Rigid Panel Adhesion Method and a Smearing Module Utilized Thereby
    2.
    发明申请
    Rigid Panel Adhesion Method and a Smearing Module Utilized Thereby 审中-公开
    刚性面板粘合方法和由此使用的涂抹模块

    公开(公告)号:US20120312470A1

    公开(公告)日:2012-12-13

    申请号:US13465067

    申请日:2012-05-07

    Applicant: Chin-Ho Chen

    Inventor: Chin-Ho Chen

    Abstract: The invention discloses a rigid panel adhesion method including a smearing step and a pressing step. The smearing step smears glue on a surface of a first rigid panel to form a glue layer. The glue layer has a single contact portion being in one-dimensional form of a dot or line. The glue layer has a coverage ratio of no less than 50% over the surface of the first rigid panel. The pressing step touches the contact portion of the glue layer with a second rigid panel, and slowly presses the first and second rigid panels together to discharge gases between the first and second rigid panels, thereby adhering the first and second rigid panels to each other.

    Abstract translation: 本发明公开了一种包括涂抹步骤和压制步骤的刚性面板粘合方法。 涂抹步骤在第一刚性面板的表面上涂抹胶水以形成胶层。 胶层具有单点或一线的单一接触部分。 胶层在第一刚性面板的表面上具有不小于50%的覆盖率。 按压步骤用第二刚性面板接触胶层的接触部分,并且将第一和第二刚性面板缓慢地压在一起以排出第一和第二刚性面板之间的气体,从而将第一和第二刚性面板彼此粘合。

    BETULINIC ACID DERIVATIVES AS ANTI-HIV AGENTS
    5.
    发明申请
    BETULINIC ACID DERIVATIVES AS ANTI-HIV AGENTS 审中-公开
    作为抗艾滋病毒药物的白蛋白酸衍生物

    公开(公告)号:US20110152229A1

    公开(公告)日:2011-06-23

    申请号:US11943956

    申请日:2007-11-21

    CPC classification number: C07J63/008

    Abstract: The present invention provides compounds of the general structure: which are substituted at the 3 and 28 positions, along with pharmaceutical formulations containing the same and methods of treating viral infections employing the same.

    Abstract translation: 本发明提供了一般结构的化合物:其在3和28位被取代,以及含有该化合物的药物制剂以及使用其的治疗病毒感染的方法。

    Anti-HIV agents with dual sites of action
    6.
    发明授权
    Anti-HIV agents with dual sites of action 有权
    具有双重作用地点的抗艾滋病毒药物

    公开(公告)号:US07381717B2

    公开(公告)日:2008-06-03

    申请号:US11348052

    申请日:2006-02-06

    CPC classification number: A61K31/56 C07J53/00

    Abstract: The present invention provides compounds of the general structure: which are substituted at the 3 and 28 positions, along with pharmaceutical formulations containing the same and methods of treating viral infections employing the same.

    Abstract translation: 本发明提供了一般结构的化合物:其在3和28位被取代,以及含有该化合物的药物制剂以及使用其的治疗病毒感染的方法。

    Anti-HIV agents with dual sites of action
    8.
    发明授权
    Anti-HIV agents with dual sites of action 有权
    具有双重作用地点的抗艾滋病毒药物

    公开(公告)号:US07026305B2

    公开(公告)日:2006-04-11

    申请号:US10413193

    申请日:2003-04-14

    CPC classification number: A61K31/56 C07J53/00

    Abstract: The present invention provides compounds of the general structure: which are substituted at the 3 and 28 positions, along with pharmaceutical formulations containing the same and methods of treating viral infections employing the same.

    Abstract translation: 本发明提供了一般结构的化合物:其在3和28位被取代,以及含有该化合物的药物制剂以及使用其的治疗病毒感染的方法。

    Suppressor of HIV-1 replication and transcription
    9.
    发明授权
    Suppressor of HIV-1 replication and transcription 失效
    HIV-1复制和转录抑制因子

    公开(公告)号:US06586174B1

    公开(公告)日:2003-07-01

    申请号:US09450141

    申请日:1999-11-29

    CPC classification number: C12Q1/703 A61K38/00 C07K14/4703 C12Q1/6897

    Abstract: The present invention relates to a bioactive molecule, herein referred to as the CD8+ suppressor molecule, that is produced by the CD8+ subset of human T-lymphocytes and suppresses type-1 human immunodeficiency virus (HIV-1) replication through inhibition of viral transcription. The invention relates to isolation of clonal CD8+ cells lines that produce the antiviral activity and the development of an assay system for detection of the antiviral activity. The clonal cell lines and the assay system, described herein, may be utilized to purify, characterize and clone the CD8+ suppressor molecule. The CD8+ suppressor molecule may have therapeutic applications for treatment of diseases associated with HIV-1 infection.

    Abstract translation: 本发明涉及由人T淋巴细胞的CD8 +亚群产生并通过抑制病毒转录抑制1型人类免疫缺陷病毒(HIV-1)复制的生物活性分子(本文中称为CD8 +抑制分子)。 本发明涉及产生抗病毒活性的克隆CD8 +细胞系的分离和用于检测抗病毒活性的测定系统的开发。 本文所述的克隆细胞系和测定系统可用于纯化,表征和克隆CD8 +抑制分子。 CD8 +抑制分子可能具有用于治疗与HIV-1感染相关的疾病的治疗应用。

    Suppressor of HIV replication and transcription
    10.
    发明授权
    Suppressor of HIV replication and transcription 失效
    HIV复制和转录抑制因子

    公开(公告)号:US5627023A

    公开(公告)日:1997-05-06

    申请号:US38387

    申请日:1993-03-29

    CPC classification number: C12Q1/6897 C07K14/4703 A61K38/00 Y10S435/974

    Abstract: The present invention relates to a bioactive molecule, herein referred to as the CD8 suppressor molecule, that is produced by the CD8 subset of human T-lymphocytes and suppresses type-1 human immunodeficiency virus (HIV-1) replication through inhibition of vital transcription. The invention relates to isolation of clonal CD8 cells lines that produce the antiviral activity and the development of an assay system for detection of the antiviral activity. The clonal cell lines and the assay system, described herein, may be utilized to purify, characterize and clone the CD8 suppressor molecule. The CD8 suppressor molecule may have therapeutic applications for treatment of diseases associated with HIV-1 infection.

    Abstract translation: 本发明涉及由人T淋巴细胞的CD8子集产生并通过抑制重要转录抑制1型人类免疫缺陷病毒(HIV-1)复制的生物活性分子(本文中称为CD8抑制分子)。 本发明涉及产生抗病毒活性的克隆CD8细胞系的分离和用于检测抗病毒活性的测定系统的开发。 本文所述的克隆细胞系和测定系统可用于纯化,表征和克隆CD8抑制分子。 CD8抑制分子可能具有用于治疗与HIV-1感染相关的疾病的治疗应用。

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