CA2378409A1 - Control of crustacean infestation of aquatic animals - Google Patents
Control of crustacean infestation of aquatic animals Download PDFInfo
- Publication number
- CA2378409A1 CA2378409A1 CA002378409A CA2378409A CA2378409A1 CA 2378409 A1 CA2378409 A1 CA 2378409A1 CA 002378409 A CA002378409 A CA 002378409A CA 2378409 A CA2378409 A CA 2378409A CA 2378409 A1 CA2378409 A1 CA 2378409A1
- Authority
- CA
- Canada
- Prior art keywords
- compound
- juvenile hormone
- group
- species
- fish
- 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.)
- Abandoned
Links
- 241000238424 Crustacea Species 0.000 title claims abstract description 48
- 206010061217 Infestation Diseases 0.000 title claims abstract description 28
- 241001465754 Metazoa Species 0.000 title claims description 47
- 150000001875 compounds Chemical class 0.000 claims abstract description 188
- 241000251468 Actinopterygii Species 0.000 claims abstract description 118
- 229930014550 juvenile hormone Natural products 0.000 claims abstract description 104
- 239000002949 juvenile hormone Substances 0.000 claims abstract description 104
- 150000003633 juvenile hormone derivatives Chemical class 0.000 claims abstract description 104
- 239000003814 drug Substances 0.000 claims abstract description 36
- 241000277263 Salmo Species 0.000 claims abstract description 17
- 241000277331 Salmonidae Species 0.000 claims abstract description 11
- 241001405819 Caligus elongatus Species 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 46
- -1 2,2-dimethylcyclopropyl Chemical group 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 28
- 230000003054 hormonal effect Effects 0.000 claims description 23
- 241000894007 species Species 0.000 claims description 22
- 239000004530 micro-emulsion Substances 0.000 claims description 21
- 241001247234 Lepeophtheirus salmonis Species 0.000 claims description 19
- 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 claims description 18
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 18
- FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 claims description 18
- 229930000073 hydroprene Natural products 0.000 claims description 18
- 229930002897 methoprene Natural products 0.000 claims description 18
- 229950003442 methoprene Drugs 0.000 claims description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 15
- 239000001301 oxygen Substances 0.000 claims description 15
- 229910052760 oxygen Inorganic materials 0.000 claims description 15
- 229920002101 Chitin Polymers 0.000 claims description 13
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 13
- 229910052717 sulfur Inorganic materials 0.000 claims description 13
- 239000011593 sulfur Chemical group 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000000243 solution Substances 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 241000277334 Oncorhynchus Species 0.000 claims description 10
- 230000002401 inhibitory effect Effects 0.000 claims description 10
- 230000015572 biosynthetic process Effects 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 238000003786 synthesis reaction Methods 0.000 claims description 9
- 241001266069 Livoneca Species 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 230000003071 parasitic effect Effects 0.000 claims description 8
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 claims description 7
- 239000008187 granular material Substances 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 7
- 150000003505 terpenes Chemical class 0.000 claims description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 6
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 6
- 239000000839 emulsion Substances 0.000 claims description 6
- FZRBKIRIBLNOAM-UHFFFAOYSA-N (E,E)-2-propynyl 3,7,11-trimethyl-2,4-dodecadienoate Chemical compound CC(C)CCCC(C)CC=CC(C)=CC(=O)OCC#C FZRBKIRIBLNOAM-UHFFFAOYSA-N 0.000 claims description 5
- YHDXOFFTMOZZPE-UHFFFAOYSA-N 2-ethyl-3-[3-ethyl-5-(4-ethylphenoxy)pentyl]-2-methyloxirane Chemical compound O1C(CC)(C)C1CCC(CC)CCOC1=CC=C(CC)C=C1 YHDXOFFTMOZZPE-UHFFFAOYSA-N 0.000 claims description 5
- QAEVVTVIOGTPLI-UHFFFAOYSA-N 3-[(4-phenoxyphenyl)methoxy]pyridine Chemical compound C=1C=C(OC=2C=CC=CC=2)C=CC=1COC1=CC=CN=C1 QAEVVTVIOGTPLI-UHFFFAOYSA-N 0.000 claims description 5
- 241000277275 Oncorhynchus mykiss Species 0.000 claims description 5
