RU2013133704A - Комбинации эктопаразитицидных активных соединений - Google Patents
Комбинации эктопаразитицидных активных соединений Download PDFInfo
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- RU2013133704A RU2013133704A RU2013133704/13A RU2013133704A RU2013133704A RU 2013133704 A RU2013133704 A RU 2013133704A RU 2013133704/13 A RU2013133704/13 A RU 2013133704/13A RU 2013133704 A RU2013133704 A RU 2013133704A RU 2013133704 A RU2013133704 A RU 2013133704A
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- Prior art keywords
- alkyl
- haloalkyl
- group
- alkoxy
- pyrazol
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- 150000001875 compounds Chemical class 0.000 title claims abstract 10
- 230000001984 ectoparasiticidal effect Effects 0.000 title 1
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract 19
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 18
- 125000000217 alkyl group Chemical group 0.000 claims abstract 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 12
- 229910052736 halogen Inorganic materials 0.000 claims abstract 11
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract 7
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract 7
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 6
- 125000004438 haloalkoxy group Chemical group 0.000 claims abstract 6
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 claims abstract 6
- 125000005843 halogen group Chemical group 0.000 claims abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract 5
- 125000001424 substituent group Chemical group 0.000 claims abstract 5
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims abstract 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract 4
- 125000003277 amino group Chemical group 0.000 claims abstract 4
- 125000003302 alkenyloxy group Chemical group 0.000 claims abstract 3
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims abstract 3
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims abstract 3
- 125000003282 alkyl amino group Chemical group 0.000 claims abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract 3
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims abstract 3
- 125000004665 trialkylsilyl group Chemical group 0.000 claims abstract 3
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 claims abstract 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
- 125000004122 cyclic group Chemical group 0.000 claims abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims abstract 2
- 125000005432 dialkylcarboxamide group Chemical group 0.000 claims abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 2
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 2
- 239000001301 oxygen Substances 0.000 claims abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract 2
- -1 benzyloxyalkyloxy Chemical group 0.000 claims 11
- 150000002367 halogens Chemical group 0.000 claims 10
- 239000000556 agonist Substances 0.000 claims 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 6
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 6
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 6
