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1.发明授权2-aryl-&Dgr;2-1,3,4-(oxa and thia)diazoline insecticidal and acaricidal agents 失效2-芳基-DDTA2-1,3,4-（氧杂和硫杂）二唑啉杀虫剂和杀螨剂公开(公告)号：US06235762B1
公开(公告)日：2001-05-22
申请号：US09435343
申请日：1999-11-05
IPC分类号： A01N4734
CPC分类号： C07D271/10 , A01N47/38 , C07D271/107 , C07D271/12 , C07D285/12 , C07D413/04
摘要： The present invention relates to 2-aryl-&Dgr;2-1,3,4-(oxa and thia)diazoline compounds having the structural formula and compositions and methods comprising those compounds for the control of insect and acarid pests.
摘要翻译： 本发明涉及具有结构式和组成的2-芳基-ΔTTA2-1,3,4-（氧杂和硫杂）二唑啉化合物和包含用于防治昆虫和螨类害虫的化合物的方法。
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公开(公告)号：US06534492B2
公开(公告)日：2003-03-18
申请号：US09848881
申请日：2001-05-04
IPC分类号： A61K3133
CPC分类号： C07D239/54 , A01N41/02 , A01N43/40 , A01N43/54 , A01N43/56 , A01N43/58 , A01N43/64 , A01N43/653 , A01N43/707 , A01N43/90 , C07D213/61 , C07D231/20 , C07D237/14 , C07D249/12 , C07D471/04
摘要： Novel uracil substituted phenyl sulfamoyl carboxamides I and salts thereof, where A=oxygen or sulfur; X1=H, halogen, C1-C4-alkyl; X2=H, CN, CS—NH2, halogen, C1-C4-alkyl, C1-C4-haloalkyl; X3=H, CN, C1-C6-alkyl, C1-C6-alkoxyalkyl, C3-C7-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, optionally substituted benzyl; R1, R2=H, halogen, optionally substituted hydroxy, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkynyl, C3-C7-cycloalkyl, phenyl, benzyl or C5-C7-cycloalkenyl, or R1+R2 together with the atom to which they are attached form 3- to 7-membered heterocyclic ring; Q is selected from Q1 to Q40 as defined in the description. Use: As herbicides; for the desiccation/defoliation of plants.
摘要翻译： 新型尿嘧啶取代苯基氨磺酰甲酰胺其中A =氧或硫; X 1 = H，卤素，C 1 -C 4烷基; X 2 = H，CN，CS-NH 2，卤素，C 1 -C 4烷基，C 1 -C 4 - 卤代烷基; X3 = H，CN，C1-C6-烷基，C1-C6-烷氧基烷基，C3-C7-环烷基，C3-C6-烯基，C3-C6-炔基，任意取代的苄基; R1，R2 = 任选取代的羟基，C 1 -C 10 - 烷基，C 2 -C 10 - 烯基，C 3 -C 10 - 炔基，C 3 -C 7 - 环烷基，苯基，苄基或C 5 -C 7 - 环烯基，或者R 1 + 连接形式3-至7-元杂环; Q如说明书所定义，选自Q1至Q40。用途：作为除草剂; 用于植物的干燥/脱叶。
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公开(公告)号：US06689773B2
公开(公告)日：2004-02-10
申请号：US10347920
申请日：2003-01-22
IPC分类号： A61K3133
CPC分类号： C07D239/54 , A01N41/02 , A01N43/40 , A01N43/54 , A01N43/56 , A01N43/58 , A01N43/64 , A01N43/653 , A01N43/707 , A01N43/90 , C07D213/61 , C07D231/20 , C07D237/14 , C07D249/12 , C07D471/04
摘要： Novel uracil substituted phenyl sulfamoyl carboxamides I and salts thereof, where A=oxygen or sulfur; X1=H, halogen, C1-C4-alkyl; X2=H, CN, CS—NH2, halogen, C1-C4-alkyl, C1-C4-haloalkyl; X3=H, CN, C1-C6-alkyl, C1-C6-alkoxyalkyl, C3-C7-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, optionally substituted benzyl; R1, R2=H, halogen, optionally substituted hydroxy, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkynyl, C3-C7-cycloalkyl, phenyl, benzyl or C5-C7-cycloalkenyl, or R1+R2 together with the atom to which they are attached form a 3- to 7-membered heterocyclic ring; Q is selected from Q1 to Q40 as defined in the description. Use: As herbicides; for the desiccation/defoliation of plants.
