Nuclease resistant compounds
    1.
    发明授权
    Nuclease resistant compounds 失效
    核酸酶抗性化合物

    公开(公告)号:US5567810A

    公开(公告)日:1996-10-22

    申请号:US456017

    申请日:1995-05-31

    CPC分类号: C07H21/00

    摘要: Compounds, compositions and methods for inhibiting gene expression are disclosed. The compounds comprise oligonucleotide sequences of from about 9 to about 200 bases having a diol at either or both termini. Preferred diols are polyalkyleneglycols, preferably polyethyleneglycols. Pharmaceutical compositions comprising the compounds and a physiologically acceptable carrier and methods of inhibiting gene expression in mammals comprising administering such compounds are also provided. Methods for inhibiting nuclease cleavage of compounds are also provided.

    摘要翻译: 公开了抑制基因表达的化合物,组合物和方法。 所述化合物包含约9至约200个碱基的寡核苷酸序列,在任一端或两端具有二醇。 优选的二醇是聚亚烷基二醇,优选聚乙二醇。 还提供了包含化合物和生理上可接受的载体的药物组合物和抑制哺乳动物中基因表达的方法,包括给予这些化合物。 还提供了抑制化合物核酸酶切割的方法。

    2,5-benzodiazocine antiarrhythmic agents
    3.
    发明授权
    2,5-benzodiazocine antiarrhythmic agents 失效
    2,5-苯并二氮辛类抗心律失常药

    公开(公告)号:US5206231A

    公开(公告)日:1993-04-27

    申请号:US757167

    申请日:1991-09-10

    申请人: Robert E. Johnson

    发明人: Robert E. Johnson

    IPC分类号: C07D245/06 C07D487/08

    CPC分类号: C07D487/08 C07D245/06

    摘要: Novel 2,5-benzodiazocines of formulas II and IV, pharmaceutical compositions containing them, processes for preparing them and methods of treating cardiac arrhythmias in mammals utilizing them. ##STR1##

    摘要翻译: 式II和IV的新型2,5-苯并二氮茚,含有它们的药物组合物,其制备方法以及利用它们治疗哺乳动物心脏心律失常的方法。 IV。图像IV

    1,2,4-oxadiazolyl-phenoxyalkylisoxazoles and their use as antiviral
agents
    4.
    发明授权
    1,2,4-oxadiazolyl-phenoxyalkylisoxazoles and their use as antiviral agents 失效
    1,2,4-恶二唑基 - 苯氧基烷基异恶唑及其作为抗病毒剂的用途

    公开(公告)号:US5175178A

    公开(公告)日:1992-12-29

    申请号:US532480

    申请日:1990-06-04

    摘要: Compounds of the formulas ##STR1## wherein: Y is an alkylene bridge of 3-9 carbon atoms;R' is lower-alkyl or hydroxy-lower-alkyl of 1-5 carbon atoms;R.sub.1 and R.sub.2 are hydrogen, halogen, lower-alkyl, lower-alkoxy, nitro, lower-alkoxycarbonyl or trifluoromethyl; andR.sub.8 is hydrogen or lower-alkyl of 1-5 carbon atoms, with the proviso that when R.sub.8 is hydrogen R' is hydroxy-lower-alkyl,are useful as antiviral agents, particularly against picornaviruses, including numerous strains of rhinovirus.

    摘要翻译: 下式化合物其中:Y是3-9个碳原子的亚烷基桥; R'是1-5个碳原子的低级烷基或羟基 - 低级 - 烷基; R 1和R 2是氢,卤素,低级烷基,低级烷氧基,硝基,低级烷氧基羰基或三氟甲基; 并且R 8为氢或1-5个碳原子的低级烷基,条件是当R 8为氢时R'为羟基 - 低级 - 烷基,可用作抗病毒剂,特别是针对小核糖核酸病毒,包括许多鼻病毒株。

    Trap for catching mice and rats
    5.
    发明授权
    Trap for catching mice and rats 失效
    捕捉小鼠和老鼠的陷阱

    公开(公告)号:US5172512A

    公开(公告)日:1992-12-22

    申请号:US747161

    申请日:1991-08-19

    IPC分类号: A01M23/30

    CPC分类号: A01M23/30

    摘要: A trap for catching mice and rats includes a standard mousetrap mounted within a two-part housing. The standard mousetrap includes a tab which projects through a slot an arcuate upper wall of one portion of the housing, allowing one to cock the trap from the exterior of the housing. The first portion of the housing is pivoted to the second portion of the housing so that the housing can be conveniently opened to dispose of a mouse or rat caught in the trap. The housing shields the cocked trap so as to enhance the safety thereof while allowing one to empty the trap without running the risk of touching the mouse or rat caught therein.

