JP5474347B2 - 製薬学的使用のためのマラチオンの調製方法 - Google Patents
製薬学的使用のためのマラチオンの調製方法 Download PDFInfo
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- JP5474347B2 JP5474347B2 JP2008520372A JP2008520372A JP5474347B2 JP 5474347 B2 JP5474347 B2 JP 5474347B2 JP 2008520372 A JP2008520372 A JP 2008520372A JP 2008520372 A JP2008520372 A JP 2008520372A JP 5474347 B2 JP5474347 B2 JP 5474347B2
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- JP
- Japan
- Prior art keywords
- malathion
- less
- water
- solution
- dimethyldithiophosphoric acid
- 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.)
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- 239000005949 Malathion Substances 0.000 title claims description 327
- 229960000453 malathion Drugs 0.000 title claims description 327
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 title claims description 268
- 238000000034 method Methods 0.000 title claims description 72
- 230000008569 process Effects 0.000 title claims description 14
- 238000002360 preparation method Methods 0.000 title description 8
- 239000012535 impurity Substances 0.000 claims description 80
- -1 alkali metal bisulfites Chemical class 0.000 claims description 75
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 71
- CZGGKXNYNPJFAX-UHFFFAOYSA-N Dimethyldithiophosphate Chemical compound COP(S)(=S)OC CZGGKXNYNPJFAX-UHFFFAOYSA-N 0.000 claims description 66
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 64
- 239000000243 solution Substances 0.000 claims description 63
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 54
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 claims description 49
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 claims description 44
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 claims description 44
- 239000000203 mixture Substances 0.000 claims description 34
- LPQDGVLVYVULMX-UHFFFAOYSA-N isomalathion Chemical compound CCOC(=O)CC(SP(=O)(OC)SC)C(=O)OCC LPQDGVLVYVULMX-UHFFFAOYSA-N 0.000 claims description 31
- 239000007864 aqueous solution Substances 0.000 claims description 28
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 27
- 229910052717 sulfur Inorganic materials 0.000 claims description 24
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 23
- 229910052760 oxygen Inorganic materials 0.000 claims description 23
- 239000011593 sulfur Substances 0.000 claims description 23
- 239000003960 organic solvent Substances 0.000 claims description 20
- 239000000725 suspension Substances 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 238000010533 azeotropic distillation Methods 0.000 claims description 15
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical group [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 claims description 14
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 claims description 14
- 239000003153 chemical reaction reagent Substances 0.000 claims description 13
- WSORODGWGUUOBO-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphoryl)thio]succinate Chemical compound CCOC(=O)CC(SP(=O)(OC)OC)C(=O)OCC WSORODGWGUUOBO-UHFFFAOYSA-N 0.000 claims description 13
- 238000006116 polymerization reaction Methods 0.000 claims description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 12
- 239000003112 inhibitor Substances 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 238000000605 extraction Methods 0.000 claims description 10
- 238000001914 filtration Methods 0.000 claims description 10
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N 1,4-Benzenediol Natural products OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 9