- 229930001540 kinoprene Natural products 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims description 5
- 239000002728 pyrethroid Substances 0.000 claims description 5
- YGBMMMOLNODPBP-GWGZPXPZSA-N s-ethyl (2e,4e)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienethioate Chemical compound CCSC(=O)\C=C(/C)\C=C\CC(C)CCCC(C)(C)OC YGBMMMOLNODPBP-GWGZPXPZSA-N 0.000 claims description 5
- OQJRUUUFRQCENE-UHFFFAOYSA-N 1-octylpiperidine Chemical compound CCCCCCCCN1CCCCC1 OQJRUUUFRQCENE-UHFFFAOYSA-N 0.000 claims description 4
- QKJJUQOUDLVMCG-UHFFFAOYSA-N 2-[2-(4-phenoxyphenoxy)ethoxy]pyridine Chemical compound C=1C=C(OC=2C=CC=CC=2)C=CC=1OCCOC1=CC=CC=N1 QKJJUQOUDLVMCG-UHFFFAOYSA-N 0.000 claims description 4
- 125000006020 2-methyl-1-propenyl group Chemical group 0.000 claims description 4
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 claims description 4
- NMLNNXGEQCSYGQ-UHFFFAOYSA-N 4-octylmorpholine Chemical compound CCCCCCCCN1CCOCC1 NMLNNXGEQCSYGQ-UHFFFAOYSA-N 0.000 claims description 4
- 241000009885 Anilocra physodes Species 0.000 claims description 4
- 241001611011 Caligus Species 0.000 claims description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 4
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
- 239000002270 dispersing agent Substances 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 4
- 125000001072 heteroaryl group Chemical group 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 239000008188 pellet Substances 0.000 claims description 4
- 239000000725 suspension Substances 0.000 claims description 4
- JDEPNKUINYBORA-UHFFFAOYSA-N 1,4-dioctylpiperazine Chemical compound CCCCCCCCN1CCN(CCCCCCCC)CC1 JDEPNKUINYBORA-UHFFFAOYSA-N 0.000 claims description 3
- TWOLMUQSOOZPPE-UHFFFAOYSA-N 2-(3,7-dimethyloctylsulfanyl)thiophene Chemical compound CC(C)CCCC(C)CCSC1=CC=CS1 TWOLMUQSOOZPPE-UHFFFAOYSA-N 0.000 claims description 3
- 241000009884 Anilocra Species 0.000 claims description 3
- 241000473391 Archosargus rhomboidalis Species 0.000 claims description 3
- 241000790794 Argulus Species 0.000 claims description 3
- 241000239250 Copepoda Species 0.000 claims description 3
- 241001149911 Isopoda Species 0.000 claims description 3
- 241001247233 Lepeophtheirus Species 0.000 claims description 3
- 241000277326 Oncorhynchus gorbuscha Species 0.000 claims description 3
- 241000277329 Oncorhynchus keta Species 0.000 claims description 3
- 241000277338 Oncorhynchus kisutch Species 0.000 claims description 3
- 241001280377 Oncorhynchus tshawytscha Species 0.000 claims description 3
- 241000277289 Salmo salar Species 0.000 claims description 3
- 241000277295 Salvelinus Species 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- 241000269858 Anarhichas lupus Species 0.000 claims description 2
- 241000040006 Elthusa vulgaris Species 0.000 claims description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical group OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 2
- 241000013856 Olencira Species 0.000 claims description 2
- 241000013857 Olencira praegustator Species 0.000 claims description 2
- 241000269908 Platichthys flesus Species 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000004067 bulking agent Substances 0.000 claims description 2
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical group [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- 229960005349 sulfur Drugs 0.000 claims 7
- 235000001508 sulfur Nutrition 0.000 claims 7
- 229960005419 nitrogen Drugs 0.000 claims 6
- JOZSNVOTRXIUNJ-UHFFFAOYSA-N 3-[2-(4-phenoxyphenoxy)ethoxy]pyridine Chemical compound C=1C=C(OC=2C=CC=CC=2)C=CC=1OCCOC1=CC=CN=C1 JOZSNVOTRXIUNJ-UHFFFAOYSA-N 0.000 claims 2
- 241000239265 Branchiura <Crustacea> Species 0.000 claims 2
- 239000005898 Fenoxycarb Substances 0.000 claims 2
- 241000277288 Salmo trutta Species 0.000 claims 2
- 229910001369 Brass Inorganic materials 0.000 claims 1
- 241000276438 Gadus morhua Species 0.000 claims 1
- 241000269980 Pleuronectidae Species 0.000 claims 1
- 239000010951 brass Substances 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 229960003903 oxygen Drugs 0.000 claims 1
- 235000019688 fish Nutrition 0.000 abstract description 118
- 238000011282 treatment Methods 0.000 abstract description 32
- 229940079593 drug Drugs 0.000 abstract description 21
