Zhejiang Huahai Pharmaceutical Co., Ltd.

Yangtze River Pharmaceutical Group Co., Ltd.

Shanghai Haiyan Pharmaceutical Technology Co., Ltd.

Shanghai Aobo Pharmtech, Inc., Ltd.

Huawei Technologies Co., Limited

Emc IP Holding Company LLC

Emc Corporation

Ito Luggage Co., Ltd.

Shanghai Huahong Grace Semiconductor Manufacturing Corporation

Signify Holding B.v.

Shanghai Syncores Technologies Inc. Ltd.

Shanghai Hua Nec Electronics Co., Ltd.

Koninklijke Philips Corporation N.v.

Yang Liu

Ziye Yang

Hong Gu

Lintao Wan

Chenhui Fan

Jiong Lan

Kai Zhang

Jun Wei Zhang

Ying Lin Cai

Jing Xie

Luning Huang

Xiang Chen

Fusheng Zhou

Dong Huang

Shuchun Guo

Jinzhu Zhao

Han Yu

Zhengliang Zhou

Wan He

Changjiang Qiao

Steven Chen

Ping Chen

David Lionel Black

Qing Shan Zhang

Xiaoye Jiang

Fan Chen

Tao Wang

Donald Mace

Yuhong Fang

Ningjiang Chen

Anping Tao

Jianbiao Peng

Zhiqiang Zou

Wei Xu

Kai Xue

Xiaohong Qin

Xiaowen Guo

Jia Pan

Joan Jun Xiong

Xiongbin Chen

Lei Fang

Weiguang Cai

YinKee Yee

Yingtao Liu

Jintao Yang

Boyu Wang

Smitha Mave

Jianguo An

Kaiqiang Shi

Harshitha Gudipati

Jiangwei Wang

Wangbin Sun

Lixiao Wang

Yukun Liang

Zhihua Fang

Zonglei Fei

Shifeng Xu

Kang He

Yinglu Jiao

Handa Li

Hailan Chen

Hu Su

Jia Xin

Keran Xue

Yonggang Chen

Rong Song

Baoxin Xi

Adriana Johanna Pas

Provided herein is a method for preparing an Escitalopram bis-hydroxynaphtoate ((S)-(+)-1-(3-(-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydro-5-cyanisob enzofuranone) crystal form A. Said method is ecofriendly and non pollutive, and the obtained Escitalopram bis-hydroxynaphtoate crystal form A is highly pure and easy to reproduce.

Method for preparing escitalopram bis-hydroxynaphtoate crystal form a

The present invention relates to a method for preparing an intermediate (Formula IV) of sodium elagolix. The intermediate is prepared by the following route. The method has advantages of simple and safe operation, high yield, less environmental pollution, good economic effect and suitability for industrial production, wherein R represents C1-C4 substituted or unsubstituted benzyl or allyl. 

Method for preparing elagolix intermediate and composition thereof

One example method includes copying code and a security signature of a first off-chip boot to a static random access memory (SRAM) for signature verification, where a function implemented by the first off-chip boot includes initializing a double data rate synchronous dynamic random access memory (DDR), and the DDR initialization includes configuring a DDR secure zone, executing, in the SRAM, the code of the first off-chip boot after the signature verification on the first off-chip boot succeeds to initialize the DDR and configure the DDR secure zone, copying code and a security signature of a second off-chip boot to the DDR secure zone for signature verification, where the second off-chip boot is all of other boots in off-chip boots except the first off-chip boot, and executing, in the DDR secure zone, the code of the second off-chip boot after the signature verification on the second off-chip boot succeeds.

Secure boot and apparatus, and terminal device

The present invention relates to a 1,2-dihydropyrrol[3,4-c]pyridin/pyrimidin-3-one derivative substituted by N-(3-aminophenyl)acrylamide and a preparation method and pharmaceutical use thereof. In particular, the present invention relates to a compound of formula (II) or a pharmaceutically acceptable salt, stereoisomer, solvate, or prodrug thereof and a preparation method and application of the same. The definition of each substituent in the formula is described in detail in the specification and claims. 

Aniline-substituted 1,2-dihydropyrrol[3,4-C]pyridin/pyrimidin-3-one derivative and use thereof

The present invention relates to a new preparation method for escitalopram pamoate ((S)-(+)-1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-cyanoisob enzofuran pamoate), wherein the method is environmentally friendly and pollution-free, and the escitalopram pamoate prepared by means of the method has a high purity and a good repeatability.

Preparation method for escitalopram pamoate

The present disclosure relates to pyridinamine-substituted heterotricyclo compounds, a preparation method thereof, and a use thereof in medicines. Specifically, a compound of formula (I), or a pharmaceutically acceptable salt, stereoisomer, solvate, or prodrug thereof, a preparation method and a use thereof are disclosed, wherein the groups in the formula (I) are as defined in the Description and claims. 

