);棉花、稻、马铃薯、坪草、玉米、油菜、马铃薯、糖用甜菜、蔬菜和多种其他植物上的丝核菌属(Rhizoctonia)物种,例如大豆上的立枯丝核菌(R.solani)(根茎腐病)、稻上的立枯丝核菌(R.solani)(纹枯病)或者小麦或大麦上的禾谷丝核菌(R.cerealis)(丝核菌春叶枯病);草莓、胡萝卜、卷心菜、藤本植物和番茄上的匐枝根霉(Rhizopus stolonifer)(黑霉病、软腐病);大麦、黑麦和黑小麦上的黑麦喙孢(Rhynchosporium secalis)和R.commune(灼枯病(scald));稻上的稻帚枝杆孢菌(Sarocladium oryzae)和S.attenuatum(鞘腐病);蔬菜(小核盘菌(S.minor)和核盘菌(S.sclerotiorum))和大田作物,例如油菜、向日葵(例如核盘菌)和大豆上的核盘菌属(Sclerotinia)物种(茎腐病或白霉),大豆、花生、蔬菜、玉米、谷物和观赏植物上的齐整小核菌(S.rolfsii)(同义词Athelia rolfsii);多种植物上的壳针孢属(Septoria)物种,例如大豆上的大豆壳针孢(S.glycines))(褐斑病)、小麦上的小麦壳针孢(S.tritici)(同义词小麦发酵壳针孢(Zymoseptoria tritici),壳针孢斑枯病)和谷物上的颖枯壳针孢(S.nodorum)(同义词颖枯壳多孢(Stagonospora nodorum)(壳多孢属斑枯病);藤本植物上的葡萄钩丝壳(Uncinula necator)(同义词葡萄白粉菌(Erysiphe necator))(白粉病,无性型:葡萄粉孢(Oidium tuckeri));玉米(例如玉米大斑病菌(S.turcicum),同义词大斑病长蠕孢(Helminthosporium turcicum))和坪草上的大斑病菌属(Setosphaeria)物种(叶枯病);玉米(例如,丝轴黑粉菌(S.reiliana),同义词Ustilago reiliana:丝黑穗病)、高粱和甘蔗上的轴黑粉菌属(Sphacelotheca)物种(黑穗病);葫芦上的单丝壳菌(Sphaerothecafuliginea)(同义词瓜类单囊壳(Podosphaera xanthii):白粉病);马铃薯上的马铃薯粉痂菌(Spongospora subterranea)(粉痂病)和由此传播的病毒病;谷物上的壳多孢属(Stagonospora)物种,例如小麦上的颖枯壳多孢(S.nodorum)(壳多孢属斑枯病,有性型:颖枯小球腔菌(Leptosphaeria nodorum)[同义词颖枯暗球腔菌(Phaeosphaeria nodorum)],同义词颖枯壳针孢(Septoria nodorum));马铃薯上的内生集壶菌(Synchytriumendobioticum)(马铃薯癌肿病);外囊菌属(Taphrina)物种,例如桃上的畸形外囊菌(T.deformans)(缩叶病)和李树上的李外囊菌(T.pruni)(李囊果病(plum pocket));烟草、梨果、蔬菜、大豆和棉花上的根串珠霉属(Thielaviopsis)物种(黑根腐病),例如根串珠霉(T.basicola)(同义词Chalara elegans);谷物上的腥黑粉菌属(Tilletia)物种(腥黑穗病(common bunt或stinking smut)),例如像小麦上的小麦腥黑粉菌(T.tritici)(同义词小麦网腥黑粉菌(T.caries),小麦腥黑穗病)和小麦矮腥黑粉菌(T.controversa)(矮腥黑穗病);蘑菇上的哈茨木霉(Trichoderma harzianum);大麦或小麦上的肉孢核瑚菌(Typhulaincarnate)(灰雪腐霉病(grey snow mold));条黑粉菌属(Urocystis)物种,例如黑麦上的隐条黑粉菌(U.occulta)(秆黑穗病(stem smut));蔬菜例如菜豆(例如疣顶单胞锈菌(U.appendiculatus),同义词菜豆单胞锈菌(U.phaseoli))、糖用甜菜(例如甜菜单胞锈菌(U.betae)或甜菜生胞锈菌(U.beticola))和干豆(例如豇豆单胞锈菌(U.vignae)、U.pisi、野豌豆单胞锈菌(U.viciae-fabae)和蚕豆单胞锈菌(U.fabae))上的单胞锈菌属(Uromyces)物种(锈病);谷物(例如麦散黑粉菌(U.nuda)和燕麦散黑粉菌(U.avaenae))、玉米(例如玉蜀黍黑粉菌(U.maydis):玉米黑粉病)和甘蔗上的黑粉菌属(Ustilago)物种(散黑穗病(loose smut));苹果(例如苹果黑星菌(V.inaequalis))和梨上的黑星菌属(Venturia)物种(疮痂病(scab));以及多种植物例如水果和观赏植物、藤本植物、软果、蔬菜和大田作物上的轮枝孢属(Verticillium)物种(萎蔫),例如油菜上的长孢轮枝孢(V.longisporum),草莓、油菜、马铃薯和番茄上的大丽花轮枝孢(V.dahliae)以及蘑菇上的真菌轮枝孢(V.fungicola);谷物上的小麦发酵壳针孢。
化合物I及其组合物分别特别适用于控制以下植物病害的致病病原:大豆和谷物上的锈病(例如大豆上的豆薯层锈菌和山马蝗层锈菌;小麦上的小麦叶锈菌(Pucciniatritici)和条纹锈菌(P.striiformis));特色作物、大豆、油菜和向日葵上的霉病(例如草莓和藤本植物上的灰葡萄孢菌,油菜、向日葵和大豆上的核盘菌、小核盘菌和齐整小核菌(S.rolfsii));谷物上的镰孢菌属病害(例如小麦上的黄色镰孢菌和禾谷镰孢菌);特色作物上的霜霉病(例如藤本植物上的葡萄霜霉病菌,马铃薯上的晚疫菌);特色作物和谷物上的白粉病(例如藤本植物上的葡萄钩丝壳,各种特色作物上的白粉菌属物种,谷物上的禾本科布氏白粉菌);以及谷物、大豆和玉米上的叶斑病(例如谷物上的小麦壳针孢和颖枯壳针孢,大豆上的大豆壳针孢,玉米和大豆上的尾孢属物种)。
化合物I及其组合物还分别在储存产品或收获物的保护以及材料的保护中适合用于控制有害微生物。
术语“储存产品或收获物”应理解为表示植物或动物来源的天然物质以及长期保护所需的其加工形式。植物来源的储存产品,例如茎秆、叶子、块茎、种子、果实或谷粒可以以新鲜收割的状态或者以预干燥的、弄湿的、粉碎的、磨碎的、压榨的或烘烤的等加工形式(该加工也被称为收割后处理)进行保护。同样落在储存产品定义下的是木材,无论为原木形式,如建筑木材、输电塔和栅栏,或为制成品形式,如由木头制造的家具或物体。动物来源的储存产品是兽皮、皮革、毛皮、毛发等。优选地,“储存产品”应理解为表示植物来源的天然物质及其加工形式,更优选果实及其加工形式,如梨果、核果、软果和柑橘类水果及其加工形式,其中化合物I及其组合物的施用还可以防止腐烂、变色或发霉等不利影响。
术语“材料的保护”应理解为表示保护技术和非生命材料如粘合剂、胶、木料、纸、纸板、纺织品、皮革、油漆分散体、塑料、冷却润滑剂、纤维、或织物以防有害微生物(如真菌和细菌)侵染和破坏。
当用于材料或储存产品的保护中时,所施用的活性物质的量取决于应用领域的种类和期望的效果。通常施用于材料的保护中的量是0.001g至2kg、优选0.005g至1kg活性物质/立方米经处理的材料。
化合物I及其组合物可以分别用于改善植物的健康。本发明还涉及一种用于通过以下方式改善植物健康的方法:分别用有效量的化合物I及其组合物处理植物、其繁殖材料和/或植物正在生长或将要生长的场所。
术语“植物健康”应理解为表示植物和/或其产品的状况,其通过单独或彼此组合的多项指标确定,如产量(例如增加的生物质和/或增加的有价值成分的含量)、植物活力(例如改善的植物生长和/或更绿的叶子(“绿化效果”))、品质(例如改善的某些成分的含量或组成)、以及对非生物和/或生物胁迫的耐受性。以上确定的植物健康状况指标可以相互依存或者可以相互影响。
化合物I按原样或以组合物的形式使用,通过用杀真菌有效量的活性物质处理真菌,植物,植物繁殖材料(如种子),待保护免受真菌侵袭的土壤、表面、材料或房间。施用可以在植物、植物繁殖材料(如种子)、土壤、表面、材料或房间受真菌感染之前和之后进行。
农用化学组合物包含杀真菌有效量的化合物I。术语“杀真菌有效量”表示足以用于控制栽培植物上、或储存产品或收获物的保护、或材料的保护中的有害真菌,并且不会对经处理的植物、经处理的储存产品或收获物、或对经处理的材料产生实质损害的组合物或化合物I的量。此种量可以在广泛的范围内变化并且取决于各种因素,诸如待控制的真菌物种,经处理的栽培植物、储存产品、收获物或材料,气候条件和所使用的具体化合物I。
植物繁殖材料可以在种植或移植时或在种植或移植之前用化合物I本身或包含至少一种化合物I的组合物预防性地处理。
当用于植物保护中时,取决于期望的效果类型,所施用的活性物质的量是0.001至2kg/ha、优选0.005至2kg/ha、更优选0.05至0.9kg/ha、并且特别是0.1至0.75kg/ha。
在植物繁殖材料(如种子)的处理中,例如通过撒粉、涂覆或浸透,每100kg的植物繁殖材料(优选种子)需要通常0.1至1000g、优选1至1000g、更优选1至100g、并且最优选5至100g的活性物质的量。
使用者通常由预先给药装置、背负式喷雾器、喷雾罐、喷雾飞机、或灌溉系统施用农用化学组合物。通常,农用化学组合物用水、缓冲液、和/或另外的辅助剂制成至期望的施用浓度,并且因此获得根据本发明的即用型喷雾液或农用化学组合物。通常,每公顷农业可用面积施用20至2000升、优选地50至400升的即用型喷雾液。
化合物I、其N-氧化物和盐可以转化成常用类型的农用化学组合物,例如溶液、乳液、悬浮液、粉尘剂、粉剂、糊剂、颗粒剂、压片剂、胶囊、及其混合物。组合物类型的实例(还参见“Catalogue of pesticide formulation types and international coding system[杀有害生物剂配制品类型和国际编码系统目录]”,Technical Monograph[技术专论]第2期,第6版,2008年5月,CropLife International[国际作物生命协会])是悬浮液(例如SC、OD、FS)、可乳化浓缩液(例如EC)、乳液(例如EW、EO、ES、ME)、胶囊(例如CS、ZC)、糊剂、锭剂、可湿性粉末或粉剂(例如WP、SP、WS、DP、DS)、压制剂(例如BR、TB、DT)、颗粒剂(例如WG、SG、GR、FG、GG、MG)、杀昆虫制品(例如LN)以及用于处理植物繁殖材料(如种子)的凝胶配制品(例如GF)。这些组合物以已知的方式制备,诸如由以下所描述的:Mollet和Grubemann,Formulation technology[配制品技术],Wiley VCH,Weinheim,2001;或Knowles,Newdevelopments in crop protection product formulation[作物保护产品配制的新发展],Agrow Reports[世界农作物保护新闻报告]DS243,T&F Informa[泰勒-弗朗西斯英富曼公司],London[伦敦],2005。本发明还涉及包含助剂和至少一种化合物I的农用化学组合物。
合适的助剂是溶剂、液体载体、固体载体或填料、表面活性剂、分散剂、乳化剂、湿润剂、辅助剂、增溶剂、渗透增强剂、保护性胶体、粘着剂、增稠剂、保湿剂、忌避剂、引诱剂、取食刺激剂、相容剂、杀菌剂、防冻剂、防沫剂、着色剂、增粘剂和粘合剂。
合适的溶剂和液体载体是水和有机溶剂,例如中至高沸点的矿物油级分,如煤油、柴油;植物或动物来源的油;脂肪族烃、环烃和芳香族烃,例如甲苯、石蜡、四氢化萘和烷基化萘;醇,例如乙醇、丙醇、丁醇、苯甲醇、环己醇、乙二醇;DMSO;酮,例如环己酮;酯,例如乳酸盐、碳酸盐、脂肪酸酯、γ-丁内酯;脂肪酸;膦酸酯;胺;酰胺,例如N-甲基吡咯烷酮,脂肪酸二甲基酰胺;及其混合物。
合适的固体载体或填料是矿物土,例如硅酸盐、硅胶、滑石粉、高岭土、石灰石、石灰、白垩、粘土、白云石、硅藻土、膨润土、硫酸钙、硫酸镁、氧化镁;多糖,例如纤维素、淀粉;肥料,例如硫酸铵、磷酸铵、硝酸铵、尿素;植物来源的产品,例如谷物粉、树皮粉、木粉、坚果壳粉及其混合物。
合适的表面活性剂是表面活性化合物,诸如阴离子、阳离子、非离子和两性表面活性剂,嵌段聚合物,聚电解质,以及其混合物。此类表面活性剂可以被用作乳化剂、分散剂、增溶剂、润湿剂、渗透增强剂、保护胶体、或辅助剂。表面活性剂的实例列于McCutcheon’s,第1卷:Emulsifiers&Detergents[乳化剂和洗涤剂],McCutcheon’s Directories,GlenRock,USA,2008(国际版或北美洲版)中。
合适的阴离子表面活性剂是磺酸盐、硫酸盐、磷酸盐、羧酸盐的碱金属盐、碱土金属盐或铵盐及其混合物。磺酸盐的实例是烷基芳基磺酸盐、二苯基磺酸盐、α-烯烃磺酸盐、木质素磺酸盐、脂肪酸和油的磺酸盐、乙氧基化烷基酚的磺酸盐、烷氧基化芳基酚的磺酸盐、缩合萘的磺酸盐、十二烷基苯和十三烷基苯的磺酸盐、萘和烷基萘的磺酸盐、磺基琥珀酸盐或琥珀酰胺磺酸盐(sulfosuccinamate)。硫酸盐的实例是脂肪酸、油、乙氧基化烷基酚、醇、乙氧基化醇或脂肪酸酯的硫酸盐。磷酸盐的实例是磷酸盐酯。羧酸盐的实例是烷基羧酸盐以及羧化醇或烷基酚乙氧基化物。
合适的非离子表面活性剂是烷氧基化物、N-取代的脂肪酸酰胺、胺氧化物、酯、糖基表面活性剂、聚合物表面活性剂及其混合物。烷氧基化物的实例是化合物如已经被1至50当量烷氧基化的醇、烷基酚、胺、酰胺、芳基酚、脂肪酸或脂肪酸酯。环氧乙烷和/或环氧丙烷可以用于烷氧基化,优选环氧乙烷。N-取代的脂肪酸酰胺的实例是脂肪酸葡糖酰胺或脂肪酸链烷醇酰胺。酯的实例是脂肪酸酯、甘油酯或甘油单酯。糖基表面活性剂的实例是山梨聚糖、乙氧基化山梨聚糖、蔗糖和葡萄糖酯或烷基聚葡萄糖苷。聚合物表面活性剂的实例是乙烯基吡咯烷酮、乙烯醇或乙酸乙烯酯的同源物或共聚物。
合适的阳离子表面活性剂是季铵表面活性剂,例如具有一个或两个疏水基团的季铵化合物、或长链伯胺的盐。合适的两性表面活性剂是烷基甜菜碱和咪唑啉。合适的嵌段聚合物是包含聚氧化乙烯和聚环氧丙烷嵌段的A-B或A-B-A型嵌段聚合物,或包含烷醇、聚氧化乙烯和聚环氧丙烷的A-B-C型嵌段聚合物。合适的聚电解质是多酸或多碱。多酸的实例是聚丙烯酸或多酸梳状聚合物的碱金属盐。多元碱的实例是聚乙烯基胺或聚乙烯胺。
合适的辅助剂是化合物,这些化合物本身具有可忽略不计的杀有害生物活性甚至没有杀有害生物活性,并且可提高化合物I对靶标的生物学性能。实例是表面活性剂、矿物油或植物油以及其他辅助剂。另外的实例由Knowles,Adjuvants and additives[辅助剂和添加剂],Agrow Reports DS256,T&F Informa UK,2006,第5章列出。合适的增稠剂是多糖(例如黄原胶、羧甲基纤维素)、无机粘土(有机改性的或未改性的)、聚羧酸盐和硅酸盐。
合适的杀菌剂是溴硝醇(bronopol)和异噻唑啉酮衍生物,如烷基异噻唑啉酮和苯并异噻唑啉酮。合适的防冻剂是乙二醇、丙二醇、脲和甘油。
合适的消泡剂是硅酮、长链醇和脂肪酸的盐。
合适的着色剂(例如红色、蓝色或绿色)是低水溶性颜料和水溶性染料。实例是无机着色剂(如氧化铁、氧化钛、六氰合铁酸铁(iron hexacyanoferrate))和有机着色剂(如茜素、偶氮和酞菁着色剂)。
合适的增粘剂或粘合剂是聚乙烯吡咯烷酮、聚乙酸乙烯酯、聚乙烯醇、聚丙烯酸酯、生物蜡或合成蜡以及纤维素醚。
农用化学组合物通常包含按重量计0.01%至95%、优选0.1%至90%、更优选1%至70%,并且特别是10%至60%的活性物质(例如至少一种化合物I)。农用化学组合物通常包含按重量计5%至99.9%、优选10%至99.9%、更优选30%至99%,并且特别是40%至90%的至少一种助剂。活性物质(例如化合物I)以90%至100%、优选95%至100%的纯度(根据NMR谱图)采用。
出于处理植物繁殖材料特别是种子的目的,通常使用种子处理用溶液(LS)、悬浮乳液(SE)、可流动浓缩液(FS)、干法处理用粉末(DS)、浆料处理用水分散性粉末(WS)、水溶性粉末(SS)、乳液(ES)、可乳化浓缩液(EC)和凝胶(GF)。在2至10倍稀释后,所讨论的组合物的即用制剂中活性物质浓度为按重量计0.01%至60%,优选地0.1%至40%。施用可以在播种之前或期间进行。用于分别将化合物I及其组合物施用于植物繁殖材料、尤其是种子的方法包括拌制、涂覆、造粒、撒粉、浸泡以及沟内施用方法。优选地,将化合物I或其组合物通过使得不诱发萌发的方法,例如通过拌种、造粒、涂覆和撒粉分别施用到植物繁殖材料上。
各种类型的油、湿润剂、辅助剂、肥料或微量营养物质以及另外的杀有害生物剂(例如杀真菌剂、生长调节剂、除草剂、杀昆虫剂、安全剂)可以作为预混料添加到化合物I或其组合物中,或者直到使用前才加入(罐式混合(tank mix))。这些试剂可以以1:100至100:1、优选地1:10至10:1的重量比与根据本发明的组合物掺合。
杀有害生物剂通常是通过其效果将有害生物阻止、失能、杀灭或在其他方面受挫的化学或生物药剂(如杀有害生物活性成分、化合物、组合物、病毒、细菌、抗微生物剂或消毒剂)。目标有害生物可以包括破坏财产、引起妨害、传播疾病或为疾病的媒介的昆虫、植物病原体、杂草、软体动物、鸟、哺乳动物、鱼、线虫(蛔虫)和微生物。术语“杀有害生物剂”还包括改变植物的预期生长、开花或繁殖率的植物生长调节剂;引起叶子或其他枝叶从植物脱落的落叶剂,通常促进收获;促进活体组织,如不想要的植物地上部分的干燥的干燥剂;活化植物生理机能以防御某些有害生物的植物活化剂;降低杀有害生物剂对作物植物的不想要的除草作用的安全剂;以及影响植物生理机能例如以增强植物生长、生物质、产量或作物植物的可收获物品的任何其他质量参数的植物生长促进剂。
生物杀有害生物剂被定义为基于微生物(细菌、真菌、病毒、线虫等)的杀有害生物剂或天然产品(化合物,如代谢物、蛋白质或来自生物或其他天然来源的提取物)的形式(美国环境保护署(U.S.Environmental Protection Agency):http://www.epa.gov/pesticides/biopesticides/)。生物杀有害生物剂落入两个主要类别,微生物和生物化学杀有害生物剂:
(1)微生物杀有害生物剂由细菌、真菌或病毒组成(并且通常包括细菌和真菌产生的代谢物)。昆虫病原线虫也被归类为微生物杀有害生物剂,尽管它们是多细胞的。
(2)生物化学杀有害生物剂是防治有害生物或提供如下文所定义的其他作物保护用途,但对哺乳动物相对无毒的天然存在的物质。
将作为杀真菌剂的使用形式的化合物I或包含它们的组合物与其他杀真菌剂混合在许多情况下致使杀真菌活性谱的扩展或防止杀真菌剂抗性的发展。此外,在许多情况下,获得了协同效果(协同混合物)。
可以与化合物I结合使用的以下杀有害生物剂II清单旨在说明可能的组合,但不限制它们:
A)呼吸抑制剂
-在Qo位点的配合物III抑制剂:嘧菌酯(A.1.1)、甲香菌酯(A.1.2)、丁香菌酯(A.1.3)、醚菌胺(A.1.4)、烯肟菌酯(A.1.5)、烯肟菌胺(A.1.6)、氟菌螨酯(fenoxystrobin/flufenoxystrobin)(A.1.7)、氟嘧菌酯(A.1.8)、醚菌酯(A.1.9)、甲苯醚菌酯(mandestrobin)(A.1.10)、苯氧菌胺(A.1.11)、肟醚菌胺(A.1.12)、啶氧菌酯(A.1.13)、唑菌胺酯(A.1.14)、唑胺菌酯(A.1.15)、唑菌酯(A.1.16)、肟菌酯(A.1.17)、2-(2-(3-(2,6-二氯苯基)-1-甲基-亚烯丙基氨基氧基甲基)-苯基)-2-甲氧亚氨基-N-甲基-乙酰胺(A.1.18)、吡菌苯威(A.1.19)、氯啶菌酯(triclopyricarb/chlorodincarb)(A.1.20)、噁唑酮菌(A.1.21)、咪唑菌酮(A.1.21)、甲基-N-[2-[(1,4-二甲基-5-苯基-吡唑-3-基)氧基甲基]苯基]-N-甲氧基-氨基甲酸酯(A.1.22)、四唑菌酮(A.1.25)、(Z,2E)-5-[1-(2,4-二氯苯基)吡唑-3-基]氧基-2-甲氧亚氨基-N,3-二甲基-戊-3-烯酰胺(A.1.34)、(Z,2E)-5-[1-(4-氯苯基)吡唑-3-基]氧基-2-甲氧亚氨基-N,3-二甲基-戊-3-烯酰胺(A.1.35)、嘧螨胺(A.1.36)、吡氟菌酯(A.1.37)、2-(邻-((2,5-二甲基苯基-氧基亚甲基)苯基)-3-甲氧基-丙烯酸甲酯(A.1.38);
-在Qi位点的配合物III抑制剂:氰霜唑(A.2.1)、吲唑磺菌胺(A.2.2)、2-甲基丙酸[(6S,7R,8R)-8-苄基-3-[(3-羟基-4-甲氧基-吡啶-2-羰基)氨基]-6-甲基-4,9-二氧代-1,5-二氧壬环-7-基]酯(A.2.3)、吡啶菌胺(fenpicoxamid)(A.2.4)、吡啶菌酰胺(A.2.5)、吡啶草酰胺(metarylpicoxamid)(A.2.6);