- VKCLPVFDVVKEKU-UHFFFAOYSA-N S=[P] Chemical compound S=[P] VKCLPVFDVVKEKU-UHFFFAOYSA-N 0.000 claims description 9
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 claims description 7
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 6
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- 238000001816 cooling Methods 0.000 claims description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000008096 xylene Substances 0.000 claims description 4
- JUNYLKWIDRWTHV-UHFFFAOYSA-N 3-(1,2-dicarboxy-2-ethylbutyl)sulfanyl-2,2-diethylbutanedioic acid Chemical compound CCC(CC)(C(C(=O)O)SC(C(=O)O)C(CC)(CC)C(=O)O)C(=O)O JUNYLKWIDRWTHV-UHFFFAOYSA-N 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 claims 1
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 claims 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims 1
- 238000003860 storage Methods 0.000 description 45
- 239000010410 layer Substances 0.000 description 20
- 238000004821 distillation Methods 0.000 description 15
- 238000004128 high performance liquid chromatography Methods 0.000 description 15
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 13
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- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 239000006210 lotion Substances 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 11
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- 230000002378 acidificating effect Effects 0.000 description 8
- 230000008901 benefit Effects 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- 238000004817 gas chromatography Methods 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 239000000523 sample Substances 0.000 description 8
- 231100000331 toxic Toxicity 0.000 description 8
- 230000002588 toxic effect Effects 0.000 description 8
- LUNBZJCLRCHGPN-UHFFFAOYSA-N 3-[(1,2-dicarboxy-2-ethylbutyl)disulfanyl]-2,2-diethylbutanedioic acid Chemical compound CCC(CC)(C(C(=O)O)SSC(C(=O)O)C(CC)(CC)C(=O)O)C(=O)O LUNBZJCLRCHGPN-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 239000012044 organic layer Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- WTUNGUOZHBRADH-UHFFFAOYSA-N [methoxy(methylsulfanyl)phosphoryl]oxymethane Chemical compound COP(=O)(OC)SC WTUNGUOZHBRADH-UHFFFAOYSA-N 0.000 description 4
- 239000012491 analyte Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000001514 detection method Methods 0.000 description 4
- 239000000539 dimer Substances 0.000 description 4
- 230000036541 health Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 230000035945 sensitivity Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 238000004364 calculation method Methods 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- BZVCTTJRBWHTOF-UHFFFAOYSA-N diethoxy-ethylsulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(OCC)SCC BZVCTTJRBWHTOF-UHFFFAOYSA-N 0.000 description 3
- KLXFSKITMRWDPM-UHFFFAOYSA-N diethyl 2-sulfanylbutanedioate Chemical compound CCOC(=O)CC(S)C(=O)OCC KLXFSKITMRWDPM-UHFFFAOYSA-N 0.000 description 3
- ILDHFYGNYDICFB-UHFFFAOYSA-N dimethoxy-methylsulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SC ILDHFYGNYDICFB-UHFFFAOYSA-N 0.000 description 3
- 238000006317 isomerization reaction Methods 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 238000002953 preparative HPLC Methods 0.000 description 3
- 238000011002 quantification Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 238000012958 reprocessing Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 231100000419 toxicity Toxicity 0.000 description 3
- 230000001988 toxicity Effects 0.000 description 3
