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    • 2. 发明授权
    • Optimization design method for the chassis structure of an electronic device based on mechanical, electrical and thermal three-field coupling
    • 基于机械,电和热三场耦合的电子设备底盘结构的优化设计方法
    • US08744824B2
    • 2014-06-03
    • US13259262
    • 2009-09-24
    • Baoyan DuanHui QiaoPeng LiShibo JiangBoyuan MaNing HanLizhi ZengYu He
    • Baoyan DuanHui QiaoPeng LiShibo JiangBoyuan MaNing HanLizhi ZengYu He
    • G06F17/50
    • G06F17/5018G06F2217/16G06F2217/80
    • An optimizing design method for a chassis structure of electronic equipment is disclosed, including: investigating from the point of view of mechanical, electric and thermal three-field coupling, determining the preliminary design size of the chassis, performing a mechanical analysis by using a mechanical analysis software such as ANSYS; converting the mesh model among the three-fields, obtaining the mesh model used for the electromagnetic and thermal analyses; setting the thermal analysis parameters, performing the thermal analysis by using an electromagnetic analysis software such as ICEPAK; determining a resonance frequency of the chassis and an electric parameter of the absorbing material, performing an electromagnetic analysis by using a thermal analysis software such as FEKO; correcting the analysis result by sample testing; determining whether the chassis satisfies the design requirement, if it satisfies the requirement, the optimizing design will be finished, otherwise, modifying the preliminary computer assisted design model, the electromagnetic analysis parameter and the thermal analysis parameter, repeating the above processes until the requirement is satisfied.
    • 公开了一种用于电子设备底盘结构的优化设计方法,包括:从机械,电和热三场耦合的角度考察,确定底盘的初步设计尺寸,通过使用机械 分析软件如ANSYS; 在三场中转换网格模型,获得用于电磁和热分析的网格模型; 设置热分析参数,使用ICEPAK等电磁分析软件进行热分析; 确定底盘的共振频率和吸收材料的电参数,通过使用诸如FEKO的热分析软件执行电磁分析; 通过样本测试纠正分析结果; 确定底盘是否满足设计要求,如果满足要求,优化设计将完成,否则,修改初步计算机辅助设计模型,电磁分析参数和热分析参数,重复上述过程,直到要求为 满意。
    • 5. 发明授权
    • Compounds for inhibition of HIV infection by blocking HIV entry
    • 通过阻止HIV进入来抑制HIV感染的化合物
    • US07241803B2
    • 2007-07-10
    • US10706027
    • 2003-11-12
    • Shibo JiangAsim Kumar Debnath
    • Shibo JiangAsim Kumar Debnath
    • C07D207/327A61K31/402
    • C07D207/327
    • A group of compounds that inhibit HIV replication by blocking HIV entry was identified. Two representative compounds, designated NB-2 and NB-64, inhibited HIV replication (p24 production) with IC50 values
    • 鉴定了一组通过阻断HIV进入而抑制HIV复制的化合物。 两种代表性的化合物(称为NB-2和NB-64)抑制HIV复制(p24产生),IC <50μg/ ml。 证明NB-2和NB-64是通过靶向HIV gp41的HIV进入抑制因子,因为:1)它们抑制HIV介导的细胞融合; 2)只有当病毒加入不到1小时后,才能抑制HIV复制; 3)它们不阻断gp120-CD4结合; 4)它们没有与共受体CXCR4相互作用,因为它们不能阻断抗CXCR4抗体结合CXCR4表达细胞; 5)它们阻断了使用构象特异性MAb NC-1通过夹心酶联免疫吸附测定(ELISA)检测到的gp41核心的形成; 6)它们抑制荧光天然 - 聚丙烯酰胺凝胶电泳(FN-PAGE)显示的gp41六螺旋束的形成; 和7)它们阻断了肽肽与肽IQN17模拟的gp41卷曲螺旋结构域内的疏水空穴的结合。 这些结果表明NB-2和NB-64可能与疏水腔相互作用并阻断融合活性gp41卷曲螺旋结构域的形成,导致HIV-1介导的膜融合和病毒进入的抑制。