| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 61 | ANTIMICROBIAL PERACID COMPOSITIONS WITH SELECTED CATALASE ENZYMES AND METHODS OF USE IN ASEPTIC PACKAGING | PCT/IB2009/051610 | 2009-04-17 | WO2009128049A2 | 2009-10-22 | HERDT, Brandon L.; MAGNUSON, Joshua P.; MCSHERRY, David D.; LI, Junzhong; OWENS, Krista L. |
The present invention relates to specially selected catalase enzymes and their use in reducing hydrogen peroxide in applications, and particularly in aseptic packaging applications. |
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| 62 | 以取代的環酮烯醇類及安全劑為底之選擇性殺蟲劑 SELECTIVE INSECTICIDES BASED ON SUBSTITUTED CYCLIC KETOENOLS AND SAFENERS | TW094124480 | 2005-07-20 | TW200616543A | 2006-06-01 | 佛倫恩 FISCHER, REINER; 若又得 RECKMANN, UDO; 羅克根 ROSINGER, CHRISTOPHER HUGH; 孫愛其 SANWALD, ERICH; 羅克亭 ARNOLD, CHRISTIAN |
| 本發明係有關選擇性殺蟲組合物於控制昆蟲與／或蜱上之用途，其特徵在於其包含有效量之活性化合物組合，其包含(a)至少一種式(I)化合物094124480-p01.bmp其中CKE、W、X、Y與Z如說明書中之定義，及(b)至少一種改善作物相容性之化合物，其係選自本說明書所述及之群中，及使用該組合物控制昆蟲與／或蜱之方法。 | ||||||
| 63 | 以取代的環酮烯醇類及安全劑為底之選擇性殺蟲劑 SELECTIVE INSECTICIDES BASED ON SUBSTITUTED CYCLIC KETOENOLS AND SAFENERS | TW094124480 | 2005-07-20 | TWI368481B | 2012-07-21 | 佛倫恩; 若又得; 羅克根; 孫愛其; 羅克亭 |
| 本發明係有關選擇性殺蟲組合物於控制昆蟲與/或蜱蟎上之用途，其特徵在於其包含有效量之活性化合物組合，其包含(a)至少一種式(I)化合物 其中CKE、W、X、Y與Z如說明書中之定義，及(b)至少一種改善作物相容性之化合物，其係選自本說明書所述及之群中，及使用該組合物控制昆蟲與/或蜱蟎之方法。 | ||||||
| 64 | Insecticidal N-(optionally substituted) - N'-substituted-N,N'-disubstituted- hydrazines | EP87303296.5 | 1987-04-15 | EP0286746B1 | 1991-02-27 | Hsu, Adam Chi-Tung; Hamp, Donald Wesley |
| 65 | SELEKTIVE INSEKTIZIDE UND/ODER AKARIZIDE AUF BASIS VON SUBSTITUIERTEN, CYCLISCHEN DICARBONYLVERBINDUNGEN UND SAFENERN | EP05762457.9 | 2005-07-18 | EP1773126A1 | 2007-04-18 | FISCHER, Reiner; RECKMANN, Udo; ROSINGER, Chris; SANWALD, Erich; ARNOLD, Christian |
| The invention relates to the use of selective insecticidal and/or acaricidal agents for controlling insects and/or arachnids. Said insecticidal and/or acaricidal agents are characterized by an active moiety of an active substance combination comprising (a) at least one substituted, cyclic dicarbonyl compound of formula (I), wherein W, X, Y, and Z have the meaning indicated in the description while CDC represents one of the dicarbonyl radicals mentioned in the description, and (b) at least one compound that improves crop plant tolerance and is part of the group of compounds indicated in the description. Also disclosed is a method for controlling insects and/or arachnids using the inventive agents. | ||||||
| 66 | ANTIMICROBIAL PERACID COMPOSITIONS WITH SELECTED CATALASE ENZYMES AND METHODS OF USE IN ASEPTIC PACKAGING | PCT/IB2009051253 | 2009-03-25 | WO2009127986A2 | 2009-10-22 | HERDT BRANDON L; MAGNUSON JOSHUA PM; MCSHERRY DAVID D; LI ZUNZHONG; OWENS KRISTA L |
| The present invention relates to specially selected catalase enzymes and their use in reducing hydrogen peroxide in applications, and particularly in aseptic packaging applications. | ||||||
| 67 | Selective insecticides based on anthranilic acid diamides and safeners | US14095509 | 2013-12-03 | US08841328B2 | 2014-09-23 | Reiner Fischer; Rüdiger Fischer; Christian Funke; Achim Hense; Wolfram Andersch; Heike Hungenberg; Wolfgang Thielert; Udo Reckmann; Lothar Willms; Christian Arnold |