- CCHCXJQUURNGPO-UHFFFAOYSA-N 2,2,3,3-tetraethylbutanebis(thioic S-acid) Chemical compound CCC(CC)(C(S)=O)C(CC)(CC)C(S)=O CCHCXJQUURNGPO-UHFFFAOYSA-N 0.000 description 2
- 102100033639 Acetylcholinesterase Human genes 0.000 description 2
- 108010022752 Acetylcholinesterase Proteins 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- IDWUAONPQIKAHB-UHFFFAOYSA-N CCOC(=O)C(CC(=O)OC)SS(=O)P(OC)OC Chemical compound CCOC(=O)C(CC(=O)OC)SS(=O)P(OC)OC IDWUAONPQIKAHB-UHFFFAOYSA-N 0.000 description 2
- CCSVVFFYZKAWTG-UHFFFAOYSA-N CCOC(=O)CC(C(=O)OC)SS(=O)P(OC)OC Chemical compound CCOC(=O)CC(C(=O)OC)SS(=O)P(OC)OC CCSVVFFYZKAWTG-UHFFFAOYSA-N 0.000 description 2
- 102000003914 Cholinesterases Human genes 0.000 description 2
- 108090000322 Cholinesterases Proteins 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 229940022698 acetylcholinesterase Drugs 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- NIJIQSOYZWDHAQ-UHFFFAOYSA-N bis(methylsulfanyl)phosphoryloxymethane Chemical compound COP(=O)(SC)SC NIJIQSOYZWDHAQ-UHFFFAOYSA-N 0.000 description 2
- 230000005587 bubbling Effects 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 230000008029 eradication Effects 0.000 description 2
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- 230000008020 evaporation Effects 0.000 description 2
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- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
- 230000008520 organization Effects 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 230000005180 public health Effects 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000012502 risk assessment Methods 0.000 description 2
- 239000012488 sample solution Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000012086 standard solution Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- LOZDOQJARMKMFN-UHFFFAOYSA-N tetraphosphorus pentasulfide Chemical compound S1P(S2)P3SP2SP1S3 LOZDOQJARMKMFN-UHFFFAOYSA-N 0.000 description 2
- 231100000027 toxicology Toxicity 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- XUKUURHRXDUEBC-SXOMAYOGSA-N (3s,5r)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-propan-2-ylpyrrol-1-yl]-3,5-dihydroxyheptanoic acid Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-SXOMAYOGSA-N 0.000 description 1
- LUOZTUYAYLNGTG-UHFFFAOYSA-N 1,3,2-dioxathiepane-4,7-dione Chemical compound O=C1CCC(=O)OSO1 LUOZTUYAYLNGTG-UHFFFAOYSA-N 0.000 description 1
- AOSFMYBATFLTAQ-UHFFFAOYSA-N 1-amino-3-(benzimidazol-1-yl)propan-2-ol Chemical compound C1=CC=C2N(CC(O)CN)C=NC2=C1 AOSFMYBATFLTAQ-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- VGGBOAAZBVMVKB-UHFFFAOYSA-N COC(=O)CC(C(=O)OC)SS(=O)P(OC)OC Chemical compound COC(=O)CC(C(=O)OC)SS(=O)P(OC)OC VGGBOAAZBVMVKB-UHFFFAOYSA-N 0.000 description 1
- 206010012442 Dermatitis contact Diseases 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- 206010062016 Immunosuppression Diseases 0.000 description 1
- 206010067125 Liver injury Diseases 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- 206010046742 Urticaria contact Diseases 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- UYJXRRSPUVSSMN-UHFFFAOYSA-P ammonium sulfide Chemical compound [NH4+].[NH4+].[S-2] UYJXRRSPUVSSMN-UHFFFAOYSA-P 0.000 description 1
- 238000012863 analytical testing Methods 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000003637 basic solution Substances 0.000 description 1
- 239000012455 biphasic mixture Substances 0.000 description 1