- 208000028454 lice infestation Diseases 0.000 abstract description 5
- 241001674048 Phthiraptera Species 0.000 description 57
- 241000133262 Nauplius Species 0.000 description 37
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 36
- 230000000694 effects Effects 0.000 description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 30
- 229930191400 juvenile hormones Natural products 0.000 description 29
- 238000011161 development Methods 0.000 description 24
- 230000018109 developmental process Effects 0.000 description 24
- 238000012360 testing method Methods 0.000 description 23
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- 241000238631 Hexapoda Species 0.000 description 18
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 18
- 239000000126 substance Substances 0.000 description 17
- 239000013535 sea water Substances 0.000 description 16
- 230000001276 controlling effect Effects 0.000 description 14
- 239000013543 active substance Substances 0.000 description 13
- 238000002474 experimental method Methods 0.000 description 13
- 238000009472 formulation Methods 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- 244000045947 parasite Species 0.000 description 11
- 229940022682 acetone Drugs 0.000 description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 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 8
- 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 8
- 244000078703 ectoparasite Species 0.000 description 8
- 229960002418 ivermectin Drugs 0.000 description 8
- FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical compound C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 210000001672 ovary Anatomy 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 230000004083 survival effect Effects 0.000 description 7
- 241000972773 Aulopiformes Species 0.000 description 6
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 6
- 239000005556 hormone Substances 0.000 description 6
- 229940088597 hormone Drugs 0.000 description 6
- 230000000366 juvenile effect Effects 0.000 description 6
- 235000019515 salmon Nutrition 0.000 description 6
- 231100000331 toxic Toxicity 0.000 description 6
- 230000002588 toxic effect Effects 0.000 description 6
- 239000005893 Diflubenzuron Substances 0.000 description 5
- 241000124008 Mammalia Species 0.000 description 5
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 5
- 239000005938 Teflubenzuron Substances 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 239000012141 concentrate Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 description 5
- 229940019503 diflubenzuron Drugs 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 230000001418 larval effect Effects 0.000 description 5
- 230000029052 metamorphosis Effects 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 229950001327 dichlorvos Drugs 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000013505 freshwater Substances 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- WEGQSMDVKYYUPG-UHFFFAOYSA-N 3-(3,7-dimethyloctoxy)pyridine Chemical compound CC(C)CCCC(C)CCOC1=CC=CN=C1 WEGQSMDVKYYUPG-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 206010014143 Ectoparasitic Infestations Diseases 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- WPPOGHDFAVQKLN-UHFFFAOYSA-N N-Octyl-2-pyrrolidone Chemical compound CCCCCCCCN1CCCC1=O WPPOGHDFAVQKLN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000000540 analysis of variance Methods 0.000 description 3
- 230000002141 anti-parasite Effects 0.000 description 3
- 238000003287 bathing Methods 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 235000010980 cellulose Nutrition 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 230000001524 infective effect Effects 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229960001952 metrifonate Drugs 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 208000029380 parasitic ectoparasitic infectious disease Diseases 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 230000000699 topical effect Effects 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
- LVQFGKMCIGFCST-UHFFFAOYSA-N 2-methyl-5-octoxypyridine Chemical compound CCCCCCCCOC1=CC=C(C)N=C1 LVQFGKMCIGFCST-UHFFFAOYSA-N 0.000 description 2
- MKXPLUCMXAMDBY-UHFFFAOYSA-N 3,7-dimethyloctoxybenzene Chemical compound CC(C)CCCC(C)CCOC1=CC=CC=C1 MKXPLUCMXAMDBY-UHFFFAOYSA-N 0.000 description 2
