CN1738828A - 在4"-或4′-位上有烷氧基甲基取代基的阿维菌素b1和阿维菌素b1单糖衍生物 - Google Patents
在4"-或4′-位上有烷氧基甲基取代基的阿维菌素b1和阿维菌素b1单糖衍生物 Download PDFInfo
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- CN1738828A CN1738828A CNA2003801088575A CN200380108857A CN1738828A CN 1738828 A CN1738828 A CN 1738828A CN A2003801088575 A CNA2003801088575 A CN A2003801088575A CN 200380108857 A CN200380108857 A CN 200380108857A CN 1738828 A CN1738828 A CN 1738828A
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- 238000001179 sorption measurement Methods 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000005936 tau-Fluvalinate Substances 0.000 description 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
- AWYOMXWDGWUJHS-UHFFFAOYSA-N tebupirimfos Chemical compound CCOP(=S)(OC(C)C)OC1=CN=C(C(C)(C)C)N=C1 AWYOMXWDGWUJHS-UHFFFAOYSA-N 0.000 description 1
- 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 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 210000005239 tubule Anatomy 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/22—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom rings with more than six members
-
- 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
- A61P33/10—Anthelmintics
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Tropical Medicine & Parasitology (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Description
HPLC梯度条件 | |||
溶剂A | 0.01%三氟乙酸的水溶液 | ||
溶剂B | 0.01%三氟乙酸的CH3CN溶液 | ||
时间[分钟] | A[%] | B[%] | 流速[μl/分钟] |
0 | 80 | 20 | 500 |
0.1 | 50 | 50 | 500 |
10 | 5 | 95 | 500 |
15 | 0 | 100 | 500 |
17 | 0 | 100 | 500 |
17.1 | 80 | 20 | 500 |
22 | 80 | 20 | 500 |
柱 | YMC-Pack ODS-AQ | ||
柱长 | 125mm | ||
柱内径 | 2mm | ||
温度 | 40℃ |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
1.11.21.31.41.51.61.71.81.91.101.111.121.131.141.151.161.171.18 | CH2C6H5p-ClC6H5(CH2)7CH3(CH2)3CH3CH2CH3CH3CH(CH3)2CH2CH2OCH3CH2CH2OHCH(CH3)CH2OHCH2CH2CH2OHCH(CH3)CH2CH2OHCH2CH2OC(=O)CH3CH2(CH2)2OC(=O)CH3CH(CH3)CH2OC(=O)CH3CH(CH3)(CH2)2OC(=O)CH3CH2CH2N3CH2(CH2)2N3 | HHHHHHHHHHHHHHHHHH | 12.1610.0210.4910.468.5310.9810.0811.1816.16 | 11.649.369.7210.679.3910.50 |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
1.501.511.521.531.541.551.561.571.581.591.601.611.621.631.641.651.661.671.68 | CH2CH2NH(C=O)CH2OCH3CH2CH2NH(C=O)CH2CO2CH3CH2CH2NH(C=O)OCH2CH=CH2CH2CH2OCH2CH=CH2CH2CH2SCH3CH2CH2S(O)CH3CH2CH2S(O)2CH3CH2CH2NH(C=O)CH2OCH3CH2CH2NH(C=O)CH2CO2CH3CH2CH2NH(C=O)OCH2CH=CH2CH2CH2OCH2CH=CH2CH2CH2SCH3CH2CH2S(O)CH3CH2CH2S(O)2CH3 | HHHHHHHHHHHHHH | ||
