Agents for treatment of diabetic retinopathy and drusen formation in macular degeneration
    2.
    发明申请
    Agents for treatment of diabetic retinopathy and drusen formation in macular degeneration 审中-公开
    用于治疗黄斑变性的糖尿病性视网膜病变和玻璃体变形的药剂

    公开(公告)号:US20050137147A1

    公开(公告)日:2005-06-23

    申请号:US11016116

    申请日:2004-12-17

    摘要: Agents that stimulate nuclear translocation of Nrf2 protein and the subsequent increases in gene products that detoxify and eliminate cytotoxic metabolites are provided in a method for treating diabetic retinopathy or drusen formation in age-related macular degeneration. The structurally diverse agents that act on the Nrf2/ARE pathway induce the expression of enzymes and proteins that possess chemically versatile cytoprotective properties and are a defense against toxic metabolites and xenobiotics. Agents include certain electrophiles and oxidants such as a Michael Addition acceptor, diphenol, thiocarbamate, quinone, 1,2-dithiole-3-thione, butylated hydroxyanisole, flavonoid other than genistein, an isothiocyanate, 3,5-di-tert-butyl-4-hydroxytoluene, ethoxyquin, a coumarin, combinations thereof, or a pharmacologically active derivative or analog thereof.

    摘要翻译: 在年龄相关性黄斑变性中治疗糖尿病性视网膜病变或玻璃疣形成的方法中提供了刺激Nrf2蛋白的核易位和随后增加解毒和消除细胞毒性代谢物的基因产物的试剂。 作用于Nrf2 / ARE途径的结构不同的试剂诱导具有化学通用的细胞保护性质的酶和蛋白质的表达,并且是防止有毒代谢物和异生物。 药剂包括某些亲电试剂和氧化剂如迈克尔加成受体,二酚,硫代氨基甲酸酯,醌,1,2-二硫杂环戊烯-3-硫酮,丁基化羟基苯甲醚,除了染料木黄酮以外的类黄酮,异硫氰酸酯,3,5-二叔丁基 - 4-羟基甲苯,乙氧喹,香豆素,其组合,或其药理活性衍生物或类似物。

    Time division multiplexed switch core using multiple write ports
    3.
    发明申请
    Time division multiplexed switch core using multiple write ports 审中-公开
    使用多个写端口的时分复用交换机核心

    公开(公告)号:US20050078693A1

    公开(公告)日:2005-04-14

    申请号:US10683038

    申请日:2003-10-10

    IPC分类号: H04L12/56

    CPC分类号: H04L49/103

    摘要: ASIC libraries generally have some form of multi-port register file with 2 or more write ports and 2-8 read ports. Such register files can be exploited to implement a memory system using less external logic (fewer external-to-the memory MUXes to achieve desired narrow read ports) and/or fewer RAM instances. The desired memory system (including a single multi-port RAM that is configured to have a single very-wide write port and multiple narrow read ports) will then no longer require multiple instances of RAMs, and will therefore require less area due to overall reduced bit density.

    摘要翻译: ASIC库通常具有一些形式的多端口寄存器文件,具有2个或更多写入端口和2-8个读取端口。 这样的寄存器文件可以被利用来实现使用更少的外部逻辑(更少的外部到存储器MUX来实现期望的窄读取端口)和/或更少的RAM实例的存储器系统。 所需的存储系统(包括配置为具有单个非常宽的写入端口和多个窄读取端口的单个多端口RAM)将不再需要多个RAM实例,因此总体上将减少面积 位密度。

    Agents for treatment of glaucomatous retinopathy and optic neuropathy
    6.
    发明申请
    Agents for treatment of glaucomatous retinopathy and optic neuropathy 审中-公开
    用于治疗青光眼性视网膜病变和视神经病变的药剂

    公开(公告)号:US20050137146A1

    公开(公告)日:2005-06-23

    申请号:US11015888

    申请日:2004-12-17

    摘要: Agents that stimulate nuclear translocation of Nrf2 protein and the subsequent increases in gene products that detoxify and eliminate cytotoxic metabolites are provided in a method for treating glaucomatous retinopathy or optic neuropathy. The structurally diverse agents that act on the Nrf2/ARE pathway induce the expression of enzymes and proteins that possess chemically versatile cytoprotective properties and are a defense against toxic metabolites and xenobiotics. Agents include certain electrophiles and oxidants such as a Michael Addition acceptor, diphenol, thiocarbamate, quinone, 1,2-dithiole-3-thione, butylated hydroxyanisole, flavonoid, an isothiocyanate, 3,5-di-tert-butyl-4-hydroxytoluene, ethoxyquin, a coumarin, combinations thereof, or a pharmacologically active derivative or analog thereof.

    摘要翻译: 在治疗青光眼性视网膜病变或视神经病变的方法中提供了刺激Nrf2蛋白的核易位的药物和随后增加的解毒和消除细胞毒性代谢物的基因产物。 作用于Nrf2 / ARE途径的结构不同的试剂诱导具有化学通用的细胞保护性质的酶和蛋白质的表达,并且是防止有毒代谢物和异生物。 药剂包括某些亲电试剂和氧化剂如迈克尔加成受体,二酚,硫代氨基甲酸酯,醌,1,2-二硫杂环戊烯-3-硫酮,丁基化羟基苯甲醚,类黄酮,异硫氰酸酯,3,5-二叔丁基-4-羟基甲苯 ,乙氧喹啉,香豆素,其组合,或其药理学活性衍生物或类似物。