- 239000003112 inhibitor Substances 0.000 claims 6
- 241001465754 Metazoa Species 0.000 claims 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 4
- 244000078703 ectoparasite Species 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 claims 3
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 claims 3
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 3
- 230000027756 respiratory electron transport chain Effects 0.000 claims 3
- VOKAJVSKGOCKRU-UHFFFAOYSA-N 4-(3,5-dichloro-4-methoxyphenyl)-2-(3-ethoxypyrazin-2-yl)-5-(trifluoromethyl)pyrazol-3-amine Chemical compound CCOC1=NC=CN=C1N1C(N)=C(C=2C=C(Cl)C(OC)=C(Cl)C=2)C(C(F)(F)F)=N1 VOKAJVSKGOCKRU-UHFFFAOYSA-N 0.000 claims 2
- 229920002101 Chitin Polymers 0.000 claims 2
- 108010009685 Cholinergic Receptors Proteins 0.000 claims 2
- 108010052164 Sodium Channels Proteins 0.000 claims 2
- 102000018674 Sodium Channels Human genes 0.000 claims 2
- 102000034337 acetylcholine receptors Human genes 0.000 claims 2
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 claims 2
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 2
- 230000003281 allosteric effect Effects 0.000 claims 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 2
- 230000015572 biosynthetic process Effects 0.000 claims 2
- 150000003857 carboxamides Chemical class 0.000 claims 2
- 239000003467 chloride channel stimulating agent Substances 0.000 claims 2
- 239000000544 cholinesterase inhibitor Substances 0.000 claims 2
- 230000001419 dependent effect Effects 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 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 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 230000010627 oxidative phosphorylation Effects 0.000 claims 2
- 239000000018 receptor agonist Substances 0.000 claims 2
- 229940044601 receptor agonist Drugs 0.000 claims 2
- 239000003195 sodium channel blocking agent Substances 0.000 claims 2
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 claims 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 claims 1
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 claims 1
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 claims 1
- SIERAXDNRKTKLY-UHFFFAOYSA-N 2-(3-ethoxypyrazin-2-yl)-5-(trifluoromethyl)-4-[7-(trifluoromethyl)-1,3-benzodioxol-5-yl]pyrazol-3-amine Chemical compound CCOC1=NC=CN=C1N1C(N)=C(C=2C=C(C=3OCOC=3C=2)C(F)(F)F)C(C(F)(F)F)=N1 SIERAXDNRKTKLY-UHFFFAOYSA-N 0.000 claims 1
- WCVSHZYZHUZQOF-UHFFFAOYSA-N 2-(3-methoxypyrazin-2-yl)-5-(trifluoromethyl)-4-[7-(trifluoromethyl)-1,3-benzodioxol-5-yl]pyrazol-3-amine Chemical compound COC1=NC=CN=C1N1C(N)=C(C=2C=C(C=3OCOC=3C=2)C(F)(F)F)C(C(F)(F)F)=N1 WCVSHZYZHUZQOF-UHFFFAOYSA-N 0.000 claims 1
- FXJRDUKXWHFPND-NSHDSACASA-N 2-[(1s)-1-(2,3-dimethylphenyl)ethyl]-1h-imidazole Chemical compound C1([C@@H](C)C=2C(=C(C)C=CC=2)C)=NC=CN1 FXJRDUKXWHFPND-NSHDSACASA-N 0.000 claims 1
- FYELSNVLZVIGTI-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-5-ethylpyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1CC)CC(=O)N1CC2=C(CC1)NN=N2 FYELSNVLZVIGTI-UHFFFAOYSA-N 0.000 claims 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 claims 1
