会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明申请
    • ROLE OF PLD1 IN THROMBUS FORMATION AND INTEGRIN ALPHA IIB BETA 3 ACTIVATION
    • PLD1在血栓形成和INTEGRIN ALPHA IIB BETA 3激活中的作用
    • WO2011003809A1
    • 2011-01-13
    • PCT/EP2010/059405
    • 2010-07-01
    • CSL BEHRING GMBHJULIUS-MAXIMILIANS-UNIVERSITÄT-WÜRZBURGNIESWANDT, BernhardSTOLL, Guido
    • NIESWANDT, BernhardSTOLL, Guido
    • C07K16/40C12N9/20A61K39/395G01N33/50
    • C07K16/40A01K2217/075A61K2039/505C12N9/20
    • The present invention relates to an inhibitor of phospholipase D1(PLD1) or an inhibitor of a direct activator of PLD1 for use in treating or preventing a disorder related to venous or arterial thrombus formation. Alternatively the present invention relates to the use of such an inhibitor as a lead compound for developing a drug for treating or preventing a disorder related to venous or arterial thrombus formation. The present invention also relates to a method of treating and/or preventing a disorder related to venous or arterial thrombus formation comprising administering a pharmaceutically effective amount of an inhibitor of phospholipase D1(PLD1) or an inhibitor of a direct activator of PLD1 to a subject in need thereof. The present invention further relates to methods of identifying a compound suitable as a lead compound and/or as a medicament for the treatment and/or prevention of a disorder related to venous or arterial thrombus formation.
    • 本发明涉及磷脂酶D1(PLD1)的抑制剂或PLD1的直接活化剂的抑制剂,其用于治疗或预防与静脉或动脉血栓形成相关的病症。 或者,本发明涉及这种抑制剂作为引导化合物用于开发用于治疗或预防与静脉或动脉血栓形成相关的病症的药物的用途。 本发明还涉及治疗和/或预防与静脉或动脉血栓形成相关的病症的方法,其包括向受试者施用药学有效量的磷脂酶D1(PLD1)抑制剂或PLD1直接激活剂的抑制剂 需要它。 本发明还涉及鉴定适合作为铅化合物的化合物和/或用于治疗和/或预防与静脉或动脉血栓形成相关的障碍的药物的方法。
    • 4. 发明申请
    • CLEC-2 IS AN ESSENTIAL PLATELET ACTIVATING RECEPTOR IN HEMOSTASIS AND THROMBOSIS
    • CLEC-2是HEMOSTASIS和THROMBOSIS中的基础药物活化受体
    • WO2010149664A1
    • 2010-12-29
    • PCT/EP2010/058840
    • 2010-06-22
    • CSL Behring GmbHJulius-Maximilians-Universität-WürzburgNIESWANDT, BernhardMAY, Frauke
    • NIESWANDT, BernhardMAY, Frauke
    • A61P7/02
    • G01N33/5044A61K39/39541A61K39/3955A61K2039/505C07K16/2803C07K2317/55C07K2319/30G01N2333/4724A61K2300/00
    • The present invention relates to a pharmaceutical composition comprising an inhibitor of C-type lectin-like receptor 2 (CLEC-2) or an inhibitor of an activator of CLEC-2, each of which induces an irreversible inactivation or degradation of CLEC-2 on platelets, and optionally a pharmaceutically acceptable carrier, excipient and/or diluent. Furthermore, the present invention relates to an inhibitor of C-type lectin-like receptor 2 (CLEC-2) or an inhibitor of an activator of CLEC-2, each of which induces an irreversible inactivation or degradation of CLEC-2 on platelets, for use in treating or preventing a disorder related to venous or arterial thrombus formation and to the use of such an inhibitor as a lead compound for developing a drug for treating or preventing a disorder related to venous or arterial thrombus formation. The present invention also relates to a method of treating and/or preventing a disorder related to venous or arterial thrombus formation comprising administering a pharmaceutically effective amount of an inhibitor of C-type lectin-like receptor 2 (CLEC-2) or an inhibitor of an activator of CLEC-2, each of which induces an irreversible inactivation or degradation of CLEC-2 on platelets, to a subject in need thereof. The present invention further relates to methods of identifying a compound suitable as a lead compound and/or as a medicament for the treatment and/or prevention of a disorder related to venous or arterial thrombus formation.
