摘要:
An Active Directory (AD) is utilized to authenticate a remote user to a server or node by providing an object corresponding to the node. The object include an Access Control Entry (ACE) that is listed within an Access Control List (ACL). The ACE also lists privileges that are designated for each specified user. The AD is then queried by the Remote Access Card of a node to authenticate the username and password of a remote user and to determine the privileges granted to such user.
摘要:
A printed circuit board trace coupling system for providing high voltage isolation includes a driving circuit, a coupling transformer including a printed circuit board trace, and a receiving circuit.
摘要:
A compound of the formula (I): or a pharmaceutically acceptable salt thereof is disclosed, as well as processes for and intermediates in the preparation thereof, a method of antagonizing endothelin, methods for the inhibition of bone metastases, methods for the prevention of growth of new metastases, methods for the inhibition of bone turnover, and methods for the prevention of bone loss in patients, including cancer patients, using an endothelin ET-A receptor antagonist.
摘要:
The present invention is directed to compounds of formula (I), or a pharmaceutically suitable salt or prodrug thereof, which are useful for the selective inhibition of protein tyrosine phosphatase-1B (PTP1B), and are useful for the treatment of disorders caused by overexpressed or altered protein tyrosine phosphatase 1B.
摘要:
The present invention relates to compounds of formula (I), which inhibit acetyl-CoA carboxylase (ACC) and are useful for the prevention or treatment of metabolic syndrome, type II diabetes, obesity, atherosclerosis and cardiovascular diseases in humans.
摘要:
The present invention relates to compounds that are inhibitors of c-jun N-terminal kinase 1, 2, or 3 (JNK1, JNK2, or JNK3), compositions containing the compounds and the use of the compounds in the prevention or treatment of disorders regulated by the activation of JNK1, JNK2 and JNK3.
摘要:
A system for remote controlling of a media player includes a host computer (1), a display (2), and a remote controller (3). The remote controller is used for inputting commands for controlling a media player (8), and generating consumer infrared (CIR) signals according to the commands. The host computer includes: a CIR signal processing module (14) for receiving and modulating the CIR signals from the remote controller; an audio DJ data processing module (15) for analyzing and transforming the CIR signals to audio DJ data, and sending the audio DJ data to control the media player; and a Liquid Crystal Display (LCD) controlling module (16) for receiving and controlling media information to be displayed on an LCD panel (10). A related method is also disclosed.
摘要:
A computer system for displaying media playing information includes: media playing software installed in a host computer (1) for playing media files; a media playing controller (11) enchased on a front panel of the host computer for receiving user-input commands to control the media playing software; an LCD (Liquid Crystal Display) panel (12); a motherboard (2) including a CPU (Central Processing Unit) (21) and a south bridge chipset (22) for obtaining the media playing information from the media playing software; and a plug-in board (3) including: a PCI (Peripheral Component Interface) chipset (31) for receiving the media playing information from the motherboard; a media information obtaining module (32) for obtaining the media playing information from the PCI; and a media information displaying module (33) for controlling the LCD panel to display the media playing information. A related method is also disclosed.
摘要:
A compound of the formula (I): or a pharmaceutically acceptable salt thereof is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.
摘要:
The present invention encompasses structures of the Formula or the pharmaceutically acceptable non-toxic salts thereof wherein: X is hydrogen, halogen, (un)substituted alkyl, (un)substituted alkoxy or amino; and Y is (un)substituted alkyl, aryl, or heteroaryl, which compounds are highly selective agonists, antagonists or inverse agonists for GABAa brain receptors or prodrugs of agonists, antagonists or inverse agonists for GABAa brain receptors. These compounds are useful in the diagnosis and treatment of anxiety, Down Syndrome, sleep, cognitive and seizure disorders, and overdose with benzodiazepine drugs and for enhancement of alertness.