- MSHKRQZNUARPFF-UHFFFAOYSA-N 3-(4,8-dimethylnonyl)pyridine Chemical compound CC(C)CCCC(C)CCCC1=CC=CN=C1 MSHKRQZNUARPFF-UHFFFAOYSA-N 0.000 description 2
- 239000005660 Abamectin Substances 0.000 description 2
- 229940122041 Cholinesterase inhibitor Drugs 0.000 description 2
- 239000005892 Deltamethrin Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 241000269951 Labridae Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 208000030852 Parasitic disease Diseases 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 241000382353 Pupa Species 0.000 description 2
- 241000316146 Salmo trutta trutta Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- IOSLINNLJFQMFF-XMMPIXPASA-N [(2R)-1-[[4-[[3-[(4-fluorophenyl)methylsulfanyl]phenoxy]methyl]phenyl]methyl]pyrrolidin-2-yl]methanol Chemical compound FC1=CC=C(CSC=2C=C(OCC3=CC=C(CN4[C@H](CCC4)CO)C=C3)C=CC=2)C=C1 IOSLINNLJFQMFF-XMMPIXPASA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 238000005273 aeration Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000003674 animal food additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000003096 antiparasitic agent Substances 0.000 description 2
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 2
- 230000008499 blood brain barrier function Effects 0.000 description 2
- 210000001218 blood-brain barrier Anatomy 0.000 description 2
- 210000004556 brain Anatomy 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000544 cholinesterase inhibitor Substances 0.000 description 2
- 230000009850 completed effect Effects 0.000 description 2
- 229940125900 compound 59 Drugs 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
- 235000013601 eggs Nutrition 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 235000021323 fish oil Nutrition 0.000 description 2
- 239000007972 injectable composition Substances 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 210000003097 mucus Anatomy 0.000 description 2
- 150000002903 organophosphorus compounds Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000009372 pisciculture Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 230000000979 retarding effect Effects 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- 239000004546 suspension concentrate Substances 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- HZDZRGKULMGCJE-NCZFFCEISA-N (2e,6e)-1-methoxy-3,7,11-trimethyldodeca-2,6,10-triene Chemical compound COC\C=C(/C)CC\C=C(/C)CCC=C(C)C HZDZRGKULMGCJE-NCZFFCEISA-N 0.000 description 1
- BZJTUOGZUKFLQT-UHFFFAOYSA-N 1,3,5,7-tetramethylcyclooctane Chemical group CC1CC(C)CC(C)CC(C)C1 BZJTUOGZUKFLQT-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VLZLAARBPXSSPH-UHFFFAOYSA-N 1,4-dioctylpiperidine Chemical compound CCCCCCCCC1CCN(CCCCCCCC)CC1 VLZLAARBPXSSPH-UHFFFAOYSA-N 0.000 description 1
- QXOGPTXQGKQSJT-UHFFFAOYSA-N 1-amino-4-[4-(3,4-dimethylphenyl)sulfanylanilino]-9,10-dioxoanthracene-2-sulfonic acid Chemical compound Cc1ccc(Sc2ccc(Nc3cc(c(N)c4C(=O)c5ccccc5C(=O)c34)S(O)(=O)=O)cc2)cc1C QXOGPTXQGKQSJT-UHFFFAOYSA-N 0.000 description 1
- NJPQAIBZIHNJDO-UHFFFAOYSA-N 1-dodecylpyrrolidin-2-one Chemical compound CCCCCCCCCCCCN1CCCC1=O NJPQAIBZIHNJDO-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- FZNJWZDBSDVBAE-UHFFFAOYSA-N 2-(3,7-dimethyloctylsulfanyl)pyridine Chemical compound CC(C)CCCC(C)CCSC1=CC=CC=N1 FZNJWZDBSDVBAE-UHFFFAOYSA-N 0.000 description 1
- HMYUFOBJJSHXFK-UHFFFAOYSA-N 2-methyl-5-nonoxypyridine Chemical compound CCCCCCCCCOC1=CC=C(C)N=C1 HMYUFOBJJSHXFK-UHFFFAOYSA-N 0.000 description 1
- IMZXGVAUGRDJMQ-UHFFFAOYSA-N 3-(3,7-dimethyloctylsulfanyl)pyridine Chemical compound CC(C)CCCC(C)CCSC1=CC=CN=C1 IMZXGVAUGRDJMQ-UHFFFAOYSA-N 0.000 description 1
- FWUMGMDRJBFSOD-UHFFFAOYSA-N 4,8-dimethyl-1-pyridin-3-ylnonan-1-ol Chemical compound CC(C)CCCC(C)CCC(O)C1=CC=CN=C1 FWUMGMDRJBFSOD-UHFFFAOYSA-N 0.000 description 1
- DCNHHEKYZFLGIF-UHFFFAOYSA-N 4,8-dimethyl-1-pyridin-3-ylnonan-1-one Chemical compound CC(C)CCCC(C)CCC(=O)C1=CC=CN=C1 DCNHHEKYZFLGIF-UHFFFAOYSA-N 0.000 description 1
- IPYRAUOTBYUFIK-UHFFFAOYSA-N 5-(3,7-dimethyloctoxy)-1,3-benzodioxole Chemical compound CC(C)CCCC(C)CCOC1=CC=C2OCOC2=C1 IPYRAUOTBYUFIK-UHFFFAOYSA-N 0.000 description 1
- HJKHVUURJUFFRF-UHFFFAOYSA-N 5-(3,7-dimethyloctoxy)-2-methylpyridine Chemical compound CC(C)CCCC(C)CCOC1=CC=C(C)N=C1 HJKHVUURJUFFRF-UHFFFAOYSA-N 0.000 description 1