Pyridylamino substituted heterotricyclic compounds, and preparation method and pharmaceutical use thereof

The present disclosure relates to 4,6,7-trisubstituted 1,2-dihydropyrrolo[3,4-c]pyridin/pyrimidin-3-one derivatives, and their preparations and medicinal use. Specifically, the present disclosure discloses a compound of formula (I) or a pharmaceutically acceptable salt, stereoisomer, solvate or prodrug thereof, and a preparation method and use thereof, wherein the definition of each group is as described in the specification and claims. 

4,6,7-trisubstituted 1,2-dihydropyrrolo[3,4-c]pyridin/pyrimidin-3-one derivatives and uses thereof

Provided are 4,5,6-tri-substituted indazoles derivatives, a preparation method therefor, and a use thereof in medicines. Specifically, provided are compounds of formula (I) or pharmaceutically acceptable salts, stereoisomers, solvates, or prodrugs thereof, a preparation method therefor, and a use thereof. 

4,5,6-trisubstituted indazole derivatives, and preparation method and pharmaceutical use thereof

A computer system and a memory access technology are provided. In the computer system, when load/store instructions having a dependency relationship is processed, dependency information between a producer load/store instruction and a consumer load/store instruction can be obtained from a processor. A consumer load/store request is sent to a memory controller in the computer system based on the obtained dependency information, so that the memory controller can terminate a dependency relationship between load/store requests in the memory controller locally based on the dependency information in the received consumer load/store request, and execute the consumer load/store request.

Computer system and memory access technology

Disclosed is a new method for preparing a donepezil pamoate (1-benzyl-4-[(5,6-dimethoxyindan-2-one)methyl]piperidine pamoate). The donepezil pamoate prepared by using the method has a high purity and a good flowability.

Method for preparing donepezil pamoate

A lighting driver () receives an AC Mains voltage (), employs a rectifier () to produce a rectified voltage, and supplies an output current () to a lighting device () in response to the rectified voltage. A surge protection circuit () of the lighting driver includes a voltage clamping device (MOV) connected across the output of the rectifier, and a differentiator circuit () configured to differentiate between a temporary voltage spike at the input to the rectifier and a loss of neutral connection to the lighting driver. When a temporary voltage spike is detected, the voltage clamping device is activated to clamp the rectified voltage until the temporary voltage spike ends. When a loss of neutral is detected, the voltage clamping device is latched into a disabled state until the AC Mains voltage input to the lighting driver is turned off.

Method of lighting driver protection in case of loss of neutral connection, and lighting driver including such protection

Disclosed are a crystal form of brexpiprazole and a preparation method therefor. The X-ray powder diffraction pattern, which is detected with Cu&#x2014;K&#x3b1; radiation, of the crystal form of brexpiprazole has characteristic peaks at the positions where 2&#x3b8; is about 9.1&#xb1;0.2, 15.2&#xb1;0.2, 15.7&#xb1;0.2, 17.6&#xb1;0.2, 18.1&#xb1;0.2, 24.4&#xb1;0.2. The crystal form I of brexpiprazole has a high purity, good stability and good reproducibility, and is suitable for industrial production.

Crystal form of brexpiprazole and preparation method therefor

Embodiments of the present invention provide an adaptive narrowband interference cancellation method and an apparatus. A receiving apparatus in the present invention includes: a channel type determining module, configured to: measure a delay spread of a multipath channel passed by a received time-domain signal, and determine a channel type according to a measurement result; a weighting coefficient selection module, configured to select a weighting coefficient according to the channel type; a time-domain windowing processing module, configured to perform time-domain windowing processing on the time-domain signal according to the weighting coefficient; and a frequency-domain interference cancellation processing module, configured to perform, according to the weighting coefficient, frequency-domain interference cancellation processing on the signal that is output after the time-domain windowing processing.

Adaptive narrowband interference cancellation method, and apparatus

The present disclosure relates to a method and apparatus for measuring performance of a storage system. The method comprises: causing one or more entities to execute a task set comprising multiple tasks, each of the multiple tasks being used for accessing the storage system; obtaining an indicator set of the storage system based on a result of the execution, the indicator set comprising one or more indicators for indicating performance of the storage system; and adjusting the task set based on the indicator set, for subsequent execution by the one or more entities. The method can be executed iteratively. By means of the present invention, workloads for the next round's execution can be intelligently improved according to execution results after each round's execution of workloads, so that performance of the storage system can be obtained more pertinently and efficiently so as to better utilize the storage system.

Measuring performance of storage system

A plurality of network cables are physically connected to a plurality of network ports on an appliance, wherein the appliance comprises a plurality of nodes each associated with a corresponding chassis slot position in which the node is located within a chassis of the appliance and each node having at least one management network port and one host network port. A network address is identified for each of the plurality of network ports. A first subset of network addresses is identified as being associated with a management network port and a second subset of network addresses is identified as being associated with a host network port based at least in part on a respective response received from each network address to a management request using a management interface protocol. For each management network port, a corresponding chassis slot position is associated with that management network port based at least in part on a response to a slot request using the management interface protocol. For each host network port, a corresponding chassis slot position is associated with that host network port based at least in part on a response to an identification request using the management interface protocol.

Self-identifying cable assignment

Growing community of inventors

Shanghai, China

Yang Liu