CN101616905B - 苯并呋喃杀寄生物剂 - Google Patents
苯并呋喃杀寄生物剂 Download PDFInfo
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- CN101616905B CN101616905B CN2008800057820A CN200880005782A CN101616905B CN 101616905 B CN101616905 B CN 101616905B CN 2008800057820 A CN2008800057820 A CN 2008800057820A CN 200880005782 A CN200880005782 A CN 200880005782A CN 101616905 B CN101616905 B CN 101616905B
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- compound
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- alkyl
- haloalkyl
- dihydro
- Prior art date
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- 239000003096 antiparasitic agent Substances 0.000 title abstract description 8
- 229940125687 antiparasitic agent Drugs 0.000 title abstract description 3
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- 150000001875 compounds Chemical class 0.000 claims abstract description 251
- 150000003839 salts Chemical class 0.000 claims abstract description 35
- 238000002360 preparation method Methods 0.000 claims description 99
- 125000000217 alkyl group Chemical group 0.000 claims description 93
- 125000001188 haloalkyl group Chemical group 0.000 claims description 67
- 239000003795 chemical substances by application Substances 0.000 claims description 35
- 229910052736 halogen Inorganic materials 0.000 claims description 27
- 150000002367 halogens Chemical class 0.000 claims description 27
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 25
- 241001465754 Metazoa Species 0.000 claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 23
- 229910052794 bromium Inorganic materials 0.000 claims description 22
- 229910052801 chlorine Inorganic materials 0.000 claims description 22
- 239000003814 drug Substances 0.000 claims description 18
- 229910052731 fluorine Inorganic materials 0.000 claims description 17
- 229910052760 oxygen Inorganic materials 0.000 claims description 15
- 239000008194 pharmaceutical composition Substances 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 claims description 9
- 230000001225 therapeutic effect Effects 0.000 claims description 9
- HLFSDGLLUJUHTE-SNVBAGLBSA-N Levamisole Chemical group C1([C@H]2CN3CCSC3=N2)=CC=CC=C1 HLFSDGLLUJUHTE-SNVBAGLBSA-N 0.000 claims description 8
- 241000244206 Nematoda Species 0.000 claims description 8
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- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 7
- 239000011737 fluorine Substances 0.000 claims description 7
- REEJOFMTJPOBAY-UHFFFAOYSA-N benzene;1h-pyrrole Chemical class C=1C=CNC=1.C1=CC=CC=C1 REEJOFMTJPOBAY-UHFFFAOYSA-N 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 244000045947 parasite Species 0.000 claims description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
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- 150000002825 nitriles Chemical class 0.000 claims description 4
- BEZZFPOZAYTVHN-UHFFFAOYSA-N oxfendazole Chemical compound C=1C=C2NC(NC(=O)OC)=NC2=CC=1S(=O)C1=CC=CC=C1 BEZZFPOZAYTVHN-UHFFFAOYSA-N 0.000 claims description 4
- 229960004454 oxfendazole Drugs 0.000 claims description 4
- FSVJFNAIGNNGKK-UHFFFAOYSA-N 2-[cyclohexyl(oxo)methyl]-3,6,7,11b-tetrahydro-1H-pyrazino[2,1-a]isoquinolin-4-one Chemical compound C1C(C2=CC=CC=C2CC2)N2C(=O)CN1C(=O)C1CCCCC1 FSVJFNAIGNNGKK-UHFFFAOYSA-N 0.000 claims description 3
- QOVTVIYTBRHADL-UHFFFAOYSA-N 4-amino-6-(1,2,2-trichloroethenyl)benzene-1,3-disulfonamide Chemical compound NC1=CC(C(Cl)=C(Cl)Cl)=C(S(N)(=O)=O)C=C1S(N)(=O)=O QOVTVIYTBRHADL-UHFFFAOYSA-N 0.000 claims description 3
- NQPDXQQQCQDHHW-UHFFFAOYSA-N 6-chloro-5-(2,3-dichlorophenoxy)-2-(methylthio)-1H-benzimidazole Chemical compound ClC=1C=C2NC(SC)=NC2=CC=1OC1=CC=CC(Cl)=C1Cl NQPDXQQQCQDHHW-UHFFFAOYSA-N 0.000 claims description 3
- 101000807541 Homo sapiens Ubiquitin carboxyl-terminal hydrolase 24 Proteins 0.000 claims description 3