- XZWBLRMBDRWQKM-UHFFFAOYSA-N 5-(3,7-dimethyloctoxy)-2-methylpyrimidine Chemical compound CC(C)CCCC(C)CCOC1=CN=C(C)N=C1 XZWBLRMBDRWQKM-UHFFFAOYSA-N 0.000 description 1
- JKJBGRJNTIJAJQ-UHFFFAOYSA-N 5-[5-(2,2-dimethylcyclopropyl)-3-methylpentoxy]-2-methylpyridine Chemical compound C1C(C)(C)C1CCC(C)CCOC1=CC=C(C)N=C1 JKJBGRJNTIJAJQ-UHFFFAOYSA-N 0.000 description 1
- RZRRIGCRQHCDRS-UHFFFAOYSA-N 5-dodecoxy-2-methylpyridine Chemical compound CCCCCCCCCCCCOC1=CC=C(C)N=C1 RZRRIGCRQHCDRS-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000252087 Anguilla japonica Species 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241000239201 Argulidae Species 0.000 description 1
- 241000238421 Arthropoda Species 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 241001195214 Brachiella Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000276694 Carangidae Species 0.000 description 1
- 241000369098 Chondracanthidae Species 0.000 description 1
- 241000276616 Cichlidae Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000005946 Cypermethrin Substances 0.000 description 1
- 241000252210 Cyprinidae Species 0.000 description 1
- 241000252233 Cyprinus carpio Species 0.000 description 1
- 241000723298 Dicentrarchus labrax Species 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000618288 Ergasilidae Species 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 241001205608 Hatschekia Species 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 241000442132 Lactarius lactarius Species 0.000 description 1
- 241000696958 Lernaea Species 0.000 description 1
- 241001206069 Lernaeocera Species 0.000 description 1
- 241001593519 Liza affinis Species 0.000 description 1
- LVDRREOUMKACNJ-BKMJKUGQSA-N N-[(2R,3S)-2-(4-chlorophenyl)-1-(1,4-dimethyl-2-oxoquinolin-7-yl)-6-oxopiperidin-3-yl]-2-methylpropane-1-sulfonamide Chemical compound CC(C)CS(=O)(=O)N[C@H]1CCC(=O)N([C@@H]1c1ccc(Cl)cc1)c1ccc2c(C)cc(=O)n(C)c2c1 LVDRREOUMKACNJ-BKMJKUGQSA-N 0.000 description 1
- WXOMTJVVIMOXJL-BOBFKVMVSA-A O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)OS(=O)(=O)OC[C@H]1O[C@@H](O[C@]2(COS(=O)(=O)O[Al](O)O)O[C@H](OS(=O)(=O)O[Al](O)O)[C@@H](OS(=O)(=O)O[Al](O)O)[C@@H]2OS(=O)(=O)O[Al](O)O)[C@H](OS(=O)(=O)O[Al](O)O)[C@@H](OS(=O)(=O)O[Al](O)O)[C@@H]1OS(=O)(=O)O[Al](O)O Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)O.O[Al](O)OS(=O)(=O)OC[C@H]1O[C@@H](O[C@]2(COS(=O)(=O)O[Al](O)O)O[C@H](OS(=O)(=O)O[Al](O)O)[C@@H](OS(=O)(=O)O[Al](O)O)[C@@H]2OS(=O)(=O)O[Al](O)O)[C@H](OS(=O)(=O)O[Al](O)O)[C@@H](OS(=O)(=O)O[Al](O)O)[C@@H]1OS(=O)(=O)O[Al](O)O WXOMTJVVIMOXJL-BOBFKVMVSA-A 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 206010033799 Paralysis Diseases 0.000 description 1
- 241000101788 Pennella <fungus> Species 0.000 description 1
- 241001600434 Plectroglyphidodon lacrymatus Species 0.000 description 1
- 241000269907 Pleuronectes platessa Species 0.000 description 1
- 239000005927 Pyriproxyfen Substances 0.000 description 1
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
- 241000231739 Rutilus rutilus Species 0.000 description 1
- 241000258242 Siphonaptera Species 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 241000766285 Sphyriidae Species 0.000 description 1
- 241000269319 Squalius cephalus Species 0.000 description 1
- 241000886165 Symphodus Species 0.000 description 1
- 240000004460 Tanacetum coccineum Species 0.000 description 1
- 241000276707 Tilapia Species 0.000 description 1
- 229920001615 Tragacanth Polymers 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
- 230000003187 abdominal effect Effects 0.000 description 1
- 230000037374 absorbed through the skin Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000036528 appetite Effects 0.000 description 1
- 235000019789 appetite Nutrition 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000000305 astragalus gummifer gum Substances 0.000 description 1
- VNKBTWQZTQIWDV-UHFFFAOYSA-N azamethiphos Chemical compound C1=C(Cl)C=C2OC(=O)N(CSP(=O)(OC)OC)C2=N1 VNKBTWQZTQIWDV-UHFFFAOYSA-N 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- 235000012216 bentonite Nutrition 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
- 125000005605 benzo group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 230000002508 compound effect Effects 0.000 description 1