- SNLURJJQQAHQQH-UHFFFAOYSA-N 4-(7-bromo-1,3-benzodioxol-5-yl)-2-(3-ethoxypyrazin-2-yl)-5-(trifluoromethyl)pyrazol-3-amine Chemical compound CCOC1=NC=CN=C1N1C(N)=C(C=2C=C(Br)C=3OCOC=3C=2)C(C(F)(F)F)=N1 SNLURJJQQAHQQH-UHFFFAOYSA-N 0.000 claims 1
- IUQGWFGDVKNQGP-UHFFFAOYSA-N 4-(7-bromo-1,3-benzodioxol-5-yl)-2-(3-ethoxypyrazin-2-yl)-5-ethylpyrazol-3-amine Chemical compound CCOC1=NC=CN=C1N1C(N)=C(C=2C=C(Br)C=3OCOC=3C=2)C(CC)=N1 IUQGWFGDVKNQGP-UHFFFAOYSA-N 0.000 claims 1
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- AZRFANQWLXXYFD-UHFFFAOYSA-N 4-(7-bromo-1,3-benzodioxol-5-yl)-5-ethyl-2-(3-methoxypyrazin-2-yl)pyrazol-3-amine Chemical compound NC1=C(C=2C=C(Br)C=3OCOC=3C=2)C(CC)=NN1C1=NC=CN=C1OC AZRFANQWLXXYFD-UHFFFAOYSA-N 0.000 claims 1
- DECNEEFTPNHYJH-UHFFFAOYSA-N 4-(7-chloro-1,3-benzodioxol-5-yl)-2-(3-ethoxypyrazin-2-yl)-5-(trifluoromethyl)pyrazol-3-amine Chemical compound CCOC1=NC=CN=C1N1C(N)=C(C=2C=C(Cl)C=3OCOC=3C=2)C(C(F)(F)F)=N1 DECNEEFTPNHYJH-UHFFFAOYSA-N 0.000 claims 1
- IPPUSMIYYOLNLB-UHFFFAOYSA-N 4-(7-chloro-1,3-benzodioxol-5-yl)-2-(3-ethoxypyrazin-2-yl)-5-ethylpyrazol-3-amine Chemical compound CCOC1=NC=CN=C1N1C(N)=C(C=2C=C(Cl)C=3OCOC=3C=2)C(CC)=N1 IPPUSMIYYOLNLB-UHFFFAOYSA-N 0.000 claims 1
- AUOKOFDRRYMXSD-UHFFFAOYSA-N 4-(7-chloro-1,3-benzodioxol-5-yl)-2-(3-methoxypyrazin-2-yl)-5-(trifluoromethyl)pyrazol-3-amine Chemical compound COC1=NC=CN=C1N1C(N)=C(C=2C=C(Cl)C=3OCOC=3C=2)C(C(F)(F)F)=N1 AUOKOFDRRYMXSD-UHFFFAOYSA-N 0.000 claims 1
- AJYXNACWDGAEGG-UHFFFAOYSA-N 4-(7-chloro-1,3-benzodioxol-5-yl)-2-(3-methoxypyrazin-2-yl)-5-methylpyrazol-3-amine Chemical compound COC1=NC=CN=C1N1C(N)=C(C=2C=C(Cl)C=3OCOC=3C=2)C(C)=N1 AJYXNACWDGAEGG-UHFFFAOYSA-N 0.000 claims 1
- UITZXRUBVLCZLS-UHFFFAOYSA-N 4-(7-chloro-1,3-benzodioxol-5-yl)-2-(3-methoxypyrazin-2-yl)-5-propan-2-ylpyrazol-3-amine Chemical compound COC1=NC=CN=C1N1C(N)=C(C=2C=C(Cl)C=3OCOC=3C=2)C(C(C)C)=N1 UITZXRUBVLCZLS-UHFFFAOYSA-N 0.000 claims 1
- GVHJKXWYLJSDBY-UHFFFAOYSA-N 4-(7-chloro-1,3-benzodioxol-5-yl)-5-cyclopropyl-2-(3-methoxypyrazin-2-yl)pyrazol-3-amine Chemical compound COC1=NC=CN=C1N1C(N)=C(C=2C=C(Cl)C=3OCOC=3C=2)C(C2CC2)=N1 GVHJKXWYLJSDBY-UHFFFAOYSA-N 0.000 claims 1
- VTXJDRAVWPFFFK-UHFFFAOYSA-N 4-(7-chloro-1,3-benzodioxol-5-yl)-5-ethyl-2-(3-methoxypyrazin-2-yl)pyrazol-3-amine Chemical compound NC1=C(C=2C=C(Cl)C=3OCOC=3C=2)C(CC)=NN1C1=NC=CN=C1OC VTXJDRAVWPFFFK-UHFFFAOYSA-N 0.000 claims 1
- PUAAPBBXXVGAJX-UHFFFAOYSA-N 4-[3,5-dichloro-4-(dimethylamino)phenyl]-2-(3-ethoxypyrazin-2-yl)-5-(trifluoromethyl)pyrazol-3-amine Chemical compound CCOC1=NC=CN=C1N1C(N)=C(C=2C=C(Cl)C(N(C)C)=C(Cl)C=2)C(C(F)(F)F)=N1 PUAAPBBXXVGAJX-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 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 claims 1
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- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
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- QLFZZSKTJWDQOS-YDBLARSUSA-N doramectin 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](C3CCCCC3)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 QLFZZSKTJWDQOS-YDBLARSUSA-N 0.000 claims 1
