Inks containing water-soluble perylene dyes and their use in ink-jet printing
    3.
    发明授权
    Inks containing water-soluble perylene dyes and their use in ink-jet printing 失效
    含有水溶性苝染料的油墨及其在喷墨印刷中的用途

    公开(公告)号:US07214259B2

    公开(公告)日:2007-05-08

    申请号:US10558072

    申请日:2004-04-07

    IPC分类号: C09D11/02 B41J2/01 C07D221/22

    摘要: An ink comprising a liquid medium and a colorant, wherein the liquid medium comprises water and a water-miscible organic solvent and the colorant is of Formula (1), wherein the colorant is dissolved in the liquid medium: Formula (1) wherein: each independently is a water-solubilising group selected from sulfo, carboxy, phosphato and poly(ethylene oxide); each Z independently is optionally substituted alkyl, optionally substituted aryl or optionally substituted aralkyl; each Q independently is a direct bond or —NR— wherein R is H, optionally substituted aryl or optionally substituted alkyl; rings A,B,C and D are each independently unsubstituted or carry a substituent selected from optionally substituted alkyl, optionally substituted aryl and optionally substituted aralkyl; each n independently is from 1 to 3; and each m independently is 0, 1 or 2; provided that when either or both of the groups represented by Q is a direct bond then at least one n has a value of at least 2. Also colourants and ink-jet printing processes, cartridges and prints

    摘要翻译: 一种包含液体介质和着色剂的油墨,其中所述液体介质包括水和水混溶性有机溶剂,并且所述着色剂具有式(1),其中所述着色剂溶解在液体介质中:式(1)其中: 独立地是选自磺基,羧基,磷酸酯和聚(环氧乙烷)的水溶性基团; 每个Z独立地是任选取代的烷基,任选取代的芳基或任选取代的芳烷基; 每个Q独立地是直接键或-NR-,其中R是H,任选取代的芳基或任选取代的烷基; 环A,B,C和D各自独立地是未取代的或携带选自任选取代的烷基,任选取代的芳基和任选取代的芳烷基的取代基; 每个n独立地为1至3; 并且每个m独立地为0,1或2; 条件是当由Q表示的基团中的任一个或两个是直接键合时,至少一个n的值至少为2.还有着色剂和喷墨印刷方法,墨盒和印刷品

    Inks containing water-soluble perylene dyes and their use in ink-jet printing
    5.
    发明申请
    Inks containing water-soluble perylene dyes and their use in ink-jet printing 失效
    含有水溶性苝染料的油墨及其在喷墨印刷中的用途

    公开(公告)号:US20060272546A1

    公开(公告)日:2006-12-07

    申请号:US10558072

    申请日:2004-04-07

    摘要: An ink comprising a liquid medium and a colorant, wherein the liquid medium comprises water and a water-miscible organic solvent and the colorant is of Formula (1), wherein the colorant is dissolved in the liquid medium: Formula (1) wherein: each independently is a water-solubilising group selected from sulfo, carboxy, phosphato and poly(ethylene oxide); each Z independently is optionally substituted alkyl, optionally substituted aryl or optionally substituted aralkyl; each Q independently is a direct bond or —NR— wherein R is H, optionally substituted aryl or optionally substituted alkyl; rings A,B,C and D are each independently unsubstituted or carry a substituent selected from optionally substituted alkyl, optionally substituted aryl and optionally substituted aralkyl; each n independently is from 1 to 3; and each m independently is 0, 1 or 2; provided that when either or both of the groups represented by Q is a direct bond then at least one n has a value of at least 2. Also colourants and ink-jet printing processes, cartridges and prints.

    摘要翻译: 一种包含液体介质和着色剂的油墨,其中所述液体介质包括水和水混溶性有机溶剂,并且所述着色剂具有式(1),其中所述着色剂溶解在液体介质中:式(1)其中: 独立地是选自磺基,羧基,磷酸酯和聚(环氧乙烷)的水溶性基团; 每个Z独立地是任选取代的烷基,任选取代的芳基或任选取代的芳烷基; 每个Q独立地是直接键或-NR-,其中R是H,任选取代的芳基或任选取代的烷基; 环A,B,C和D各自独立地是未取代的或携带选自任选取代的烷基,任选取代的芳基和任选取代的芳烷基的取代基; 每个n独立地为1至3; 并且每个m独立地为0,1或2; 条件是当由Q表示的基团中的任一个或两个是直接键合时,至少一个n的值至少为2.还有着色剂和喷墨印刷方法,墨盒和印刷品。