- 230000002844 continuous effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 210000002251 corpora allata Anatomy 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
- 230000007423 decrease Effects 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000001083 documented effect Effects 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical class CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 150000002058 ecdysones Chemical class 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- MXYHUYGRMOJHIQ-UHFFFAOYSA-N ethyl 9-(2,2-dichloro-3,3-dimethylcyclopropyl)-7-methylnona-2,4-dienoate Chemical compound CCOC(=O)C=CC=CCC(C)CCC1C(C)(C)C1(Cl)Cl MXYHUYGRMOJHIQ-UHFFFAOYSA-N 0.000 description 1
- NAWFMEHNGFMVSM-UHFFFAOYSA-N ethyl 9-(2,2-dimethylcyclopropyl)-7-methylnona-2,4-dienoate Chemical compound CCOC(=O)C=CC=CCC(C)CCC1CC1(C)C NAWFMEHNGFMVSM-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009313 farming Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000021050 feed intake Nutrition 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
- 238000001914 filtration Methods 0.000 description 1
- 208000010824 fish disease Diseases 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 210000004392 genitalia Anatomy 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 229940071676 hydroxypropylcellulose Drugs 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000201 insect hormone Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229930000024 juvenile hormones I Natural products 0.000 description 1
- 229930002340 juvenile hormones II Natural products 0.000 description 1
- 229930000772 juvenile hormones III Natural products 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
- 150000002576 ketones Chemical class 0.000 description 1
- 230000000974 larvacidal effect Effects 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- NOPCRSLRJIYLJH-UHFFFAOYSA-N methyl 9-(2,2-dichloro-3,3-dimethylcyclopropyl)-7-methylnona-2,4-dienoate Chemical compound COC(=O)C=CC=CCC(C)CCC1C(C)(C)C1(Cl)Cl NOPCRSLRJIYLJH-UHFFFAOYSA-N 0.000 description 1
- FNTGCXPLWNAYQT-UHFFFAOYSA-N methyl 9-(2,2-dimethylcyclopropyl)-7-methylnona-2,4-dienoate Chemical compound COC(=O)C=CC=CCC(C)CCC1CC1(C)C FNTGCXPLWNAYQT-UHFFFAOYSA-N 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000001537 neural effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000036281 parasite infection Effects 0.000 description 1
- 239000004466 pelleted feed Substances 0.000 description 1
- 229960000490 permethrin Drugs 0.000 description 1
- 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 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- NSVDOFGFOYFGEV-UHFFFAOYSA-N propan-2-yl 9-(2,2-dichloro-3,3-dimethylcyclopropyl)-7-methylnona-2,4-dienoate Chemical compound CC(C)OC(=O)C=CC=CCC(C)CCC1C(C)(C)C1(Cl)Cl NSVDOFGFOYFGEV-UHFFFAOYSA-N 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-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
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229940108410 resmethrin Drugs 0.000 description 1
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 150000005846 sugar alcohols Polymers 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
- FODHIQQNHOPUKH-UHFFFAOYSA-N tetrapropylene-benzenesulfonic acid Chemical compound CC1CC11C2=C3S(=O)(=O)OC(C)CC3=C3C(C)CC3=C2C1C FODHIQQNHOPUKH-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229960001005 tuberculin Drugs 0.000 description 1
- 210000003934 vacuole Anatomy 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000009736 wetting 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
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N49/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds containing the group, wherein m+n>=1, both X together may also mean —Y— or a direct carbon-to-carbon bond, and the carbon atoms marked with an asterisk are not part of any ring system other than that which may be formed by the atoms X, the carbon atoms in square brackets being part of any acyclic or cyclic structure, or the group, wherein A means a carbon atom or Y, n>=0, and not more than one of these carbon atoms being a member of the same ring system, e.g. juvenile insect hormones or mimics thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P15/00—Biocides for specific purposes not provided for in groups A01P1/00 - A01P13/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