-配合物II抑制剂:麦锈灵(A.3.1)、苯并烯氟菌唑(A.3.2)、联苯吡菌胺(A.3.3)、啶酰菌胺(A.3.4)、萎锈灵(A.3.5)、甲呋酰胺(A.3.6)、氟吡菌酰胺(A.3.7)、氟酰胺(A.3.8)、氟唑菌酰胺(A.3.9)、呋吡菌胺(A.3.10)、异丙噻菌胺(A.3.11)、吡唑萘菌胺(A.3.12)、灭锈胺(A.3.13)、氧化萎锈灵(A.3.14)、氟唑菌苯胺(A.3.15)、吡噻菌胺(A.3.16)、氟唑菌酰羟胺(A.3.17)、联苯吡嗪菌胺(A.3.18)、氟唑环菌胺(A.3.19)、叶枯酞(A.3.20)、噻呋酰胺(A.3.21)、茚吡菌胺(inpyrfluxam)(A.3.22)、吡炔虫酰胺(pyrapropoyne)(A.3.23)、氟茚唑菌胺(A.3.28)、N-[2-[2-氯-4-(三氟甲基)苯氧基]苯基]-3-(二氟甲基)-5-氟-1-甲基-吡唑-4-甲酰胺(A.3.29)、(E)-2-[2-[(5-氰基-2-甲基-苯氧基)甲基]苯基]-3-甲氧基-丙-2-烯酸甲酯(A.3.30)、异丙氟吡菌胺(isoflucypram)(A.3.31)、2-(二氟甲基)-N-(1,1,3-三甲基-茚满-4-基)吡啶-3-甲酰胺(A.3.32)、2-(二氟甲基)-N-[(3R)-1,1,3-三甲基茚满-4-基]吡啶-3-甲酰胺(A.3.33)、2-(二氟甲基)-N-(3-乙基-1,1-二甲基-茚满-4-基)吡啶-3-甲酰胺(A.3.34)、2-(二氟甲基)-N-[(3R)-3-乙基-1,1-二甲基-茚满-4-基]吡啶-3-甲酰胺(A.3.35)、2-(二氟甲基)-N-(1,1-二甲基-3-丙基-茚满-4-基)吡啶-3-甲酰胺(A.3.36)、2-(二氟甲基)-N-[(3R)-1,1-二甲基-3-丙基-茚满-4-基]吡啶-3-甲酰胺(A.3.37)、2-(二氟甲基)-N-(3-异丁基-1,1-二甲基-茚满-4-基)吡啶-3-甲酰胺(A.3.38)、2-(二氟甲基)-N-[(3R)-3-异丁基-1,1-二甲基-茚满-4-基]吡啶-3-甲酰胺(A.3.39)、三氟吡啶胺(A.3.24);
-其他呼吸抑制剂:二氟林(A.4.1);硝基苯基衍生物:乐杀螨(A.4.2)、敌螨通(A.4.3)、敌螨普(A.4.4)、氟啶胺(A.4.5)、消螨多(A.4.6)、嘧菌腙(A.4.7);有机金属化合物:三苯锡盐,例如三苯基乙酸锡(A.4.8)、三苯基氯化锡(A.4.9)或三苯基氢氧化锡(A.4.10);唑嘧菌胺(A.4.11);硅噻菌胺(A.4.12);
B)甾醇生物合成抑制剂(SBI杀真菌剂)
-C14脱甲基酶抑制剂:三唑:戊环唑(B.1.1)、联苯三唑醇(B.1.2)、糠菌唑(B.1.3)、环唑醇(B.1.4)、噁醚唑(B.1.5)、烯唑醇(B.1.6)、烯唑醇-M(B.1.7)、氟环唑(B.1.8)、腈苯唑(B.1.9)、氟喹唑(B.1.10)、氟硅唑(B.1.11)、粉唑醇(B.1.12)、己唑醇(B.1.13)、酰胺唑(B.1.14)、种菌唑(B.1.15)、叶菌唑(B.1.17)、腈菌唑(B.1.18)、噁咪唑(B.1.19)、多效唑(B.1.20)、戊菌唑(B.1.21)、丙环唑(B.1.22)、丙硫菌唑(B.1.23)、硅氟唑(B.1.24)、戊唑醇(B.1.25)、氟醚唑(B.1.26)、三唑酮(B.1.27)、唑菌醇(B.1.28)、灭菌唑(B.1.29)、烯效唑(B.1.30)、2-(2,4-二氟苯基)-1,1-二氟-3-(四唑-1-基)-1-[5-[4-(2,2,2-三氟乙氧基)苯基]-2-吡啶基]丙-2-醇(B.1.31)、2-(2,4-二氟苯基)-1,1-二氟-3-(四唑-1-基)-1-[5-[4-(三氟甲氧基)苯基]-2-吡啶基]丙-2-醇(B.1.32)、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(5-硫烷基-1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈(B.1.33)、伊芬三氟康唑(ipfentrifluconazole)(B.1.37)、氯氟醚菌唑(B.1.38)、(2R)-2-[4-(4-氯苯氧基)-2-(三氟甲基)苯基]-1-(1,2,4-三唑-1-基)丙-2-醇、(2S)-2-[4-(4-氯苯氧基)-2-(三氟甲基)苯基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-(氯甲基)-2-甲基-5-(对甲苯基甲基)-1-(1,2,4-三唑-1-基甲基)环戊醇(B.1.43);咪唑:抑霉唑(B.1.44)、稻瘟酯(B.1.45)、咪鲜胺(B.1.46)、氟菌唑(B.1.47);嘧啶、吡啶、哌嗪:氯苯嘧啶醇(B.1.49)、啶斑肟(B.1.50)、嗪氨灵(B.1.51)、[3-(4-氯-2-氟-苯基)-5-(2,4-二氟苯基)异噁唑-4-基]-(3-吡啶基)甲醇(B.1.52)、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈(B.1.53)、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇(B.1.54)、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇(B.1.55);
-δ14-还原酶抑制剂:4-十二烷基-2,6-二甲基吗啉(Aldimorph)(B.2.1)、吗菌灵(B.2.2)、吗菌灵乙酸酯(B.2.3)、丁苯吗啉(B.2.4)、克啉菌(B.2.5)、苯锈啶(B.2.6)、粉病灵(B.2.7)、螺环菌胺(B.2.8);
-3-酮基还原酶抑制剂:环酰菌胺(B.3.1);
-其他甾醇生物合成抑制剂:氯苯肟唑(B.4.1);
C)核酸合成抑制剂
-苯基酰胺类或酰基氨基酸杀真菌剂:苯霜灵(C.1.1)、精苯霜灵(Benalaxyl-M)(C.1.2)、精苯霜灵(kiralaxyl)(C.1.3)、甲霜灵(C.1.4)、精甲霜灵(C.1.5)、呋酰胺(C.1.6)、噁霜灵(C.1.7);
-其他核酸合成抑制剂:噁霉灵(C.2.1)、辛噻酮(C.2.2)、噁喹酸(C.2.3)、乙嘧酚磺酸酯(C.2.4)、5-氟胞嘧啶(C.2.5)、5-氟-2-(对甲苯基甲氧基)嘧啶-4-胺(C.2.6)、5-氟-2-(4-氟苯基甲氧基)嘧啶-4-胺(C.2.7)、5-氟-2-(4-氯苯基甲氧基)嘧啶-4-胺(C.2.8);
D)细胞分裂和细胞骨架抑制剂
-微管蛋白抑制剂:苯菌灵(D.1.1)、多菌灵(D.1.2)、麦穗宁(D1.3)、涕必灵(D.1.4)、甲基托布津(D.1.5)、氟苯菌哒嗪(pyridachlometyl)(D.1.6)、N-乙基-2-[(3-乙炔基-8-甲基-6-喹啉基)氧基]丁酰胺(D.1.8)、N-乙基-2-[(3-乙炔基-8-甲基-6-喹啉基)氧基]-2-甲基硫烷基-乙酰胺(D.1.9)、2-[(3-乙炔基-8-甲基-6-喹啉基)氧基]-N-(2-氟乙基)丁酰胺(D.1.10)、2-[(3-乙炔基-8-甲基-6-喹啉基)氧基]-N-(2-氟乙基)-2-甲氧基-乙酰胺(D.1.11)、2-[(3-乙炔基-8-甲基-6-喹啉基)氧基]-N-丙基-丁酰胺(D.1.12)、2-[(3-乙炔基-8-甲基-6-喹啉基)氧基]-2-甲氧基-N-丙基-乙酰胺(D.1.13)、2-[(3-乙炔基-8-甲基-6-喹啉基)氧基]-2-甲基硫烷基-N-丙基-乙酰胺(D.1.14)、2-[(3-乙炔基-8-甲基-6-喹啉基)氧基]-N-(2-氟乙基)-2-甲基硫烷基-乙酰胺(D.1.15)、4-(2-溴-4-氟-苯基)-N-(2-氯-6-氟-苯基)-2,5-二甲基-吡唑-3-胺(D.1.16);
-其他细胞分裂抑制剂:乙霉威(D.2.1)、噻唑菌胺(D.2.2)、戊菌隆(D.2.3)、氟吡菌胺(D.2.4)、苯酰菌胺(D.2.5)、苯菌酮(D.2.6)、苯啶菌酮(pyriofenone)(D.2.7)、氰烯菌酯(D.2.8);
E)氨基酸和蛋白质合成抑制剂
-蛋氨酸合成抑制剂:嘧菌环胺(E.1.1)、嘧菌胺(E.1.2)、嘧霉胺(E.1.3);
-蛋白质合成抑制剂:杀稻瘟菌素-S(E.2.1)、春雷霉素(E.2.2)、春雷霉素盐酸盐水合物(E.2.3)、米多霉素(E.2.4)、链霉素(E.2.5)、土霉素(E.2.6);
F)信号转导抑制剂
-MAP/组氨酸激酶抑制剂:氟氯菌核利(luoroimid)(F.1.1)、异菌脲(F.1.2)、腐霉利(F.1.3)、乙烯菌核利(F.1.4)、咯菌腈(F.1.5);
-G蛋白抑制剂:喹氧灵(F.2.1);
G)脂质和膜合成抑制剂
-磷脂生物合成抑制剂:克瘟散(G.1.1)、异稻瘟净(G.1.2)、定菌磷(G.1.3)、稻瘟灵(G.1.4);
-脂质过氧化:氯硝胺(G.2.1)、五氯硝基苯(G.2.2)、四氯硝基苯(G.2.3)、甲基立枯磷(G.2.4)、联苯(G.2.5)、地茂散(G.2.6)、氯唑灵(G.2.7)、噻唑锌(G.2.8);
-磷脂生物合成和细胞壁沉积:烯酰吗啉(G.3.1)、氟吗啉(G.3.2)、双炔酰菌胺(G.3.3)、丁吡吗啉(G.3.4)、苯噻菌胺(G.3.5)、异丙菌胺(G.3.6)、缬菌胺(G.3.7);
-影响细胞膜渗透性的化合物和脂肪酸:霜霉威(G.4.1);
-氧化甾醇结合蛋白抑制剂:氟噻唑吡乙酮(G.5.1)、氟沙普罗林(fluoxapiprolin)(G.5.3)、4-[1-[2-[3-二氟甲基-5-甲基-吡唑-1-基]乙酰基]-4-哌啶基]-N-四氢萘-1-基-吡啶-2-甲酰胺(G.5.4)、4-[1-[2-[3,5-双(二氟甲基)吡唑-1-基]乙酰基]-4-哌啶基]-N-四氢萘-1-基-吡啶-2-甲酰胺(G.5.5)、4-[1-[2-[3-(二氟甲基)-5-(三氟甲基)吡唑-1-基]乙酰基]-4-哌啶基]-N-四氢萘-1-基-吡啶-2-甲酰胺(G.5.6)、4-[1-[2-[5-环丙基-3-(二氟甲基)吡唑-1-基]乙酰基]-4-哌啶基]-N-四氢萘-1-基-吡啶-2-甲酰胺(G.5.7)、4-[1-[2-[5-甲基-3-(三氟甲基)吡唑-1-基]乙酰基]-4-哌啶基]-N-四氢萘-1-基-吡啶-2-甲酰胺(G.5.8)、4-[1-[2-[5-(二氟甲基)-3-(三氟甲基)吡唑-1-基]乙酰基]-4-哌啶基]-N-四氢萘-1-基-吡啶-2-甲酰胺(G.5.9)、4-[1-[2-[3,5-双(三氟甲基)吡唑-1-基]乙酰基]-4-哌啶基]-N-四氢萘-1-基-吡啶-2-甲酰胺(G.5.10)、(4-[1-[2-[5-环丙基-3-(三氟甲基)吡唑-1-基]乙酰基]-4-哌啶基]-N-四氢萘-1-基-吡啶-2-甲酰胺(G.5.11);
H)具有多位点作用的抑制剂
-无机活性物质:波尔多混合剂(H.1.1)、铜(H.1.2)、乙酸铜(H.1.3)、氢氧化铜(H.1.4)、氯氧化铜(H.1.5)、碱式硫酸铜(H.1.6)、硫(H.1.7);
-硫代-和二硫代氨基甲酸酯:福美铁(H.2.1)、代森锰锌(H.2.2)、代森锰(H.2.3)、威百亩(H.2.4)、代森联(H.2.5)、甲基代森锌(H.2.6)、福美双(H.2.7)、代森锌(H.2.8)、福美锌(H.2.9);
-有机氯化合物:敌菌灵(H.3.1)、百菌清(H.3.2)、敌菌丹(H.3.3)、克菌丹(H.3.4)、灭菌丹(H.3.5)、抑菌灵(H.3.6)、双氯酚(H.3.7)、六氯苯(H.3.8)、五氯酚(H.3.9)及其盐、四氯苯酞(H.3.10)、对甲抑菌灵(H.3.11);
-胍及其他:胍(H.4.1)、多果定(H.4.2)、多果定游离碱(H.4.3)、双胍辛盐(guazatine)(H.4.4)、双胍辛乙酸盐(guazatine-acetate)(H.4.5)、双胍辛胺(H.4.6)、双胍辛胺三乙酸盐(H.4.7)、双胍三辛烷基苯磺酸盐(H.4.8)、二噻农(H.4.9)、2,6-二甲基-1H,5H-[1,4]二噻英并[2,3-c:5,6-c’]二吡咯-1,3,5,7(2H,6H)-四酮(H.4.10);
I)细胞壁合成抑制剂
-葡聚糖合成抑制剂:有效霉素(I.1.1)、多氧菌素(I.1.2);
-黑色素合成抑制剂:咯喹酮(I.2.1)、三环唑(I.2.2)、环丙酰菌胺(I.2.3)、双氯氰菌胺(Dicyclomet)(I.2.4)、稻瘟酰胺(I.2.5);
J)植物防御诱导剂
-阿拉酸式苯-S-甲基(J.1.1)、噻菌灵(J.1.2)、异噻菌胺(J.1.3)、噻酰菌胺(J.1.4)、调环酸-钙(J.1.5);膦酸酯:乙膦酸(J.1.6)、乙膦铝(J.1.7)、亚磷酸及其盐(J.1.8)、膦酸钙(J.1.11)、膦酸钾(J.1.12)、碳酸氢钾或钠(J.1.9)、4-环丙基-N-(2,4-二甲氧基苯基)噻二唑-5-甲酰胺(J.1.10);
K)未知作用模式
-溴硝醇(K.1.1)、灭螨蜢(K.1.2)、环氟菌胺(K.1.3)、霜脲氰(K.1.4)、棉隆(K.1.5)、咪菌威(K.1.6)、双氯氰菌胺(K.1.7)、哒菌清(K.1.8)、野燕枯(K.1.9)、野燕枯-甲基硫酸盐(K.1.10)、二苯胺(K.1.11)、种衣酯(K.1.12)、胺苯吡菌酮(K.1.13)、氟联苯菌(flumetover)(K.1.14)、磺菌胺(K.1.15)、氟噻唑菌腈(K.1.16)、超敏蛋白(K.1.17)、磺菌威(K.1.18)、三氯甲基吡啶(K.1.19)、酞菌酯(K.1.20)、三氟甲氧威(tolprocarb)(K.1.21)、喹啉铜(K.1.22)、丙氧喹啉(K.1.23)、异丁乙氧喹啉(tebufloquin)(K.1.24)、叶枯酞(K.1.25)、唑菌嗪(K.1.26)、N’-(4-(4-氯-3-三氟甲基-苯氧基)-2,5-二甲基-苯基)-N-乙基-N-甲基甲脒(K.1.27)、N’-(4-(4-氟-3-三氟甲基-苯氧基)-2,5-二甲基-苯基)-N-乙基-N-甲基甲脒(K.1.28)、N’-[4-[[3-[(4-氯苯基)甲基]-1,2,4-噻二唑-5-基]氧基]-2,5-二甲基-苯基]-N-乙基-N-甲基-甲脒(K.1.29)、N’-(5-溴-6-茚满-2-基氧基-2-甲基-3-吡啶基)-N-乙基-N-甲基-甲脒(K.1.30)、N’-[5-溴-6-[1-(3,5-二氟苯基)乙氧基]-2-甲基-3-吡啶基]-N-乙基-N-甲基-甲脒(K.1.31)、N’-[5-溴-6-(4-异丙基环己氧基)-2-甲基-3-吡啶基]-N-乙基-N-甲基-甲脒(K.1.32)、N’-[5-溴-2-甲基-6-(1-苯基乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒(K.1.33)、N’-(2-甲基-5-三氟甲基-4-(3-三甲基硅烷基-丙氧基)苯基)-N-乙基-N-甲基甲脒(K.1.34)、N’-(5-二氟甲基-2-甲基-4-(3-三甲基硅烷基-丙氧基)-苯基)-N-乙基-N-甲基甲脒(K.1.35)、2-(4-氯-苯基)-N-[4-(3,4-二甲氧基-苯基)异噁唑-5-基]-2-丙-2-炔氧基-乙酰胺(K.1.36)、3-[5-(4-氯-苯基)-2,3-二甲基-异噁唑烷-3-基]-吡啶(啶菌噁唑)(K.1.37)、3-[5-(4-甲基苯基)-2,3-二甲基-异噁唑烷-3-基]-吡啶(K.1.38)、5-氯-1-(4,6-二甲氧基-嘧啶-2-基)-2-甲基-1H-苯并咪唑(K.1.39)、(Z)-3-氨基-2-氰基-3-苯基-丙-2-烯酸乙酯(K.1.40)、四唑吡氨酯(K.1.41)、N-[6-[[(Z)-[(1-甲基四唑-5-基)-苯基-亚甲基]氨基]氧基甲基]-2-吡啶基]氨基甲酸戊酯(K.1.42)、N-[6-[[(Z)-[(1-甲基四唑-5-基)-苯基-亚甲基]氨基]氧基甲基]-2-吡啶基]氨基甲酸丁-3-炔基酯(K.1.43)、伊氟芬喹(ipflufenoquin)(K.1.44)、氟菌喹啉(quinofumelin)(K.1.47)、噻霉酮(K.1.48)、溴菌腈(K.1.49)、2-(6-苄基-2-吡啶基)喹唑啉(K.1.50)、2-[6-(3-氟-4-甲氧基-苯基)-5-甲基-2-吡啶基]喹唑啉(K.1.51)、二氯菌噻(dichlobentiazox)(K.1.52)、N’-(2,5-二甲基-4-苯氧基-苯基)-N-乙基-N-甲基-甲脒(K.1.53)、氨吡菌酯(K.1.54)、氟醚菌酰胺(K.1.55)、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒(K.1.56)、N'-[4-(4,5-二氯噻唑-2-基)氧基-2,5-二甲基-苯基]-N-乙基-N-甲基-甲脒(K.1.57)、N-(2-氟苯基)-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺(K.1.58)、N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]硫代苯甲酰胺(K.1.59)、N-甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]环丙烷甲酰胺(WO 2018/177894、WO 2020/212513);
L)生物杀有害生物剂
L1)具有杀真菌、杀细菌、杀病毒和/或植物防御活化剂活性的微生物杀有害生物剂:白粉寄生孢、黄曲霉、出芽短梗霉菌、高地芽孢杆菌、解淀粉芽孢杆菌、解淀粉芽孢杆菌植物亚种(也称为贝莱斯芽孢杆菌)、巨大芽孢杆菌、莫海威芽孢杆菌、蕈状芽孢杆菌、短小芽孢杆菌、简单芽孢杆菌、盐土芽孢杆菌、枯草芽孢杆菌、解淀粉枯草芽孢杆菌变种、贝莱斯芽孢杆菌、橄榄假丝酵母、齐藤假丝酵母(C.saitoana)、番茄溃疡病菌(Clavibactermichiganensis)(噬菌体)、盾壳霉、寄生隐丛赤壳菌、白色隐球菌、秃发双孢菌(Dilophosphora alopecuri)、尖孢镰刀菌、链孢粘帚霉(Clonostachys roseaf.catenulate)(也称为链孢粘帚菌(Gliocladium catenulatum))、粉红粘帚霉、抗生素溶杆菌、产霉溶杆菌、核果梅奇酵母、双胞镰孢(Microdochium dimerum)、小球壳孢、白色产气霉(Muscodor albus)、蜂房芽孢杆菌、附生类芽孢杆菌、多粘类芽孢杆菌、成团泛菌、拜赖青霉、大伏革菌、假单胞菌属物种、绿镇假单胞菌、絮状假酶菌(Pseudozyma flocculosa)、异常毕赤酵母、寡雄腐霉、球形孢子菌(Sphaerodes mycoparasitica)、灰绿链霉菌、利迪链霉菌、紫黑链霉菌、黄蓝状菌、类棘孢木霉(Trichoderma asperelloides)、棘孢木霉、深绿木霉、顶孢木霉、盖姆斯木霉、钩状木霉(T.harmatum)、哈茨木霉、多孢木霉(T.polysporum)、子座木霉(T.stromaticum)、绿木霉(T.virens)、绿色木霉(T.viride)、透根核瑚菌(Typhula phacorrhiza)、奥德曼细基格孢、大丽轮枝菌、小西葫芦黄花叶病毒(无毒菌株);
L2)具有杀真菌、杀细菌、杀病毒和/或植物防御活化剂活性的生物化学杀有害生物剂:超敏蛋白,大虎杖提取物;
L3)具有杀昆虫、杀螨、杀螺和/或杀线虫活性的微生物杀有害生物剂:放射形土壤杆菌、蜡样芽孢杆菌、坚强芽孢杆菌、苏云金芽孢杆菌、苏云金芽孢杆菌鲇泽亚种、苏云金芽孢杆菌以色列亚种、苏云金芽孢杆菌蜡螟亚种、苏云金芽孢杆菌库尔斯塔克亚种、苏云金芽孢杆菌拟步行甲亚种、球孢白僵菌、布氏白僵菌、伯克霍尔德氏菌物种、活性紫色细菌(Chromobacterium subtsugae)、苹果蠹蛾颗粒体病毒(CpGV)、伪苹果蠹蛾颗粒体病毒(CrleGV)、黄杆菌属物种、棉铃虫核型多角体病毒(HearNPV)、玉米夜蛾核型多角体病毒(HzNPV)、玉米夜蛾单衣壳核型多角体病毒(HzSNPV)、嗜菌异小杆线虫、玫烟色棒束孢、长孢蜡蚧菌(Lecanicillium longisporum)、蝇蚧疥霉(L.muscarium)、金龟子绿僵菌、金龟子绿僵菌小孢变种、金龟子绿僵菌蝗变种、莱氏野村菌、玫烟色拟青霉、淡紫色拟青霉、日本甲虫类芽孢杆菌、巴斯德氏芽菌属物种、拟斯扎瓦巴氏杆菌、穿刺巴氏杆菌、分支巴斯德氏菌(P.ramosa)、李氏巴斯德氏菌(P.thornea)、乌斯巴斯德氏菌(P.usgae)、荧光假单胞菌、灰翅夜蛾核型多角体病毒(SpliNPV)、斯氏小卷蛾线虫、斯氏夜蛾线虫、锯蜂线虫、鲜黄链霉菌、细黄链霉菌;
L4)具有杀昆虫、杀螨、杀螺、信息素和/或杀线虫活性的生物化学杀有害生物剂:L-香芹酮、柠檬醛、乙酸(E,Z)-7,9-十二碳二烯-1-基酯、甲酸乙酯、(E,Z)-2,4-癸二烯酸乙酯(梨酯)、(Z,Z,E)-7,11,13-十六碳三烯醛、丁酸庚酯、肉豆蔻酸异丙酯、千里酸熏衣草酯、顺式-茉莉酮、2-甲基1-丁醇、甲基丁香酚、茉莉酮酸甲酯、(E,Z)-2,13-十八碳二烯-1-醇、乙酸(E,Z)-2,13-十八碳二烯-1-醇酯、(E,Z)-3,13-十八碳二烯-1-醇、(R)-1-辛烯-3-醇、白蚁信息素(pentatermanone)、乙酸(E,Z,Z)-3,8,11-十四碳三烯基酯、乙酸(Z,E)-9,12-十四碳二烯-1-基酯、(Z)-7-十四碳烯-2-酮、乙酸(Z)-9-十四碳烯-1-基酯、(Z)-11-十四碳烯醛、(Z)-11-十四碳烯-1-醇、土荆芥(Chenopodium ambrosiodes)提取物、印楝油、皂树(Quillay)提取物;
L5)具有植物胁迫降低、植物生长调节剂、植物生长促进和/或产量提高活性的微生物杀有害生物剂:无乳固氮螺菌、巴西固氮螺菌、生脂固氮螺菌、伊拉克固氮螺菌、高盐固氮螺菌、慢生根瘤菌属物种、埃氏慢生根瘤菌、大豆慢生根瘤菌、辽宁慢生根瘤菌、慢生羽扇豆根瘤菌、食酸戴尔福特菌、丛枝菌根真菌、中生根瘤菌属物种、豌豆根瘤菌菜豆生物型、豌豆根瘤菌三叶草生物型、豌豆根瘤菌蚕豆生物型、热带根瘤菌和苜蓿中华根瘤菌;
O)来自O.1至O.29类的杀昆虫剂