| The present invention relates to the use of selective insecticidal compositions, characterized by an effective amount of an active compound combination comprising (a) (1) at least one haloalkylnicotinic acid derivative of the formula (I) in which AA and R1A are as defined in the description, or (2) at least one phthalic acid diamide of the formula (II) in which XB, R1B, R2B, R3B, L1B, L2B and L3B are as defined in the description, or (3) at least one anthranilamide of the formula (III) in which A1C, A2C, XC, R1C, R2C, R3C, R4C, R5C, R7C, R8C and R9C are as defined in the description, and (b) at least one crop plant compatibility-improving compound from the group of compounds given in the description, in particular cloquintocet-mexyl, isoxadifen-ethyl and mefenpyr-diethyl for controlling insects and/or arachnids, and a method for controlling insects and/or arachnids using the compositions. | ||||||
| 68 | Selective insecticides based on anthranilic acid diamides and safeners | US12944074 | 2010-11-11 | US08685985B2 | 2014-04-01 | Reiner Fischer; Rüdiger Fischer; Christian Funke; Achim Hense; Wolfram Andersch; Heike Hungenberg; Wolfgang Thielert; Udo Reckmann; Lothar Willms; Christian Arnold |
| The present invention relates to the use of selective insecticidal compositions, characterized by an effective amount of an active compound combination comprising (a) (1) at least one haloalkylnicotinic acid derivative of the formula (I) in which AA and R1A are as defined in the description, or (2) at least one phthalic acid diamide of the formula (II) in which XB, R1B, R2B, R3B, L1B, L2B and L3B are as defined in the description, or (3) at least one anthranilamide of the formula (III) in which A1C, A2C, XC,R1C, R2C, R3C, R4C, R5C, R7C, R8Cand R9C are as defined in the description, and (b) at least one crop plant compatibility-improving compound from the group of compounds given in the description, in particular cloquintocet-mexyl, isoxadifen-ethyl and mefenpyr-diethyl for controlling insects and/or arachnids, and a method for controlling insects and/or arachnids using the compositions. | ||||||
| 69 | INSECTICIDAL CARBAMATES EXHIBITING SPECIES-SELECTIVE INHIBITION OF ACETYLCHOLINESTERASE (AChE) | US13358586 | 2012-01-26 | US20120122970A1 | 2012-05-17 | Paul Carlier; Jeffrey Bloomquist; Sally Paulson; Eric Wong |
| The present invention includes insecticidal carbamates that are useful, for example, for the control of insects, such as mosquitoes, which can be used in applications where exposure to and/or contact with humans is likely. The insecticides of the present invention include phenyl N-methyl carbamates and compositions comprising them that exhibit species-selective inhibition of acetylcholinesterase (AChE) and are preferably toxic to mosquitoes but not humans. Of particular interest are compounds of Formula (I) and Formula (II): Compounds of Formula (I) and Formula (II) are especially suitable for insecticide treated nets and indoor residual spraying for mosquito control. | ||||||
| 70 | INSECTICIDAL CARBAMATES EXHIBITING SPECIES-SELECTIVE INHIBITION OF ACETYLCHOLINESTERASE (AChE) | US12209301 | 2008-09-12 | US20090068242A1 | 2009-03-12 | Paul Carlier; Jeffrey Bloomquist; Sally Paulson; Eric Wong |
| The present invention includes insecticidal carbamates that are useful, for example, for the control of insects, such as mosquitoes, which can be used in applications where exposure to and/or contact with humans is likely. The insecticides of the present invention include phenyl N-methyl carbamates and compositions comprising them that exhibit species-selective inhibition of acetylcholinesterase (AChE) and are preferably toxic to mosquitoes but not humans. Of particular interest are compounds of Formula (I) and Formula (II): Compounds of Formula (I) and Formula (II) are especially suitable for insecticide treated nets and indoor residual spraying for mosquito control. | ||||||
| 71 | S-difluoromethylhomocysteines, preparation process, and selective insecticides containing them | US706266 | 1991-05-28 | US5166425A | 1992-11-24 | Tadahiko Tsushima; Shoichi Ishihara |