- A61K31/231—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms having one or two double bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/255—Esters, e.g. nitroglycerine, selenocyanates of sulfoxy acids or sulfur analogues thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/336—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having three-membered rings, e.g. oxirane, fumagillin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Agronomy & Crop Science (AREA)
- Insects & Arthropods (AREA)
- Dentistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Farming Of Fish And Shellfish (AREA)
- Fodder In General (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DKPA199901054 | 1999-07-23 | ||
DKPA199901054 | 1999-07-23 | ||
PCT/IB2000/001002 WO2001007047A2 (en) | 1999-07-23 | 2000-07-20 | Control of crustacean infestation of aquatic animals |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2378409A1 true CA2378409A1 (en) | 2001-02-01 |
Family
ID=8100468
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002378409A Abandoned CA2378409A1 (en) | 1999-07-23 | 2000-07-20 | Control of crustacean infestation of aquatic animals |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1204413A2 (de) |
AU (1) | AU5837900A (de) |
CA (1) | CA2378409A1 (de) |
NO (1) | NO20020360L (de) |
WO (1) | WO2001007047A2 (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU5838000A (en) * | 1999-07-23 | 2001-02-13 | Bioparken As | Novel juvenile hormone analogues and their use as antifouling agents |
GB2371053A (en) * | 2001-01-13 | 2002-07-17 | David R Harper | Microbiological control of sea lice |
GB0605900D0 (en) * | 2006-03-23 | 2006-05-03 | Lipigen As | Modulators of nuclear receptors |
AR101474A1 (es) * | 2014-08-12 | 2016-12-21 | Inst De Rech En Semiochimie Et Ethologie Appliquee | Composición semioquímica inhibidora de la fijación de copepoditos de piojos de mar |
Family Cites Families (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3970758A (en) * | 1969-04-10 | 1976-07-20 | Stauffer Chemical Company | Certain geranyl phenyl ethers and their epoxides and their use in controlling insects |
US4001339A (en) * | 1969-04-30 | 1977-01-04 | Hoffmann-La Roche Inc. | Phenyl derivatives |
CH568708A5 (de) * | 1969-04-30 | 1975-11-14 | Hoffmann La Roche | |
CH526258A (de) * | 1970-03-25 | 1972-08-15 | Hoffmann La Roche | Schädlingsbekämpfungsmittel |
US3709914A (en) * | 1970-07-30 | 1973-01-09 | Zoecon Corp | Methylenedioxyphenyl compounds |
US3868406A (en) * | 1970-08-03 | 1975-02-25 | Zoecon Corp | P-alkenyloxybenzoic acid esters useful for the control of insects |
US3832385A (en) * | 1970-08-03 | 1974-08-27 | Zoecon Corp | Substituted 4-alkylthiobenzoic acid esters |
DE2144936B2 (de) * | 1970-10-20 | 1974-02-21 | Ciba-Geigy Ag, Basel (Schweiz) | Terpen-aryläther, Verfahren zu deren Herstellung und diese enthaltende Schädlingsbekämpfungsmittel |
US3810989A (en) * | 1970-11-16 | 1974-05-14 | Stauffer Chemical Co | Control of confused flour beetles using geranyl phenyl ethers |
AU3666671A (en) * | 1970-12-22 | 1973-06-14 | Zoecon Corp | Compounds and syntheses |
CA1005821A (en) * | 1971-02-01 | 1977-02-22 | Clive A. Henrick | 2,4-diolefinic compounds and the control of insects |
CA919685A (en) * | 1971-03-15 | 1973-01-23 | The Dow Chemical Company | Ethers having juvenile hormone activity |
GB1339764A (en) * | 1971-03-29 | 1973-12-05 | Ici Ltd | Pyridine derivatives |
GB1420533A (en) * | 1971-09-27 | 1976-01-07 | Cheminova As | Pyridine derivatives having juvenile hormone activity |
DE2210230A1 (de) * | 1972-03-03 | 1973-09-06 | Kolmar Laboratories | Verwendung bestimmter thioaether als antimikrobielle und zytostatische mittel |
JPS4892529A (de) * | 1972-03-11 | 1973-11-30 | ||
JPS49421A (de) * | 1972-04-21 | 1974-01-05 | ||
AU5620873A (en) * | 1972-06-16 | 1974-11-28 | F. Hoffmann-Laroche & Co. Aktiengesellschaft | Polyene derivatives |
DE2947648A1 (de) * | 1979-11-27 | 1981-08-06 | C.F. Spiess & Sohn GmbH & Co, 6719 Kleinkarlbach | Verwendung tertiaerer heterocyclischer amine als potenzierungsmittel fuer insektizide |
JPS59199673A (ja) * | 1983-04-25 | 1984-11-12 | Sumitomo Chem Co Ltd | 含窒素複素環化合物、その製造法およびそれを有効成分とする有害生物防除剤 |