    • 本发明涉及包含C型凝集素样受体2(CLEC-2)抑制剂或CLEC-2活化剂抑制剂的药物组合物,其各自诱导CLEC-2的不可逆失活或降解 血小板和任选的药学上可接受的载体,赋形剂和/或稀释剂。 此外,本发明涉及C型凝集素样受体2(CLEC-2)的抑制剂或CLEC-2的活化剂的抑制剂,其各自诱导血小板上的CLEC-2的不可逆失活或降解, 用于治疗或预防与静脉或动脉血栓形成相关的病症,以及使用这种抑制剂作为引导化合物用于开发用于治疗或预防与静脉或动脉血栓形成相关的病症的药物。 本发明还涉及治疗和/或预防与静脉或动脉血栓形成相关的病症的方法,其包括给予药学有效量的C型凝集素样受体2(CLEC-2)抑制剂或 CLEC-2的活化剂,其各自诱导血小板上的CLEC-2的不可逆失活或降解,需要其受试者。 本发明还涉及鉴定适合作为铅化合物的化合物和/或用于治疗和/或预防与静脉或动脉血栓形成相关的障碍的药物的方法。
    • 5. 发明申请
    • STIM2-MEDIATED CAPACITIVE CALCIUM ENTRY
    • STIM2介导的电容钙入侵
    • WO2010136577A1
    • 2010-12-02
    • PCT/EP2010/057443
    • 2010-05-28
    • CSL BEHRING GMBHJULIUS-MAXIMILIANS-UNIVERSITÄT-WÜRZBURGNIESWANDT, BernhardSTOLL, Guido
    • NIESWANDT, BernhardSTOLL, Guido
    • A61K39/395C07K16/18C12N15/113
    • C07K16/18A61K39/39541C07K14/705
    • The present invention relates to a pharmaceutical composition comprising an inhibitor of STIM2 or an inhibitor of STIM2-regulated plasma membrane calcium channel activity and optionally a pharmaceutically acceptable carrier, excipient and/or diluent. Furthermore, the present invention relates to an inhibitor of STIM2 or an inhibitor of STIM2-regulated plasma membrane calcium channel activity for the treatment and/or prevention of a neurological disorder associated with pathologically increased cytosolic calcium concentrations. The present invention also relates to a method of treating and/or preventing a neurological disorder associated with pathologically increased cytosolic calcium concentrations comprising administering a pharmaceutically effective amount of an inhibitor of STIM2 or of an inhibitor of STIM2-regulated plasma membrane calcium channel activity to a subject in need thereof. The present invention further relates to methods of identifying a compound suitable as a lead compound and/or as a medicament for the treatment and/or prevention of a neurological disorder associated with pathologically increased cytosolic calcium concentrations.
    • 本发明涉及包含STIM2抑制剂或STIM2调节的质膜钙通道活性抑制剂和任选的药学上可接受的载体,赋形剂和/或稀释剂的药物组合物。 此外,本发明涉及用于治疗和/或预防与病理性增加的细胞溶质钙浓度相关的神经障碍的STIM2抑制剂或STIM2调节的质膜钙通道活性抑制剂。 本发明还涉及治疗和/或预防与病理增加的细胞溶质钙浓度相关的神经障碍的方法,其包括将药物有效量的STIM2抑制剂或STIM2调节的质膜钙通道活性抑制剂施用于 受到需要。 本发明还涉及鉴定适合作为铅化合物的化合物和/或用于治疗和/或预防与病理增加的细胞溶质钙浓度相关的神经障碍的药物的方法。