- JMPFSEBWVLAJKM-UHFFFAOYSA-N N-{5-chloro-4-[(4-chlorophenyl)(cyano)methyl]-2-methylphenyl}-2-hydroxy-3,5-diiodobenzamide Chemical group ClC=1C=C(NC(=O)C=2C(=C(I)C=C(I)C=2)O)C(C)=CC=1C(C#N)C1=CC=C(Cl)C=C1 JMPFSEBWVLAJKM-UHFFFAOYSA-N 0.000 claims description 3
- 102100037176 Ubiquitin carboxyl-terminal hydrolase 24 Human genes 0.000 claims description 3
- 150000003851 azoles Chemical class 0.000 claims description 3
- 229950004178 closantel Drugs 0.000 claims description 3
- LGUDKOQUWIHXOV-UHFFFAOYSA-N epsiprantel Chemical compound C1C(C2=CC=CC=C2CCC2)N2C(=O)CN1C(=O)C1CCCCC1 LGUDKOQUWIHXOV-UHFFFAOYSA-N 0.000 claims description 3
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- 229960001920 niclosamide Drugs 0.000 claims description 3
- RJMUSRYZPJIFPJ-UHFFFAOYSA-N niclosamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC=C([N+]([O-])=O)C=C1Cl RJMUSRYZPJIFPJ-UHFFFAOYSA-N 0.000 claims description 3
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- VTGXDWHWZQHAPU-UHFFFAOYSA-N 2-(aminomethyl)phenol iodo hypoiodite Chemical compound C(C=1C(O)=CC=CC1)N.IOI VTGXDWHWZQHAPU-UHFFFAOYSA-N 0.000 claims description 2
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- UVZZDDLIOJPDKX-ITKQZBBDSA-N paraherquamide Chemical compound O1C(C)(C)C=COC2=C1C=CC1=C2NC(=O)[C@]11C(C)(C)[C@@H]2C[C@]3(N(C4)CC[C@@]3(C)O)C(=O)N(C)[C@]42C1 UVZZDDLIOJPDKX-ITKQZBBDSA-N 0.000 description 1
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- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- FRYANWYSCROOCU-UHFFFAOYSA-N pentafluoro-(4-iodophenyl)-$l^{6}-sulfane Chemical compound FS(F)(F)(F)(F)C1=CC=C(I)C=C1 FRYANWYSCROOCU-UHFFFAOYSA-N 0.000 description 1
- 238000005897 peptide coupling reaction Methods 0.000 description 1
- 108010021753 peptide-Gly-Leu-amide Proteins 0.000 description 1
- XCRBXWCUXJNEFX-UHFFFAOYSA-N peroxybenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1 XCRBXWCUXJNEFX-UHFFFAOYSA-N 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229940023488 pill Drugs 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229940068968 polysorbate 80 Drugs 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 description 1
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QZWHWHNCPFEXLL-UHFFFAOYSA-N propan-2-yl n-[2-(1,3-thiazol-4-yl)-3h-benzimidazol-5-yl]carbamate Chemical compound N1C2=CC(NC(=O)OC(C)C)=CC=C2N=C1C1=CSC=N1 QZWHWHNCPFEXLL-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 229960000996 pyrantel pamoate Drugs 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 229940043131 pyroglutamate Drugs 0.000 description 1
- 229940072132 quinolone antibacterials Drugs 0.000 description 1
- YJQZYXCXBBCEAQ-UHFFFAOYSA-N ractopamine Chemical compound C=1C=C(O)C=CC=1C(O)CNC(C)CCC1=CC=C(O)C=C1 YJQZYXCXBBCEAQ-UHFFFAOYSA-N 0.000 description 1
- 229940074095 ractopamine Drugs 0.000 description 1
- 229940074092 ractopamine hydrochloride Drugs 0.000 description 1
- NEMNPWINWMHUMR-UHFFFAOYSA-N rafoxanide Chemical compound OC1=C(I)C=C(I)C=C1C(=O)NC(C=C1Cl)=CC=C1OC1=CC=C(Cl)C=C1 NEMNPWINWMHUMR-UHFFFAOYSA-N 0.000 description 1
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 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 description 1
- 229960002245 selamectin Drugs 0.000 description 1
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- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 229940045902 sodium stearyl fumarate Drugs 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 229930185156 spinosyn Natural products 0.000 description 1
- 239000004544 spot-on Substances 0.000 description 1
- 229940032147 starch Drugs 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 210000001562 sternum Anatomy 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- KQKPFRSPSRPDEB-UHFFFAOYSA-N sumatriptan Chemical compound CNS(=O)(=O)CC1=CC=C2NC=C(CCN(C)C)C2=C1 KQKPFRSPSRPDEB-UHFFFAOYSA-N 0.000 description 1