| A compound of the formula: ##STR1## wherein R and R' each is hydrogen or a protecting group, or acid addition salts thereof, useful as a selective insecticide. | ||||||
| 72 | Selective pyrazoline insecticides and fungicides, compositions and use | US478881 | 1990-02-12 | US4999368A | 1991-03-12 | John J. Delany |
| A pyrazoline having the formula: ##STR1## wherein: R.sup.1 and R.sup.2 are selected independently from a group consisting of hydrogen with the proviso that only one of R.sup.1 and R.sup.2 can be hydrogen, substituted or unsubstituted alkyl of from 1-20 carbon atoms and substituted or unsubstituted aryl of 6 to 20 carbons, or R.sup.1 and R.sup.2 can together comprise the atoms necessary to complete a heterocyclic group of 5 to 6 nuclear carbon and hetero atoms;R.sup.3 and R.sup.4 are selected independently from a group consisting of hydrogen, substituted or unsubstituted alkyl of from 1-20 carbon atoms, substituted or unsubstituted aryl of 6-20 carbon atoms, alkoxy, alkylthio, cycloalkyl or heterocyclyl of 5 to 6 nuclear carbon and hetero atoms, or R.sup.3 and R.sup.4 together are an alkylene group of 4 to 5 carbon atoms.R.sup.5 is selected from a group consisting of substituted or unsubstituted alkyl of 1-10 carbon atoms, alkenyl of 1-10 carbon atoms, substituted or unsubstituted aryl of 6-20 carbon atoms and cycloalkyl of 5 to 6 nuclear carbon atoms.Compounds of the above formula are useful as aphicides and fungicides. | ||||||
| 73 | 제초활성을 갖는2-(5-옥시란일메톡시페닐)-4,5,6,7-테트라히드로-2Ｈ-인다졸유도체 | KR1020030021052 | 2003-04-03 | KR1020040086696A | 2004-10-12 | 전동주; 김형래; 송종환; 장규환; 황인택 |
| PURPOSE: Herbicidal2-(5-oxiranylmethoxyphenyl)-4,5,6,7-tetrahydro-2H-indazole derivatives are provided, which compounds have improved herbicidal effects and selectivity, so that the compounds can selectively kill weeds. CONSTITUTION: The herbicidal2-(5-oxiranylmethoxyphenyl)- 4,5,6,7-tetrahydro-2H-indazole derivatives represented by formula (1) are provided, wherein R1, R2 and R3 are independently hydrogen, C1-C5 alkyl, phenyl or substituted phenyl with 1 to 3 of halogen atoms. The method for preparing the herbicidal2-(5-oxiranylmethoxyphenyl)- 4,5,6,7-tetrahydro-2H-indazole derivatives of formula (1) comprises the steps of: reacting a compound of formula (2) with allyl halide in the presence of base to prepare a compound of formula (3); and introducing epoxy group into a double bond of the compound of formula (3), wherein X is halogen. | ||||||
| 74 | Compounds with antidotal activity for the defence of cultivations of agrarian interest from the action of non-selective weed-killers | EP84108943.6 | 1984-07-27 | EP0133970B1 | 1989-05-31 | Palla, Ottorino, Dr.; Camaggi, Giovanni; Gozzo, Franco, Dr.; Signorini, Ernesto |
| 75 | Selective Insecticides and/or Acaricides Based on Substituted Cyclic Dicarbonyl Compounds and Safeners | US11632501 | 2005-07-18 | US20080200499A1 | 2008-08-21 | Reiner Fischer; Udo Reckmann; Chris Rosinger; Erich Sanwald; Christian Arnold |
| The present invention relates to the use of selective insecticidal and/or acaricidal compositions, characterized in that they comprise an effective amount of an active compound combination comprising (a) at least one substituted cyclic dicarbonyl compound of the formula (I) in which W, X, Y and Z are as defined in the description and CDC is one of the dicarbonyl radicals mentioned in the description, and (b) at least one crop plant compatibility-improving compound from the group of compounds given in the description. for controlling insects and/or arachnids, and also to a method for controlling insects and/or arachnids using the compositions. | ||||||
