专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

61. 发明授权

US2906770A Production of phosphoric and thiophosphoric-dialkyl ester-hydrazides 失效
标题翻译：磷酸和硫代磷酸二烷基酯 - 酰肼的生产
公开(公告)号：US2906770A
公开(公告)日：1959-09-29
申请号：US68345857
申请日：1957-09-12
申请人： BENCKISER GMBH JOH A
发明人： ARNO DEBO
IPC分类号： C07F9/22 , C07F9/24
CPC分类号： C07F9/2491 , C07F9/228

62. 发明授权

US07030103B2 Sulfonamidomethyl phosphonate inhibitors of β-lactamase 失效
公开(公告)号：US07030103B2
公开(公告)日：2006-04-18
申请号：US10266213
申请日：2002-10-08
申请人： Jeffrey M. Besterman , Daniel Delorme , Jubrail Rahil
发明人： Jeffrey M. Besterman , Daniel Delorme , Jubrail Rahil
IPC分类号： C07F9/40 , C07F9/44 , A61K31/662 , A61K31/67 , A61K31/664
CPC分类号： C07F9/655354 , C07F9/2491 , C07F9/3808 , C07F9/4006 , C07F9/425 , C07F9/4407 , C07F9/572 , C07F9/5728 , C07F9/58 , C07F9/60 , C07F9/6539 , C07F9/65395 , C07F9/6541 , C07F9/65515 , C07F9/65517 , C07F9/655345
摘要： The intention relates to bacterial antibiotic resistance and, in particular, to compositions and methods for overcoming bacterial antibiotic resistance. The invention provides novel β-lactamase inhibitors, which are structurally unrelated to the natural product and semi-synthetic β-lactamase inhibitors presently available, and which do not require a β-lactam pharmacophore. The invention also provides pharmaceutical compositions and methods for inhibiting bacterial growth.

63. 发明授权

US06969528B1 Phosphorus-containing dendrimers as transfection agents 失效
标题翻译：含磷树枝状大分子作为转染剂
公开(公告)号：US06969528B1
公开(公告)日：2005-11-29
申请号：US10130739
申请日：2000-11-23
申请人： Jean-Pierre Majoral , Bernard Meunier , Anne-Marie Caminade , Christophe Loup , Maria-Antonietta Zanta-Boussif
发明人： Jean-Pierre Majoral , Bernard Meunier , Anne-Marie Caminade , Christophe Loup , Maria-Antonietta Zanta-Boussif
IPC分类号： A61K47/48 , A61K31/7088 , A61K48/00 , C07F9/24 , C07F9/6593 , C08G83/00 , C12N15/87 , A61K9/00 , A61K31/74 , A61K47/30 , C07C209/06 , C07F9/02
CPC分类号： C08G83/003 , C07F9/2491 , C07F9/65815 , C12N15/87
摘要： The invention concerns phosphorus-containing dendrimers and their uses, as gene transfection agents, in vitro and in vivo, including in the treatment of human and animal diseases. These agents or vectors are in particular suited for delivering to appropriate target cells, nucleic acid sequences of interest.
摘要翻译：本发明涉及含磷树枝状大分子及其在体外和体内作为基因转染试剂的用途，包括治疗人和动物疾病。这些试剂或载体特别适合于将合适的靶细胞输送到感兴趣的核酸序列。