-CH2CH2CH2--CH2CH2CH2CH2--CH2CH2-O-CH2--CH2CH2-N(CH3)-CH2--CH2(C=O)CH2CH2- |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
2.12.22.32.42.52.62.72.82.92.102.112.122.132.142.152.162.172.182.192.202.212.222.232.242.252.262.272.282.292.302.31 | CH2C6H5pClC6H5(CH2)7CH3(CH2)3CH3CH2CH3CH3CH(CH3)2CH2CH2OCH3CH2CH2OHCH(CH3)CH2OHCH2CH2CH2OHCH(CH3)CH2CH2OHCH2CH2OC(=O)CH3CH2(CH2)2OC(=O)CH3CH2CH2SCH2CH3CH2CH2S(O)CH2CH3CH2CH2S(O)2CH2CH3CH2CH2N3CH2CH2NH2CH2CH2NHCHOCH2CH2NH(C=O)CH3CH2CH2NH(C=O)OCH3CH2CH2NH(C=O)OCH2CH3CH2CH2NH(C=O)CH2OCH3CH2CH2NH(C=O)CH2CO2CH3CH2CH2NH(C=O)OCH2CH=CH2CH2CH2OCH2CH=CH2CH2CH2SCH3CH2CH2S(O)CH3CH2CH2S(O)2CH3CH2CH2CH2NH2 | HHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH | 7.149.659.399.8411.2012.4212.438.859.9811.526.09 | 8.918.6911.7211.848.119.23 |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
2.322.332.342.352.362.372.382.392.40 | CH2CH2NHCH3CH2CH2N(CH3)2CH2CH2N(CH3)CH2CH3CH2CH2N+(CH3)2.C6H5CO2 - | HHHH | ||
-CH2CH2CH2--CH2CH2CH2CH2--CH2CH2-O-CH2--CH2CH2-N(CH3)-CH2--CH2(C=O)CH2CH2- |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
3.13.23.33.43.53.63.73.8 | CH2C6H5pClC6H5(CH2)7CH3(CH2)3CH3CH2CH3CH3CH(CH3)2CH2CH2OCH3 | HHHHHHHH | 13.8111.369.3911.20 | 10.618.6910.45 |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
3.403.413.423.433.443.453.463.473.483.493.50 | CH2CH2N(CH3)2CH2CH2N(CH3)CH2CH3CH2CH2N+(CH3)2.C6H5CO2 -CH3CH2CH=CH2 | HHHCH2BrCH2Br | 4.6910.56,10.3511.26,11.099.07/9.4910.0710.94/11.699.98/10.5111.87 | 4.4810.7,10.610.45/10.9311.20 |
-CH2CH2CH2--CH2CH2-O-CH2--CH2CH2-N(CH3)-CH2--CH2(C=O)CH2CH2--CH2CH(CH3)CH2--CH2CH2CH(CH3)CH2- |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
4.14.24.34.44.54.6 | CH2C6H5pClC6H5(CH2)7CH3(CH2)3CH3CH2CH3CH3 | HHHHHH | 10.7211.6313.7111.15 | 10.0313.1710.29 |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
4.74.84.94.104.114.124.134.144.154.164.174.184.194.204.214.224.234.244.254.264.274.284.294.304.314.324.334.344.354.364.374.38 | CH(CH3)2CH2CH2OCH3CH2CH2OHCH(CH3)CH2OHCH2CH2CH2OHCH(CH3)CH2CH2OHCH2CH2OC(=O)CH3CH2(CH2)2OC(=O)CH3CH(CH3)CH2OC(=O)CH3CH(CH3)(CH2)2OC(=O)CH3CH2CH2N3CH2(CH2)2N3CH2CH2NH2CH2CH2SCH2CH3CH2CH2S(O)CH2CH3CH2CH2S(O)2CH2CH3CH(CH3)CH2CH2N3CH2CH2SCH3CH2CH2S(O)CH3CH2CH2S(O)2CH3CH2CH2NHCHOCH2CH2NH(C=O)CH3CH2CH2NH(C=O)OCH3CH2CH2NH(C=O)OCH2CH3CH2CH2NH(C=O)CH2OCH3CH2CH2NH(C=O)CH2CO2CH3CH2CH2NH(C=O)OCH2CH=CH2CH2CH2OCH2CH=CH2CH2CH2CH2NH2CH2CH2NHCH3CH2CH2N(CH3)2CH2CH2N(CH3)CH2CH3 | HHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH | 9.926.246.946.456.898.168.698.498.978.759.3311.0911.206.938.11 | 9.175.666.455.876.257.578.057.958.328.118.6910.3510.516.297.52 |