- 229960000658 sumatriptan succinate Drugs 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
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- 238000010189 synthetic method Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 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
- 229940095064 tartrate Drugs 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- 125000005958 tetrahydrothienyl group Chemical group 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- UURAUHCOJAIIRQ-QGLSALSOSA-N tiamulin Chemical compound CCN(CC)CCSCC(=O)O[C@@H]1C[C@@](C)(C=C)[C@@H](O)[C@H](C)[C@@]23CC[C@@H](C)[C@]1(C)[C@@H]2C(=O)CC3 UURAUHCOJAIIRQ-QGLSALSOSA-N 0.000 description 1
- 229960004885 tiamulin Drugs 0.000 description 1
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- 238000004448 titration Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
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- 239000012137 tryptone Substances 0.000 description 1
- 210000003708 urethra Anatomy 0.000 description 1
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- 229960002675 xylitol Drugs 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/81—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
- 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
Abstract
Description
实施例 | 结构评述 | 停留时间(分) | MH+实测值/预测值 | H.c.(L3)MED微克/毫升 |
1a | 4种非对映体的混合物 | - | 402.0402.1 | 3 |
1b | 洗脱的第二对对映体 | - | 402.1402.1 | |
1c | 单个对映体 | 15.36 | 402.2402.1 | |
1d | 单个对映体 | 33.87 | 402.2402.1 |
制备例号 | 名称 | MH+实测值/预测值 | 来自制备例 |
2 | 2-氨基-2-(2,3-二氢-1-苯并呋喃-2-基)丙腈 | 189.7189.1 | 11 |
3 | 2-氨基-2-(5-溴-2,3-二氢-1-苯并呋喃-2-基)丙腈 | 269.6267.0 | 13 |
4 | 2-氨基-2-(5-氯-2,3-二氢-1-苯并呋喃-2-基)丙腈 | 223.6223.1 | 14 |
5 | 2-(1-氨基-1-氰乙基)-2,3-二氢-1-苯并呋喃-7-甲腈 | 15 |
Claims (25)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US89091407P | 2007-02-21 | 2007-02-21 | |
US60/890,914 | 2007-02-21 | ||
PCT/IB2008/000362 WO2008102232A1 (en) | 2007-02-21 | 2008-02-08 | Benzofuran antiparasitic agents |
Publications (2)
Publication Number | Publication Date |
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CN101616905A CN101616905A (zh) | 2009-12-30 |
CN101616905B true CN101616905B (zh) | 2012-06-27 |
Family
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CN2008800057820A Expired - Fee Related CN101616905B (zh) | 2007-02-21 | 2008-02-08 | 苯并呋喃杀寄生物剂 |
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US (2) | US7622500B2 (zh) |
EP (1) | EP2125766B1 (zh) |
JP (1) | JP5327876B2 (zh) |
CN (1) | CN101616905B (zh) |
AR (1) | AR065432A1 (zh) |
AT (1) | ATE515503T1 (zh) |
AU (1) | AU2008217028B2 (zh) |
BR (1) | BRPI0807354A2 (zh) |
CA (1) | CA2678149C (zh) |
CL (1) | CL2008000463A1 (zh) |
ES (1) | ES2367332T3 (zh) |
MX (1) | MX2009008028A (zh) |
NZ (1) | NZ578378A (zh) |
TW (1) | TW200900388A (zh) |
UY (1) | UY30933A1 (zh) |
WO (1) | WO2008102232A1 (zh) |
ZA (1) | ZA200904908B (zh) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005023943A1 (de) * | 2005-05-20 | 2006-11-23 | Grünenthal GmbH | Pentafluorsulfanyl-substituierte Verbindung und deren Verwendung zur Herstellung von Arzneimitteln |
ES2367332T3 (es) * | 2007-02-21 | 2011-11-02 | Pfizer Limited | Agentes antiparasitarios de benzofurano. |
GB0905365D0 (en) | 2009-03-27 | 2009-05-13 | Norbrook Lab Ltd | A topical parasiticide composition |
EP2314292A1 (en) * | 2009-10-20 | 2011-04-27 | Novartis AG | Endoparasiticidal compositions |
CN104271128A (zh) | 2011-10-19 | 2015-01-07 | 佐蒂斯有限责任公司 | 氨基乙腈衍生物针对体内寄生虫的用途 |
CA2858157A1 (en) * | 2011-12-06 | 2013-06-13 | Ube Industries, Ltd. | Method for producing pentafluorosulfanyl benzoic acid |
AR094961A1 (es) | 2013-03-15 | 2015-09-09 | Lilly Co Eli | 1-hidroxi-benzooxaboroles como agentes antiparasitarios |
CN104208656B (zh) * | 2014-09-10 | 2016-04-20 | 河南牧翔动物药业有限公司 | 一种维吉尼亚霉素微乳及其制备方法 |