O.1乙酰胆碱酯酶(AChE)抑制剂:涕灭威、棉铃威、噁虫威、丙硫克百威、丁酮威、丁酮砜威、甲萘威、卡巴呋喃、丁硫克百威、乙硫苯威、仲丁威、伐虫脒、呋线威、异丙威、灭虫威、灭多虫、速灭威、杀线威、抗蚜威、残杀威、硫双威、久效威、混杀威、XMC、灭杀威、唑蚜威;高灭磷、甲基吡啶磷、乙基谷硫磷、谷硫磷、硫线磷、氯氧磷、毒虫畏、氯甲磷、毒死蜱、甲基毒死蜱、蝇毒磷、杀螟腈、内吸磷-S-甲基、二嗪农、敌敌畏/DDVP、百治磷、乐果、甲基毒虫畏、乙拌磷、EPN、乙硫磷、丙线磷、伐灭磷、苯线磷、杀螟松、倍硫磷、噻唑磷、庚烯磷、氰咪唑硫磷、异丙胺磷、O-(甲氧基氨基硫代-磷酰基)水杨酸异丙酯、异噁唑磷、马拉硫磷、灭蚜磷、甲胺磷、杀扑磷、速灭磷、久效磷、二溴磷、氧乐果、砜吸磷、对硫磷、甲基对硫磷、稻丰散、甲拌磷、伏杀磷、亚胺硫磷、磷胺、辛硫磷、甲基嘧啶磷、丙溴磷、烯虫磷、丙硫磷、吡唑硫磷、哒嗪硫磷、喹硫磷、治螟磷、丁基嘧啶磷、双硫磷、特丁磷、杀虫畏、甲基乙拌磷、三唑磷、敌百虫、蚜灭磷;
O.2GABA门控氯离子通道拮抗剂:硫丹、氯丹;乙虫腈、氟虫腈、丁烯氟虫腈、啶吡唑虫胺(pyrafluprole)、吡唑虫啶(pyriprole);
O.3钠通道调节剂:氟丙菊酯、丙烯菊酯、右旋-顺式-反式丙烯菊酯、右旋反式丙烯菊酯、联苯菊酯、k-联苯菊酯、生物丙烯菊酯、生物丙烯菊酯S-环戊烯基、生物苄呋菊酯、乙氰菊酯、氟氯氰菊酯、β-氟氯氰菊酯、三氟氯氰菊酯、λ-三氟氯氰菊酯、γ-三氟氯氰菊酯、氯氰菊酯、α-氯氰菊酯、β-氯氰菊酯、θ-氯氰菊酯、ζ-氯氰菊酯、苯醚氰菊酯、溴氰菊酯、烯炔菊酯、高氰戊菊酯、醚菊酯、甲氰菊酯、杀灭菊酯、氟氰戊菊酯、氟氯苯菊酯、τ-氟胺氰菊酯、溴氟醚菊酯、七氟甲醚菊酯、咪炔菊酯、氯氟醚菊酯、甲氧苄氟菊酯、甲氧氟菊酯、ε-甲氧氟菊酯、氯菊酯、苯醚菊酯、炔丙菊酯、丙氟菊酯、除虫菊酯(除虫菊)、灭虫菊、氟硅菊酯、七氟菊酯、κ-七氟菊酯、四氟醚菊酯、胺菊酯、四溴菊酯、四氟苯菊酯;DDT、甲氧滴滴涕;
O.4烟碱型乙酰胆碱受体(nAChR)激动剂:啶虫脒、噻虫胺、环氧虫啶、呋虫胺、吡虫啉、烯啶虫胺、噻虫啉、噻虫嗪;4,5-二氢-N-硝基-1-(2-环氧乙烷基甲基)-1H-咪唑-2-胺、(2E)-1-[(6-氯吡啶-3-基)甲基]-N’-硝基-2-亚戊基氨基胍;1-[(6-氯吡啶-3-基)甲基]-7-甲基-8-硝基-5-丙氧基-1,2,3,5,6,7-六氢咪唑并[1,2-a]吡啶;烟碱;氟啶虫胺腈、氟吡呋喃酮、三氟苯嘧啶、(3R)-3-(2-氯噻唑-5-基)-8-甲基-5-氧代-6-苯基-2,3-二氢噻唑并[3,2-a]嘧啶-8-鎓-7-酚盐、(3S)-3-(6-氯-3-吡啶基)-8-甲基-5-氧代-6-苯基-2,3-二氢噻唑并[3,2-a]嘧啶-8-鎓-7-酚盐、(3S)-8-甲基-5-氧代-6-苯基-3-嘧啶-5-基-2,3-二氢噻唑并[3,2-a]嘧啶-8-鎓-7-酚盐、(3R)-3-(2-氯噻唑-5-基)-8-甲基-5-氧代-6-[3-(三氟甲基)苯基]-2,3-二氢噻唑并[3,2-a]嘧啶-8-鎓-7-酚盐;(3R)-3-(2-氯噻唑-5-基)-6-(3,5-二氯苯基)-8-甲基-5-氧代-2,3-二氢噻唑并[3,2-a]嘧啶-8-鎓-7-酚盐、(3R)-3-(2-氯噻唑-5-基)-8-乙基-5-氧代-6-苯基-2,3-二氢噻唑并[3,2-a]嘧啶-8-鎓-7-酚盐;
O.5烟碱型乙酰胆碱受体变构活化剂:多杀菌素、乙基多杀菌素;
O.6氯离子通道活化剂:阿巴美丁、甲氨基阿维菌素苯甲酸盐、伊维菌素、雷皮菌素、弥拜菌素;
O.7保幼激素模拟物:烯虫乙酯、烯虫炔酯、烯虫酯;苯氧威、蚊蝇醚;
O.8各种各样非特异性(多位点)抑制剂:溴甲烷和其他烷基卤化物;三氯硝基甲烷、磺酰氟、硼砂、吐酒石;
O.9弦音器官TRPV通道调节剂:吡蚜酮、氟虫吡喹;
O.10螨生长抑制剂:四螨嗪、噻螨酮、氟螨嗪;乙螨唑;
O.11昆虫中肠膜的微生物干扰剂:苏云金芽孢杆菌、球形芽孢杆菌以及它们产生的杀昆虫蛋白:苏云金芽孢杆菌以色列亚种、球形芽孢杆菌、苏云金芽孢杆菌鲇泽亚种、苏云金芽孢杆菌库尔斯塔克亚种、苏云金芽孢杆菌拟步行甲亚种,Bt作物蛋白:Cry1Ab、Cry1Ac、Cry1Fa、Cry2Ab、mCry3A、Cry3Ab、Cry3Bb、Cry34/35Ab1;
O.12线粒体ATP合成酶抑制剂:丁醚脲;三唑锡、三环锡、苯丁锡、克螨特、三氯杀螨砜;
O.13经由质子梯度干扰的氧化磷酸化去偶剂:溴虫腈、DNOC、氟虫胺;
O.14烟碱型乙酰胆碱受体(nAChR)通道阻断剂:杀虫磺、杀螟丹、杀虫环、杀虫双;
O.15甲壳素生物合成抑制剂0型:双三氟虫脲、氟啶脲、二氟脲、氟环脲、氟虫脲、氟铃脲、虱螨脲、氟酰脲、多氟脲、氟苯脲、杀铃脲;
O.16甲壳素生物合成抑制剂1型:噻嗪酮;
O.17蜕皮干扰剂:灭蝇胺;
O.18蜕皮激素受体激动剂:甲氧虫酰肼、虫酰肼、氯虫酰肼、呋喃虫酰肼、环虫酰肼;
O.19章鱼胺受体激动剂:双甲脒;
O.20线粒体配合物III电子传输抑制剂:氟蚁腙、灭螨醌、嘧螨酯、联苯肼酯;
O.21线粒体配合物I电子传输抑制剂:喹螨醚、唑螨酯、嘧螨醚、哒螨酮、吡螨胺、唑虫酰胺;鱼藤酮;
O.22电压依赖型钠通道阻断剂:茚虫威、氰氟虫腙、2-[2-(4-氰基苯基)-1-[3-(三氟甲基)苯基]亚乙基]-N-[4-(二氟甲氧基)苯基]-肼甲酰胺、N-(3-氯-2-甲基苯基)-2-[(4-氯苯基)-[4-[甲基(甲基磺酰基)氨基]苯基]亚甲基]-肼甲酰胺;
O.23乙酰辅酶A羧化酶抑制剂:螺螨酯、螺甲螨酯、螺虫乙酯、甲氧哌啶乙酯;
O.24线粒体配合物IV电子传输抑制剂:磷化铝、磷化钙、膦、磷化锌、氰化物;
O.25线粒体配合物II电子传输抑制剂:腈吡螨酯、丁氟螨酯;
O.26利阿诺定受体调节剂:氟虫双酰胺、氯虫苯甲酰胺、溴氰虫酰胺、环溴虫酰胺、氟氰虫酰胺;(R)-3-氯-N1-{2-甲基-4-[1,2,2,2–四氟-1-(三氟甲基)乙基]苯基}-N2-(1-甲基-2-甲基磺酰基乙基)酞酰胺、(S)-3-氯-N1-{2-甲基-4-[1,2,2,2–四氟-1-(三氟甲基)乙基]苯基}-N2-(1-甲基-2-甲基磺酰基乙基)酞酰胺、甲基-2-[3,5-二溴-2-({[3-溴-1-(3-氯吡啶-2-基)-1H-吡唑-5-基]羰基}氨基)苯甲酰基]-1,2-二甲基肼羧酸酯;N-[4,6-二氯-2-[(二乙基-λ-4-亚硫烷基)氨基甲酰基]苯基]-2-(3-氯-2-吡啶基)-5-(三氟甲基)吡唑-3-甲酰胺;N-[4-氯-2-[(二乙基-λ-4-亚硫烷基)氨基甲酰基]-6-甲基-苯基]-2-(3-氯-2-吡啶基)-5-(三氟甲基)吡唑-3-甲酰胺;N-[4-氯-2-[(二-2-丙基-λ-4-亚硫烷基)氨基甲酰基]-6-甲基-苯基]-2-(3-氯-2-吡啶基)-5-(三氟甲基)吡唑-3-甲酰胺;N-[4,6-二氯-2-[(二-2-丙基-λ-4-亚硫烷基)氨基甲酰基]苯基]-2-(3-氯-2-吡啶基)-5-(三氟甲基)吡唑-3-甲酰胺;N-[4,6-二溴-2-[(二乙基-λ-4-亚硫烷基)氨基甲酰基]苯基]-2-(3-氯-2-吡啶基)-5-(三氟甲基)吡唑-3-甲酰胺;N-[2-(5-氨基-1,3,4-噻二唑-2-基)-4-氯-6-甲基苯基]-3-溴-1-(3-氯-2-吡啶基)-1H-吡唑-5-甲酰胺;3-氯-1-(3-氯-2-吡啶基)-N-[2,4-二氯-6-[[(1-氰基-1-甲基乙基)氨基]羰基]苯基]-1H-吡唑-5-甲酰胺;四氯虫酰胺;N-[4-氯-2-[[(1,1-二甲基乙基)氨基]羰基]-6-甲基苯基]-1-(3-氯-2-吡啶基)-3-(氟甲氧基)-1H-吡唑-5-甲酰胺;氯氟氰虫酰胺;
O.27弦音器官调节剂-未限定的目标位点:氟啶虫酰胺;
O.28未知或不确定作用模式的杀昆虫化合物:双丙环虫酯、阿福拉纳、印楝素、磺胺螨酯、苯螨特、溴虫氟苯双酰胺、溴螨酯、灭螨猛、冰晶石、环丙氟虫胺(cyproflanilide)、二氯噻吡嘧啶、三氯杀螨醇、嘧虫胺、氟虫碳酸酯(flometoquin)、氟噻虫砜、氟己虫腈(fluhexafon)、氟吡菌酰胺、氟雷拉纳、噁虫酮、增效醚、吡唑酰苯胺(pyflubumide)、啶虫丙醚、线噻吩(tioxazafen)、11-(4-氯-2,6-二甲基苯基)-12-羟基-1,4-二氧杂-9-氮杂二螺[4.2.4.2]十四碳-11-烯-10-酮、3-(4’-氟-2,4-二甲基二苯基-3-基)-4-羟基-8-氧杂-1-氮杂螺[4.5]癸-3-烯-2-酮、1-[2-氟-4-甲基-5-[(2,2,2-三氟乙基)亚磺酰基]苯基]-3-(三氟甲基)-1H-1,2,4-三唑-5-胺、坚强芽孢杆菌I-1582;氟虫啶胺(flupyrimin);三氟咪啶酰胺;4-[5-(3,5-二氯苯基)-5-(三氟甲基)-4H-异噁唑-3-基]-2-甲基-N-(1-氧代硫杂环丁烷-3-基)苯甲酰胺;氟噁唑酰胺;5-[3-[2,6-二氯-4-(3,3-二氯烯丙氧基)苯氧基]丙氧基]-1H-吡唑;4-氰基-N-[2-氰基-5-[[2,6-二溴-4-[1,2,2,3,3,3-六氟-1-(三氟甲基)丙基]苯基]氨基甲酰基]苯基]-2-甲基-苯甲酰胺;4-氰基-3-[(4-氰基-2-甲基-苯甲酰基)氨基]-N-[2,6-二氯-4-[1,2,2,3,3,3-六氟-1-(三氟甲基)丙基]苯基]-2-氟-苯甲酰胺;N-[5-[[2-氯-6-氰基-4-[1,2,2,3,3,3-六氟-1-(三氟甲基)丙基]苯基]氨基甲酰基]-2-氰基-苯基]-4-氰基-2-甲基-苯甲酰胺;N-[5-[[2-溴-6-氯-4-[2,2,2-三氟-1-羟基-1-(三氟甲基)乙基]苯基]氨基甲酰基]-2-氰基-苯基]-4-氰基-2-甲基-苯甲酰胺;N-[5-[[2-溴-6-氯-4-[1,2,2,3,3,3-六氟-1-(三氟甲基)丙基]苯基]氨基甲酰基]-2-氰基-苯基]-4-氰基-2-甲基-苯甲酰胺;4-氰基-N-[2-氰基-5-[[2,6-二氯-4-[1,2,2,3,3,3-六氟-1-(三氟甲基)丙基]苯基]氨基甲酰基]苯基]-2-甲基-苯甲酰胺;4-氰基-N-[2-氰基-5-[[2,6-二氯-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基]氨基甲酰基]苯基]-2-甲基-苯甲酰胺;N-[5-[[2-溴-6-氯-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基]氨基甲酰基]-2-氰基-苯基]-4-氰基-2-甲基-苯甲酰胺;2-(1,3-二噁烷-2-基)-6-[2-(3-吡啶基)-5-噻唑基]-吡啶;2-[6-[2-(5-氟-3-吡啶基)-5-噻唑基]-2-吡啶基]-嘧啶;2-[6-[2-(3-吡啶基)-5-噻唑基]-2-吡啶基]-嘧啶;N-甲基磺酰基-6-[2-(3-吡啶基)噻唑-5-基]吡啶-2-甲酰胺;N-甲基磺酰基-6-[2-(3-吡啶基)噻唑-5-基]吡啶-2-甲酰胺;1-[(6-氯-3-吡啶基)甲基]-1,2,3,5,6,7-六氢-5-甲氧基-7-甲基-8-硝基-咪唑并[1,2-a]吡啶;1-[(6-氯吡啶-3-基)甲基]-7-甲基-8-硝基-1,2,3,5,6,7-六氢咪唑并[1,2-a]吡啶-5-醇;1-异丙基-N,5-二甲基-N-哒嗪-4-基-吡唑-4-甲酰胺;1-(1,2-二甲基丙基)-N-乙基-5-甲基-N-哒嗪-4-基-吡唑-4-甲酰胺;N,5-二甲基-N-哒嗪-4-基-1-(2,2,2-三氟-1-甲基-乙基)吡唑-4-甲酰胺;1-[1-(1-氰基环丙基)乙基]-N-乙基-5-甲基-N-哒嗪-4-基-吡唑-4-甲酰胺;N-乙基-1-(2-氟-1-甲基-丙基)-5-甲基-N-哒嗪-4-基-吡唑-4-甲酰胺;1-(1,2-二甲基丙基)-N,5-二甲基-N-哒嗪-4-基-吡唑-4-甲酰胺;1-[1-(1-氰基环丙基)乙基]-N,5-二甲基-N-哒嗪-4-基-吡唑-4-甲酰胺;N-甲基-1-(2-氟-1-甲基-丙基]-5-甲基-N-哒嗪-4-基-吡唑-4-甲酰胺;1-(4,4-二氟环己基)-N-乙基-5-甲基-N-哒嗪-4-基-吡唑-4-甲酰胺;1-(4,4-二氟环己基)-N,5-二甲基-N-哒嗪-4-基-吡唑-4-甲酰胺、N-(1-甲基乙基)-2-(3-吡啶基)-2H-吲唑-4-甲酰胺;N-环丙基-2-(3-吡啶基)-2H-吲唑-4-甲酰胺;N-环己基-2-(3-吡啶基)-2H-吲唑-4-甲酰胺;2-(3-吡啶基)-N-(2,2,2-三氟乙基)-2H-吲唑-4-甲酰胺;2-(3-吡啶基)-N-[(四氢-2-呋喃基)甲基]-2H-吲唑-5-甲酰胺;2-[[2-(3-吡啶基)-2H-吲唑-5-基]羰基]肼甲酸甲酯;N-[(2,2-二氟环丙基)甲基]-2-(3-吡啶基)-2H-吲唑-5-甲酰胺;N-(2,2-二氟丙基)-2-(3-吡啶基)-2H-吲唑-5-甲酰胺;2-(3-吡啶基)-N-(2-嘧啶基甲基)-2H-吲唑-5-甲酰胺;N-[(5-甲基-2-吡嗪基)甲基]-2-(3-吡啶基)-2H-吲唑-5-甲酰胺、氯吡唑虫胺(tyclopyrazoflor);沙罗拉纳(sarolaner)、洛替拉纳(lotilaner)、N-[4-氯-3-[[(苯基甲基)氨基]羰基]苯基]-1-甲基-3-(1,1,2,2,2-五氟乙基)-4-(三氟甲基)-1H-吡唑-5-甲酰胺;2-(3-乙基磺酰基-2-吡啶基)-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、2-[3-乙基磺酰基-5-(三氟甲基)-2-吡啶基]-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、异噁唑虫酰胺、N-[4-氯-3-(环丙基氨基甲酰基)苯基]-2-甲基-5-(1,1,2,2,2-五氟乙基)-4-(三氟甲基)吡唑-3-甲酰胺、N-[4-氯-3-[(1-氰基环丙基)氨基甲酰基]苯基]-2-甲基-5-(1,1,2,2,2-五氟乙基)-4-(三氟甲基)吡唑-3-甲酰胺;氟螨啶(acynonapyr);苯嘧虫噁烷(benzpyrimoxan);替戈拉纳(tigolaner);氯-N-(1-氰基环丙基)-5-[1-[2-甲基-5-(1,1,2,2,2-五氟乙基)-4-(三氟甲基)吡唑-3-基]吡唑-4-基]苯甲酰胺、噁唑磺酰虫啶、[(2S,3R,4R,5S,6S)-3,5-二甲氧基-6-甲基-4-丙氧基-四氢吡喃-2-基]-N-[4-[1-[4-(三氟甲氧基)苯基]-1,2,4-三唑-3-基]苯基]氨基甲酸酯、[(2S,3R,4R,5S,6S)-3,4,5-三甲氧基-6-甲基-四氢吡喃-2-基]N-[4-[1-[4-(三氟甲氧基)苯基]-1,2,4-三唑-3-基]苯基]氨基甲酸酯、[(2S,3R,4R,5S,6S)-3,5-二甲氧基-6-甲基-4-丙氧基-四氢吡喃-2-基]-N-[4-[1-[4-(1,1,2,2,2-五氟乙氧基)苯基]-1,2,4-三唑-3-基]苯基]氨基甲酸酯、[(2S,3R,4R,5S,6S)-3,4,5-三甲氧基-6-甲基-四氢吡喃-2-基]-N-[4-[1-[4-(1,1,2,2,2-五氟乙氧基)苯基]-1,2,4-三唑-3-基]苯基]氨基甲酸酯、(2Z)-3-(2-异丙基苯基)-2-[(E)-[4-[1-[4-(1,1,2,2,2-五氟乙氧基)苯基]-1,2,4-三唑-3-基]苯基]亚甲基亚肼基]噻唑烷-4-酮;2-(6-氯-3-乙基磺酰基-咪唑并[1,2-a]吡啶-2-基)-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、2-(6-溴-3-乙基磺酰基-咪唑并[1,2-a]吡啶-2-基)-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、2-(3-乙基磺酰基-6-碘-咪唑并[1,2-a]吡啶-2-基)-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、2-[3-乙基磺酰基-6-(三氟甲基)咪唑并[1,2-a]吡啶-2-基]-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、2-(7-氯-3-乙基磺酰基-咪唑并[1,2-a]吡啶-2-基)-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、2-(3-乙基磺酰基-7-碘-咪唑并[1,2-a]吡啶-2-基)-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、3-乙基磺酰基-6-碘-2-[3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶-2-基]咪唑并[1,2-a]吡啶-8-甲腈、2-[3-乙基磺酰基-8-氟-6-(三氟甲基)咪唑并[1,2-a]吡啶-2-基]-3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶、2-[3-乙基磺酰基-7-(三氟甲基)咪唑并[1,2-a]吡啶-2-基]-3-甲基-6-(三氟甲基亚磺酰基)咪唑并[4,5-b]吡啶、2-[3-乙基磺酰基-7-(三氟甲基)咪唑并[1,2-a]吡啶-2-基]-3-甲基-6-(三氟甲基)咪唑并[4,5-c]吡啶、2-(6-溴-3-乙基磺酰基-咪唑并[1,2-a]吡啶-2-基)-6-(三氟甲基)吡唑并[4,3-c]吡啶。
被称为组分2的活性物质、其制备及其例如抗有害真菌的活性是已知的(参见:http://www.alanwood.net/pesticides/);这些物质是可商购的。由IUPAC命名法描述的化合物、其制备及其杀有害生物活性也是已知的(参见Can.J.Plant Sci.[加拿大植物科学杂志]48(6),587-94,1968;EP-A 141 317;EP-A 152 031;EP-A 226 917;EP-A 243 970;EP-A256503;EP-A 428 941;EP-A 532 022;EP-A 1 028 125;EP-A 1 035 122;EP-A 1 201648;EP-A 1 122 244,JP 2002316902;DE 19650197;DE 10021412;DE 102005009458;US3,296,272;US 3,325,503;WO 98/46608;WO 99/14187;WO 99/24413;WO 99/27783;WO 00/29404;WO 00/46148;WO 00/65913;WO 01/54501;WO 01/56358;WO 02/22583;WO 02/40431;WO 03/10149;WO 03/11853;WO 03/14103;WO 03/16286;WO 03/53145;WO 03/61388;WO 03/66609;WO 03/74491;WO 04/49804;WO 04/83193;WO 05/120234;WO 05/123689;WO 05/123690;WO 05/63721;WO 05/87772;WO 05/87773;WO 06/15866;WO 06/87325;WO 06/87343;WO 07/82098;WO 07/90624,WO 10/139271,WO 11/028657,WO 12/168188,WO 07/006670,WO 11/77514;WO 13/047749,WO 10/069882,WO 13/047441,WO 03/16303,WO 09/90181,WO 13/007767,WO 13/010862,WO 13/127704,WO 13/024009,WO 13/24010,WO 13/047441,WO 13/162072,WO 13/092224,WO 11/135833,CN 1907024,CN1456054,CN 103387541,CN 1309897,WO 12/84812,CN 1907024,WO 09094442,WO 14/60177,WO 13/116251,WO 08/013622,WO 15/65922,WO 94/01546,EP 2865265,WO 07/129454,WO 12/165511,WO 11/081174,WO 13/47441,WO 16/156241,WO 16/162265)。一些化合物通过其CAS登记号来标识,该登记号被连字符分成三个部分,第一部分由两个至七个数字组成,第二部分由两个数字组成,并且第三部分由单个数字组成。
根据本发明,生物杀有害生物剂(油如印楝油等除外)的固体材料(干物质)被认为是活性组分(例如在微生物杀有害生物剂的液体配制品的情况下在干燥或蒸发提取或悬浮介质之后得到)。对生物提取物如皂树提取物所使用的重量比和百分比基于相应提取物的干含量(固体材料)的总重量。
以活微生物细胞形式(包括休眠形式)包含至少一种微生物杀有害生物剂的组合物的总重量比可以使用相应微生物的CFU的量来用以下等式计算相应活性组分的总重量来确定:1×1010CFU等于一克相应活性组分的总重量。菌落形成单位是活微生物细胞的量度。此外,“CFU”在线虫生物杀有害生物剂如斯氏夜蛾线虫(Steinernema feltiae)的情况下还可以理解为(幼年)个体线虫的数目。
在二元混合物中,组分1)与组分2)的重量比通常取决于所使用的组分的特性,通常其在1:10,000至10,000:1、时常在1:100至100:1、经常在1:50至50:1、优选在1:20至20:1、更优选在1:10至10:1、甚至更优选在1:4至4:1、并且特别是在1:2至2:1的范围内。根据另一个实施例,组分1)与组分2)的重量比通常在1000:1至1:1、时常在100:1至1:1、经常在50:1至1:1、优选在20:1至1:1、更优选在10:1至1:1、甚至更优选在4:1至1:1、并且特别是在2:1至1:1的范围内。根据另一个实施例,组分1)与组分2)的重量比通常在20,000:1至1:10、时常在10,000:1至1:1、经常在5,000:1至5:1、优选在5,000:1至10:1、更优选在2,000:1至30:1、甚至更优选在2,000:1至100:1、并且特别是在1,000:1至100:1的范围内。根据另一个实施例,组分1)与组分2)的重量比通常在1:1至1:1000、时常在1:1至1:100、经常在1:1至1:50、优选在1:1至1:20、更优选在1:1至1:10、甚至更优选在1:1至1:4、并且特别是在1:1至1:2的范围内。根据另一个实施例,组分1)与组分2)的重量比通常在10:1至1:20,000、时常在1:1至1:10,000、经常在1:5至1:5,000、优选在1:10至1:5,000、更优选在1:30至1:2,000、甚至更优选在1:100至1:2,000、并且特别是在1:100至1:1,000的范围内。