    Tissue-specific and pathogen-specific toxic agents and ribozymes
    6.
    发明授权
    Tissue-specific and pathogen-specific toxic agents and ribozymes 失效
    组织特异性和病原体特异性毒素和核酶

    公开(公告)号:US06271359B1

    公开(公告)日:2001-08-07

    申请号:US09291902

    申请日:1999-04-14

    IPC分类号: C07H2102

    摘要: The present invention relates to the discovery, identification and characterization of toxic agents which are lethal to pathogens and methods for targeting such toxic agents to a pathogen or pathogen infected cells in order to treat and/or eradicate the infection. In particular, the present invention relates to toxic agents which target bacteria at different stages of the bacterial life cycle, which are delivered alone or in combination to bacteria or bacteria-infected cells. The invention relates to toxic agents which are lethal to diseased cells and methods for targeting such toxic agents to a diseased cell in order to treat and/or eradicate the disease. The present invention relates to promoter elements which are pathogen-specific or tissue-specific and the use of such promoter elements to achieve pathogen-specific or tissue-specific expression of the toxic agent(s) and/or ribozyme(s) of the present invention. Specifically, the invention relates to the delivery of one or more toxic gene products, antisense RNAs, or ribozymes, or combination thereof. The invention provides a novel system by which multiple pathogenic targets may be simultaneously targeted to cause the death of a pathogen, or cell infected with a pathogen. Further, the invention has important implications in the eradication of drug-resistant bacterium and bacterial pathogens. The invention provides a novel system by which multiple targets may be simultaneously targeted to cause the death of a diseased cell. The invention also has important implications in the eradication of drug-resistant pathogens and drug-resistant diseased cells (such as cancer cells).

    摘要翻译: 本发明涉及对病原体致死的毒性试剂的发现,鉴定和表征以及将这些毒性试剂靶向病原体或病原体感染的细胞以便治疗和/或根除感染的方法。 特别地,本发明涉及针对细菌生命周期不同阶段的细菌的毒性试剂,它们单独或组合递送至细菌或细菌感染细胞。 本发明涉及对患病细胞致死的毒物剂和用于将这些毒物剂靶向病变细胞以便治疗和/或根除疾病的方法。 本发明涉及作为病原体特异性或组织特异性的启动子元件以及这些启动子元件用于实现本发明的毒性剂和/或核酶的病原体特异性或组织特异性表达的启动子元件 发明。 具体地,本发明涉及递送一种或多种有毒基因产物,反义RNA或核酶或其组合。 本发明提供了一种新的系统,通过该系统可以同时靶向多种致病性靶标以引起病原体或感染病原体的细胞的死亡。 此外,本发明对消除耐药细菌和细菌病原体具有重要的意义。 本发明提供了一种新颖的系统,通过该系统可以同时靶向多个靶标以引起患病细胞的死亡。 本发明也对消除耐药病原体和耐药性疾病细胞(如癌细胞)具有重要意义。

    Substituted naphthalenyloxy-1,2-diaminocyclohexyl amide compounds
    7.
    发明授权
    Substituted naphthalenyloxy-1,2-diaminocyclohexyl amide compounds 失效
    取代萘氧基-1,2-二氨基环己基酰胺化合物

    公开(公告)号:US4663343A

    公开(公告)日:1987-05-05

    申请号:US756634

    申请日:1985-07-19

    CPC分类号: C07D295/135

    摘要: Substituted naphthalenyloxy- or naphthalenylthiooxyamides of trans-1,2-diaminocyclohexanes possess selective kappa opioid receptor site binding activity and are thus useful as analgesic or diuretic agents. Methods of preparing the compounds, pharmaceutical compositions, and a method for their use as analgesic agents are also disclosed.

    摘要翻译: 反式-1,2-二氨基环己烷的取代萘氧基或萘基硫代氧酰胺具有选择性κ阿片受体位点结合活性,因此可用作止痛剂或利尿剂。 还公开了制备化合物的方法,药物组合物及其用作止痛剂的方法。

    Process for the preparation of butane triols
    8.
    发明授权
    Process for the preparation of butane triols 失效
    制备丁三醇的方法

    公开(公告)号:US06479714B1

    公开(公告)日:2002-11-12

    申请号:US09242899

    申请日:1999-02-26

    IPC分类号: C07C2700

    CPC分类号: C07C29/147 C07C31/22

    摘要: A process for the preparation of butane triols is provided. In the process, a malic acid diester is reduced with sodium borohydride in the presence of an ether and an alcohol. Preferably, the malic acid diester is an ethyl or methyl ester, the ether is tetrahydrofuran or bis(2-methoxyethyl) ether (diglyme), and the alcohol comprises ethanol. Advantageously, the reaction is carried out at ambient temperature.