JPS6036403A (ja) * | 1983-08-08 | 1985-02-25 | Sumitomo Chem Co Ltd | 混合殺虫組成物 |
JPS6038303A (ja) * | 1983-08-11 | 1985-02-27 | Sumitomo Chem Co Ltd | ハエ類の駆除方法 |
JPS60215671A (ja) * | 1984-04-10 | 1985-10-29 | Sumitomo Chem Co Ltd | 含窒素複素環化合物、その製造法およびそれを有効成分とする有害生物防除剤 |
DE3522905A1 (de) * | 1985-06-27 | 1987-01-08 | Basf Ag | O-substituierte 3-oxypyridiniumsalze, verfahren zu ihrer herstellung und ihre verwendung als fungizide fuer den pflanzenschutz |
JPS6287528A (ja) * | 1985-10-15 | 1987-04-22 | Nitto Electric Ind Co Ltd | N−アルキルモルホリン含有外皮投与用組成物 |
DE3614706A1 (de) * | 1986-04-30 | 1987-11-05 | Basf Ag | Mittel zur bekaempfung von mikroben |
JP2522941B2 (ja) * | 1987-04-28 | 1996-08-07 | 住友化学工業株式会社 | 防蟻組成物 |
JP2707617B2 (ja) * | 1987-08-11 | 1998-02-04 | 住友化学工業株式会社 | 釣餌用ハチミツガ幼虫の調製法 |
JPH01168602A (ja) * | 1987-12-24 | 1989-07-04 | Nichibai Boeki Kk | 衛生害虫忌避剤 |
DE3825172A1 (de) * | 1988-07-23 | 1990-01-25 | Bayer Ag, 5090 Leverkusen | Mittel zur bekaempfung von floehen |
GB9105694D0 (en) * | 1991-03-18 | 1991-05-01 | Hand Peter Animal Health | Control of sea lice in salmon |
AU660205B2 (en) * | 1991-12-23 | 1995-06-15 | Virbac, Inc | Systemic control of parasites |
DE4232561A1 (de) * | 1992-09-29 | 1994-03-31 | Bayer Ag | Bekämpfung von Fischparasiten |
US5707639A (en) * | 1993-10-18 | 1998-01-13 | Sumitomo Chemical Company, Limited | Solid insect growth regulating compositions |
IL112721A0 (en) * | 1994-03-10 | 1995-05-26 | Zeneca Ltd | Azole derivatives |
GB9418328D0 (en) * | 1994-09-12 | 1994-11-02 | Grampian Pharm Ltd | Control of sea lice in seawater fish |
NO179816C (no) * | 1995-06-13 | 1996-12-27 | Nutreco Aquaculture Res Centre | Middel for bekjempelse av parasitter hos oppdrettsfisk |
US5902808A (en) * | 1995-09-29 | 1999-05-11 | Buckman Laboratories International Inc. | Methods and compositions for controlling biofouling using N-alkyl heterocyclic compounds |
PT874549E (pt) * | 1995-12-11 | 2002-05-31 | Novartis Ag | Metodo de controlo de parasitas do peixe |
-
2000
- 2000-07-20 WO PCT/IB2000/001002 patent/WO2001007047A2/en not_active Application Discontinuation
- 2000-07-20 AU AU58379/00A patent/AU5837900A/en not_active Abandoned
- 2000-07-20 EP EP00944146A patent/EP1204413A2/de not_active Withdrawn
- 2000-07-20 CA CA002378409A patent/CA2378409A1/en not_active Abandoned
-
2002
- 2002-01-23 NO NO20020360A patent/NO20020360L/no unknown
Also Published As
Publication number | Publication date |
---|---|
WO2001007047A2 (en) | 2001-02-01 |
WO2001007047A3 (en) | 2001-12-20 |
NO20020360L (no) | 2002-03-14 |
AU5837900A (en) | 2001-02-13 |
EP1204413A2 (de) | 2002-05-15 |
NO20020360D0 (no) | 2002-01-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5728719A (en) | Systemic control of parasites | |
EP1119256B1 (de) | Orale kombination von lufenuron und nitenpyram gegen flöhe | |
EP0255803A1 (de) | Verfahren zur Verhinderung des Wiederbefalls von Hunden und Katzen mit Flöhen | |
WO2012001668A1 (en) | Anti-sea lice compositions and their use | |
JP2854097B2 (ja) | 海ジラミの抑制方法 | |
NZ302661A (en) | Composition for controlling parasites comprising n phenyl-n'-benzoylurea derivatives | |
JP6267188B2 (ja) | ルフェヌロンによる魚類個体群の処理 | |
AU764007B2 (en) | Injectable preparation for controlling fish live comprising benzoyl urea derivatives | |
EP1306084B1 (de) | Zusammensetzungen zur Bekämpfung von parasitischen Befallen in Fischen | |
JP4530307B2 (ja) | 魚類寄生虫の治療剤、その使用方法および用途 | |
KR100236586B1 (ko) | 가축에서 벼룩을 방제하기 위한 1-(n-(할로-3-피리딜메틸))-n-메틸아미노-1-알킬아미노-2-니트로에틸렌 유도체 | |
JP3170077B2 (ja) | 寄生生物の全身的駆除 | |
US5416102A (en) | Method of preventing the reinfestation of dogs and cats by fleas | |
CA2378409A1 (en) | Control of crustacean infestation of aquatic animals | |
MXPA02005245A (es) | Combinacion de un derviado de n-fenil-n'benzoilurea y compuestos de nectina para el control de parasitos. | |
EP0917822B1 (de) | Verfahren zur Bekämpfung von Tier-Ektoparasiten | |
MX2012012196A (es) | Composiciones y metodos para el control de las moscas de arena y otros insectos que succionan la sangre. | |
CN107920531B (zh) | 用于对抗鱼类寄生虫的试剂 | |
CA2267978A1 (en) | Method for the prevention of the reinfestation of warm-blooded animals by ectoparasites | |
MXPA97006416A (en) | Composition to control parasi |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Discontinued | ||
FZDE | Discontinued |
Effective date: 20050720 |