- 239000012496 blank sample Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- JGIATAMCQXIDNZ-UHFFFAOYSA-N calcium sulfide Chemical compound [Ca]=S JGIATAMCQXIDNZ-UHFFFAOYSA-N 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 229940048961 cholinesterase Drugs 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 208000010247 contact dermatitis Diseases 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- ZKEARLMRNPOULL-UHFFFAOYSA-N dimethoxy-sulfanyl-sulfanylidene-lambda5-phosphane 1,3,5,7-tetrakis(sulfanylidene)-2,4,6,8,9,10-hexathia-1lambda5,3lambda5,5lambda5,7lambda5-tetraphosphatricyclo[3.3.1.13,7]decane Chemical compound P12(=S)SP3(=S)SP(=S)(S1)SP(=S)(S2)S3.COP(S)(OC)=S ZKEARLMRNPOULL-UHFFFAOYSA-N 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-K dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [O-]P([O-])([S-])=S NAGJZTKCGNOGPW-UHFFFAOYSA-K 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000007701 flash-distillation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 231100000234 hepatic damage Toxicity 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- PQPVPZTVJLXQAS-UHFFFAOYSA-N hydroxy-methyl-phenylsilicon Chemical class C[Si](O)C1=CC=CC=C1 PQPVPZTVJLXQAS-UHFFFAOYSA-N 0.000 description 1
- 230000007954 hypoxia Effects 0.000 description 1
- 230000001506 immunosuppresive effect Effects 0.000 description 1
- 238000001727 in vivo Methods 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
- 230000008818 liver damage Effects 0.000 description 1
- LPHFLPKXBKBHRW-UHFFFAOYSA-L magnesium;hydrogen sulfite Chemical compound [Mg+2].OS([O-])=O.OS([O-])=O LPHFLPKXBKBHRW-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012022 methylating agents Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003986 organophosphate insecticide Substances 0.000 description 1
- 229940061319 ovide Drugs 0.000 description 1
- LUGHFUPPCAAIHD-UHFFFAOYSA-N p4-s7 Chemical compound S1P(S2)SP3SP2SP1(=S)S3 LUGHFUPPCAAIHD-UHFFFAOYSA-N 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- DPLVEEXVKBWGHE-UHFFFAOYSA-N potassium sulfide Chemical compound [S-2].[K+].[K+] DPLVEEXVKBWGHE-UHFFFAOYSA-N 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- XWSLYQXUTWUIKM-UHFFFAOYSA-N trimethoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound COP(=S)(OC)OC XWSLYQXUTWUIKM-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000010200 validation analysis Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/17—Esters of thiophosphoric acids with hydroxyalkyl compounds without further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Dentistry (AREA)
- Veterinary Medicine (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69701005P | 2005-07-06 | 2005-07-06 | |
| US60/697,010 | 2005-07-06 | ||
| US74136005P | 2005-12-01 | 2005-12-01 | |
| US60/741,360 | 2005-12-01 | ||
| US74374106P | 2006-03-24 | 2006-03-24 | |
| US60/743,741 | 2006-03-24 | ||
| PCT/US2006/026251 WO2007005988A2 (en) | 2005-07-06 | 2006-07-06 | Process for preparing malathion for pharmaceutical use |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012255574A Division JP2013032405A (ja) | 2005-07-06 | 2012-11-21 | 製薬学的使用のためのマラチオンの調製方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009500422A JP2009500422A (ja) | 2009-01-08 |
| JP5474347B2 true JP5474347B2 (ja) | 2014-04-16 |
Family
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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008520372A Expired - Fee Related JP5474347B2 (ja) | 2005-07-06 | 2006-07-06 | 製薬学的使用のためのマラチオンの調製方法 |
| JP2012255574A Pending JP2013032405A (ja) | 2005-07-06 | 2012-11-21 | 製薬学的使用のためのマラチオンの調製方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012255574A Pending JP2013032405A (ja) | 2005-07-06 | 2012-11-21 | 製薬学的使用のためのマラチオンの調製方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (6) | US7560445B2 (enExample) |