在三元混合物,即包含组分1)和组分2)和化合物III(组分3)的组合物中,组分1)与组分2)的重量比取决于所使用的活性物质的特性,通常其在1:100至100:1、经常在1:50至50:1、优选在1:20至20:1、更优选在1:10至10:1、并且特别是在1:4至4:1的范围内,并且组分1)与组分3)的重量比通常在1:100至100:1、经常在1:50至50:1、优选在1:20至20:1、更优选在1:10至10:1、并且特别是在1:4至4:1的范围内。如果需要,任何另外活性组分以20:1至1:20的比率添加到组分1)中。这些比率也适合于通过种子处理施用的混合物。
当包含微生物杀有害生物剂的混合物用于作物保护时,施用率范围为1×106至5×1016(或更大)CFU/ha、优选1×108至1×1013CFU/ha,并且甚至更优选1×109至5×1015CFU/ha、并且特别是1×1012至5×1014CFU/ha。在线虫作为微生物杀有害生物剂(例如斯氏夜蛾线虫)的情况下,施用率范围经常为1×105至1×1012(或更大)、优选1×108至1×1011、更优选5×108至1×1010个个体(例如呈卵、幼虫或任何其他活体阶段形式,优选处于非繁殖性(infetive)幼虫阶段)/ha。
当包含微生物杀有害生物剂的混合物用于种子处理时,施用率范围通常为1×106至1×1012(或更大)CFU/种子、优选1×106至1×109CFU/种子。此外,关于种子处理的施用率范围通常为1×107至1×1014(或更大)CFU/100kg种子、优选1×109至1×1012CFU/100kg种子。
优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组A)的在Qo位点的配合物III抑制剂,更优选地选自化合物(A.1.1)、(A.1.4)、(A.1.8)、(A.1.9)、(A.1.10)、(A.1.12)、(A.1.13)、(A.1.14)、(A.1.17)、(A.1.21)、(A.1.25)、(A.1.34)和(A.1.35);特别地选自(A.1.1)、(A.1.4)、(A.1.8)、(A.1.9),(A.1.13)、(A.1.14)、(A.1.17)、(A.1.25)、(A.1.34)和(A.1.35)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组A)的在Qi位点的配合物III抑制剂,更优选地选自化合物(A.2.1)、(A.2.3)、(A.2.4)和(A.2.6);特别地选自(A.2.3)、(A.2.4)和(A.2.6)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组A)的配合物II抑制剂,更优选地选自化合物(A.3.2)、(A.3.3)、(A.3.4)、(A.3.7)、(A.3.9)、(A.3.11)、(A.3.12)、(A.3.15)、(A.3.16)、(A.3.17)、(A.3.18)、(A.3.19)、(A.3.20)、(A.3.21)、(A.3.22)、(A.3.23)、(A.3.24)、(A.3.28)、(A.3.31)、(A.3.32)、(A.3.33)、(A.3.34)、(A.3.35)、(A.3.36)、(A.3.37)、(A.3.38)和(A.3.39);特别地选自(A.3.2)、(A.3.3)、(A.3.4)、(A.3.7)、(A.3.9)、(A.3.12)、(A.3.15)、(A.3.17)、(A.3.19)、(A.3.22)、(A.3.23)、(A.3.24)、(A.3.31)、(A.3.32)、(A.3.33)、(A.3.34)、(A.3.35)、(A.3.36)、(A.3.37)、(A.3.38)和(A.3.39)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组A)的其他呼吸抑制剂,更优选地选自化合物(A.4.5)和(A.4.11);特别是(A.4.11)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组B)的C14脱甲基酶抑制剂,更优选地选自化合物(B.1.4)、(B.1.5)、(B.1.8)、(B.1.10)、(B.1.11)、(B.1.12)、(B.1.13)、(B.1.17)、(B.1.18)、(B.1.21)、(B.1.22)、(B.1.23)、(B.1.25)、(B.1.26)、(B.1.29)、(B.1.34)、(B.1.37)、(B.1.38)、(B.1.43)、(B.1.46)、(B.1.53)、(B.1.54)和(B.1.55);特别地选自(B.1.5)、(B.1.8)、(B.1.10)、(B.1.17)、(B.1.22)、(B.1.23)、(B.1.25)、(B.1.33)、(B.1.34)、(B.1.37)、(B.1.38)、(B.1.43)和(B.1.46)。还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组B)的δ14-还原酶抑制剂,更优选地选自化合物(B.2.4)、(B.2.5)、(B.2.6)和(B.2.8);特别是(B.2.4)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组C)的苯基酰胺和酰基氨基酸杀真菌剂,更优选地选自化合物(C.1.1)、(C.1.2)、(C.1.4)和(C.1.5);特别地选自(C.1.1)和(C.1.4)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组C)的其他核酸合成抑制剂,更优选地选自化合物(C.2.6)、(C.2.7)和(C.2.8)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组D),更优选地选自化合物(D.1.1)、(D.1.2)、(D.1.5)、(D.2.4)和(D.2.6);特别地选自(D.1.2)、(D.1.5)和(D.2.6)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组E),更优选地选自化合物(E.1.1)、(E.1.3)、(E.2.2)和(E.2.3);特别是(E.1.3)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组F),更优选地选自化合物(F.1.2)、(F.1.4)和(F.1.5)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组G),更优选地选自化合物(G.3.1)、(G.3.3)、(G.3.6)、(G.5.1)、(G.5.3)、(G.5.4)、(G.5.5)、G.5.6)、G.5.7)、(G.5.8)、(G.5.9)、(G.5.10)和(G.5.11);特别地选自(G.3.1)、(G.5.1)和(G.5.3)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组H),更优选地选自化合物(H.2.2)、(H.2.3)、(H.2.5)、(H.2.7)、(H.2.8)、(H.3.2)、(H.3.4)、(H.3.5)、(H.4.9)和(H.4.10);特别地选自(H.2.2)、(H.2.5)、(H.3.2)、(H.4.9)和(H.4.10)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组I),更优选地选自化合物(I.2.2)和(I.2.5)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组J),更优选地选自化合物(J.1.2)、(J.1.5)、(J.1.8)、(J.1.11)和(J.1.12);特别是(J.1.5)。
还优选的是包含作为组分2)的至少一种活性物质的混合物,该至少一种活性物质选自组K),更优选地选自化合物(K.1.41)、(K.1.42)、(K.1.44)、(K.1.47)、(K.1.57)、(K.1.58)和(K.1.59);特别地选自(K.1.41)、(K.1.44)、(K.1.47)、(K.1.57)、(K.1.58)和(K.1.59)。
来自组L1)和/或L2)的生物杀有害生物剂还可以具有杀昆虫、杀螨、杀螺、信息素、杀线虫、植物胁迫降低、植物生长调节剂、植物生长促进和/或产量提高活性。来自组L3)和/或L4)的生物杀有害生物剂还可以具有杀真菌、杀细菌、杀病毒、植物防御活化剂、植物胁迫降低、植物生长调节剂、植物生长促进和/或产量提高活性。来自组L5)的生物杀有害生物剂还可以具有杀真菌、杀细菌、杀病毒、植物防御活化剂、杀昆虫、杀螨、杀螺、信息素和/或杀线虫活性。
微生物杀有害生物剂,特别是来自组L1)、L3)和L5)的那些,不仅包括如本文定义的相应微生物的分离的纯培养物,而且包括其无细胞提取物、其在全肉汤培养物和含代谢物的培养基中的悬浮液、或从微生物的全肉汤培养物获得的纯化的代谢物。
这些生物杀有害生物剂中的许多以本文所提及的保藏号保藏(前缀如ATCC或DSM是指相应培养物保藏的首字母缩写,详情在这里参见例如:http://www.wfcc.info/ ccinfo/collection/by_acronym/),在文献中被提及,被注册和/或可商购:出芽短梗霉DSM14940和DSM 14941的混合物于1989年在德国康斯坦茨分离(例如芽生孢子,来自奥地利bio-ferm有限公司的),巴西固氮螺菌Sp245至少在1980年以前最初在巴西南部(帕苏风杜)的小麦区分离(BR 11005;例如来自巴西巴斯夫农业产品有限公司(BASF Agricultural Specialties Ltd.)的/>Gramíneas),巴西固氮螺菌菌株Ab-V5和Ab-V6(例如来自巴西夸特鲁巴拉斯Novozymes BioAg Produtos papraAgricultura Ltda.的AzoMax或来自巴西Simbiose-Agro的Simbiose-/>Plant Soil331,413-425,2010),解淀粉芽孢杆菌菌株AP-188(NRRL B-50615和B-50331;US 8,445,255);解淀粉芽孢杆菌植物亚种菌株,以前有时也被称为枯草芽孢杆菌,最近与甲基营养型芽孢杆菌(B.methylotrophicus)和贝莱斯芽孢杆菌一起被归类为贝莱斯芽孢杆菌(Int.J.Syst.Evol.Microbiol.[国际系统与进化微生物学杂志]66,1212–1217,2016);在日本菊川市从空气中分离的解淀粉芽孢杆菌植物亚种或贝莱斯芽孢杆菌D747(US20130236522 A1;FERM BP-8234;例如来自美国Certis LLC的Double NickelTM55WDG),在德国勃兰登堡从土壤中分离的解淀粉芽孢杆菌植物亚种或贝莱斯芽孢杆菌FZB24(也称为SB3615;DSM 96-2;J.Plant Dis.Prot.[植物病害与防治杂志]105,181-197,1998;例如来自美国诺维信生物公司(Novozyme Biologicals,Inc.)的/>),在德国勃兰登堡从土壤中分离的解淀粉芽孢杆菌植物亚种或贝莱斯芽孢杆菌FZB42(DSM 23117;J.PlantDis.Prot.[植物病害与防治杂志]105,181-197,1998;例如来自德国AbiTEP有限公司的42),至少在1988年以前在英国诺丁汉郡Sutton Bonington从蚕豆中分离的解淀粉芽孢杆菌植物亚种或贝莱斯芽孢杆菌MBI600(也被称为1430;NRRL B-50595;US2012/0149571A1;例如来自美国巴斯夫公司的/>),1995年在美国加利福尼亚从桃园分离的解淀粉芽孢杆菌植物亚种或贝莱斯芽孢杆菌QST-713(NRRL B-21661;例如来自美国拜耳作物科学公司(Bayer Crop Science LP)的/>MAX),1992年在美国南达科他州(South Dakoda)分离的解淀粉芽孢杆菌植物亚种或贝莱斯芽孢杆菌TJ1000(也被称为1BE;ATCC BAA-390;CA 2471555 A1;例如来自美国南达科他州沃特敦TJ Technologies的QuickRootsTM);坚强芽孢杆菌CNCM I-1582,由以色列中原地区的土壤分离的亲代菌株EIP-N1的变体(CNCM I-1556)(WO 2009/126473,US 6,406,690;例如来自美国拜耳作物科学有限合伙公司(Bayer CropScience LP)的/>),短小芽孢杆菌GHA 180在墨西哥由苹果树根际分离(IDAC 260707-01;例如来自加拿大魁北克Premier Horticulture的PRO-/>BX),另外称为BU-F22和BU-F33的短小芽孢杆菌INR-7至少在1993年以前由嗜维管束欧文氏菌(Erwinia tracheiphila)侵染的黄瓜分离(NRRL B-50185、NRRL B-50153;US 8,445,255),短小芽孢杆菌KFP9F至少在2008年以前在南非由禾草根际分离(NRRL B-50754;WO 2014/029697;例如来自南非巴斯夫农业产品有限公司(BASF AgriculturalSpecialities(Pty)Ltd.)的BAC-UP或FUSION-P),短小芽孢杆菌QST 2808于1998年由在密克罗尼西亚联邦波纳佩(Pohnpei,Federated States of Micronesia)采集的土壤分离(NRRL B-30087;例如来自美国拜耳作物科学公司的/>或/>Plus),简单芽孢杆菌ABU 288(NRRL B-50304;US 8,445,255),也称为UD 1022或UD10-22的枯草芽孢杆菌FB17在北美由红甜菜根分离(ATCC PTA-11857;System.Appl.Microbiol.[系统和应用微生物学]27,372-379,2004;US2010/0260735;WO 2011/109395);苏云金芽孢杆菌鲇泽亚种ABTS-1857于1987年由取自美国威斯康星州以法莲(Ephraim)草坪的土壤分离(也称为ABG-6346;ATCC SD-1372;例如来自德国明辛根BioFa AG的/>),苏云金芽孢杆菌库尔斯塔克亚种ABTS-351等同于在1967年由美国德克萨斯州布朗斯维尔的患病棉红铃虫黑幼虫分离的HD-1(ATCC SD-1275;例如来自美国伊利诺伊州Valent BioSciences的/>DF),苏云金芽孢杆菌库尔斯塔克亚种SB4由非洲茎螟(E.saccharina)幼虫尸体分离(NRRLB-50753;例如来自南非巴斯夫农业产品有限公司(BASF Agricultural Specialities(Pty)Ltd.)的Beta/>),苏云金芽孢杆菌拟步行甲亚种NB-176-1,菌株NB-125的突变体,于1982年由甲虫大黄粉虫的死蛹分离的野生型菌株(DSM 5480;EP 585 215B1;例如来自瑞士Valent BioSciences的/>),球孢白僵菌GHA(ATCC 74250;例如来自美国Laverlam Int.Corp.的/>22WGP),球孢白僵菌JW-1(ATCC 74040;例如来自意大利CBC(Europe)S.r.l.的/>),球孢白僵菌PPRI 5339由龟甲虫Conchylocteniapunctata的幼虫分离(NRRL 50757;例如来自南非巴斯夫农业产品有限公司(BASFAgricultural Specialities(Pty)Ltd.)的/>),埃氏慢生根瘤菌菌株SEMIA5019(也称为29W)在巴西里约热内卢分离并且SEMIA 587于1967年在南里奥格兰德州(State of Rio Grande do Sul)分离,来自先前用北美分离物接种的区域,并且自1968年开始用于商用接种体(Appl.Environ.Microbiol.[应用与环境微生物学]73(8),2635,2007;例如来自巴西巴斯夫农业产品有限公司(BASF Agricultural Specialties Ltd.)的GELFIX 5),大豆慢生根瘤菌532c由美国威斯康星州田间分离(Nitragin 61A152;Can.J.Plant.Sci.[加拿大植物科学杂志]70,661-666,1990;例如来自加拿大巴斯夫农业产品有限公司(BASF Agricultural Specialties Ltd.)的Super),菌株USDA 138的大豆慢生根瘤菌E-109变体(INTA E109,SEMIA 5085;Eur.J.Soil Biol.[欧洲土壤生物学杂志]45,28-35,2009;Biol.Fertil.Soils[土壤的生物学和肥力]47,81–89,2011);由Appl.Environ.Microbiol.[应用与环境微生物学]73(8),2635,2007已知保藏在SEMIA的大豆慢生根瘤菌菌株:SEMIA5079在巴西塞拉多(Cerrados)区由Embrapa-Cerrados由土壤分离,自1992开始用于商用接种体(CPAC 15;例如来自巴西巴斯夫农业产品有限公司(BASF Agricultural SpecialtiesLtd.)的GELFIX 5或ADHERE 60),大豆慢生根瘤菌SEMIA 5080在巴西由Embrapa-Cerrados在实验室条件下得到并且自1992年开始用于商用接种体,为最初在美国分离的SEMIA 586的天然变体(CB1809)(CPAC 7;例如来自巴西巴斯夫农业产品有限公司(BASFAgricultural Specialties Ltd.)的GELFIX 5或ADHERE 60);伯克霍尔德氏菌物种A396于2008年在日本日光由土壤分离(NRRL B-50319;WO 2013/032693;美国马罗尼生物创新公司(Marrone Bio Innovations,Inc.)),盾壳霉CON/M/91-08由油籽油菜分离(WO 1996/021358;DSM 9660;例如来自德国拜耳作物科学股份公司(Bayer CropScience AG)的WG、/>WG),超敏蛋白(α-β)蛋白(Science[科学]257,85-88,1992;例如来自英国植物保健公司(Plant Health Care plc)的MessengerTM或HARP-N-Tek),棉铃虫核型多角体病毒(HearNPV)(J.Invertebrate Pathol[无脊椎动物病理学杂志].107,112-126,2011;例如来自瑞士Adermatt Biocontrol的/>来自巴西科伯特(Koppert)的/>来自澳大利亚昆士兰AgBiTech Pty Ltd.的/>Max),玉米夜蛾单衣壳核型多角体病毒(HzSNPV)(例如来自美国Certis LLC的/>),玉米夜蛾核型多角体病毒ABA-NPV-U(例如来自澳大利亚昆士兰AgBiTech Pty Ltd.的),嗜菌异小杆线虫(例如来自英国巴斯夫农业产品有限公司(BASFAgricultural Specialities Limited)的/>G),玫烟色棒束孢Apopka-97在美国佛罗里达州阿波普卡由紫背天葵上的粉蚧分离(ATCC 20874;Biocontrol ScienceTechnol[生物防治科学与技术].22(7),747-761,2012;例如来自美国Certis LLC的PFR-97TM或/>),也称为275或V275的金龟子绿僵菌小孢变种F52在奥地利由苹果蠹蛾分离(DSM 3884,ATCC 90448;例如/>Novozymes Biologicals BioAg Group,加拿大),核果梅奇酵母277在以色列中部地区由葡萄分离(US 6,994,849;NRRL Y-30752;例如以前的来自以色列Agrogreen的/>),淡紫色拟青霉251在菲律宾由感染的线虫卵分离(AGAL 89/030550;WO 1991/02051;Crop Protection[作物保护]27,352-361,2008;例如来自德国拜耳作物科学股份公司的/>和来自美国Certis的/>),蜂房芽孢杆菌NAS6G6至少在2008年以前在南非由禾草根际分离(WO 2014/029697;NRRL B-50755;例如来自南非巴斯夫农业产品有限公司(BASF Agricultural Specialities(Pty)Ltd.)的BAC-UP),从各欧洲地区包括德国的土壤样品中分离的类芽孢杆菌菌株:附生类芽孢杆菌Lu17015(WO 2016/020371;DSM 26971),多粘类芽孢杆菌植物亚种Lu16774(WO2016/020371;DSM 26969),多粘类芽孢杆菌植物亚种菌株Lu17007(WO 2016/020371;DSM26970);拟斯扎瓦巴氏杆菌Pn1于2000年代中期在美国伊利诺斯州由大豆田分离(ATCC SD-5833;Federal Register[联邦公报]76(22),5808,2011年2月2日;例如来自美国先正达作物保护有限公司(Syngenta Crop Protection,LLC)的ClarivaTMPN),拜赖青霉(也称为P.bilaii)菌株ATCC 18309(=ATCC 74319)、ATCC 20851和/或ATCC 22348(=ATCC 74318)最初在加拿大亚伯达由土壤分离(Fertilizer Res[肥料研究].39,97-103,1994;Can.J.Plant Sci.[加拿大植物科学杂志]78(1),91-102,1998;US 5,026,417,WO 1995/010006;例如来自加拿大Novozymes Biologicals BioAg Group的Jump/> ),大虎杖提取物(EP 0307510 B1;例如来自美国加利福尼亚州戴维斯马罗尼生物创新公司(Marrone BioInnovations,Davis,CA,USA)的/>SC或来自德国BioFaAG的/>),斯氏小卷蛾线虫(例如来自英国巴斯夫农业产品有限公司(BASFAgricultural Specialities Limited)的/>),斯氏夜蛾线虫(例如来自美国BioWorks,Inc.的/>来自英国巴斯夫农业产品有限公司(BASFAgricultural Specialities Limited)的/>),细黄链霉菌NRRL B-50550(WO2014/124369;德国拜耳作物科学公司),类棘孢木霉JM41R在南非分离(NRRL 50759;也称为顶孢木霉;例如来自南非巴斯夫农业产品有限公司(BASF Agricultural Specialities(Pty)Ltd.)的/>),哈茨木霉T-22也称为KRL-AG2(ATCC 20847;BioControl[生物防治]57,687-696,2012;例如来自美国BioWorks Inc.的/>或来自美国俄亥俄州范沃特Advanced Biological Marketing Inc.的SabrExTM)。根据混合物的另一个实施例,至少一种杀有害生物剂II选自组L1)至L5):