- 229960003997 doramectin Drugs 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- UPEZCKBFRMILAV-JMZLNJERSA-N ecdysone Chemical compound C1[C@@H](O)[C@@H](O)C[C@]2(C)[C@@H](CC[C@@]3([C@@H]([C@@H]([C@H](O)CCC(C)(C)O)C)CC[C@]33O)C)C3=CC(=O)[C@@H]21 UPEZCKBFRMILAV-JMZLNJERSA-N 0.000 claims 1
- 239000012636 effector Substances 0.000 claims 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 claims 1
- WPNHOHPRXXCPRA-TVXIRPTOSA-N eprinomectin Chemical compound O1[C@@H](C)[C@@H](NC(C)=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 WPNHOHPRXXCPRA-TVXIRPTOSA-N 0.000 claims 1
- 229960002346 eprinomectin Drugs 0.000 claims 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 claims 1
- 229950005085 etofenprox Drugs 0.000 claims 1
- 229940013764 fipronil Drugs 0.000 claims 1
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 claims 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 claims 1
- 239000003966 growth inhibitor Substances 0.000 claims 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229940056881 imidacloprid Drugs 0.000 claims 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims 1
- 229960002418 ivermectin Drugs 0.000 claims 1
- 229930014550 juvenile hormone Natural products 0.000 claims 1
- 239000002949 juvenile hormone Substances 0.000 claims 1
- 150000003633 juvenile hormone derivatives Chemical class 0.000 claims 1
- 229930191400 juvenile hormones Natural products 0.000 claims 1
- 102000035110 latrophilin Human genes 0.000 claims 1
- 108091005543 latrophilin Proteins 0.000 claims 1
- 229960002809 lindane Drugs 0.000 claims 1
- 230000010534 mechanism of action Effects 0.000 claims 1
- CKVMAPHTVCTEMM-ALPQRHTBSA-N milbemycin oxime 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(=N/O)/[C@H]3OC\2)O)C[C@H]4C1.C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\1)O)C[C@H]4C2 CKVMAPHTVCTEMM-ALPQRHTBSA-N 0.000 claims 1
- 229940099245 milbemycin oxime Drugs 0.000 claims 1
- YZBLFMPOMVTDJY-CBYMMZEQSA-N moxidectin Chemical compound O1[C@H](C(\C)=C\C(C)C)[C@@H](C)C(=N/OC)\C[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 YZBLFMPOMVTDJY-CBYMMZEQSA-N 0.000 claims 1
- 229960004816 moxidectin Drugs 0.000 claims 1
- 229940079888 nitenpyram Drugs 0.000 claims 1
- 229960000490 permethrin Drugs 0.000 claims 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 claims 1
- 229960005235 piperonyl butoxide Drugs 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims 1
- 102000042094 ryanodine receptor (TC 1.A.3.1) family Human genes 0.000 claims 1
- 108091052345 ryanodine receptor (TC 1.A.3.1) family Proteins 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- AFJYYKSVHJGXSN-KAJWKRCWSA-N selamectin Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1C(/C)=C/C[C@@H](O[C@]2(O[C@@H]([C@@H](C)CC2)C2CCCCC2)C2)C[C@@H]2OC(=O)[C@@H]([C@]23O)C=C(C)C(=N\O)/[C@H]3OC\C2=C/C=C/[C@@H]1C AFJYYKSVHJGXSN-KAJWKRCWSA-N 0.000 claims 1
- 229960002245 selamectin Drugs 0.000 claims 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 claims 1
- 229940014213 spinosad Drugs 0.000 claims 1