| EP (1) | EP1898707A4 (enExample) |
| JP (2) | JP5474347B2 (enExample) |
| CN (2) | CN103087095A (enExample) |
| BR (1) | BRPI0612686A2 (enExample) |
| CA (1) | CA2612578A1 (enExample) |
| IL (1) | IL188512A0 (enExample) |
| WO (1) | WO2007005988A2 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8012498B2 (en) * | 2004-07-12 | 2011-09-06 | Sandhya Goyal | Topical gel formulation comprising organophosphate insecticide and preparation thereof |
| US7560445B2 (en) * | 2005-07-06 | 2009-07-14 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| EP2170078B1 (en) | 2007-07-09 | 2014-03-26 | Suven Life Sciences Limited | Process for the preparation of malathion and its intermediate |
| CA2977732C (en) | 2015-03-10 | 2021-02-23 | Rhodes Technologies | Acetate salt of buprenorphine and methods for preparing buprenorphine |
| HUE065408T2 (hu) * | 2018-09-27 | 2024-05-28 | Cheminova As | Malation katalizált és zöld elõállítási eljárása |
| JP6827687B1 (ja) * | 2019-11-15 | 2021-02-10 | 長谷川香料株式会社 | 香味付与剤としてのジエチル メルカプトサクシネート |
| CN111100163A (zh) * | 2019-12-30 | 2020-05-05 | 江苏腾龙生物药业有限公司 | 一种马拉硫磷原药及其制备方法 |
| CN111440211B (zh) * | 2020-04-28 | 2023-02-07 | 宁波大学科学技术学院 | 一种一锅法催化合成马拉硫磷的方法 |
| CN113372381A (zh) * | 2021-05-13 | 2021-09-10 | 西北矿冶研究院 | 烃基二硫代磷酸硫醚酯的合成方法 |
Family Cites Families (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE501609A (enExample) * | 1950-03-02 | |||
| NL92943C (enExample) * | 1954-09-08 | |||
| GB834814A (en) | 1955-06-14 | 1960-05-11 | Montedison Spa | ª‡-substituted o, o-dialkyl-dithiophosphorylacetic esters and process for their preparation |
| US2879284A (en) * | 1955-08-12 | 1959-03-24 | American Cyanamid Co | Odor removal and stabilization of phosphate-containing pesticides |
| BE562612A (enExample) * | 1956-12-12 | |||
| US2962521A (en) * | 1957-11-26 | 1960-11-29 | Sumitomo Chemical Co | Method for purification of organo phosphoric acid ester |
| BE626519A (enExample) * | 1959-06-16 | |||
| GB1018460A (en) * | 1963-03-19 | 1966-01-26 | Allied Chem | Ketone adducts and their use as pesticides |
| US3352664A (en) * | 1963-12-16 | 1967-11-14 | American Cyanamid Co | Viscosity stable insecticidal and herbicidal compositions |
| US3515782A (en) * | 1964-11-27 | 1970-06-02 | American Cyanamid Co | Method for controlling insects |
| US3403201A (en) * | 1964-12-08 | 1968-09-24 | Mini Ind Chimice | Method for the preparation of o, o-dimethyl-s-(1, 2-dicarbethoxyethyl)dithiophosphate |
| US3440305A (en) * | 1965-09-30 | 1969-04-22 | American Cyanamid Co | Process for upgrading malathion |
| US3309432A (en) * | 1965-10-23 | 1967-03-14 | American Cyanamid Co | Process for upgrading thiophosphates |
| US3396223A (en) * | 1965-10-23 | 1968-08-06 | American Cyanamid Co | Insecticidal composition consisting of technical grade malathion as a carrier having dissolved therein certain other malathion-soluble technical grade synthetic organic insecticides |
| US3470272A (en) * | 1966-10-24 | 1969-09-30 | Mobil Oil Corp | Process for making phosphorothioates |
| US3463841A (en) * | 1966-11-01 | 1969-08-26 | American Cyanamid Co | Malathion manufacture |
| FR1541883A (fr) | 1966-11-01 | 1968-10-11 | American Cyanamid Co | Procédé perfectionné de préparation d'o, o-diméthylphosphorodithioate de mercaptosuccinate de diéthyle |
| JPS4429647Y1 (enExample) | 1967-12-29 | 1969-12-08 | ||
| US3671612A (en) | 1968-04-05 | 1972-06-20 | Knapsack Ag | Process for the manufacture of ammonium dialkyldithiophosphates |
| DK118016B (da) * | 1968-12-23 | 1970-06-29 | Cheminova As | Fremgangsmåde til desodorisering af eller hæmning af udviklingen af dårlig lugt i produkter, bestående af eller indeholdende organiske thiophosphater. |