L1)具有杀真菌、杀细菌、杀病毒和/或植物防御活化剂活性的微生物杀有害生物剂:出芽短梗霉DSM 14940和DSM 14941(L1.1)、解淀粉芽孢杆菌AP-188(L.1.2)、解淀粉芽孢杆菌植物亚种D747(L.1.3)、解淀粉芽孢杆菌植物亚种FZB24(L.1.4)、解淀粉芽孢杆菌植物亚种FZB42(L.1.5)、解淀粉芽孢杆菌植物亚种MBI600(L.1.6)、解淀粉芽孢杆菌植物亚种QST-713(L.1.7)、解淀粉芽孢杆菌植物亚种TJ1000(L.1.8)、短小芽孢杆菌GB34(L.1.9)、短小芽孢杆菌GHA 180(L.1.10)、短小芽孢杆菌INR-7(L.1.11)、短小芽孢杆菌KFP9F(L.1.12)、短小芽孢杆菌QST 2808(L.1.13)、简单芽孢杆菌ABU 288(L.1.14)、枯草芽孢杆菌FB17(L.1.15)、盾壳霉CON/M/91-08(L.1.16)、核果梅奇酵母NRRL Y-30752(L.1.17)、蜂房芽孢杆菌NAS6G6(L.1.18)、附生类芽孢杆菌Lu17015(L.1.25)、多粘类芽孢杆菌植物亚种Lu16774(L.1.26)、多粘类芽孢杆菌植物亚种菌株Lu17007(L.1.27)、拜赖青霉ATCC 22348(L.1.19)、拜赖青霉ATCC 20851(L.1.20)、拜赖青霉ATCC 18309(L.1.21)、细黄链霉菌NRRLB-50550(L.1.22)、类棘孢木霉JM41R(L.1.23)、哈茨木霉T-22(L.1.24);
L2)具有杀真菌、杀细菌、杀病毒和/或植物防御活化剂活性的生物化学杀有害生物剂:超敏蛋白(L.2.1)、大虎杖提取物(L.2.2);
L3)具有杀昆虫、杀螨、杀螺和/或杀线虫活性的微生物杀有害生物剂:坚强芽孢杆菌I-1582(L.3.1);苏云金芽孢杆菌鲇泽亚种ABTS-1857(L.3.2)、苏云金芽孢杆菌库尔斯塔克亚种ABTS-351(L.3.3)、苏云金芽孢杆菌库尔斯塔克亚种SB4(L.3.4)、苏云金芽孢杆菌拟步行甲亚种NB-176-1(L.3.5)、球孢白僵菌GHA(L.3.6)、球孢白僵菌JW-1(L.3.7)、球孢白僵菌PPRI 5339(L.3.8)、伯克霍尔德氏菌物种A396(L.3.9)、棉铃虫核型多角体病毒(HearNPV)(L.3.10)、玉米夜蛾核型多角体病毒(HzNPV)ABA-NPV-U(L.3.11)、玉米夜蛾单衣壳核型多角体病毒(HzSNPV)(L.3.12)、嗜菌异小杆线虫(Heterohabditis bacteriophora)(L.3.13)、玫烟色棒束孢Apopka-97(L.3.14)、金龟子绿僵菌小孢变种F52(L.3.15)、淡紫色拟青霉251(L.3.16)、拟斯扎瓦巴氏杆菌Pn1(L.3.17)、斯氏小卷蛾线虫(L.3.18)、斯氏夜蛾线虫(L.3.19);
L4)具有杀昆虫、杀螨、杀螺、信息素和/或杀线虫活性的生物化学杀有害生物剂:顺式-茉莉酮(L.4.1)、茉莉酮酸甲酯(L.4.2)、皂树提取物(L.4.3);
L5)具有植物胁迫降低、植物生长调节剂、植物生长促进和/或产量提高活性的微生物杀有害生物剂:巴西固氮螺菌Ab-V5和Ab-V6(L.5.1)、巴西固氮螺菌Sp245(L.5.2)、埃氏慢生根瘤菌SEMIA 587(L.5.3)、埃氏慢生根瘤菌SEMIA 5019(L.5.4)、大豆慢生根瘤菌(B.japonicum)532c(L.5.5)、大豆慢生根瘤菌E-109(L.5.6)、大豆慢生根瘤菌SEMIA 5079(L.5.7)、大豆慢生根瘤菌SEMIA 5080(L.5.8)。
此外,本发明涉及农用化学组合物,其包含以下项的混合物:至少一种化合物I(组分1)和至少一种选自组L)的生物杀有害生物剂(组分2)、特别是至少一种选自如上所述的组L1)和L2)的生物杀有害生物剂、以及(如果需要)至少一种合适的助剂。此外,本发明涉及农用化学组合物,其包含以下项的混合物:至少一种化合物I(组分1)和至少一种选自组L)的生物杀有害生物剂(组分2)、特别是至少一种选自如上所述的组L3)和L4)的生物杀有害生物剂、以及(如果需要)至少一种合适的助剂。
还优选的是包含作为杀有害生物剂II(组分2)的生物杀有害生物剂的混合物,该生物杀有害生物剂选自组L1)、L3)和L5),优选地选自上文表示为(L.1.2)、(L.1.3)、(L.1.4)、(L.1.5)、(L.1.6)、(L.1.7)、(L.1.8)、(L.1.10)、(L.1.11)、(L.1.12)、(L.1.13)、(L.1.14)、(L.1.15)、(L.1.17)、(L.1.18)、(L.1.19)、(L.1.20)、L.1.21)、(L.1.25)、(L.1.26)、(L.1.27)、(L.3.1);(L.3.9)、(L.3.16)、(L.3.17)、(L.5.1)、(L.5.2)、(L.5.3)、(L.5.4)、(L.5.5)、(L.5.6)、L.5.7)、(L.5.8);(L.4.2)和(L.4.1)的菌株;甚至更优选地选自(L.1.2)、(L.1.6)、(L.1.7)、(L.1.8)、(L.1.11)、(L.1.12)、(L.1.13)、(L.1.14)、(L.1.15)、(L.1.18)、(L.1.19)、(L.1.20)、(L.1.21)、(L.3.1);(L.3.9)、(L.3.16)、(L.3.17)、(L.5.1)、(L.5.2)、(L.5.5)、(L.5.6);(L.4.2)和(L.4.1)。这些混合物特别适合用于处理繁殖材料,即种子处理目的,并且同样适用于土壤处理。这些种子处理混合物特别适合用于作物如谷物、玉米和豆科植物如大豆。
还优选的是包含作为杀有害生物剂II(组分2)的生物杀有害生物剂的混合物,该生物杀有害生物剂选自组L1)、L3)和L5),优选地选自上文表示为(L1.1)、(L.1.2)、(L.1.3)、(L.1.6)、(L.1.7)、(L.1.9)、(L.1.11)、(L.1.12)、(L.1.13)、(L.1.14)、(L.1.15)、(L.1.17)、(L.1.18)、(L.1.22)、(L.1.23)、L.1.24)、(L.1.25)、(L.1.26)、(L.1.27)、(L.2.2);(L.3.2)、(L.3.3)、(L.3.4)、(L.3.5)、(L.3.6)、(L.3.7)、(L.3.8)、(L.3.10)、(L.3.11)、(L.3.12)、(L.3.13)、(L.3.14)、(L.3.15)、(L.3.18)、(L.3.19);(L.4.2)的菌株,甚至更优选地选自(L.1.2)、(L.1.7)、(L.1.11)、(L.1.13)、(L.1.14)、(L.1.15)、(L.1.18)、(L.1.23)、(L.3.3)、(L.3.4)、(L.3.6)、(L.3.7)、(L.3.8)、(L.3.10)、(L.3.11)、(L.3.12)、(L.3.15)和(L.4.2)。这些混合物特别适合于栽培植物,优选蔬菜、水果、藤本植物、谷物、玉米和豆科作物如大豆的叶处理。
包含活性成分的混合物的组合物可以通过常用手段制备,例如通过对于化合物I的组合物所给出的手段。
当活的微生物如来自组L1)、L3)和L5)的杀有害生物剂II形成组合物的一部分时,此类组合物可以通过常用手段制备(例如H.D.Burges:Formulation of MicrobialBiopesticides[微生物生物杀有害生物剂配制品],施普林格(Springer),1998;WO 2008/002371,US 6,955,912,US 5,422,107)。
I.合成实例
实例1-(8-氟-3-喹啉基)-(2-硝基苯基)甲醇
在0℃下在N2下,向8-氟-3-碘-喹啉(15g,0.055mol)在THF(200mL)中的混合物中逐滴添加i-PrMgCl(2M)(36mL,0.0715mol),并且将混合物在0℃下搅拌20min。然后,在0℃下逐滴添加2-硝基苯甲醛(10g,0.066mol)在THF(10mL)中的溶液,并且将混合物在20℃下搅拌16h。将反应混合物用NH4Cl水溶液(200mL)淬灭,并且用EtOAc(100mL)萃取。将有机层经无水硫酸镁干燥、真空浓缩,并且将残余物通过硅胶柱(PE:EtOAc=47%-100%)纯化,以得到呈绿色固体的标题化合物。
1H NMR:(400MHz,氯仿-d):δ=3.56-3.92(m,1H)6.70(s,1H)7.37-7.43(m,1H)7.46-7.55(m,2H)7.59(d,J=8.16Hz,1H)7.70(td,J=7.62,1.19Hz,1H)7.83(dd,J=7.91,1.25Hz,1H)8.03(dd,J=8.16,1.25Hz,1H)8.19(s,1H)8.90(d,J=2.01Hz,1H)
实例2-(8-氟-3-喹啉基)-(2-硝基苯基)甲醇
将(8-氟-3-喹啉基)-(2-硝基苯基)甲醇(1.6g,5.4mmol)在EtOH(200mL)中的溶液添加到雷尼Ni(500mg)在EtOH(10mL)中的混合物中,并且将混合物在20℃下在H2(15PSi)下搅拌2h。将反应混合物过滤,将滤液在减压下浓缩,并且将粗产物用MTBE(30mL)洗涤,以得到呈黄色固体的标题化合物。直接使用标题化合物而无需进一步纯化。
1H NMR(400MHz,CDCl3):μ[ppm]:2.78-2.92(m,1H)4.01-4.17(m,2H)6.14(s,1H)6.74(d,J=8.03Hz,1H)6.80(t,J=7.47Hz,1H)7.09(br d,J=7.78Hz,1H)7.20(br t,J=7.78Hz,1H)7.39-7.44(m,1H)7.51(td,J=7.91,4.89Hz,1H)7.62(d,J=7.91Hz,1H)8.21(s,1H)8.99(d,J=1.63Hz,1H)。
实例3-(2-氨基苯基)-(8-氟-3-喹啉基)甲酮
向(8-氟-3-喹啉基)-(2-硝基苯基)甲醇(1g,3.73mmol)在DMF(15mL)中的溶液中添加CuCl(37mg,0.373mmol)和K2CO3(1.03g,7.46mmol),然后将混合物在60℃下在O2气氛下搅拌16h。将反应溶液用盐水(100mL)淬灭,并且用EtOAc(80mL)萃取。将有机物用盐水(100mL×2)洗涤、经无水硫酸镁干燥、并真空浓缩。通过硅胶液相色谱法(PE:EtOAc=约30%)纯化提供呈黄色固体的标题化合物。
1H NMR(400MHz,CDCl3):μ[ppm]:6.03-6.34(m,2H)6.57(ddd,J=8.06,7.06,1.07Hz,1H)6.72(dd,J=8.41,0.75Hz,1H)7.29(ddd,J=8.41,7.03,1.51Hz,1H)7.37(dd,J=8.09,1.44Hz,1H)7.42-7.55(m,2H)7.65(d,J=8.03Hz,1H)8.37(t,J=1.76Hz,1H)9.13(d,J=2.13Hz,1H)
实例4-4-(8-氟-3-喹啉基)-2,2-二甲基-1H-喹唑啉
在N2下,向(2-氨基苯基)-(8-氟-3-喹啉基)甲酮(700mg,2.63mmol)在丙酮(10mL)中的混合物中添加NH4OAc(1g,13.2mmol)和分子筛(1.5g),并且将混合物在60℃下搅拌2h。将反应混合物过滤,将滤液用NaHCO3水溶液(50mL)和盐水(50mL)洗涤。然后,将有机物经无水硫酸镁干燥并真空浓缩。将粗产物通过硅胶液相色谱法(PE:EtOAc=3:1)纯化以得到呈黄色固体的标题化合物。
1H NMR(400MHz,CDCl3):μ[ppm]:9.02(d,J=1.88Hz,1H),8.33(br s,1H),7.62(d,J=8.00Hz,1H),7.32-7.51(m,2H),7.19-7.23(m,1H),6.98(d,J=7.63Hz,1H),6.55-6.66(m,2H),3.96-4.14(br,1H),1.55(s,6H)
实例5-4-(8-氟-3-喹啉基)-1,2,2-三甲基-喹唑啉
在0℃下在N2下,向4-(8-氟-3-喹啉基)-2,2-二甲基-1H-喹唑啉(250mg,0.82mmol)在DMF(10mL)中的混合物中添加NaH(约60%)(66mg,1.64mmol),并且将混合物在0℃下搅拌0.5h。然后,添加碘甲烷(175mg,1.23mmol),并且将混合物在20℃下搅拌16h。将反应混合物用盐水(50mL)稀释、用EtOAc(50mL)萃取,将合并的有机层用盐水(80mL×2)洗涤、经无水硫酸镁干燥并真空浓缩。将粗产物通过硅胶液相色谱法(PE:EtOAc=约30%)纯化以得到呈黄色油状物的标题化合物。
1H NMR(400MHz,CDCl3):μ[ppm]:9.02(d,J=1.88Hz,1H),8.31(br s,1H),7.61(d,J=8.16Hz,1H),7.28-7.48(m,3H),6.98(dd,J=7.65,1.25Hz,1H),6.70(d,J=8.28Hz,1H),6.60(t,J=7.47Hz,1H),2.88(s,3H),1.53(s,6H)
实例6-1-[8-氟-4-(8-氟-3-喹啉基)-2,2-二甲基-喹唑啉-1-基]乙酮
在25℃下在N2下,将8-氟-4-(8-氟-3-喹啉基)-2,2-二甲基-1H-喹唑啉(200mg,0.31mmol)添加到Ac2O(4mL)和吡啶(0.2mL)的溶液中,并且将混合物在145℃下搅拌16h。将反应混合物在减压下浓缩,并且将粗产物通过硅胶高效液相色谱法纯化(HPLC-柱KinetexXB C181.7μ(50×2.1mm);洗脱液:乙腈/水(在60℃下在1.5min内梯度为5:95至100:0,在1.5min内流量梯度为0.8至1.0ml/min)),以得到呈黄色固体的标题化合物。
1H NMR(400MHz,CDCl3):μ[ppm]:9.24(d,J=2.1Hz,1H),8.51(t,J=1.7Hz,1H),7.72(d,J=8.2Hz,1H),7.61-7.48(m,2H),7.35-7.29(m,1H),7.22(dt,J=4.9,7.9Hz,1H),7.13(dd,J=1.0,7.6Hz,1H),2.22(d,J=4.8Hz,3H),1.79(s,6H)
表I中列出的化合物以类似的方式制备。
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
温室
将化合物溶解在溶剂-乳化剂之比(体积)为99:1的丙酮和/或二甲亚砜和基于乙氧基化烷基酚的润湿剂/乳化剂Wettol的混合物中以得到5ml的总体积。随后,添加水至100ml的总体积。
然后将此储备溶液用所述溶剂-乳化剂-水混合物稀释至下表中给出的最终浓度。
实例1-青椒叶上的灰葡萄孢菌的预防性杀真菌控制
青椒幼苗在盆中生长至4至5叶阶段。用前述喷雾溶液喷雾这些植物至滴流,该喷雾溶液含有下表中所提及的浓度的活性成分或混合物。第二天,用含灰葡萄孢菌孢子悬浮液的生物麦芽水溶液或DOB溶液接种植物。然后立即将植物转移至潮湿室。在22℃至24℃和饱和相对湿度下5天后,目视评估叶子上真菌侵袭的程度,作为%病叶面积。
在此测试中,经250ppm分别来自Ex-2、Ex-3、Ex-4、Ex-6、Ex-7、Ex-8、Ex-9、Ex-10、Ex-11、Ex-12、Ex-13、Ex-14、Ex-15、Ex-18、Ex-20、Ex-22、Ex-23、Ex-25、Ex-26、Ex-28、Ex-31、Ex-39、Ex-42、Ex-43、Ex-45、Ex-46、Ex-47、Ex-54、Ex-55、Ex-60、Ex-61、Ex-65和Ex-76的实例的活性物质处理的样品显示出最高达至多13%的病原体增长率,而未处理的植物80%被感染。
实例2-由核盘菌(Slerotinia sclerotiorum)SCLESC P1 OSR引起的油菜上白霉的预防性杀真菌控制
油菜在盆中生长至13至14叶阶段。用前述喷雾溶液喷雾这些植物至滴流(run-off),该喷雾溶液含有下表中所提及的浓度的活性成分或其混合物。
植物可以风干。第二天,用25μl的2.5%甲基纤维素将施药后的油菜花瓣固定在叶1上,并将2.25μl的核盘菌孢子悬浮液用移液管移至每个固定好的油菜花瓣上。在20℃和60%的相对湿度下14天后,目视评估叶子上真菌侵袭的程度,作为%病叶面积。
在此测试中,经100g/ha分别来自Ex-2、Ex-3、Ex-4、Ex-6、Ex-7、Ex-8、Ex-9、Ex-10、Ex-11、Ex-12、Ex-13、Ex-15、Ex-22、Ex-25、Ex-26的实例的活性物质处理的样品显示出最高达至多12%的病原体增长率,而未处理的植物80%被感染。
实例3-由核盘菌(SCLESC P1)引起的大豆上白霉的预防性杀真菌控制
将大豆幼苗种植在盆中。用前述喷雾溶液喷雾这些植物至滴流,该喷雾溶液含有下表中所提及的浓度的活性成分或混合物。第二天,用含核盘菌菌丝的生物麦芽悬浮液接种经处理的植物。然后,将试验植物在23℃且相对湿度在80%与85%之间的温室中培育6天。目视评估叶子上真菌侵袭的程度,作为%病叶面积。
在此测试中,经250ppm分别来自Ex-8、Ex-11、Ex-13、Ex-14、Ex-22、Ex-25、Ex-26、Ex-28、Ex-31、Ex-39、Ex-42、Ex-43、Ex-45、Ex-47、Ex-55、Ex-60、Ex-65、Ex-76和Ex-77的实例的活性物质处理的样品显示出最高达至多15%的病原体增长率,而未处理的植物80%被感染。
微测试
将活性化合物单独配制为在二甲亚砜中的浓度为10000ppm的储备溶液。
按比例混合储备溶液,将其用移液管移到微量滴定板(MTP)上并用水稀释至规定浓度。
实例1-微量滴定板测试中的抗灰霉灰葡萄孢菌活性
然后添加灰葡萄孢菌(Botrci cinerea)在生物麦芽水溶液或酵母-细菌蛋白胨-乙酸钠溶液中的孢子悬浮液。
在此测试中,经31ppm分别来自实例Ex-1、Ex-2、Ex-3、Ex-4、Ex-5、Ex-6、Ex-7、Ex-8、Ex-9、Ex-10、Ex-11、Ex-12、Ex-13、Ex-14、Ex-15、Ex-16、Ex-17、Ex-18、Ex-19、Ex-20、Ex-21、Ex-22、Ex-23,Ex-24、Ex-25、Ex-26、Ex-27、Ex-28、Ex-29、Ex-30、Ex-31、Ex-32、Ex-33、Ex-34、Ex-35、Ex-36、Ex-37、Ex-38、Ex-39、Ex-40、Ex-41、Ex-42、Ex-43、Ex-44、Ex-45、Ex-46、Ex-47、Ex-48、Ex-49、Ex-49″、Ex-50、Ex-51、Ex-52、Ex-53、Ex-54、Ex-55、Ex-56、Ex-57、Ex-58、Ex-59、Ex-60、Ex-61、Ex-62、Ex-63、Ex-64、Ex-65、Ex-66、Ex-67、Ex-68的活性物质处理的样品显示出最高达14%的病原体增长率。
实例2-微量滴定板测试中的抗黄色镰孢菌活性
然后添加黄色镰孢菌在生物麦芽水溶液或酵母-细菌蛋白胨-甘油或DOB溶液中的孢子悬浮液。
在此测试中,经8ppm分别来自实例Ex-6、Ex-7、Ex-8、Ex-10和Ex-11的活性物质处理的样品显示出最高达1%的病原体增长率。
在此测试中,经31ppm分别来自实例Ex-2、Ex-3、Ex-4、Ex-6、Ex-7、Ex-8、Ex-10、Ex-11、Ex-12、Ex-13、Ex-14、Ex-17、Ex-18、Ex-19、Ex-20、Ex-22、Ex-23、Ex-25、Ex-26、Ex-27、Ex-28、Ex-29、Ex-30、Ex-31、Ex-33、Ex-34、Ex-35、Ex-36、Ex-37、Ex-38、Ex-39、Ex-40、Ex-41、Ex-42、Ex-43、Ex-44、Ex-45、Ex-46、Ex-47、Ex-49、Ex-50、Ex-51、Ex-53、Ex-54、Ex-55、Ex-57、Ex-60、Ex-61、Ex-62、Ex-64、Ex-65、Ex-67、Ex-68的活性物质处理的样品显示出最高达20%的病原体增长率。