64. 发明授权

US06884791B2 Inhibitors of β-lactamase 失效
标题翻译： β-内酰胺酶抑制剂
公开(公告)号：US06884791B2
公开(公告)日：2005-04-26
申请号：US10302124
申请日：2002-11-22
申请人： Jeffrey M. Besterman , Jubrail Rahil , Arkadii Vaisburg
发明人： Jeffrey M. Besterman , Jubrail Rahil , Arkadii Vaisburg
IPC分类号： C07F9/24 , C07F9/38 , C07F9/40 , C07F9/42 , C07F9/44 , C07F9/572 , C07F9/58 , C07F9/60 , C07F9/6506 , C07F9/6524 , C07F9/653 , C07F9/6539 , C07F9/6541 , C07F9/655 , C07F9/6553 , C07F9/6558 , A61K31/662 , A61K31/66 , A61P31/04
CPC分类号： C07F9/2491 , C07F9/3808 , C07F9/4006 , C07F9/4084 , C07F9/425 , C07F9/4407 , C07F9/572 , C07F9/5728 , C07F9/58 , C07F9/60 , C07F9/6506 , C07F9/6524 , C07F9/65312 , C07F9/6539 , C07F9/65395 , C07F9/6541 , C07F9/65515 , C07F9/65517 , C07F9/655345 , C07F9/655354 , C07F9/65583 , C07F9/65586
摘要： The intention relates to bacterial antibiotic resistance and, in particular, to compositions and methods for overcoming bacterial antibiotic resistance. The invention provides novel β-lactamase inhibitors, which are structurally unrelated to the natural product and semi-synthetic β-lactamase inhibitors presently available, and which do not require a β-lactam pharmacophore. The invention also provides pharmaceutical compositions and methods for inhibiting bacterial growth.
摘要翻译：意图涉及细菌抗生素抗性，特别涉及克服细菌抗生素抗性的组合物和方法。本发明提供了新型β-内酰胺酶抑制剂，其在结构上与目前可获得的天然产物和半合成β-内酰胺酶抑制剂无关，并且不需要β-内酰胺药效团。本发明还提供用于抑制细菌生长的药物组合物和方法。

65. 发明申请

US20050043276A1 Novel inhibitors of beta-lactamase 失效
标题翻译： β-内酰胺酶的新型抑制剂
公开(公告)号：US20050043276A1
公开(公告)日：2005-02-24
申请号：US10884435
申请日：2004-07-02
申请人： Jeffrey Besterman , Jubrail Rahil , Arkadii Vaisburg
发明人： Jeffrey Besterman , Jubrail Rahil , Arkadii Vaisburg
IPC分类号： C07F9/24 , C07F9/38 , C07F9/40 , C07F9/42 , C07F9/44 , C07F9/572 , C07F9/58 , C07F9/60 , C07F9/6506 , C07F9/6524 , C07F9/653 , C07F9/6539 , C07F9/6541 , C07F9/655 , C07F9/6553 , C07F9/6558 , A61K31/675 , A61K31/66
CPC分类号： C07F9/2491 , C07F9/3808 , C07F9/4006 , C07F9/4084 , C07F9/425 , C07F9/4407 , C07F9/572 , C07F9/5728 , C07F9/58 , C07F9/60 , C07F9/6506 , C07F9/6524 , C07F9/65312 , C07F9/6539 , C07F9/65395 , C07F9/6541 , C07F9/65515 , C07F9/65517 , C07F9/655345 , C07F9/655354 , C07F9/65583 , C07F9/65586
摘要： The intention relates to bacterial antibiotic resistance and, in particular, to compositions and methods for overcoming bacterial antibiotic resistance. The invention provides novel β-lactamase inhibitors, which are structurally unrelated to the natural product and semi-synthetic β-lactamase inhibitors presently available, and which do not require a β-lactam pharmacophore. The invention also provides pharmaceutical compositions and methods for inhibiting bacterial growth.
摘要翻译：意图涉及细菌抗生素抗性，特别涉及克服细菌抗生素抗性的组合物和方法。本发明提供了新型β-内酰胺酶抑制剂，其在结构上与目前可获得的天然产物和半合成β-内酰胺酶抑制剂无关，并且不需要β-内酰胺药效团。本发明还提供用于抑制细菌生长的药物组合物和方法。