摘要翻译： 新型尿嘧啶取代苯基氨磺酰甲酰胺其中A =氧或硫; X 1 = H，卤素，C 1 -C 4烷基; X 2 = H，CN，CS-NH 2，卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基; X 3 = H，CN，C 1 -C 6 - 烷基，C 1 -C 6 - 烷氧基烷基，C 3 -C 7 - 环烷基，C 3 -C 6 - 烯基，C 3 -C 6 - 炔基，任选取代的苄基 R 1，R 2 = H，卤素，任选取代的羟基，C 1 -C 10 - 烷基，C 2 -C 10 - 烯基，C 3 -C 10炔基，C 3 -C 7 - 环烷基，苯基，苄基或C 5 -C 7 环烯基或R 1 + R 2与它们所连接的原子一起形成3-至7-元杂环; Q选自Q 1至Q 40如 描述：用作除草剂; 用于植物的干燥/脱叶。
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公开(公告)号：US07868037B2
公开(公告)日：2011-01-11
申请号：US11331180
申请日：2006-01-13
申请人： Gary Mitchell Karp , Peter Seongwoo Hwang , James Jan Takasugi , Hongyu Ren , Richard Gerald Wilde , Anthony Allan Turpoff , Alexander Arefolov , Guangming Chen , Jeffrey Allen Campbell
发明人： Gary Mitchell Karp , Peter Seongwoo Hwang , James Jan Takasugi , Hongyu Ren , Richard Gerald Wilde , Anthony Allan Turpoff , Alexander Arefolov , Guangming Chen , Jeffrey Allen Campbell
IPC分类号： C07D209/10 , A61K31/404
CPC分类号： C07D403/12 , C07D209/14 , C07D209/42 , C07D401/12 , C07D403/10 , C07D413/10 , C07D413/12 , C07D413/14 , C07D417/10 , C07D417/12 , C07D417/14
摘要： The present invention provides compounds, pharmaceutical compositions, and methods of using such compounds or compositions for treating infection by a virus, or for affecting viral IRES activity.
摘要翻译： 本发明提供化合物，药物组合物和使用这些化合物或组合物治疗病毒感染或影响病毒IRES活性的方法。
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5.发明授权Use of Acetylamino benzoic acid compounds for nonsense suppression and the treatment of disease 失效使用乙酰氨基苯甲酸化合物进行无味抑制和治疗疾病公开(公告)号：US07763656B2
公开(公告)日：2010-07-27
申请号：US11789625
申请日：2007-04-24
申请人： Richard G. Wilde , Ellen M. Welch , James Jan Takasugi , Neil G. Almstead , Steven Marc Rubenstein , Holger Beckmann
发明人： Richard G. Wilde , Ellen M. Welch , James Jan Takasugi , Neil G. Almstead , Steven Marc Rubenstein , Holger Beckmann
IPC分类号： A61K31/19
CPC分类号： C07C235/24 , C07C235/74 , C07C323/60 , C07C327/42 , C07C2601/08 , C07C2602/08 , C07C2602/10 , C07D207/273 , C07D209/48 , C07D213/74 , C07D239/38 , C07D257/04 , C07D271/10 , C07D317/64
摘要： Novel acetylamino benzoic acid compounds, methods of using and pharmaceutical compositions comprising an acetylamino benzoic acid derivative are disclosed. The methods include methods of treating or preventing a disease ameliorated by modulation of premature translation termination or nonsense-mediated mRNA decay, or ameliorating one or more symptoms associated therewith.
