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    • 95. 发明申请
    • MEMORY ACCESSING SYSTEM AND METHOD
    • 存储器访问系统和方法
    • US20080082764A1
    • 2008-04-03
    • US11538253
    • 2006-10-03
    • Yi Feng JangZhi-Jian LiangHai-Ping Liu
    • Yi Feng JangZhi-Jian LiangHai-Ping Liu
    • G06F13/00
    • G06F13/4239
    • A memory accessing system, including an internal memory, an external memory, a microprocessor and a controller, is provided. The internal memory is configured to have a program space with a first address range and a data space with a second address range, and the program space and the data space are for source codes and data storage respectively. The external memory is configured to have an external data space with a third address range for storing data, and the third address range covers the first and second address ranges. The microprocessor is configured to process the source codes and data. The controller is configured to control the access of the program space, data space and the external data space.
    • 提供了包括内部存储器,外部存储器,微处理器和控制器的存储器访问系统。 内部存储器被配置为具有具有第一地址范围的程序空间和具有第二地址范围的数据空间,并且程序空间和数据空间分别用于源代码和数据存储。 外部存储器被配置为具有用于存储数据的具有第三地址范围的外部数据空间,并且第三地址范围覆盖第一和第二地址范围。 微处理器配置为处理源代码和数据。 控制器配置为控制程序空间,数据空间和外部数据空间的访问。
    • 96. 发明申请
    • Acyclic Hydrazides as Cannabinoid Receptor Modulators
    • 非环状酰肼作为大麻素受体调节剂
    • US20080076805A1
    • 2008-03-27
    • US11661834
    • 2005-10-03
    • Linus LinPing Liu
    • Linus LinPing Liu
    • A61K31/4412A61K31/165A61P25/00C07C243/12C07D213/63
    • C07C255/66C07C243/28C07C243/32C07C243/36C07C2601/08C07D213/64
    • The acyclic hydrazides of the invention are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as centrally acting drugs in the treatment of psychosis, memory deficits, cognitive disorders, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson's disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders (including smoking cessation), the treatment of obesity or eating disorders, as well as the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, and cirrhosis of the liver.
    • 本发明的无环酰肼是大麻素-1(CB1)受体的拮抗剂和/或反向激动剂,可用于治疗,预防和抑制由CB1受体介导的疾病。 本发明的化合物可用作治疗精神病,记忆缺陷,认知障碍,偏头痛,神经病,包括多发性硬化和神经 - 巴利综合征的神经炎症性疾病以及病毒性脑炎的炎症性后遗症,脑血管 事故和头部创伤,焦虑症,压力,癫痫,帕金森病,运动障碍和精神分裂症。 这些化合物还可用于治疗药物滥用障碍(包括戒烟),治疗肥胖或进食障碍,以及治疗哮喘,便秘,慢性肠假性梗阻和肝硬化。
    • 97. 发明授权
    • Peak current control in wireless network interface devices
    • 无线网络接口设备的峰值电流控制
    • US07343175B2
    • 2008-03-11
    • US10439990
    • 2003-05-16
    • Ping LiuBruce MillerRachel Wong
    • Ping LiuBruce MillerRachel Wong
    • H04Q7/20
    • H04B1/38H04B2001/0416
    • Methods of and apparatuses for varying and controlling the effective series resistance (ESR) of a power supply rail configured to transmit power from a power supply of a host device to a wireless network interface device (e.g. a wireless modem). Varying and controlling the ESR of the power supply rail, relative to an ESR of a super capacitor coupled to the power supply rail, allows control of the currents drawn from the host power supply and a super capacitor. During a time when the wireless network interface device is transmitting or is about to transmit, the ESR of the power supply rail is increased so that it exceeds the ESR of the super capacitor, thereby causing current for the power amplifier (PA) of the wireless network interface device to be drawn primarily from the super capacitor, rather than from the host power supply. During a time when the wireless network interface device has completed transmitting or is about to complete transmitting, the ESR of the host power supply is lowered so that it is less than the ESR of the super capacitor, thereby causing the super capacitor to enter a charging state.
    • 用于改变和控制被配置为将功率从主机设备的电源传送到无线网络接口设备(例如,无线调制解调器)的电源轨的有效串联电阻(ESR)的方法和设备。 改变和控制电源轨的ESR相对于耦合到电源轨的超级电容的ESR允许控制从主电源和超级电容器吸取的电流。 在无线网络接口设备正在传输或正在传输的时间内,电源轨的ESR增加,使其超过超级电容器的ESR,从而导致无线电功率放大器(PA)的电流 网络接口设备主要从超级电容器中抽取,而不是从主机供电。 在无线网络接口设备完成发送或即将完成传输的时间内,主电源的ESR降低,使其小于超级电容器的ESR,从而使超级电容器进入充电状态 州。
    • 100. 发明授权
    • Device with small molecular thiophene compound having divalent linkage
    • 具有二价键的小分子噻吩化合物的装置
    • US07294850B2
    • 2007-11-13
    • US10865620
    • 2004-06-10
    • Beng S. OngPing LiuYiliang Wu
    • Beng S. OngPing LiuYiliang Wu
    • H01L35/24
    • H01L51/0036H01L51/0052H01L51/0068H01L51/0541H01L51/0545
    • An electronic device composed of a semiconductor layer in contact with a number of electrodes, wherein the semiconductor layer includes a small molecular thiophene compound consisting of: at least one divalent linkage; and a plurality of thiophene units, each thiophene unit being represented by structure (A) wherein each thiophene unit is bonded at either or both of the second ring position and the fifth ring position, wherein there is at least one thiophene unit where R1 is present at the third ring position or the fourth ring position, or at both the third ring position and the fourth ring position, wherein for any two adjacent thiophene units there is excluded the simultaneous presence of the same or different R1 at the 3-position of one thiophene unit and at the 3′-position of the other thiophene unit, and wherein the number of the thiophene units is at least 6.
    • 由与多个电极接触的半导体层构成的电子器件,其中所述半导体层包括由以下组成的小分子噻吩化合物:至少一个二价键; 和多个噻吩单元,每个噻吩单元由结构(A)表示,其中每个噻吩单元在第二环位置和第五环位置的一个或两个上键合,其中存在至少一个噻吩单元,其中R 1 存在于第三环位置或第四环位置处,或在第三环位置和第四环位置处,其中对于任何两个相邻的噻吩单元,排除了同时存在相同或不同的 R 1在一个噻吩单元的3-位和另一个噻吩单元的3'-位上,并且其中噻吩单元的数目至少为6。