No. | R2 | R3 | 保留时间(min) | |
B1a | B1b | |||
4.394.404.414.424.434.44 | CH2CH2N+(CH3)2.C6H5CO2 - | H | 10.26/11.03 | |
-CH2CH2CH2--CH2CH2CH2CH2--CH2CH2-O-CH2--CH2CH2-N(CH3)-CH2--CH2(C=O)CH2CH2- |
No. | R2 | R3 |
A.22A.23A.24A.25A.26A.27A.28A.29A.30A.31A.32A.33A.34A.35A.36A.37A.38A.39A.40A.41A.42A.43A.44A.45A.46A.47A.48A.49A.50A.51A.52A.53A.54 | n-Prn-HexylCH(CH3)CH2CH2N3CH2CH2OC(=O)OCH3CH2CH2OC(=O)NHCH3CH2CH2OC(=O)N(CH3)2CH2CH2NHC(=O)NHCH3CH2CH2NHC(=O)NHC6H5CH2CH2NHC(=O)OC6H5CH2CH2NHC(=S)NHC6H5CH2CH2NHC(=O)OCH3CH2CH2NHC(=O)NHCH3CH2CH2NHC(=O)N(CH3)2CH2CH2NHC(=S)NHCH3CH2CH2NHCH3CH2CH2N(CH3)2CH2CH2SCH3CH2CH2S(O)CH3CH2CH2S(O)2CH3CH3CH2CH=CH2CH2CH2NHCHOCH2CH2N(CH3)CHOCH2CH2NHCH2COOCH3CH2COCH3-CH2-CH2-NH-C(=O)-CH3-CH2-CH2-NH-C(=O)-CH2-O-CH3-CH2-CH2-N(CH3)-C(=O)-CH3-CH2-CH2-N(CH3)-C(=O)-CH2-O-CH3-CH2-CH2-CH2-NH-C(=O)-H-CH2-CH2-CH2-NH-C(=O)-CH3-CH2-CH2-CH2-NH-C(=O)-CH2-O-CH3-CH2-CH2-CH2-N(CH3)-C(=O)-H | HHHHHHHHHHHHHHHHHHHCH2BrCH2BrHHHHHHHHHHHH |
编号 | R2 | R3 | 保留时间(分钟) | |
B1a | B1b | |||
56.656.756.78 | CH3CH(CH3)2 | HH | 12.7513.8712.86,12.21 | 11.9513.0712.11,11.57 |
CH2CH2CH2 |
编号 | R2 | R3 | 保留时间(分钟) |
57.657.7 | CH3CH(CH3)2 | HH | 15.4215.79 |
编号 | R2 | R3 | 保留时间(分钟) |
59.659.7 | CH3CH(CH3)2 | HH | 11.3112.56 |
编号 | R2 | R3 | 保留时间(分钟) |
61.661.7 | CH3CH(CH3)2 | HH | 15.3615.79 |
编号 | R2 | R3 | 保留时间(分钟) |
63.663.7 | CH3CH(CH3)2 | HH | 11.0912.27 |
Claims (7)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0229804.0 | 2002-12-20 | ||
GBGB0229804.0A GB0229804D0 (en) | 2002-12-20 | 2002-12-20 | Avermection b1 and avermectin b1 monosaccharide derivatives having an alkoxymethyl substituent in the 4"- or 4'-position |
PCT/EP2003/014613 WO2004056844A1 (en) | 2002-12-20 | 2003-12-19 | Avermectin b1 and avermectin b1 monosaccharide derivatives having an alkoxymethyl substituent in the 4”- or 4’-position |
Publications (2)
Publication Number | Publication Date |
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CN1738828A true CN1738828A (zh) | 2006-02-22 |
CN1738828B CN1738828B (zh) | 2012-09-05 |
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CN2003801088575A Expired - Lifetime CN1738828B (zh) | 2002-12-20 | 2003-12-19 | 在4"-或4′-位上有烷氧基甲基取代基的阿维菌素b1和阿维菌素b1单糖衍生物 |
Country Status (22)
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US (3) | US7737261B2 (zh) |
EP (1) | EP1581546B1 (zh) |
JP (2) | JP4851094B2 (zh) |
KR (1) | KR101109500B1 (zh) |
CN (1) | CN1738828B (zh) |
AR (1) | AR042533A1 (zh) |
AU (1) | AU2003302284B2 (zh) |