| 76 | A PROCESS FOR THE STEREOSELECTIVE PREPARATION OF INSECTICIDE 6,7,8,9,10-10-HEXAHALO-1,5,5A,6,9,9A-HEXAHYDRO-6,9-METHANO-2,4,3-BENZODIOXATHIEPIN-3-OXIDE | PCT/IN0100092 | 2001-04-24 | WO02085884A8 | 2003-01-30 | SHROFF ASHWIN CHAMPRAJ; PUROHIT ABHIJIT PREMVALLABH; VADORARIA SANJAY DHIRAJLAL |
| A process for the stereoselective preparation of insecticide 6,7,8,9,10,10-hexahalo-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide of general formula (I), wherein X is a halogen such as fluorine, chlorine or bromine. The process comprises reacting 1,4,5,6,7,7-hexahalo-5-norbornene-2,3-dimethanol of the general formula IV: wherein X is as defined above, with a cyclic sulfite ring forming reagent optionally in an inert organic solvent at ambient to 139 DEG C, wherein the reaction is carried out in the presence of a stereo isomer directing agent comprising an isomer of the compound of the formula (I) different from the desired isomer. The molar ratio of the stereoisomer directing agent to the dimethanol compound of the formula (IV) is at least 0.07. | ||||||
| 77 | Two kind of dichloracetoamide of antidote for nonnselective herbicide particularly effective to protecting corn from toxicity given from herbicide n*nndi substituted glycine ester | JP15693778 | 1978-12-21 | JPS54106423A | 1979-08-21 | FURANKO GOTSUTSUO; RUIJI ABURUTSUESE; JIORUJIO SHIDEI |
| 78 | A PROCESS FOR THE STEREOSELECTIVE PREPARATION OF INSECTICIDE 6,7,8,9,10-10-HEXAHALO-1,5,5A,6,9,9A-HEXAHYDRO-6,9-METHANO-2,4,3-BENZODIOXATHIEPIN-3-OXIDE | PCT/IN2001/000092 | 2001-04-24 | WO2002085884A1 | 2002-10-31 | SHROFF, Ashwin, Champraj; PUROHIT, Abhijit, Premvallabh; VADORARIA, Sanjay, Dhirajlal |
A process for the stereoselective preparation of insecticide 6,7,8,9,10,10-hexahalo-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxie of the general formula 1: wherein X is a halogen such as fluorine, chlorine or bromine. The process comprises reacting 1,4,5,6,7,7-hexahalo-5-norbornene-2,3-dimethanol of the general formula IV: wherein X is as defined above, with a cyclic sulfite ring forming reagent optionally in an inert organic solvent at ambient to 139 °C, wherein the reaction is carried out in the presence of a stereo isomer directing agent comprising an isomer of the compound of the formula I different from the desired isomer. The molar ratio of the stereoisomer directing agent to the dimethanol compound of the formula IV is at least 0.07. |
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| 79 | PROCESS FOR THE SELECTIVE UTILIZATION OF THE HERBICIDE IMAZETAPIR IN POST-EMERGENCE AND CULTIVATING VARIETIES OF SUNFLOWERS WHICH ARE RESISTANT OR TOLERANT TO SAID HERBICIDE AND APPLICATION TO THE CONTROL OF THE PARASITE FOXTAIL WEEDS OROBANCHE CERNUA LOEFL./O. CUMANA WALLER | PCT/ES1999/000053 | 1999-03-03 | WO99065312A1 | 1999-12-23 | |
| The process comprises a solution of imazetapir in the post-emergence phase of said sunflower culture simply or repeatedly by means of a conventional applicator while regulating the pressure and the volume of the solution to be applied per surface unit. The process can be applied essentially to the control of the parasite weeds foxtail in emerged sunflower cultures. | ||||||
| 80 | 인간 피부 표피의 기저 케라티노사이트의 비율을 제어하고 서바이빈의 핵 형태를 발현하는 활성제로서 Ｎ-팔미토일 알라닌, Ｎ-팔미토일 글리신, Ｎ-팔미토일 이소류신 및 Ｎ-코코일 알라닌 중에서 선택된 Ｎ-아실 아미노산의 용도, 및 이를 포함하는 노화 방지 화장품 조성물 | KR1020117004925 | 2009-07-24 | KR101652541B1 | 2016-08-30 | 드몽산디; 카투자토래티시아; 스똘쯔꼬린느; 세브로나탈리 |
| 본발명은인간피부표피의기저케라티노사이트의비율을제어하고서바이빈의핵 형태를발현하는활성제로서 N-팔미토일알라닌, N-팔미토일글리신, N-팔미토일이소류신및 N-코코일알라닌중에서선택된 N-아실아미노산의용도, 이를포함하는노화방지화장품조성물, 및이의인간피부표피에서줄기세포의생존을유지하기위한치료방법의수행에있어서의용도에관한것이다. | ||||||
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