- 229960005199 tetramethrin Drugs 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 239000000664 voltage gated sodium channel blocking agent Substances 0.000 claims 1
- 125000005392 carboxamide group Chemical class NC(=O)* 0.000 abstract 1
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 abstract 1
- 0 Cc1c(*)c(*)n[n]1-c1nc(C)c(*)nc1* Chemical compound Cc1c(*)c(*)n[n]1-c1nc(C)c(*)nc1* 0.000 description 1
Classifications
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- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Tropical Medicine & Parasitology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102010063691A DE102010063691A1 (de) | 2010-12-21 | 2010-12-21 | Ektoparasitizide Wirkstoffkombinationen |
| DE102010063691.6 | 2010-12-21 | ||
| PCT/EP2011/073280 WO2012084852A2 (de) | 2010-12-21 | 2011-12-19 | Ektoparasitizide wirkstoffkombinationen |
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| RU2013133704A true RU2013133704A (ru) | 2015-01-27 |
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| RU2013133704/13A RU2013133704A (ru) | 2010-12-21 | 2011-12-19 | Комбинации эктопаразитицидных активных соединений |
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| EC (1) | ECSP13012706A (enExample) |
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| RU2641916C2 (ru) * | 2012-10-02 | 2018-01-23 | Байер Кропсайенс Аг | Гетероциклические соединения в качестве пестицидов |
| CN111246743B (zh) * | 2017-10-18 | 2022-10-11 | 拜耳公司 | 具有杀虫/杀螨性质的活性化合物结合物 |
| CN110305115A (zh) * | 2019-08-19 | 2019-10-08 | 南通大学 | 一种含1-(6-氯吡嗪-2-基)-3-甲氧基吡唑单元的吡唑肟衍生物的制备和应用 |
| KR20230043904A (ko) | 2020-07-24 | 2023-03-31 | 엘랑코 유에스 인코포레이티드 | 이속사졸린 화합물 및 이의 중간체의 제조 공정 |
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| WO2024121263A1 (en) | 2022-12-09 | 2024-06-13 | Syngenta Crop Protection Ag | Insecticidal compound based on pyrazole derivatives |
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| NO176766C (no) | 1989-02-07 | 1995-05-24 | Meiji Seika Kaisha | Fremgangsmåte for fremstilling av en forbindelse med anthelmintaktivitet |
| EP0539588A1 (en) | 1990-07-05 | 1993-05-05 | Nippon Soda Co., Ltd. | Amine derivative |
| CN1234183A (zh) * | 1999-04-23 | 1999-11-10 | 西北农业大学无公害农药研究服务中心 | 一种烟碱复配乳油杀虫剂及其制造方法 |
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| UA79404C2 (en) | 2003-10-02 | 2007-06-11 | Basf Ag | 2-cyanobenzenesulfonamide for controlling pests |
| RS52173B (sr) | 2004-02-18 | 2012-08-31 | Ishihara Sangyo Kaisha Ltd. | Antranilamid jedinjenja i postupak njihove proizvodnje i pesticida koji ih sadrže |
| CN1930136B (zh) | 2004-03-05 | 2012-02-08 | 日产化学工业株式会社 | 异*唑啉取代苯甲酰胺化合物及有害生物防除剂 |
| RU2394819C2 (ru) | 2004-10-20 | 2010-07-20 | Кумиай Кемикал Индастри Ко., Лтд. | Инсектицид, акарицид и нематоцид, содержащие в качестве активного компонента производное 3-триазолилфенилсульфида |
| DE102005008021A1 (de) | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Spiroketal-substituierte cyclische Ketoenole |
| JP5007788B2 (ja) | 2005-05-16 | 2012-08-22 | 日産化学工業株式会社 | ジヒドロアゾール置換ベンズアミド化合物及び有害生物防除剤 |
| US7491738B2 (en) | 2005-06-01 | 2009-02-17 | Meiji Seika Kaisha, Ltd. | Pest control agents |