摘要翻译： 公开了新型乙酰氨基苯甲酸化合物，使用方法和包含乙酰氨基苯甲酸衍生物的药物组合物。 所述方法包括治疗或预防通过调节过早翻译终止或无义介导的mRNA衰变而改善的疾病或改善与其相关的一种或多种症状的方法。
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6.发明授权Acetylamino benzoic acid compounds and their use for nonsense suppression and the treatment of disease 有权乙酰氨基苯甲酸化合物及其用于无意义抑制和治疗疾病公开(公告)号：US07247741B2
公开(公告)日：2007-07-24
申请号：US11048657
申请日：2005-01-21
申请人： Richard G. Wilde , Ellen M. Welch , James Jan Takasugi , Neil G. Almstead , Steven Marc Rubenstein , Holger Beckmann
发明人： Richard G. Wilde , Ellen M. Welch , James Jan Takasugi , Neil G. Almstead , Steven Marc Rubenstein , Holger Beckmann
IPC分类号： C07C229/00 , C07C205/00
CPC分类号： C07C235/24 , C07C235/74 , C07C323/60 , C07C327/42 , C07C2601/08 , C07C2602/08 , C07C2602/10 , C07D207/273 , C07D209/48 , C07D213/74 , C07D239/38 , C07D257/04 , C07D271/10 , C07D317/64
摘要： Novel acetylamino benzoic acid compounds, methods of using and pharmaceutical compositions comprising an acetylamino benzoic acid derivative are disclosed. The methods include methods of treating or preventing a disease ameliorated by modulation of premature translation termination or nonsense-mediated mRNA decay, or ameliorating one or more symptoms associated therewith.
摘要翻译： 公开了新型乙酰氨基苯甲酸化合物，使用方法和包含乙酰氨基苯甲酸衍生物的药物组合物。 所述方法包括治疗或预防通过调节过早翻译终止或无义介导的mRNA衰变而改善的疾病或改善与其相关的一种或多种症状的方法。
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公开(公告)号：US06849618B2
公开(公告)日：2005-02-01
申请号：US10684940
申请日：2003-10-15
IPC分类号： A01N41/02 , A01N43/40 , A01N43/54 , A01N43/56 , A01N43/58 , A01N43/64 , A01N43/653 , A01N43/707 , A01N43/90 , C07D213/61 , C07D231/20 , C07D237/14 , C07D239/54 , C07D249/08 , C07D249/12 , C07D471/04 , A61K31/33 , A61K31/41 , A61K31/415 , C07D257/00
CPC分类号： C07D239/54 , A01N41/02 , A01N43/40 , A01N43/54 , A01N43/56 , A01N43/58 , A01N43/64 , A01N43/653 , A01N43/707 , A01N43/90 , C07D213/61 , C07D231/20 , C07D237/14 , C07D249/12 , C07D471/04
摘要： Novel uracil substituted phenyl sulfamoyl carboxamides I and salts thereof, where A=oxygen or sulfur; X1=H, halogen, C1-C4-alkyl; X2=H, CN, CS—NH2, halogen, C1-C4-alkyl, C1-C4-haloalkyl; X3=H, CN, C1-C6-alkyl, C1-C6-alkoxyalkyl, C3-C7-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, optionally substituted benzyl; R1, R2=H, halogen, optionally substituted hydroxy, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkynyl, C3-C7-cycloalkyl, phenyl, benzyl or C5-C7-cycloalkenyl, or R1+R2 together with the atom to which they are attached form a 3- to 7-membered heterocyclic ring; Q is selected from Q1 to Q40 as defined in the description. Use: As herbicides; for the desiccation/defoliation of plants.
摘要翻译： 新型尿嘧啶取代苯基氨磺酰甲酰胺其中A =氧或硫; X 1 = H，卤素，C 1 -C 4烷基; X 2 = H，CN，CS-NH 2，卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基; X 3 = H，CN，C 1 -C 6 - 烷基，C 1 -C 6 - 烷氧基烷基，C 3 -C 7 - 环烷基，C 3 -C 6 - 烯基，C 3 -C 6 - 炔基，任选取代的苄基 R 1，R 2 = H，卤素，任选取代的羟基，C 1 -C 10 - 烷基，C 2 -C 10 - 烯基，C 3 -C 10炔基，C 3 -C 7 - 环烷基，苯基，苄基或C 5 -C 7 环烯基或R 1 + R 2与它们所连接的原子一起形成3-至7-元杂环; Q选自Q 1至Q 40如 描述：用作除草剂; 用于植物的干燥/脱叶。
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