实例3-抗小麦壳针孢引起的小麦上叶疱病的活性
然后添加小麦壳针孢在生物麦芽水溶液或酵母-细菌蛋白胨-甘油或DOB溶液中的孢子悬浮液。
在此测试中,经8ppm分别来自实例Ex-6、Ex-7、Ex-8、Ex-9、Ex-10和Ex-11的活性物质处理的样品显示出19%的病原体增长率。
在此测试中,经31ppm分别来自实例Ex-2、Ex-3、Ex-4、Ex-6、Ex-7、Ex-9、Ex-10、Ex-11、Ex-12、Ex-13、Ex-14、Ex-17、Ex-18、Ex-19、Ex-20、Ex-23、Ex-25、Ex-26、Ex-27、Ex-28、Ex-31、Ex-35、Ex-36、Ex-39、Ex-41、Ex-42、Ex-44、Ex-45、Ex-49、Ex-50、Ex-51、Ex-55、Ex-57、Ex-59、Ex-60、Ex-61的活性物质处理的样品显示出最高达18%的病原体增长率。
将测量的参数与无活性化合物的对照变体的增长率(100%)和无真菌的空白值进行比较,以确定相应活性化合物中病原体的相对增长率(以%计)。
实例4-微量滴定板测试中的抗灰霉稻瘟霉活性
然后添加稻瘟霉在生物麦芽水溶液或酵母-细菌蛋白胨-乙酸钠溶液中的孢子悬浮液。
在此测试中,经31ppm分别来自实例Ex-1、Ex-2、Ex-3、Ex-4、Ex-6、Ex-7、Ex-8、Ex-9、Ex-10、Ex-11、Ex-13、Ex-14、Ex-15、Ex-16、Ex-17、Ex-18、Ex-19、Ex-20、Ex-22、Ex-23、Ex-29的活性物质处理的样品显示出最高达20%的病原体增长率。
实例5-微量滴定板测试中的抗灰霉甜菜生尾孢(Cercospora beticula)活性
然后添加甜菜生尾孢在生物麦芽水溶液或酵母-细菌蛋白胨-乙酸钠溶液中的孢子悬浮液。
在此测试中,经31ppm分别来自实例Ex-4、Ex-6、Ex-10、Ex-12、Ex-13、Ex-14、Ex-17、Ex-18、Ex-19、Ex-25、Ex-26的活性物质处理的样品显示出最高达20%的病原体增长率。
实例6-微量滴定板测试中的抗灰霉大豆尾孢活性
然后添加大豆尾孢在生物麦芽水溶液或酵母-细菌蛋白胨-乙酸钠溶液中的孢子悬浮液。
在此测试中,经31ppm分别来自实例Ex-2、Ex-3、Ex-4、Ex-6、Ex-9、Ex-10、Ex-11、Ex-12、Ex-13、Ex-14、Ex-17、Ex-18、Ex-19、Ex-26的活性物质处理的样品显示出最高达12%的病原体增长率。
实例7-微量滴定板测试中的抗灰霉玉蜀黍尾孢菌活性
然后添加玉蜀黍尾孢菌在生物麦芽水溶液或酵母-细菌蛋白胨-乙酸钠溶液中的孢子悬浮液。
在此测试中,经31ppm分别来自实例Ex-4、Ex-8、Ex-11、Ex-13、Ex-14、Ex-18、Ex-22、Ex-25、Ex-26的活性物质处理的样品显示出最高达17%的病原体增长率。
实例8-微量滴定板测试中的抗灰霉山扁豆生棒孢菌(Corynespora cassiicola)G413A突变体活性
然后添加山扁豆生棒孢菌在生物麦芽水溶液或酵母-细菌蛋白胨-乙酸钠溶液中的孢子悬浮液。
在此测试中,经31ppm分别来自实例Ex-1、Ex-2、Ex-4、Ex-5、Ex-6、Ex-7、Ex-8、Ex-10、Ex-11、Ex-12、Ex-13、Ex-14、Ex-15、Ex-16、Ex-17、Ex-18、Ex-19、Ex-20、Ex-22、Ex-23、Ex-25、Ex-26、Ex-27、Ex-28、Ex-29、Ex-30、Ex-31、Ex-32、Ex-33、Ex-34、Ex-35、Ex-36、Ex-37、Ex-38、Ex-39、Ex-40、Ex-41、Ex-42、Ex-43、Ex-44、Ex-45、Ex-46、Ex-47、Ex-48、Ex-49、Ex-49″、Ex-50、Ex-51、Ex-52、Ex-53、Ex-54、Ex-55、Ex-56、Ex-57、Ex-58、Ex-59、Ex-60、Ex-61、Ex-62、Ex-63、Ex-64、Ex-65、Ex-66、Ex-67、Ex-68的活性物质处理的样品显示出最高达17%的病原体增长率。
Claims (11)
1.作为杀真菌剂的具有式I的化合物及其N-氧化物和农业上可接受的盐
其中
R1是H、卤素、CN、C1-C4-烷基、C1-C4-卤代烷基;
R4是H、卤素、CN、C1-C4-烷基、C1-C4-卤代烷基;
R5在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、苯基、苄基,
其中R5的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R5a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
R6在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、苯基、苄基,
其中R6的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R6a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
或者
R5和R6与它们所键合的C原子一起形成C3-C6-环烷基、或含有1、2或3个来自由O和S组成的组的杂原子的3元至6元饱和杂环;
R7在每种情况下独立地选自氢、CN、CH2CN、CH(CH3)CN、CH(=O)、C(=O)C1-C6-烷基、C(=O)C2-C6-烯基、C(=O)C2-C6-炔基、C(=O)C3-C6-环烷基、C(=O)NH-C1-C4-烷基、C(=O)N-(C1-C4-烷基)2、C1-C6-烷基、C1-C4-卤代烷基、C3-C6-环烷基、C3-C6-卤代环烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、O-C1-C6-烷基、-S(=O)2-R7a、五元或六元杂芳基和芳基或苄基;其中该杂芳基含有一个、两个或三个选自N、O和S的杂原子;其中该芳基和苄基是未取代的或带有一个、两个、三个、四个或五个选自由以下组成的组的取代基:CN、卤素、OH、C1-C4-烷基、C1-C4-卤代烷基、C1-C4-烷氧基、和C1-C4-卤代烷氧基;其中
R7a选自C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基、苯基、苄基,其中苯基和苄基可以是未取代的或被卤素、C1-C6-烷基、C1-C6-卤代烷基、C2-C6-烯基、C2-C6-卤代烯基、C2-C6-炔基、C2-C6-卤代炔基取代;
X在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基、O-C1-C6-卤代烷基;
n是0、1、2或3;
Y在每种情况下独立地选自卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基;
m是1、2或3。
2.如权利要求1所述的化合物,其中,R5是C1-C6-烷基。
3.如权利要求1至2中任一项所述的化合物,其中,R6选自C1-C6-烷基、苯基、苄基,其中R6的苯基和苄基部分是未取代的或被一至三个彼此独立地选自以下的基团R6a取代:
卤素、CN、C1-C6-烷基、C1-C6-卤代烷基、O-C1-C6-烷基。
4.如权利要求1至3中任一项所述的化合物,其中,R5和R6与它们所键合的C原子一起形成C3-C6-环烷基。
5.如权利要求1至4中任一项所述的化合物,其中,X选自卤素、C1-C6-烷基、O-C1-C6-烷基、O-C1-C6-卤代烷基。
6.如权利要求1至5中任一项所述的化合物,其中,X选自F、CH3、C2H5、OCH3、OCHF2、OCF3。
7.如权利要求1至5中任一项所述的化合物,其中,Y选自F和Cl。
8.如权利要求1至9中任一项所述的化合物,其中,R7选自H、CN、CH2CN、CH(CH3)CN、C(=O)C1-C6-烷基、C1-C6-烷基、C(=O)NH-C1-C4-烷基、C(=O)N-(C1-C4-烷基)2、S(=O)2-R7a。
9.一种组合物,该组合物包含一种如权利要求1至8中任一项所定义的具有式I的化合物、其N-氧化物或农业上可接受的盐。
10.一种用于对抗植物病原性真菌的方法,该方法包括用有效量的至少一种如权利要求1至8中任一项所定义的具有式I的化合物、或用如权利要求9中任一项所定义的组合物处理该真菌或待保护以防真菌侵袭的材料、植物、土壤或种子。
11.一种种子,该种子涂覆有0.1至10kg/100kg种子量的至少一种如权利要求1至8中任一项所定义的具有式I的化合物或其农业上可接受的盐、或如权利要求9中任一项所定义的组合物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP21189028 | 2021-08-02 | ||
EP21189028.0 | 2021-08-02 | ||
PCT/EP2022/070787 WO2023011957A1 (en) | 2021-08-02 | 2022-07-25 | (3-quinolyl)-quinazoline |
Publications (1)
Publication Number | Publication Date |
---|---|
CN117794908A true CN117794908A (zh) | 2024-03-29 |
Family
ID=77168064
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202280053834.1A Pending CN117794908A (zh) | 2021-08-02 | 2022-07-25 | (3-喹啉基)-喹唑啉 |
Country Status (8)
Country | Link |
---|---|
KR (1) | KR20240042626A (zh) |
CN (1) | CN117794908A (zh) |
AR (1) | AR126671A1 (zh) |
AU (1) | AU2022323668A1 (zh) |
CA (1) | CA3227653A1 (zh) |
CO (1) | CO2024001126A2 (zh) |
IL (1) | IL310497A (zh) |
WO (1) | WO2023011957A1 (zh) |
Family Cites Families (155)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3625959A (en) | 1964-04-10 | 1971-12-07 | Hoffmann La Roche | Preparation of 2,3,4,5-tetrahydro-5-phenyl-1h-1, 4-benzodiazepin-4-ols |
DE3338292A1 (de) | 1983-10-21 | 1985-05-02 | Basf Ag, 6700 Ludwigshafen | 7-amino-azolo(1,5-a)-pyrimidine und diese enthaltende fungizide |
CA1249832A (en) | 1984-02-03 | 1989-02-07 | Shionogi & Co., Ltd. | Azolyl cycloalkanol derivatives and agricultural fungicides |
DE3545319A1 (de) | 1985-12-20 | 1987-06-25 | Basf Ag | Acrylsaeureester und fungizide, die diese verbindungen enthalten |
CN1015981B (zh) | 1986-05-02 | 1992-03-25 | 施托福化学公司 | 吡啶基亚胺酸酯的制备方法 |
ES2011602T3 (es) | 1986-08-12 | 1994-07-16 | Mitsubishi Chem Ind | Derivados de piridinacarboxamida y su uso como fungicidas. |
EP0284236B1 (en) | 1987-03-17 | 1991-08-21 | Her Majesty in Right of Canada as represented by the Minister of Agriculture Canada | Methods and compositions for increasing the amounts of phosphorous and/or micronutrients available for plant uptake from soils |
DE3731239A1 (de) | 1987-09-17 | 1989-03-30 | Basf Ag | Verfahren zur bekaempfung von pilzen |
ES2153817T3 (es) | 1989-08-03 | 2001-03-16 | Australian Technological Innov | Miconematicida. |
US6187773B1 (en) | 1989-11-10 | 2001-02-13 | Agro-Kanesho Co., Ltd. | Hexahydrotriazine compounds and insecticides |
SK281286B6 (sk) | 1989-11-17 | 2001-02-12 | Novo Nordisk A/S | Mutant mikroorganizmu bacillus thuringiensis deponovaný ako subsp. tenebrionis dsm 5480, spôsob jeho prípravy a pesticídny prostriedok, ktorý ho obsahuje |
JP2828186B2 (ja) | 1991-09-13 | 1998-11-25 | 宇部興産株式会社 | アクリレート系化合物、その製法及び殺菌剤 |
EP0648266B1 (en) | 1992-07-01 | 2006-02-08 | Cornell Research Foundation, Inc. | Elicitor of the hypersensitive response in plants |
JP3046167B2 (ja) | 1992-12-25 | 2000-05-29 | 株式会社北海道グリーン興産 | 植物病害防除菌、これを用いた防除剤及び防除剤の製造方法並びに使用方法 |
GB9320487D0 (en) | 1993-10-05 | 1993-11-24 | Angus Fire Armour Ltd | Improvements in pipe lining |
DE19502065C2 (de) | 1995-01-14 | 1996-05-02 | Prophyta Biolog Pflanzenschutz | Pilzisolat mit fungizider Wirkung |
US6406690B1 (en) | 1995-04-17 | 2002-06-18 | Minrav Industries Ltd. | Bacillus firmus CNCM I-1582 or Bacillus cereus CNCM I-1562 for controlling nematodes |
EP1894467A3 (en) | 1997-04-03 | 2008-07-16 | DeKalb Genetics Corporation | Use of glyphosate resistant maize lines |
US6333449B1 (en) | 1998-11-03 | 2001-12-25 | Plant Genetic Systems, N.V. | Glufosinate tolerant rice |
WO2000026356A1 (en) | 1998-11-03 | 2000-05-11 | Aventis Cropscience N. V. | Glufosinate tolerant rice |
IT1303800B1 (it) | 1998-11-30 | 2001-02-23 | Isagro Ricerca Srl | Composti dipeptidici aventi elevata attivita' fungicida e loroutilizzo agronomico. |
IL142816A0 (en) | 1998-12-24 | 2002-03-10 | Du Pont Pharm Co | SUCCINOYLAMINO BENZODIAZEPINES AS INHIBITORS OF Aβ PROTEIN PRODUCTION |
AU770077B2 (en) | 1999-03-11 | 2004-02-12 | Dow Agrosciences Llc | Heterocyclic substituted isoxazolidines and their use as fungicides |
UA73307C2 (uk) | 1999-08-05 | 2005-07-15 | Куміаі Кемікал Індастрі Ко., Лтд. | Похідна карбамату і фунгіцид сільськогосподарського/садівницького призначення |
US6509516B1 (en) | 1999-10-29 | 2003-01-21 | Plant Genetic Systems N.V. | Male-sterile brassica plants and methods for producing same |
US6506963B1 (en) | 1999-12-08 | 2003-01-14 | Plant Genetic Systems, N.V. | Hybrid winter oilseed rape and methods for producing same |
IL141034A0 (en) | 2000-02-04 | 2002-02-10 | Sumitomo Chemical Co | Uracil compounds and use thereof |
CN1114590C (zh) | 2000-02-24 | 2003-07-16 | 沈阳化工研究院 | 不饱和肟醚类杀菌剂 |
EP1270717A4 (en) | 2000-03-31 | 2004-06-09 | Hokkaido Green Kosan Inc | CHLAMYDOSPORES AND METHOD FOR THE PRODUCTION THEREOF |
BR122013026754B1 (pt) | 2000-06-22 | 2018-02-27 | Monsanto Company | Molécula de dna e processos para produzir uma planta de milho tolerante à aplicação do herbicida glifosato |
US6740488B2 (en) | 2000-10-25 | 2004-05-25 | Monsanto Technology Llc | Cotton event PV-GHGT07(1445) compositions and methods for detection thereof |
WO2002036831A2 (en) | 2000-10-30 | 2002-05-10 | Monsanto Technology Llc | Canola event pv-bngt04(rt73) and compositions and methods for detection thereof |
PT1372384E (pt) | 2001-03-14 | 2013-02-05 | Israel State | Nova levedura antagonista útil no controlo da degradação de produto agrícola, seus métodos de utilização e composições contendo a mesma |
EG26529A (en) | 2001-06-11 | 2014-01-27 | مونسانتو تكنولوجى ل ل سى | Prefixes for detection of DNA molecule in cotton plant MON15985 which gives resistance to damage caused by insect of squamous lepidoptera |
US6818807B2 (en) | 2001-08-06 | 2004-11-16 | Bayer Bioscience N.V. | Herbicide tolerant cotton plants having event EE-GH1 |