| TWI388282B (zh) | 2005-06-01 | 2013-03-11 | Meiji Seika Pharma Co Ltd | 害蟲控制劑 |
| WO2007027842A1 (en) | 2005-08-31 | 2007-03-08 | Bayer Healthcare Llc | Anilinopyrazole derivatives useful for the treatment of diabetes |
| DK1937664T3 (da) | 2005-10-14 | 2011-07-18 | Sumitomo Chemical Co | Hydrazidforbindelse og pesticid anvendelse af den samme |
| WO2007048733A1 (de) | 2005-10-28 | 2007-05-03 | Basf Se | Verwendung von 5-amino-pyrazolen zur bekämpfung pflanzenpathogener schadpilze, neue 5-amino-pyrazole, verfahren zu ihrer herstellung und sie enthaltende mittel |
| TW200803740A (en) | 2005-12-16 | 2008-01-16 | Du Pont | 5-aryl isoxazolines for controlling invertebrate pests |
| TW201309635A (zh) | 2006-02-10 | 2013-03-01 | Dow Agrosciences Llc | 殺蟲性之ｎ-取代（６-鹵烷基吡啶-３-基）烷基磺醯亞胺（二） |
| DE102006015468A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| DE102006015467A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| DE102006015470A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| WO2007125984A1 (ja) | 2006-04-28 | 2007-11-08 | Nihon Nohyaku Co., Ltd. | イソキサゾリン誘導体及び有害生物防除剤並びにその使用方法 |
| TWI381811B (zh) | 2006-06-23 | 2013-01-11 | Dow Agrosciences Llc | 用以防治可抵抗一般殺蟲劑之昆蟲的方法 |
| JP5164510B2 (ja) | 2006-10-06 | 2013-03-21 | 日本曹達株式会社 | 含窒素複素環化合物および有害生物防除剤 |
| JP5164525B2 (ja) | 2006-11-01 | 2013-03-21 | 日本曹達株式会社 | 含窒素へテロ環化合物および有害生物防除剤 |
| DE102006057036A1 (de) | 2006-12-04 | 2008-06-05 | Bayer Cropscience Ag | Biphenylsubstituierte spirocyclische Ketoenole |
| EA200901143A1 (ru) | 2007-03-01 | 2010-04-30 | Басф Се | Пестицидные активные смеси, включающие аминотиазолиновые соединения |
| JP2010116389A (ja) | 2008-10-17 | 2010-05-27 | Bayer Cropscience Ag | 殺虫性アリールピロリジン類 |
| JP2008266230A (ja) | 2007-04-23 | 2008-11-06 | Bayer Cropscience Ag | 殺虫性アリールピロリジン類 |
| TWI430995B (zh) | 2007-06-26 | 2014-03-21 | Du Pont | 萘異唑啉無脊椎有害動物控制劑 |
| EP2182945B1 (en) | 2007-06-27 | 2015-08-05 | E. I. du Pont de Nemours and Company | Animal pest control method |
| TWI556741B (zh) | 2007-08-17 | 2016-11-11 | 英特威特國際股份有限公司 | 異唑啉組成物及其作為抗寄生蟲藥上的應用 |
| US8648091B2 (en) | 2007-11-09 | 2014-02-11 | Novartis Ag | Dihydroquinolinones as ectoparasiticides |
| EP2230230A4 (en) | 2007-12-07 | 2011-03-16 | Nissan Chemical Ind Ltd | SUBSTITUTED DIHYDROAZOL COMPOUND AND PESTICIDES |
| CN101939295B (zh) | 2008-02-07 | 2013-04-24 | 拜尔农作物科学股份公司 | 杀虫的芳基吡咯啉 |
| JP2009286773A (ja) | 2008-03-14 | 2009-12-10 | Bayer Cropscience Ag | 殺虫性縮環式アリール類 |
| WO2010020522A1 (en) | 2008-08-22 | 2010-02-25 | Syngenta Participations Ag | Insecticidal compounds |
| EA020661B1 (ru) * | 2008-09-24 | 2014-12-30 | Басф Се | Пиразольные соединения для борьбы с беспозвоночными вредителями |
| JP5747440B2 (ja) | 2009-02-06 | 2015-07-15 | 住友化学株式会社 | ヒドラジド化合物及びその有害生物防除用途 |
| EP2248422A1 (en) | 2009-05-08 | 2010-11-10 | Novartis AG | Ectoparasiticidal compositions |
| EP2266973A1 (de) * | 2009-05-29 | 2010-12-29 | Bayer CropScience AG | Pyrazinylpyrazole |
-
2010
- 2010-12-21 DE DE102010063691A patent/DE102010063691A1/de not_active Withdrawn
-
2011
- 2011-12-19 MX MX2013006866A patent/MX2013006866A/es unknown