    摘要翻译: 提供了制备丁三醇的方法。 在此过程中,在醚和醇的存在下,用硼氢化钠还原苹果酸二酯。 优选地,苹果酸二酯是乙基或甲酯,醚是四氢呋喃或双(2-甲氧基乙基)醚(二甘醇二甲醚),醇包括乙醇。 有利地,反应在环境温度下进行。

    Substituted benzamides
    9.
    发明授权
    Substituted benzamides 失效
    取代苯甲酰胺

    公开(公告)号:US4786747A

    公开(公告)日:1988-11-22

    申请号:US48505

    申请日:1987-05-11

    CPC分类号: C07C255/00

    摘要: Benzamides of the formula (I): ##STR1## in which Ar is optionally substituted aryl; X is O, S or NH and R is optionally substituted alkyl or alkenyl when X is O or S, or is optionally substituted alkanoyl when X is NH, are prepared by(a) reacting a compound of the formula (II):ArCONHCH.sub.2 CN (II) with a brominating agent in a solvent which is substantially chemically inert to the reactants and in which compound (II) is soluble, to form a compound of the formula (III): ##STR2## and (b) reacting the compound (III) with a compound RXH.Preferably, bromination is carried out rapidly in dried ethyl acetate.The process avoids hydration of the CN group of the compound (III) to a carbamoyl group obviating a subsequent dehydration step later.The intermediate compound (III) is novel.The substituted benzamides are useful as herbicides and fungicides.

    Tissue-specific and pathogen-specific ribozymes
    10.
    发明授权
    Tissue-specific and pathogen-specific ribozymes 失效
    组织特异性和病原体特异性毒素和核酶

    公开(公告)号:US07575918B2

    公开(公告)日:2009-08-18

    申请号:US10935962

    申请日:2004-09-08

    摘要: The present invention relates to the discovery, identification and characterization of toxic agents which are lethal to pathogens and methods for targeting such toxic agents to a pathogen or pathogen infected cells in order to treat and/or eradicate the infection. In particular, the present invention relates to toxic agents which target bacteria at different stages of the bacterial life cycle, which are delivered alone or in combination to bacteria or bacteria-infected cells. The invention relates to toxic agents which are lethal to diseased cells and methods for targeting such toxic agents to a diseased cell in order to treat and/or eradicate the disease. The present invention relates to promoter elements which are pathogen-specific or tissue-specific and the use of such promoter elements to achieve pathogen-specific or tissue-specific expression of the toxic agent(s) and/or ribozyme(s) of the present invention. Specifically, the invention relates to the delivery of one or more toxic gene products, antisense RNAs, or ribozymes, or combination thereof. The invention provides a novel system by which multiple pathogenic targets may be simultaneously targeted to cause the death of a pathogen, or cell infected with a pathogen. Further, the invention has important implications in the eradication of drug-resistant bacterium and bacterial pathogens. The invention provides a novel system by which multiple targets may be simultaneously targeted to cause the death of a diseased cell. The invention has important implications in the eradication of drug-resistant pathogens (such as antibiotic resistant bacteria) and drug-resistant diseased cells (such as drug-resistant cancer cells).

    摘要翻译: 本发明涉及对病原体致死的毒性试剂的发现,鉴定和表征以及将这些毒性试剂靶向病原体或病原体感染的细胞以便治疗和/或根除感染的方法。 特别地,本发明涉及针对细菌生命周期不同阶段的细菌的毒性试剂,它们单独或组合递送至细菌或细菌感染细胞。 本发明涉及对患病细胞致死的毒物剂和用于将这些毒物剂靶向病变细胞以便治疗和/或根除疾病的方法。 本发明涉及作为病原体特异性或组织特异性的启动子元件以及这些启动子元件用于实现本发明的毒性剂和/或核酶的病原体特异性或组织特异性表达的启动子元件 发明。 具体地,本发明涉及递送一种或多种有毒基因产物,反义RNA或核酶或其组合。 本发明提供了一种新的系统,通过该系统可以同时靶向多种致病性靶标以引起病原体或感染病原体的细胞的死亡。 此外,本发明对消除耐药细菌和细菌病原体具有重要的意义。 本发明提供了一种新颖的系统,通过该系统可以同时靶向多个靶标以引起患病细胞的死亡。 本发明对消除耐药性病原体(如抗生素抗性细菌)和耐药性疾病细胞(如耐药性癌细胞)具有重要意义。