| IT1006881B (it) * | 1974-01-11 | 1976-10-20 | Montedison Spa | Preparazione in continuo di acido o c dimetiltiofosforico e dei suoi sa li alcalini |
| DE2500452A1 (de) | 1974-01-11 | 1975-07-17 | Montedison Spa | Verbessertes kontinuierliches verfahren fuer die herstellung von n-monomethylamid der o,o-dimethyl-dithio- phosphorylessigsaeure als insektizid |
| JPS50106927U (enExample) | 1974-02-09 | 1975-09-02 | ||
| JPS5839837B2 (ja) * | 1979-08-09 | 1983-09-01 | 日本化学工業株式会社 | ０，０−ジアルキルジチオリン酸の精製方法 |
| FR2478644A1 (fr) * | 1980-03-21 | 1981-09-25 | Rhone Poulenc Agrochimie | Procede de preparation de malathion |
| US4520013A (en) * | 1983-03-10 | 1985-05-28 | Creative Research And Development, Inc. | Topical preparation and method for using same in treating skin disorders in animals |
| RO86214B1 (ro) | 1983-06-01 | 1985-03-01 | Alexandru Lucaciu | Procedeu de purificare a solutiei de 0,0-dimetil-s-(1,2-dicarbetox-etil)-ditiofosfat tehnic |
| RO87602B1 (ro) | 1983-08-05 | 1985-12-31 | îNTREPRINDEREA CHIMICA "SINTEZA" | Procedeu de sinteza a malationului |
| US4681964A (en) * | 1985-02-11 | 1987-07-21 | Fmc Corporation | Method of increasing the reactivity of phosphorus pentasulfide |
| JPH0429647Y2 (enExample) | 1986-07-17 | 1992-07-17 | ||
| GB8710784D0 (en) | 1987-05-07 | 1987-06-10 | Euro Celtique Sa | Tropical ectoparasiticidal composition |
| GB8821587D0 (en) | 1988-09-15 | 1988-10-12 | Euro Celtique Sa | Method for controlling lice/their ova |
| DE69231401T2 (de) * | 1991-03-01 | 2001-02-08 | Rhone-Poulenc Rorer International (Holdings) Inc., Greenville | Herstellung von faktor-ix |
| US5783202A (en) | 1995-03-14 | 1998-07-21 | Soltec Research Pty. Ltd. | Pediculicidal mousse composition for killing head lice |
| US6121478A (en) * | 1996-08-20 | 2000-09-19 | Cheminova Agro A/S | Malathion oil-in-water emulsion formulations and use of peroxide in such formulations |
| DK1021204T3 (da) | 1997-09-26 | 2006-05-08 | Noven Pharma | Bioadhæsive præparater og fremgangsmåder til topisk administration af aktive midler |
| US6596291B2 (en) | 1997-12-05 | 2003-07-22 | Thomas A. Bell | Compositions and methods for treating surfaces infected with ectoparasitic insects |
| US6103248A (en) * | 1998-05-22 | 2000-08-15 | Burkhart; Craig G. | Topical preparation and therapy for head lice |
| US6284234B1 (en) | 1998-08-04 | 2001-09-04 | Johnson & Johnson Consumer Companies, Inc. | Topical delivery systems for active agents |
| AU755192B2 (en) * | 1998-09-03 | 2002-12-05 | Solvay Fluor Und Derivate Gmbh | Purification of 1,1,1,3,3-pentafluorobutane |
| US6607716B1 (en) * | 1998-09-29 | 2003-08-19 | Tech Labs, Inc. | Pediculicidal compositions, a kit, and methods of use |
| US6524602B1 (en) | 1998-10-13 | 2003-02-25 | Craig G. Burkhart | Polymer delivery system in treatments for parasitic skin diseases |
| US20020009486A1 (en) | 1999-11-30 | 2002-01-24 | 3M Innovative Properties Company | Therapeutic agent delivery incorporating reflective optical film |
| DE10004084A1 (de) | 2000-01-31 | 2001-08-02 | Bayer Ag | Substituierte Imid-Derivate |
| AR027527A1 (es) * | 2000-02-17 | 2003-04-02 | Ecosmart Technologies Inc | Composiciones pesticidas que contienen aceites vegetales esenciales contra el piojo del cuerpo humano |
| AU4183301A (en) * | 2000-03-03 | 2001-09-17 | Biogal Gyogyszergyar | A process for purifying lovastatin and simvastatin with reduced levels of dimeric impurities |
| WO2001089503A1 (en) | 2000-05-19 | 2001-11-29 | Effcon Laboratories, Inc. | Pest treatment composition |