66. 发明授权

US06472406B1 Sulfonamidomethyl phosphonate inhibitors of beta-lactamase 失效
标题翻译：磺酰胺甲基膦酸酯抑制剂β-内酰胺酶
公开(公告)号：US06472406B1
公开(公告)日：2002-10-29
申请号：US09610456
申请日：2000-07-05
申请人： Jeffrey M. Besterman , Daniel Delorme , Jubrail Rahil
发明人： Jeffrey M. Besterman , Daniel Delorme , Jubrail Rahil
IPC分类号： C07F940
CPC分类号： C07F9/655354 , C07F9/2491 , C07F9/3808 , C07F9/4006 , C07F9/425 , C07F9/4407 , C07F9/572 , C07F9/5728 , C07F9/58 , C07F9/60 , C07F9/6539 , C07F9/65395 , C07F9/6541 , C07F9/65515 , C07F9/65517 , C07F9/655345
摘要： The intention relates to bacterial antibiotic resistance and, in particular, to compositions and methods for overcoming bacterial antibiotic resistance. The invention provides novel &bgr;-lactamase inhibitors, which are structurally unrelated to the natural product and semi-synthetic &bgr;-lactamase inhibitors presently available, and which do not require a &bgr;-lactam pharmacophore. The invention also provides pharmaceutical compositions and methods for inhibiting bacterial growth.
摘要翻译：意图涉及细菌抗生素抗性，特别涉及克服细菌抗生素抗性的组合物和方法。本发明提供了新型β-内酰胺酶抑制剂，其在结构上与目前可获得的天然产物和半合成β-内酰胺酶抑制剂无关，并且不需要β-内酰胺药效团。本发明还提供用于抑制细菌生长的药物组合物和方法。

67. 发明授权

US5750755A Silver halide color photosensitive material 失效
标题翻译：卤化银色感光材料
公开(公告)号：US5750755A
公开(公告)日：1998-05-12
申请号：US695636
申请日：1996-08-12
申请人： Takashi Nakamura , Hiroshi Fukuzawa , Michio Ono
发明人： Takashi Nakamura , Hiroshi Fukuzawa , Michio Ono
IPC分类号： C07F9/24 , C07F9/6568 , C07F9/6571 , C07F9/6578 , G03C7/392 , C07F9/6574 , C07F9/6584
CPC分类号： C07F9/2491 , C07F9/6568 , C07F9/657154 , C07F9/6578 , G03C7/39224 , G03C7/39236 , G03C7/39288
摘要： A silver halide color photosensitive material is disclosed, which has on a support at least one photosensitive silver halide emulsion layer, wherein at least one nondiffusible compound represented by the following formulas (I), (I-1), or (I-2) is contained to inhibit generation of color stain and color fog and to ensure excellent keeping quality: ##STR1## wherein Y.sup.1 represents atoms completing a phosphorus-containing heterocyclic ring; and ##STR2## wherein R.sup.1 represents an aryl group or a heterocyclic group; R.sup.2 represents an alkyl group, a cycloalkyl group, an aryl group (formula (I-2)), a heterocyclic group (formula CI-2)), an alkoxy group or an aryloxy group; A.sup.1 and A.sup.2 each represent a hydrogen atom or a hydrolyzable group; G represents a carbon atom or a phosphorus atom; X represents an oxygen atom or a sulfur atom; and R.sup.3 represents an alkyl group, a cycloalkyl group, an aryl group, or a heterocyclic group.
摘要翻译：公开了一种卤化银色感光材料，其在至少一种感光卤化银乳剂层上具有载体，其中至少一种由下式（I），（I-1）或（I-2）表示的不可扩散化合物，含有抑制着色斑和色雾的产生，保证质量优良：含磷杂环; 和（I-2）其中R 1表示芳基或杂环基; R2表示烷基，环烷基，芳基（式（I-2）），杂环基（式CI-2）），烷氧基或芳氧基; A1和A2each表示氢原子或可水解基团; G表示碳原子或磷原子; X表示氧原子或硫原子; R 3表示烷基，环烷基，芳基或杂环基。

