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    • 1. 发明授权
    • Method and system for operating applications for remote terminal devices
    • 用于远程终端设备操作应用的方法和系统
    • US07747683B2
    • 2010-06-29
    • US12159553
    • 2006-12-28
    • Shai KurianskiAssaf Friedler
    • Shai KurianskiAssaf Friedler
    • G06F15/16
    • H04L67/303H04L67/02H04L67/04H04L67/10
    • Method for allowing a user of a mobile terminal device having predetermined computational resources to remotely develop and operate upgraded content delivery applications. A client-side application and a corresponding remote application are installed on the terminal device and on a server connected to the terminal device. The remote application dynamically splits the tasks to be performed by the content delivery application between the client-side application and remote application, according to its computational resources and processes, in real-time, the content and its associated logic and input data to be delivered to the terminal device. The processed content is then transmitted to the terminal device over the data network and the content is rendered by the client-side application. The client-side application responds to inputs from the user and/or to messages from the server or further connected devices.
    • 允许具有预定计算资源的移动终端设备的用户远程开发和操作升级的内容传送应用的方法。 客户端应用程序和对应的远程应用程序安装在终端设备和连接到终端设备的服务器上。 远程应用程序根据其计算资源和过程实时动态地将内容交付应用执行的任务在客户端应用程序和远程应用程序之间进行动态分割,内容及其相关逻辑和要传递的输入数据 到终端设备。 然后,经处理的内容通过数据网络发送到终端设备,并且内容由客户端应用呈现。 客户端应用程序响应来自用户的输入和/或来自服务器或其他连接设备的消息。
    • 5. 发明申请
    • Method and System for Operating Applications for Remote Terminal Devices
    • 远程终端设备操作应用的方法和系统
    • US20080307048A1
    • 2008-12-11
    • US12159553
    • 2006-12-28
    • Assaf FriedlerShai Kurianski
    • Assaf FriedlerShai Kurianski
    • H04L29/08G06F15/16
    • H04L67/303H04L67/02H04L67/04H04L67/10
    • Method for allowing a user of a mobile terminal device having predetermined computational resources to remotely develop and operate upgraded content delivery applications. A client-side application and a corresponding remote application are installed on the terminal device and on a server connected to the terminal device. The remote application dynamically splits the tasks to be performed by the content delivery application between the client-side application and remote application, according to its computational resources and processes, in real-time, the content and its associated logic and input data to be delivered to the terminal device. The processed content is then transmitted to the terminal device over the data network and the content is rendered by the client-side application. The client-side application responds to inputs from the user and/or to messages from the server or further connected devices.
    • 允许具有预定计算资源的移动终端设备的用户远程开发和操作升级的内容传送应用的方法。 客户端应用程序和对应的远程应用程序安装在终端设备和连接到终端设备的服务器上。 远程应用程序根据其计算资源和过程实时动态地将内容交付应用执行的任务在客户端应用程序和远程应用程序之间进行动态分割,内容及其相关逻辑和要传递的输入数据 到终端设备。 然后,经处理的内容通过数据网络发送到终端设备,并且内容由客户端应用呈现。 客户端应用程序响应来自用户的输入和/或来自服务器或其他连接设备的消息。
    • 8. 发明授权
    • Inhibition of nuclear import by backbone cyclic peptide analogs
    • 通过骨架环肽类似物抑制核进口
    • US06664368B1
    • 2003-12-16
    • US09564677
    • 2000-05-04
    • Assaf FriedlerAbraham LoyterChaim GilonAmnon Wolf
    • Assaf FriedlerAbraham LoyterChaim GilonAmnon Wolf
    • C07K750
    • C07K14/005C12N2740/16322
    • The design and the synthesis of backbone cyclic peptide analogs which functionally mimic the nuclear localization signal (NLS) region of macromolecules is disclosed. The principles of the invention are exemplified for the NLS sequences of the human immunodeficiency virus type 1 proteins MA, Vpr, Tat and NLS-like sequences of HIV-1 protein Vif. We disclose the discovery of a novel, highly potent backbone cyclic peptide, designated BCvir, which inhibits nuclear import with an IC50 value of 35 nM. This inhibitory potency is to be compared to 12 &mgr;M exhibited by the linear parent HIV-1 MA NLS peptide. BCvir also reduced HIV-1 production by 75% in infected non-dividing cultured human T-cells and was relatively resistant to tryptic digestion. These properties render backbone cyclic peptide analogs of NLS or NLS-like sequences as candidates for novel drugs based on blocking nuclear import of viral genomes.
    • 公开了功能上模拟大分子的核定位信号(NLS)区域的骨架环肽类似物的设计和合成。 对于HIV-1蛋白Vif的人免疫缺陷病毒1型蛋白MA,Vpr,Tat和NLS样序列的NLS序列,举例说明了本发明的原理。 我们公开了一种称为BCvir的新型高效骨架环肽的发现,其抑制核导入,IC50值为35nM。 将该抑制效力与线性亲本HIV-1 MA NLS肽显示的12μM进行比较。 在感染的非分裂培养的人类T细胞中,BCvir还将艾滋病毒1的产量降低了75%,并且相对抗胰蛋白酶消化。 这些性质使NLS或NLS样序列的骨架环肽类似物作为基于阻断核进入病毒基因组的新型药物的候选物。