| BR0115100A (pt) * | 2000-11-02 | 2003-09-30 | Chromaceutical Advanced Tech | Métodos para monitorar um produto de complexo ferro-sacarìdico, para purificar uma composição, e para produzir uma composição hematìnica, complexo ferro-sacarìdico, e, complexo hematìnico reconstituìdo |
| WO2002089584A1 (en) | 2001-05-09 | 2002-11-14 | Medicis Pharmaceutical Corporation | Ectoparasiticidal compositions and methods of their use |
| GB0111314D0 (en) | 2001-05-09 | 2001-07-04 | Karobio Ab | Dermatological formulations |
| US6689394B2 (en) * | 2001-06-11 | 2004-02-10 | Schering-Plough Healthcare Products, Inc. | Removal of ectoparasites |
| CN1625394A (zh) * | 2001-12-28 | 2005-06-08 | 拜奥盖尔药厂有限公司 | 结晶和无定形莫匹罗星钙的制备方法 |
| CA2473760C (en) | 2002-02-08 | 2008-11-04 | Merck & Co., Inc. | Topical ivermectin composition |
| US7820145B2 (en) * | 2003-08-04 | 2010-10-26 | Foamix Ltd. | Oleaginous pharmaceutical and cosmetic foam |
| US8012498B2 (en) | 2004-07-12 | 2011-09-06 | Sandhya Goyal | Topical gel formulation comprising organophosphate insecticide and preparation thereof |
| US20060121073A1 (en) * | 2004-07-12 | 2006-06-08 | Sandhya Goyal | Topical gel formulation comprising insecticide and its preparation thereof |
| US7560445B2 (en) * | 2005-07-06 | 2009-07-14 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| EP2170078B1 (en) | 2007-07-09 | 2014-03-26 | Suven Life Sciences Limited | Process for the preparation of malathion and its intermediate |
| JP5152883B1 (ja) | 2012-03-30 | 2013-02-27 | 株式会社 新倉技研 | 金属管補修工法および該工法に使用する包囲カバー |
-
2006
- 2006-06-30 US US11/427,863 patent/US7560445B2/en active Active
- 2006-07-06 CN CN2012105412140A patent/CN103087095A/zh active Pending
- 2006-07-06 BR BRPI0612686-3A patent/BRPI0612686A2/pt not_active IP Right Cessation
- 2006-07-06 JP JP2008520372A patent/JP5474347B2/ja not_active Expired - Fee Related
- 2006-07-06 CA CA002612578A patent/CA2612578A1/en not_active Abandoned
- 2006-07-06 CN CN200680024802XA patent/CN101287374B/zh not_active Expired - Fee Related
- 2006-07-06 WO PCT/US2006/026251 patent/WO2007005988A2/en not_active Ceased
- 2006-07-06 EP EP06774531A patent/EP1898707A4/en not_active Withdrawn
-
2007
- 2007-12-31 IL IL188512A patent/IL188512A0/en unknown
-
2009
- 2009-01-14 US US12/353,678 patent/US8039657B2/en active Active
- 2009-01-14 US US12/353,691 patent/US7977324B2/en active Active
-
2011
- 2011-09-22 US US13/239,750 patent/US8536155B2/en active Active
-
2012
- 2012-11-21 JP JP2012255574A patent/JP2013032405A/ja active Pending
-
2013
- 2013-08-29 US US14/013,966 patent/US8957238B2/en active Active - Reinstated
-
2015
- 2015-02-16 US US14/623,463 patent/US20150158893A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US7560445B2 (en) | 2009-07-14 |
| WO2007005988A2 (en) | 2007-01-11 |
| CN101287374B (zh) | 2013-03-13 |
| CN101287374A (zh) | 2008-10-15 |
| US20150158893A1 (en) | 2015-06-11 |
| BRPI0612686A2 (pt) | 2010-11-30 |
| US8536155B2 (en) | 2013-09-17 |
| US20090124822A1 (en) | 2009-05-14 |
| CA2612578A1 (en) | 2007-01-11 |
| IL188512A0 (en) | 2008-04-13 |
| US20120010175A1 (en) | 2012-01-12 |
| US8957238B2 (en) | 2015-02-17 |
| EP1898707A2 (en) | 2008-03-19 |
| EP1898707A4 (en) | 2010-07-07 |
| US8039657B2 (en) | 2011-10-18 |
| WO2007005988A3 (en) | 2008-01-24 |
| CN103087095A (zh) | 2013-05-08 |
| US7977324B2 (en) | 2011-07-12 |
| US20130345463A1 (en) | 2013-12-26 |
| JP2009500422A (ja) | 2009-01-08 |
| US20070010496A1 (en) | 2007-01-11 |
| US20090124823A1 (en) | 2009-05-14 |
| JP2013032405A (ja) | 2013-02-14 |
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