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    • 1. 发明申请
    • INHIBITORS OF GLYCOPROTEIN VI BASED ON MONOCLONAL ANTIBODY HGP 5C4
    • 基于单克隆抗体HGP 5C4的糖蛋白Ⅵ的抑制剂
    • WO2005054294A2
    • 2005-06-16
    • PCT/EP2004013779
    • 2004-12-03
    • PROCORDE GMBHGSF FORSCHUNGSZENTRUM UMWELTGAWAZ MEINRADKREMMER ELISABETHMUENCH GOETZ
    • GAWAZ MEINRADKREMMER ELISABETHMUENCH GOETZ
    • C07K16/28C07K16/00
    • C07K16/2803A61K2039/505
    • The present invention relates to a specific inhibitor of human platelet glycoprotein VI. The inhibitor may be an optionally humanized antibody or function-conservative fragments or variants thereof, a specific fusion protein or conjugate. Moreover, the present invention relates to pharmaceutical compositions containing the specific inhibitor of the invention. The present invention also relates to hybridomas expressing the antibody of the present invention. Furthermore, the present invention relates to the use of the specific inhibitor of glycoprotein VI for the preparation of a medicament for the prevention of acute and chronic vascular diseases associated with arterial and/or intravenous thrombosis, such as acute coronary syndrome, acute carotid artery syndrome, acute myocardial infarction, acute cerebral stroke and chronic coronary or peripheral vessel disease. Finally, the present invention relates to a process for preparing the antibody of the invention and to a process for preparing a specific fragment of the antibody of the present invention.
    • 本发明涉及人血小板糖蛋白VI的特异性抑制剂。 抑制剂可以是任选人源化抗体或其功能保守性片段或变体,特异性融合蛋白或缀合物。 而且,本发明涉及含有本发明特异性抑制剂的药物组合物。 本发明还涉及表达本发明抗体的杂交瘤。 此外,本发明涉及糖蛋白VI的特异性抑制剂在制备用于预防与动脉和/或静脉内血栓形成相关的急性和慢性血管疾病如急性冠状动脉综合征,急性颈动脉综合征 ,急性心肌梗塞,急性脑卒中和慢性冠状动脉或外周血管疾病。 最后,本发明涉及制备本发明抗体的方法和制备本发明抗体特异性片段的方法。
    • 5. 发明申请
    • METHOD AND DEVICE FOR THE MASS SPECTROMETRIC DETECTION OF COMPOUNDS
    • 用于质谱法检测化合物的方法和装置
    • WO2007019982A3
    • 2007-11-29
    • PCT/EP2006007773
    • 2006-08-05
    • GSF FORSCHUNGSZENTRUM UMWELTMUEHLBERGER FABIANZIMMERMANN RALF
    • MUEHLBERGER FABIANZIMMERMANN RALF
    • H01J49/10H01J49/16
    • H01J49/107H01J49/162
    • The invention relates to a method for the mass spectrometric detection of compounds in a gas flow (2). According to said method: the volume units in the gas flow (2) are ionised, forming ions of the compounds, the ionisation being carried out by means of radiation (9, 10) crossing the gas flow, formed in the alternation of electron pulses or pulse sequences and photon pulses or pulse sequences; the ions are deviated by an electric field (13) towards a mass spectrometric method; and the ions are detected using a mass spectrometric method. The aim of the invention is to provide one such method with an extended measuring range and a significantly improved resolution. To this end, the photon pulses or pulse sequences are generated by an excimer lamp (11) and the alternation between the electron pulses or pulse sequences and the photon pulses or pulse sequences is carried out at an alternation frequency higher than 50 Hz.
    • 一种气体流(2)中的化合物的质谱表征方法,包括使气体流(2)中的体积单元离子化以形成化合物的离子,通过横过射束(9,10)的气流的电离交替交替电子脉冲 或者形成脉冲串和光子脉冲或脉冲序列,通过电场(13)使离子偏转到质谱方法并且使用质谱方法检测离子。 本发明的目的是提出一种具有扩展的测量范围和显着提高的分辨率的所述类型的方法。 该目的通过由准分子灯(11)产生光子脉冲或脉冲序列来实现,并且该改变发生在电子脉冲或脉冲序列与具有高于50Hz的交变频率的光子脉冲或脉冲序列之间。
    • 10. 发明申请
    • ANTIVIRALLY ACTIVE OLIGOPEPTIDE ISOLATED FROM ROYAL JELLY
    • 蜂王浆隔离抗病毒有效寡肽
    • WO9933866A3
    • 1999-09-10
    • PCT/EP9807811
    • 1998-12-02
    • GSF FORSCHUNGSZENTRUM UMWELT
    • BENGSCH EBERHARDKETTRUP ANTONIUSPOLSTER JUERGEN
    • A61K38/00C07K14/415C07K14/435A61K38/17
    • C07K14/415A61K38/00C07K14/43572
    • The invention relates to a family of oligopeptides with a completely new structure which occurs in selectively obtained royal jellies of certain vegetable origin and has been correlated with marked antiviral properties. The pilot structure is a molecule with 52 amino acids. Numerous analogous, nearly identical molecules are present in a satellite-like manner. The substances have a broad spectrum of antiviral activity, including against retroviruses, and have no toxic effect on humans even at high doses. A further surprising characteristic is their extreme resistance to all controlled proteases and other enzymes. The molecules are highly convoluted and resistant to attack. Despite their convolution they are geometrically very flexible and can form several conformers. The native state is easily soluble in water. Chemical synthesis results in a water insoluble form which can, however, be easily transformed into a soluble bioactive conformer which is similar to the native form. These new oligopeptides are therefore the first to combine in an optimal manner all the properties required of a potentially antiviral substance category.
    • 本发明涉及一类寡肽与发生在选择性地收集果冻royales特定植物来源一个完全新的结构,并具有较强的抗病毒效果相关。 导频结构是具有52个氨基酸的分子。 卫星状这是众多模拟几乎相同的分子。 该物质具有活性的宽谱抗病毒,包括反转录病毒甚至人类无毒高剂量。 令人惊讶的也是他们极强的抗所有受控蛋白酶等酶。 分子是高度缠结和无懈可击。 尽管纠缠他们是几何高度灵活,可形成多种构象。 在天然状态下是有易溶于水的形式。 从化学合成的结果中不溶于水的形式,但其可转化为可溶的,密切相关的天然形式的生物活性构象异构体。 新寡肽结合从而在第一时间,最佳的,所有必须由潜在的抗病毒药物类被请求的属性。