SU354630A1 - - Google Patents

Info

Publication number

SU354630A1

SU354630A1 SU1386817A SU1386817A SU354630A1 SU 354630 A1 SU354630 A1 SU 354630A1 SU 1386817 A SU1386817 A SU 1386817A SU 1386817 A SU1386817 A SU 1386817A SU 354630 A1 SU354630 A1 SU 354630A1

Authority

SU

USSR - Soviet Union

Prior art keywords

compound

flies

activity

compounds

insecticides

Prior art date

Links

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• 150000001875 compounds Chemical class 0.000 description 20
• 241000255925 Diptera Species 0.000 description 13
• 239000002917 insecticide Substances 0.000 description 11
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
• 230000000694 effects Effects 0.000 description 10
• 241001465754 Metazoa Species 0.000 description 7
• 230000000749 insecticidal effect Effects 0.000 description 7
• GVOISEJVFFIGQE-YCZSINBZSA-N n-[(1r,2s,5r)-5-[methyl(propan-2-yl)amino]-2-[(3s)-2-oxo-3-[[6-(trifluoromethyl)quinazolin-4-yl]amino]pyrrolidin-1-yl]cyclohexyl]acetamide Chemical compound CC(=O)N[C@@H]1C[C@H](N(C)C(C)C)CC[C@@H]1N1C(=O)[C@@H](NC=2C3=CC(=CC=C3N=CN=2)C(F)(F)F)CC1 GVOISEJVFFIGQE-YCZSINBZSA-N 0.000 description 7
• 241000238631 Hexapoda Species 0.000 description 5
• 239000000203 mixture Substances 0.000 description 5
• DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 4
• 239000001257 hydrogen Substances 0.000 description 4
• 229910052739 hydrogen Inorganic materials 0.000 description 4
• 238000005507 spraying Methods 0.000 description 4
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
• 241000256118 Aedes aegypti Species 0.000 description 3
• 238000000034 method Methods 0.000 description 3
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
• 230000037396 body weight Effects 0.000 description 2
• 238000001784 detoxification Methods 0.000 description 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
• 241000894007 species Species 0.000 description 2
• HBENZIXOGRCSQN-VQWWACLZSA-N (1S,2S,6R,14R,15R,16R)-5-(cyclopropylmethyl)-16-[(2S)-2-hydroxy-3,3-dimethylpentan-2-yl]-15-methoxy-13-oxa-5-azahexacyclo[13.2.2.12,8.01,6.02,14.012,20]icosa-8(20),9,11-trien-11-ol Chemical compound N1([C@@H]2CC=3C4=C(C(=CC=3)O)O[C@H]3[C@@]5(OC)CC[C@@]2([C@@]43CC1)C[C@@H]5[C@](C)(O)C(C)(C)CC)CC1CC1 HBENZIXOGRCSQN-VQWWACLZSA-N 0.000 description 1
• 241000283690 Bos taurus Species 0.000 description 1
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
• 241000256113 Culicidae Species 0.000 description 1
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
• 241000257166 Lucilia cuprina Species 0.000 description 1
• 241000699670 Mus sp. Species 0.000 description 1
• 241000257159 Musca domestica Species 0.000 description 1
• 241000257226 Muscidae Species 0.000 description 1
• CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
• WABPPBHOPMUJHV-UHFFFAOYSA-N Sesamex Chemical compound CCOCCOCCOC(C)OC1=CC=C2OCOC2=C1 WABPPBHOPMUJHV-UHFFFAOYSA-N 0.000 description 1
• 239000003377 acid catalyst Substances 0.000 description 1
• 239000004480 active ingredient Substances 0.000 description 1
• 230000007059 acute toxicity Effects 0.000 description 1
• 231100000403 acute toxicity Toxicity 0.000 description 1
• 239000000443 aerosol Substances 0.000 description 1
• 238000010171 animal model Methods 0.000 description 1
• 239000003054 catalyst Substances 0.000 description 1
• 239000000460 chlorine Substances 0.000 description 1
• 229910052801 chlorine Inorganic materials 0.000 description 1
• 229950006824 dieldrin Drugs 0.000 description 1
• NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
• 239000012153 distilled water Substances 0.000 description 1
• 239000000839 emulsion Substances 0.000 description 1
• 239000012530 fluid Substances 0.000 description 1
• 150000002367 halogens Chemical group 0.000 description 1
• 244000144980 herd Species 0.000 description 1
• 150000002431 hydrogen Chemical class 0.000 description 1
• 238000010348 incorporation Methods 0.000 description 1
• 239000003112 inhibitor Substances 0.000 description 1
• 239000003350 kerosene Substances 0.000 description 1
• 229920000609 methyl cellulose Polymers 0.000 description 1
• 239000001923 methylcellulose Substances 0.000 description 1
• 235000010981 methylcellulose Nutrition 0.000 description 1
• 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
• 239000004006 olive oil Substances 0.000 description 1
• 235000008390 olive oil Nutrition 0.000 description 1
• -1 p-ethoxyphenyl Chemical group 0.000 description 1
• DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 description 1
• 239000000377 silicon dioxide Substances 0.000 description 1
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• 231100000820 toxicity test Toxicity 0.000 description 1
• 239000004563 wettable powder Substances 0.000 description 1
• 239000008096 xylene Substances 0.000 description 1