    摘要翻译: 用于捕捉小鼠和大鼠的陷阱包括安装在两部分壳体内的标准捕鼠器。 标准的捕鼠器包括一个突出部,突出部通过一个狭槽突出一个壳体的一部分的弧形上壁,从而允许从壳体的外部使捕获器旋转。 壳体的第一部分枢转到壳体的第二部分,使得壳体可以方便地打开以处置捕获在捕获器中的鼠标或鼠标。 壳体屏蔽被锁定的陷阱,以便增强其安全性,同时允许其清空捕获器,而不会冒着接触其中捕获的鼠标或鼠标的风险。

    Preservative for aqueous products and systems
    6.
    发明授权
    Preservative for aqueous products and systems 失效
    水性产品和系统的防腐剂

    公开(公告)号:US5147884A

    公开(公告)日:1992-09-15

    申请号:US479126

    申请日:1990-02-12

    IPC分类号: A01N39/00 A01N31/14

    CPC分类号: A01N31/14

    摘要: An antimicrobial composition for preserving products or systems containing an aqueous phase comprising from 10 to 60% by weight or tert.-butyl hydroperoxide, from 3 to 50% by weight of a monophenylglycol ether of formulas I or II herein, and the remainder a diluent which is water, an organic solvent or a mixture of water and organic solvent; and a method of use of the antimicrobial composition. The antimicrobial composition may additionally include up to about 20% by weight of a biocide selected from certain non-halogenated phenols, certain heterocyclic compounds and guanidine, phthalimide and urea derivatives.

    摘要翻译: 一种用于保存含有水相的产物或体系的抗微生物组合物,其包含10至60重量%或叔丁基过氧化氢,3至50重量%的本文式I或II的单苯基二醇醚,其余为稀释剂 其为水,有机溶剂或水和有机溶剂的混合物; 和抗微生物组合物的使用方法。 抗微生物组合物可另外包括至多约20重量%的选自某些非卤化酚,某些杂环化合物和胍,邻苯二甲酰亚胺和脲衍生物的杀生物剂。

    Antiandrogenic sulfonylsteroidooxazoles
    8.
    发明授权
    Antiandrogenic sulfonylsteroidooxazoles 失效
    抗雄激素磺酰甾类恶唑

    公开(公告)号:US5134135A

    公开(公告)日:1992-07-28

    申请号:US541658

    申请日:1990-06-21

    IPC分类号: C07J1/00 C07J71/00

    CPC分类号: C07J1/0025 C07J71/0063

    摘要: 2'-Alkylsulfonylsteroido[2,3-d]oxazoles, for example 2'-methylsulfonyl-5.alpha.-pregn-2-en-20-yno[2,3-d]oxazol-17.beta.-ol, which are useful as antiandrogenic agents, and proceses for preparation, method of use and compositions thereof are disclosed.

    摘要翻译: 2'-烷基磺酰基类固醇[2,3-d]恶唑,例如2'-甲基磺酰基-5α-孕-2-烯-20-炔并[2,3-d]恶唑-17β-醇,它们可用作 公开了抗雄激素剂和制剂方法,使用方法及其组合物。

    Anticoagulant/surfactant rodenticidal compositions and method
    9.
    发明授权
    Anticoagulant/surfactant rodenticidal compositions and method 失效
    抗凝剂/表面活性剂杀鼠剂组合物及方法

    公开(公告)号:US5132321A

    公开(公告)日:1992-07-21

    申请号:US403268

    申请日:1989-09-05

    申请人: Garland G. Corey

    发明人: Garland G. Corey

    IPC分类号: A01N25/00 A01N43/16

    摘要: Rodenticidal compositions comprising an anticoagulant type rodenticide in combination with a fluorosurfactant of the amphoteric, anionic or cationic type, optionally admixed with a cereal grain bait, and a method of killing rodents by oral administration of such compositions.

    摘要翻译: 包含抗凝血型杀鼠剂与两性阴离子型或阳离子类型的含氟表面活性剂组合的任选与谷粒诱饵混合的杀鼠组合物,以及通过口服给予所述组合物杀死啮齿动物的方法。

    Antiandrogenic sulfonylsteroidofurans
    10.
    发明授权
    Antiandrogenic sulfonylsteroidofurans 失效
    抗雄激素磺酰类固醇

    公开(公告)号:US5100882A

    公开(公告)日:1992-03-31

    申请号:US541656

    申请日:1990-06-21

    IPC分类号: C07J71/00

    CPC分类号: C07J71/0047 C07J71/0005

    摘要: 5'-Alkylsulfonylsteroido[3,2-b]furans, for example 5'-methylsulfonyl-5.alpha.-pregn-2-en-20-yno[3,2-b]furan-17.beta.-ol having the structural formula, ##STR1## which are useful as antiandrogenic agents, and processes for preparation, method of use and compositions thereof are disclosed.

    摘要翻译: 5'-烷基磺酰基类似甾族化合物[3,2-b]呋喃,例如具有结构式的5'-甲基磺酰基-5α-孕-2-烯-20-炔[3,2-b]呋喃-17β-醇, 公开了可用作抗雄激素剂的及其制备方法,使用方法及其组合物。