68. 发明授权

US5543404A Pesticidal phenylhydrazinephosphates 失效
标题翻译：杀虫剂苯基肼基磷酸盐
公开(公告)号：US5543404A
公开(公告)日：1996-08-06
申请号：US498556
申请日：1995-07-05
申请人： Mark A. Dekeyser , Paul T. McDonald
发明人： Mark A. Dekeyser , Paul T. McDonald
IPC分类号： A01N57/30 , C07F9/24 , C07C243/10 , C07C245/02
CPC分类号： C07F9/2491 , A01N57/30
摘要： Compounds having the formula: ##STR1## wherein R is C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkyl, hydrogen, halogen, or C.sub.1 -C.sub.4 alkylthio; R.sup.1 is phenyl, phenoxy, or benzyl, the phenyl ring of each substituent being optionally substituted with one or more of halogen, nitro, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkyl or di(C.sub.1 -C.sub.4 alkyl)amino; and R.sup.2 is branched or straight-chained, C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, C.sub.3 -C.sub.6 cycloalkoxy, C.sub.1 -C.sub.6 haloalkyl, alkoxyalkyl, C.sub.1 -C.sub.6 alkenyl, C.sub.1 -C.sub.6 alkylthio, (C.sub.1 -C.sub.6 alkoxy)carbonyl, C.sub.1 -C.sub.6 alkylamino, C.sub.1 -C.sub.6 haloalkoxy, or C.sub.3 -C.sub.6 cycloalkyl. These compounds are effective for controlling mites.
摘要翻译：具有下式的化合物：其中R是C 1 -C 4烷氧基，C 1 -C 4烷基，氢，卤素或C 1 -C 4烷硫基; R1是苯基，苯氧基或苄基，每个取代基的苯环任选被一个或多个卤素，硝基，C 1 -C 4烷基，C 1 -C 4烷氧基，C 1 -C 4卤代烷基或二（C 1 -C 4烷基）氨基 ; C1-C6烷氧基，C3-C6环烷氧基，C1-C6卤代烷基，烷氧基烷基，C1-C6烯基，C1-C6烷硫基，（C1-C6烷氧基）羰基，C1 -C6烷基氨基，C1-C6卤代烷氧基或C3-C6环烷基。这些化合物对控制螨有效。

69. 发明授权

US5536710A Bisphosphoryl hydrazines and their use as pesticides 失效
公开(公告)号：US5536710A
公开(公告)日：1996-07-16
申请号：US467512
申请日：1995-06-06
申请人： Richard M. Jacobson , Luong T. Nguyen
发明人： Richard M. Jacobson , Luong T. Nguyen
IPC分类号： A01N57/02 , C07F9/24 , C07F9/32 , C07F9/36 , C07F9/44 , C07F9/553 , C07F9/572 , C07F9/59 , A01N57/32
CPC分类号： C07F9/2491 , C07F9/36 , C07F9/4496 , C07F9/5721 , C07F9/591
摘要： This invention relates to bisphosphoryl hydrazine compounds and to compositions thereof which are useful as pesticides. The compounds of this invention are effective against soil insects, especially the corn rootworm.

70. 发明授权

US4203979A Insecticidal 1-sec. and tert.-alkyl-2-disubstituted-phosphoryl hydrazines 失效
标题翻译：杀虫1秒和叔烷基-2-二取代的磷酰肼
公开(公告)号：US4203979A
公开(公告)日：1980-05-20
申请号：US3959
申请日：1979-01-16
申请人： Michael J. Brown
发明人： Michael J. Brown
IPC分类号： A01N57/28 , C07F9/24 , C07F9/44 , A01N9/36
CPC分类号： A01N57/28 , C07F9/2491 , C07F9/4496
摘要： Compounds of the formula: ##STR1## where R is a secondary or tertiaryalkyl, C.sub.4 -C.sub.10,R' is hydrogen, alkyl, C.sub.1 -C.sub.6 or acyl, C.sub.2 -C.sub.6,X is oxygen or sulfur, and,Y and Z are independently alkyl, alkenyl, alkoxy, thioalkoxy, alkenyloxy or thioalkenyloxy, C.sub.1 -C.sub.6,are described herein.These compounds are useful as insecticides or miticides.
摘要翻译：其中R是仲或叔烷基，C 4 -C 10，R'是氢，烷基，C 1 -C 6或酰基，C 2 -C 6，X是氧或硫，且Y和Z独立地是烷基，烯基，烷氧基，硫代烷氧基，烯氧基或硫代烯氧基，C 1 -C 6。这些化合物可用作杀虫剂或杀蜱剂。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式