- 2011-12-19 KR KR1020137018518A patent/KR20140034743A/ko not_active Ceased
- 2011-12-19 EP EP11807897.1A patent/EP2654425A2/de not_active Withdrawn
- 2011-12-19 NZ NZ612221A patent/NZ612221A/en not_active IP Right Cessation
- 2011-12-19 AU AU2011347551A patent/AU2011347551B2/en not_active Ceased
- 2011-12-19 MY MYPI2013002297A patent/MY164916A/en unknown
- 2011-12-19 CA CA2822080A patent/CA2822080A1/en not_active Abandoned
- 2011-12-19 BR BR112013015952-9A patent/BR112013015952A2/pt not_active Application Discontinuation
- 2011-12-19 CN CN201180068136.0A patent/CN103442569B/zh not_active Expired - Fee Related
- 2011-12-19 RU RU2013133704/13A patent/RU2013133704A/ru not_active Application Discontinuation
- 2011-12-19 US US13/995,958 patent/US9066945B2/en not_active Expired - Fee Related
- 2011-12-19 JP JP2013545280A patent/JP6018580B2/ja not_active Expired - Fee Related
- 2011-12-19 WO PCT/EP2011/073280 patent/WO2012084852A2/de not_active Ceased
- 2011-12-19 PH PH1/2013/501317A patent/PH12013501317A1/en unknown
- 2011-12-20 TW TW100147255A patent/TWI593685B/zh not_active IP Right Cessation
- 2011-12-20 UY UY0001033822A patent/UY33822A/es not_active Application Discontinuation
- 2011-12-21 AR ARP110104847A patent/AR084509A1/es unknown
-
2013
- 2013-06-17 CO CO13144324A patent/CO6751235A2/es unknown
- 2013-06-19 DO DO2013000143A patent/DOP2013000143A/es unknown
- 2013-06-19 CL CL2013001794A patent/CL2013001794A1/es unknown
- 2013-06-19 CR CR20130303A patent/CR20130303A/es unknown
- 2013-06-19 GT GT201300157A patent/GT201300157A/es unknown
- 2013-06-20 EC ECSP13012706 patent/ECSP13012706A/es unknown
- 2013-06-20 NI NI201300056A patent/NI201300056A/es unknown
- 2013-06-20 CU CU2013000081A patent/CU20130081A7/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DOP2013000143A (es) | 2013-08-15 |
| CU20130081A7 (es) | 2013-09-27 |
| US20140179623A1 (en) | 2014-06-26 |
| MX2013006866A (es) | 2013-07-29 |
| AU2011347551B2 (en) | 2016-03-17 |
| US9066945B2 (en) | 2015-06-30 |
| TW201305141A (zh) | 2013-02-01 |
| JP2014505677A (ja) | 2014-03-06 |
| NZ612221A (en) | 2016-01-29 |
| DE102010063691A1 (de) | 2012-06-21 |
| UY33822A (es) | 2012-07-31 |
| GT201300157A (es) | 2014-09-02 |
| CN103442569B (zh) | 2017-04-05 |
| NI201300056A (es) | 2014-06-06 |
| CR20130303A (es) | 2013-07-18 |
| WO2012084852A2 (de) | 2012-06-28 |
| JP6018580B2 (ja) | 2016-11-02 |
| CA2822080A1 (en) | 2012-06-28 |
| TWI593685B (zh) | 2017-08-01 |
| BR112013015952A2 (pt) | 2018-07-10 |
| CN103442569A (zh) | 2013-12-11 |
| CL2013001794A1 (es) | 2014-04-04 |
| CO6751235A2 (es) | 2013-09-16 |
| AU2011347551A1 (en) | 2013-07-11 |
| ECSP13012706A (es) | 2013-08-30 |
| AR084509A1 (es) | 2013-05-22 |
| EP2654425A2 (de) | 2013-10-30 |
| KR20140034743A (ko) | 2014-03-20 |
| WO2012084852A3 (de) | 2012-11-15 |
| MY164916A (en) | 2018-02-15 |
| PH12013501317A1 (en) | 2019-09-02 |
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Legal Events
| Date | Code | Title | Description |
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| FA94 | Acknowledgement of application withdrawn (non-payment of fees) |
Effective date: 20181003 |