RU2004104638A (ru) | 2001-08-20 | 2005-07-10 | Дайниппон Инк Энд Кемикалз, Инк. (Jp) | Производное тетразоилоксима и сельскохозяйственный химикат, содержащий его в качестве активного ингредиента |
US20030166476A1 (en) | 2002-01-31 | 2003-09-04 | Winemiller Mark D. | Lubricating oil compositions with improved friction properties |
DE10204390A1 (de) | 2002-02-04 | 2003-08-14 | Bayer Cropscience Ag | Disubstituierte Thiazolylcarboxanilide |
IL163692A0 (en) | 2002-03-05 | 2005-12-18 | Syngenta Participations Ag | O-cyclopropyl-carboxanilides and their use as fungicides |
UA87808C2 (ru) | 2002-07-29 | 2009-08-25 | Монсанто Текнолоджи, Ллс | Зерновые растения pv-zmir13 (mon863) и композиции и способы их обнаружения |
GB0225129D0 (en) | 2002-10-29 | 2002-12-11 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
GB0227966D0 (en) | 2002-11-29 | 2003-01-08 | Syngenta Participations Ag | Organic Compounds |
EP2298921B1 (en) | 2003-02-12 | 2016-12-21 | Monsanto Technology LLC | Cotton event mon 88913 and compositions and methods for detection thereof |
DK1597373T3 (da) | 2003-02-20 | 2012-10-15 | Kws Saat Ag | Glyphosattolerant sukkerroe |
WO2004083193A1 (ja) | 2003-03-17 | 2004-09-30 | Sumitomo Chemical Company, Limited | アミド化合物およびこれを含有する殺菌剤組成物 |
CN1201657C (zh) | 2003-03-25 | 2005-05-18 | 浙江省化工研究院 | 甲氧基丙烯酸甲酯类化合物杀菌剂 |
PT1620571E (pt) | 2003-05-02 | 2015-09-03 | Du Pont | Milho do evento tc1507 e métodos para deteção deste |
US7157281B2 (en) | 2003-12-11 | 2007-01-02 | Monsanto Technology Llc | High lysine maize compositions and event LY038 maize plants |
ES2542688T3 (es) | 2003-12-15 | 2015-08-10 | Monsanto Technology, Llc | Planta de maíz MON88017 y composiciones y procedimientos de detección de la misma |
TWI355894B (en) | 2003-12-19 | 2012-01-11 | Du Pont | Herbicidal pyrimidines |
ATE473228T1 (de) | 2004-03-10 | 2010-07-15 | Basf Se | 5,6-dialkyl-7-aminotriazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
EA009883B1 (ru) | 2004-03-10 | 2008-04-28 | Басф Акциенгезельшафт | 5, 6-диалкил-7-амино-триазолопиримидины, способ их получения и их применение для борьбы с патогенными растениями, а также содержащие их средства |
EP1737290B1 (en) | 2004-03-25 | 2015-04-15 | Syngenta Participations AG | Corn event mir604 |
US7179965B2 (en) | 2004-03-26 | 2007-02-20 | Dow Agrosciences Llc | Cry1F and Cry1Ac transgenic cotton lines and event-specific identification thereof |
EP1750508A2 (en) | 2004-06-03 | 2007-02-14 | E.I.Du pont de nemours and company | Fungicidal mixtures of amidinylphenyl compounds |
WO2005123690A1 (de) | 2004-06-18 | 2005-12-29 | Basf Aktiengesellschaft | 1-methyl-3-difluormethyl-pyrazol-4-carbonsäure-(ortho-phenyl)-anilide und ihre verwendung als fungizid |
BRPI0512121A (pt) | 2004-06-18 | 2008-02-06 | Basf Ag | composto, processo para combater fungos nocivos, agente fungicida, e, uso de compostos |
CA2471555C (en) | 2004-06-18 | 2011-05-17 | Thomas D. Johnson | Controlling plant pathogens with fungal/bacterial antagonist combinations comprising trichoderma virens and bacillus amyloliquefaciens |
GB0418048D0 (en) | 2004-08-12 | 2004-09-15 | Syngenta Participations Ag | Method for protecting useful plants or plant propagation material |
UA97088C2 (ru) | 2004-09-29 | 2012-01-10 | Пионер Хай-Бред Интернешнл, Инк. | Трансгенная кукуруза das-59122-7, стойкая к насекомым, и способы его обнаружения |
US8020343B2 (en) | 2004-12-23 | 2011-09-20 | Becker Underwood Inc. | Enhanced shelf life and on seed stabilization of liquid bacterium inoculants |
ATE400576T1 (de) | 2005-02-16 | 2008-07-15 | Basf Se | 5-alkoxyalkyl-6-alkyl-7-amino-azolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
DE102005007160A1 (de) | 2005-02-16 | 2006-08-24 | Basf Ag | Pyrazolcarbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
PT1868426T (pt) | 2005-03-16 | 2018-05-08 | Syngenta Participations Ag | Evento de milho 3272 e métodos para a sua deteção |
ES2388548T3 (es) | 2005-04-08 | 2012-10-16 | Bayer Cropscience Nv | Suceso de élite A2704-12 y métodos y estuches para identificar a dicho suceso en muestras biológicas |
CA2603949C (en) | 2005-04-11 | 2014-12-09 | Bayer Bioscience N.V. | Elite event a5547-127 and methods and kits for identifying such event in biological samples |
AP2693A (en) | 2005-05-27 | 2013-07-16 | Monsanto Technology Llc | Soybean event MON89788 and methods for detection thereof |
CN101184847B (zh) | 2005-06-02 | 2015-02-25 | 先正达参股股份有限公司 | 表达cry1ab的杀昆虫转基因棉ce43-67b |
KR101335224B1 (ko) | 2005-07-07 | 2013-11-29 | 바스프 에스이 | N-티오안트라닐아미드 화합물 및 살충제로서의 이의 용도 |
CN1907024A (zh) | 2005-08-03 | 2007-02-07 | 浙江化工科技集团有限公司 | 取代甲氧基丙烯酸甲酯类化合物杀菌剂 |
US7932439B2 (en) | 2005-08-08 | 2011-04-26 | Bayer Bioscience N.V. | Herbicide tolerant cotton plants and methods for identifying the same |
JP5059779B2 (ja) | 2006-01-13 | 2012-10-31 | ダウ アグロサイエンシィズ エルエルシー | 6−(多置換アリール)−4−アミノピコリネートおよび除草剤としてのそれらの使用 |
EP1983832A2 (en) | 2006-02-09 | 2008-10-29 | Syngeta Participations AG | A method of protecting a plant propagation material, a plant, and/or plant organs |
CN101437806B (zh) | 2006-05-08 | 2011-01-19 | 组合化学工业株式会社 | 1,2-苯并异噻唑衍生物及农业或园艺用植物病害防除剂 |
MY150655A (en) | 2006-05-26 | 2014-02-14 | Monsanto Technology Llc | Corn plant and seed corresponding to transgenic event mon89034 and methods for detection and use thereof |
ES2546255T3 (es) | 2006-06-03 | 2015-09-22 | Syngenta Participations Ag | Evento de Maíz MIR162 |
US7951995B2 (en) | 2006-06-28 | 2011-05-31 | Pioneer Hi-Bred International, Inc. | Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof |
WO2008013622A2 (en) | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Fungicidal azocyclic amides |
US7928296B2 (en) | 2006-10-30 | 2011-04-19 | Pioneer Hi-Bred International, Inc. | Maize event DP-098140-6 and compositions and methods for the identification and/or detection thereof |
CA2666754C (en) | 2006-10-31 | 2016-11-29 | E. I. Du Pont De Nemours And Company | Soybean event dp-305423-1 and compositions and methods for the identification and/or detection thereof |
EP2132320B1 (en) | 2007-04-05 | 2013-08-14 | Bayer CropScience NV | Insect resistant cotton plants and methods for identifying same |
US8210267B2 (en) | 2007-06-04 | 2012-07-03 | Baker Hughes Incorporated | Downhole pressure chamber and method of making same |
WO2009064652A1 (en) | 2007-11-15 | 2009-05-22 | Monsanto Technology Llc | Soybean plant and seed corresponding to transgenic event mon87701 and methods for detection thereof |
EP2234489B1 (en) | 2008-01-15 | 2017-04-12 | Bayer Intellectual Property GmbH | Pesticide composition comprising a tetrazolyloxime derivative and a fungicide or an insecticide active substance |
DK2562166T3 (en) | 2008-01-22 | 2015-11-23 | Dow Agrosciences Llc | 5-fluoro-pyrimidine derivatives as fungicides |
AU2009214457B2 (en) | 2008-02-14 | 2014-07-31 | E. I. Du Pont De Nemours And Company | Plant genomic DNA flanking SPT event and methods for identifying SPT event |
EP2240586A1 (en) | 2008-02-15 | 2010-10-20 | Monsanto Technology, LLC | Soybean plant and seed corresponding to transgenic event mon87769 and methods for detection thereof |
BRPI0908267B8 (pt) | 2008-02-29 | 2019-02-05 | Monsanto Technology Llc | método de produção de uma planta de milho tolerante a seca |
JP2011517461A (ja) | 2008-04-07 | 2011-06-09 | バイエル・クロツプサイエンス・エル・ピー | 安定な水性胞子含有製剤 |
US8329989B2 (en) | 2008-09-29 | 2012-12-11 | Monsanto Technology Llc | Soybean transgenic event MON87705 and methods for detection thereof |
MX346320B (es) | 2008-12-16 | 2017-03-15 | Syngenta Participations Ag | Evento 5307 del maiz. |
GB0823002D0 (en) | 2008-12-17 | 2009-01-28 | Syngenta Participations Ag | Isoxazoles derivatives with plant growth regulating properties |
BRPI1006074A2 (pt) | 2009-01-07 | 2017-03-21 | Basf Agrochemical Products Bv | método para controlar ervas daninhas, molécula de ácido nucleico, planta de soja, par isolado de iniciadores de ácidos nucleicos, kit para a identificação de um evento 127 da molécula de ácido nucleico, métodos para identificar um evento 127 na planta de soja, para identificar uma planta de soja tendo um evento 127 da molécula de ácido nucleico, para aumentar o rendimento em uma planta de soja, para a reprodução de uma planta de soja resistente ao herbicida inibidor de ahas, para detectar a presença de um evento 127 da molécula de ácido nucleico em uma amostra biológica, para o cultivo de uma planta de soja, para detectar um evento 127 do polipeptídeo de uma amostra, semente e dispositivo para uso na detenção de moléculas biológicas |
US8551919B2 (en) | 2009-04-13 | 2013-10-08 | University Of Delaware | Methods for promoting plant health |
CN101906075B (zh) | 2009-06-05 | 2012-11-07 | 中国中化股份有限公司 | 含取代苯胺基嘧啶基团的e-型苯基丙烯酸酯类化合物及其应用 |
CN102573452B (zh) | 2009-08-19 | 2015-07-22 | 陶氏益农公司 | Aad-1事件das-40278-9、相关的转基因玉米品系及其事件特异性鉴定 |
NZ598809A (en) | 2009-09-01 | 2014-02-28 | Dow Agrosciences Llc | Synergistic fungicidal compositions containing a 5-fluoropyrimidine derivative for fungal control in cereals |
SG179103A1 (en) | 2009-09-17 | 2012-05-30 | Monsanto Technology Llc | Soybean transgenic event mon 87708 and methods of use thereof |
RU2764586C2 (ru) | 2009-11-23 | 2022-01-18 | Монсанто Текнолоджи Ллс | Трансгенное событие mon 87427 маиса и относительная шкала развития |