RU2717545C2 (ru) * | 2015-04-02 | 2020-03-24 | Мериал, Инк. | Комбинации противоглистных агентов и способы их применения |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0953565A2 (en) * | 1998-05-01 | 1999-11-03 | Nihon Nohyaku Co., Ltd. | Aminoacetonitrile derivative, agricultural and horticultural insecticide containing the same, and use thereof |
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ZA821052B (en) * | 1981-03-04 | 1983-01-26 | Ici Plc | Biologically active amide derivatives |
US7700656B2 (en) * | 2000-12-20 | 2010-04-20 | Novartis Ag | Organic compounds |
AU2002224942A1 (en) * | 2000-12-20 | 2002-07-01 | Syngenta Participations Ag | N-acyl aminoacetonitriles having pesticidal properties |
AR035531A1 (es) * | 2001-01-22 | 2004-06-02 | Novartis Ag | Composicion para el control de plagas endoparasiticas en ganados y animales domesticos, un metodo para su control y el uso de dicha composicion para la preparacion de medicamentos |
TW200400932A (en) * | 2002-06-19 | 2004-01-16 | Novartis Ag | Organic compounds |
GB0402677D0 (en) * | 2003-11-06 | 2004-03-10 | Novartis Ag | Organic compounds |
TW200613251A (en) * | 2004-06-10 | 2006-05-01 | Novartis Ag | Organic compounds |
WO2006043654A1 (ja) | 2004-10-22 | 2006-04-27 | Nihon Nohyaku Co., Ltd. | アセトニトリル誘導体及び有害生物防除剤並びにその使用方法 |
ES2367332T3 (es) * | 2007-02-21 | 2011-11-02 | Pfizer Limited | Agentes antiparasitarios de benzofurano. |
-
2008
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- 2008-02-08 AU AU2008217028A patent/AU2008217028B2/en not_active Ceased
- 2008-02-08 EP EP08709831A patent/EP2125766B1/en not_active Not-in-force
- 2008-02-08 AT AT08709831T patent/ATE515503T1/de not_active IP Right Cessation
- 2008-02-08 MX MX2009008028A patent/MX2009008028A/es active IP Right Grant
- 2008-02-08 CA CA2678149A patent/CA2678149C/en not_active Expired - Fee Related
- 2008-02-08 JP JP2009550331A patent/JP5327876B2/ja not_active Expired - Fee Related
- 2008-02-08 WO PCT/IB2008/000362 patent/WO2008102232A1/en active Application Filing
- 2008-02-08 CN CN2008800057820A patent/CN101616905B/zh not_active Expired - Fee Related
- 2008-02-08 BR BRPI0807354-6A patent/BRPI0807354A2/pt not_active IP Right Cessation
- 2008-02-08 NZ NZ578378A patent/NZ578378A/en not_active IP Right Cessation
- 2008-02-13 CL CL200800463A patent/CL2008000463A1/es unknown
- 2008-02-20 TW TW097105892A patent/TW200900388A/zh unknown
- 2008-02-20 US US12/034,429 patent/US7622500B2/en not_active Expired - Fee Related
- 2008-02-21 AR ARP080100727A patent/AR065432A1/es unknown
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2009
- 2009-07-14 ZA ZA200904908A patent/ZA200904908B/xx unknown
- 2009-10-15 US US12/579,809 patent/US20100035980A1/en not_active Abandoned
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0953565A2 (en) * | 1998-05-01 | 1999-11-03 | Nihon Nohyaku Co., Ltd. | Aminoacetonitrile derivative, agricultural and horticultural insecticide containing the same, and use thereof |
Also Published As
Publication number | Publication date |
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US20100035980A1 (en) | 2010-02-11 |
CL2008000463A1 (es) | 2008-08-29 |
US20080200540A1 (en) | 2008-08-21 |
CA2678149A1 (en) | 2008-08-28 |
AU2008217028A1 (en) | 2008-08-28 |
AU2008217028B2 (en) | 2013-07-25 |
AR065432A1 (es) | 2009-06-10 |
TW200900388A (en) | 2009-01-01 |
ES2367332T3 (es) | 2011-11-02 |
ATE515503T1 (de) | 2011-07-15 |
CN101616905A (zh) | 2009-12-30 |
MX2009008028A (es) | 2009-08-07 |
WO2008102232A1 (en) | 2008-08-28 |
ZA200904908B (en) | 2010-09-29 |
US7622500B2 (en) | 2009-11-24 |
JP2010519249A (ja) | 2010-06-03 |
BRPI0807354A2 (pt) | 2014-05-06 |
JP5327876B2 (ja) | 2013-10-30 |
EP2125766A1 (en) | 2009-12-02 |
UY30933A1 (es) | 2008-09-30 |
CA2678149C (en) | 2013-04-16 |
NZ578378A (en) | 2012-03-30 |
EP2125766B1 (en) | 2011-07-06 |
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