BR (1) | BR0317601A (zh) |
CA (1) | CA2507774C (zh) |
CO (1) | CO5690647A1 (zh) |
ES (1) | ES2742899T3 (zh) |
GB (1) | GB0229804D0 (zh) |
IL (1) | IL169092A (zh) |
MA (1) | MA27646A1 (zh) |
MX (1) | MXPA05006036A (zh) |
PE (1) | PE20040713A1 (zh) |
PL (1) | PL211483B1 (zh) |
RU (1) | RU2330857C2 (zh) |
TW (1) | TW200512214A (zh) |
UA (1) | UA81281C2 (zh) |
WO (1) | WO2004056844A1 (zh) |
ZA (1) | ZA200504353B (zh) |
Cited By (5)
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CN103613625A (zh) * | 2013-12-02 | 2014-03-05 | 兰州大学 | 一种阿维菌素类化合物及其制备方法和在农药中的用途 |
CN104402953A (zh) * | 2014-11-28 | 2015-03-11 | 大庆志飞生物化工有限公司 | 阿维菌素单糖化合物及其制备方法和用途 |
CN107501368A (zh) * | 2017-09-30 | 2017-12-22 | 中国科学院成都生物研究所 | 一种新型多拉菌素衍生物的合成及其杀虫应用 |
CN113150053A (zh) * | 2020-01-22 | 2021-07-23 | 华东理工大学 | 偶氮苯类阿维菌素衍生物及其制备方法和应用 |
CN113817008A (zh) * | 2021-07-15 | 2021-12-21 | 湖州师范学院 | 新型琥珀酰基十六元大环内酯的制备方法及用途 |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
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GB0229804D0 (en) * | 2002-12-20 | 2003-01-29 | Syngenta Participations Ag | Avermection b1 and avermectin b1 monosaccharide derivatives having an alkoxymethyl substituent in the 4"- or 4'-position |
JP2010006703A (ja) * | 2006-11-07 | 2010-01-14 | Hokko Chem Ind Co Ltd | アベルメクチンモノ配糖体誘導体 |
RU2472801C1 (ru) * | 2011-05-11 | 2013-01-20 | Игорь Викторович Заварзин | 5-о-производные авермектина, способ их получения и антипаразитарные средства на их основе |
RU2453553C1 (ru) * | 2011-05-11 | 2012-06-20 | Игорь Викторович Заварзин | 5-о-сукциноилавермектин, способ его получения и антипаразитарное средство на его основе |
CN104402954A (zh) * | 2014-11-28 | 2015-03-11 | 大庆志飞生物化工有限公司 | 甲胺基阿维菌素单糖化合物及其制备方法和用途 |
JP6577184B2 (ja) | 2014-12-24 | 2019-09-18 | Ntn株式会社 | 転がり軸受 |
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CN103613625A (zh) * | 2013-12-02 | 2014-03-05 | 兰州大学 | 一种阿维菌素类化合物及其制备方法和在农药中的用途 |
CN103613625B (zh) * | 2013-12-02 | 2016-03-02 | 兰州大学 | 一种阿维菌素类化合物及其制备方法和在农药中的用途 |
CN104402953A (zh) * | 2014-11-28 | 2015-03-11 | 大庆志飞生物化工有限公司 | 阿维菌素单糖化合物及其制备方法和用途 |
CN107501368A (zh) * | 2017-09-30 | 2017-12-22 | 中国科学院成都生物研究所 | 一种新型多拉菌素衍生物的合成及其杀虫应用 |
CN107501368B (zh) * | 2017-09-30 | 2020-02-21 | 中国科学院成都生物研究所 | 一种多拉菌素衍生物的合成及其杀虫应用 |
CN113150053A (zh) * | 2020-01-22 | 2021-07-23 | 华东理工大学 | 偶氮苯类阿维菌素衍生物及其制备方法和应用 |
CN113817008A (zh) * | 2021-07-15 | 2021-12-21 | 湖州师范学院 | 新型琥珀酰基十六元大环内酯的制备方法及用途 |
CN113817008B (zh) * | 2021-07-15 | 2023-05-23 | 湖州师范学院 | 新型琥珀酰基十六元大环内酯的制备方法及用途 |
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