IN2012DN04843A (zh) | 2009-11-24 | 2015-09-25 | Dow Agrosciences Llc | |
MX2012006936A (es) | 2009-12-17 | 2012-07-17 | Pioneer Hi Bred Int | Evento de maiz dp-004114-3 y metodos para su deteccion. |
MY159705A (en) | 2009-12-22 | 2017-01-13 | Mitsui Chemicals Agro Inc | Plant disease control composition and method for controlling plant disease by applying the same |
US8772200B2 (en) | 2010-01-04 | 2014-07-08 | Nippon Soda Co., Ltd. | Nitrogen-containing heterocyclic compound and agricultural fungicide |
JP2011148714A (ja) | 2010-01-19 | 2011-08-04 | Nippon Soda Co Ltd | 病害防除方法 |
BR112012021952B8 (pt) | 2010-03-01 | 2021-08-17 | Univ Delaware | método para melhorar uma qualidade de uma planta, e semente de planta revestida |
JP2011246452A (ja) | 2010-04-28 | 2011-12-08 | Sumitomo Chemical Co Ltd | 植物病害防除組成物およびその用途 |
NZ603506A (en) | 2010-06-04 | 2013-11-29 | Monsanto Technology Llc | Transgenic brassica event mon 88302 and methods of use thereof |
CN103270173B (zh) | 2010-10-12 | 2017-11-21 | 孟山都技术公司 | 对应于转基因事件mon87712的大豆植物和种子及其检测方法 |
JP5829216B2 (ja) | 2010-11-10 | 2015-12-09 | クミアイ化学工業株式会社 | 微生物農薬組成物 |
CA2820303C (en) | 2010-12-10 | 2020-02-25 | Auburn University | Inoculants including bacillus bacteria for inducing production of volatile organic compounds in plants |
TWI667347B (zh) | 2010-12-15 | 2019-08-01 | 瑞士商先正達合夥公司 | 大豆品種syht0h2及偵測其之組合物及方法 |
IT1403275B1 (it) | 2010-12-20 | 2013-10-17 | Isagro Ricerca Srl | Indanilanilidi ad elevata attività fungicida e loro composizioni fitosanitarie |
WO2012134808A1 (en) | 2011-03-30 | 2012-10-04 | Monsanto Technology Llc | Cotton transgenic event mon 88701 and methods of use thereof |
TWI583308B (zh) | 2011-05-31 | 2017-05-21 | 組合化學工業股份有限公司 | 稻之病害防治方法 |
EP2532233A1 (en) | 2011-06-07 | 2012-12-12 | Bayer CropScience AG | Active compound combinations |
CN103857798B (zh) | 2011-06-30 | 2018-06-15 | 孟山都技术公司 | 对应于转基因事件kk179-2的苜蓿植物和种子及其检测方法 |
PE20140826A1 (es) | 2011-07-13 | 2014-07-09 | Basf Se | Compuestos sustituidos fungicidas de 2-[2-halogenalquil-4-(fenoxi)-fenil]-1-[1,2,4]triazol-1-il-etanol |
AU2012285981A1 (en) | 2011-07-15 | 2014-01-30 | Basf Se | Fungicidal alkyl-substituted 2-[2-chloro-4-(4-chloro-phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds |
BR102012019434B1 (pt) | 2011-07-26 | 2021-11-09 | Dow Agrosciences Llc | Métodos de controle de pestes, de insetos, molécula e sequência de dna diagnóstica para o evento de soja 9582.814.19.1 |
CN103857666B (zh) | 2011-08-12 | 2016-12-14 | 巴斯夫欧洲公司 | N-硫代邻氨基苯甲酰胺化合物及其作为农药的用途 |
BR112014003186A2 (pt) | 2011-08-12 | 2017-04-04 | Basf Se | composto da fórmula geral (i), combinação pesticida, composição agrícola ou veterinária, método para combater ou controlar pragas invertebradas, método para a proteção de plantas e sementes, semente, uso de um composto e método para tratar um animal |
EP2748304A4 (en) | 2011-08-27 | 2015-02-11 | Marrone Bio Innovations Inc | ISOLATED BACTERIAL STRUCTURE OF STRAIN BURKHOLDERIA, PESTICIDE METABOLITE THEREOF, AND FORMULATIONS AND USES THEREOF |
CA2849425C (en) | 2011-09-26 | 2018-02-06 | Nippon Soda Co., Ltd. | Agricultural and horticultural fungicidal compositions comprising quinoline derivatives and a second active |
PL2762473T3 (pl) | 2011-09-29 | 2017-02-28 | Mitsui Chemicals Agro, Inc. | Sposób wytwarzania pochodnej 4,4-difluoro-3,4-dihydroizochinoliny |
HUE030004T2 (en) | 2011-12-21 | 2017-04-28 | Basf Se | Use of strobilurin-type compounds to combat Qo-inhibitors resistant to phytopathogenic fungi |
CN107043816A (zh) | 2012-01-23 | 2017-08-15 | 陶氏益农公司 | 除草剂耐受性棉花事件pDAB4468.19.10.3 |
TWI568721B (zh) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
CN104244716B (zh) | 2012-02-27 | 2017-05-03 | 拜耳知识产权有限责任公司 | 包含噻唑基异噁唑啉和杀真菌剂的活性化合物组合产品 |
JP6107377B2 (ja) | 2012-04-27 | 2017-04-05 | 住友化学株式会社 | テトラゾリノン化合物及びその用途 |
AR090981A1 (es) | 2012-05-08 | 2014-12-17 | Monsanto Technology Llc | Evento de maiz mon 87411 |
CN103387541B (zh) | 2012-05-10 | 2016-02-10 | 中国中化股份有限公司 | 一种取代吡唑醚类化合物的制备方法 |
BR112015003688B1 (pt) | 2012-08-22 | 2020-09-24 | Basf Se | Mistura, composição agroquímica, semente, uso da mistura e método para o controle de fungos nocivos fitopatogênicos |
WO2014060177A1 (en) | 2012-10-16 | 2014-04-24 | Syngenta Participations Ag | Fungicidal compositions |
WO2014100913A1 (en) | 2012-12-24 | 2014-07-03 | Beijing Anxinhuaide Biotech. Co., Ltd | Improving the half life of a therapeutic polypeptide by fusing with a trimeric scaffold protein via a spacer |
US9844083B2 (en) | 2012-12-24 | 2017-12-12 | Nokia Technologies Oy | Method and network element for controlling UE's state transition in proximity wireless communication |
CL2012003727A1 (es) | 2012-12-28 | 2013-02-01 | Quiborax Sa | Uso de acidos debiles oxigenados, minerales, compuestos que los generen, para aumentar la recuperacion de cobre en el proceso de lixiviacion o biolixiviacion; procedimiento de lixiviacion o biolixiviacion de cobre que comprende a dichos acidos; y uso de desechos solidos y liquidos de planyas productoras de acidos debiles. |
WO2014116854A1 (en) | 2013-01-25 | 2014-07-31 | Pioneer Hi-Bred International, Inc. | Maize event dp-033121-3 and methods for detection thereof |
KR20150119023A (ko) | 2013-02-11 | 2015-10-23 | 바이엘 크롭사이언스 엘피 | 고제로틴 및 살진균제를 포함하는 조성물 |
WO2014178910A1 (en) | 2013-05-02 | 2014-11-06 | J.R. Simplot Company | Potato cultivar e12 |
MX356384B (es) | 2013-06-14 | 2018-05-24 | Monsanto Technology Llc | Evento transgenico de soja mon87751 y metodos para su deteccion y uso. |
EP3054764B1 (en) | 2013-10-09 | 2018-12-05 | Monsanto Technology LLC | Transgenic corn event mon87403 and methods for detection thereof |
WO2015065922A1 (en) | 2013-10-28 | 2015-05-07 | Dexcom, Inc. | Devices used in connection with continuous analyte monitoring that provide the user with one or more notifications, and related methods |
EP2865265A1 (en) | 2014-02-13 | 2015-04-29 | Bayer CropScience AG | Active compound combinations comprising phenylamidine compounds and biological control agents |
KR102308359B1 (ko) | 2014-03-20 | 2021-10-06 | 몬산토 테크놀로지 엘엘씨 | 형질전환 옥수수 이벤트 mon 87419 및 이의 사용 방법 |
PL3194566T3 (pl) | 2014-08-04 | 2019-09-30 | Basf Se | Przeciwgrzybicze szczepy paenibacillus, związki typu fuzarycydyny i ich zastosowanie |
GB201505740D0 (en) | 2015-04-02 | 2015-05-20 | Syngenta Participations Ag | Herbicidal mixtures |
GB201505852D0 (en) | 2015-04-07 | 2015-05-20 | Syngenta Participations Ag | Herbicidal mixtures |
MX2017014656A (es) | 2015-05-14 | 2018-01-23 | Simplot Co J R | Cultivar de papa v11. |
JP2018529364A (ja) | 2015-10-08 | 2018-10-11 | ジェイ.アール.シンプロット カンパニー | ジャガイモ栽培品種x17 |
CN108347894B (zh) | 2015-10-08 | 2019-10-29 | 杰.尔.辛普洛公司 | 马铃薯栽培品种y9 |
RU2649048C1 (ru) | 2016-11-25 | 2018-03-29 | Самсунг Электроникс Ко., Лтд. | Система компактного спектрометра, предназначенного для неинвазивного измерения спектров поглощения и пропускания образцов биологической ткани |
US20210007358A1 (en) | 2017-03-31 | 2021-01-14 | Syngenta Participations Ag | Fungicidal compositions |
CN107879989B (zh) | 2017-11-29 | 2020-01-03 | 重庆市中药研究院 | 具有生物活性的3,4,5-取代苯并二氮卓2-酮类药物分子及其制备方法 |
CN207973751U (zh) | 2018-01-04 | 2018-10-16 | 浙江润兰科技有限公司 | 一种细胞助推器 |
AR118673A1 (es) | 2019-04-18 | 2021-10-20 | Syngenta Crop Protection Ag | Procedimiento para la preparación de derivados de oxadiazol microbiocidas |
-
2022
- 2022-07-25 CN CN202280053834.1A patent/CN117794908A/zh active Pending
- 2022-07-25 CA CA3227653A patent/CA3227653A1/en active Pending
- 2022-07-25 KR KR1020247006619A patent/KR20240042626A/ko unknown
- 2022-07-25 AU AU2022323668A patent/AU2022323668A1/en active Pending
- 2022-07-25 WO PCT/EP2022/070787 patent/WO2023011957A1/en active Application Filing
- 2022-07-25 IL IL310497A patent/IL310497A/en unknown
- 2022-08-01 AR ARP220102056A patent/AR126671A1/es unknown
-
2024
- 2024-02-01 CO CONC2024/0001126A patent/CO2024001126A2/es unknown
Also Published As
Publication number | Publication date |
---|---|
CA3227653A1 (en) | 2023-02-09 |
IL310497A (en) | 2024-03-01 |
AR126671A1 (es) | 2023-11-01 |
AU2022323668A1 (en) | 2024-02-15 |
WO2023011957A1 (en) | 2023-02-09 |
KR20240042626A (ko) | 2024-04-02 |
CO2024001126A2 (es) | 2024-02-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN108026066B (zh) | 可用于防除植物病原性真菌的吡啶化合物 | |
JP2020518607A (ja) | 植物病原菌を駆除するための置換5−(ハロアルキル)−5−ヒドロキシ−イソオキサゾール | |
WO2019154665A1 (en) | New pyridine carboxamides | |
KR20200118091A (ko) | 신규의 피리딘 카르복스아미드 | |
WO2018149754A1 (en) | Pyridine compounds | |
JP7179777B2 (ja) | ピリジン化合物及びピラジン化合物 | |
CN117794908A (zh) | (3-喹啉基)-喹唑啉 | |
CN117794907A (zh) | (3-吡啶基)-喹唑啉 | |
WO2018184882A1 (en) | Pyridine compounds | |
CN117355518A (zh) | 用作杀真菌剂的新型取代吡啶类 | |
CN117355520A (zh) | 用作杀真菌剂的新型取代喹啉类 | |
CN117355519A (zh) | 用作杀真菌剂的新型取代吡啶类 | |
EP3970494A1 (en) | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors viii | |
EP4361126A1 (en) | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors xv | |
EP3960727A1 (en) | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors vi | |
EP3939961A1 (en) | Strobilurin type compounds and their use for combating phytopathogenic fungi | |
WO2023072671A1 (en) | Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors ix | |
EA042940B1 (ru) | Пиридиновые и пиразиновые соединения | |
EP3670501A1 (en) | Substituted [1,2,4]triazole compounds as fungicides |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication |