Abstract: A data transmission method is applied to a decoding end of a network audio and video matrix system, and the decoding end is in communication connection with an encoding end and several secondary decoding ends. The data transmission method comprises: acquiring request data signaling from a secondary decoding end, wherein the request data signaling comprises a distribution data signaling receiving address of the secondary decoding end; determining whether a currently occupied distribution capability value reaches a maximum distribution capability value; and if yes, sending a secondary distribution device table to the secondary decoding end, such that the secondary decoding end sends the request data signaling to other secondary decoding ends in the secondary distribution device table, and after the sending of the secondary distribution device table is completed, disconnecting a network connection with the secondary decoding end.

Abstract: A multi-cell protection circuit and method. The multi-cell protection circuit comprises one or more multi-cell protection chips, a charge control switch (M2) and a discharge control switch (M1). Each multi-cell protection chip comprises a multi-cell protection integrated circuit module and an expansion connection module. The input terminals (VC1, VC2, VC3, GND1, VC4, VC5, VC6, VC7, GND) of the multi-cell protection integrated circuit module are connected to the positive and negative poles of corresponding cells. The output terminals (co, do) of the multi-cell protection integrated circuit module are connected to the interior signal input terminals (Dco, Ddo) of the expansion connection module. The expansion signal input terminals (exterior.co, exterior.do) of the expansion connection module are connected to expansion signal output terminals (Co?, Do?) of an expansion connection module in a multi-cell protection chip adjacent to this multi-cell protection chip.

Abstract: A multi-cell protection circuit and method. The multi-cell protection circuit comprises one or more multi-cell protection chips, a charge control switch (M2) and a discharge control switch (M1). Each multi-cell protection chip comprises a multi-cell protection integrated circuit module and an expansion connection module. The input terminals (VC1, VC2, VC3, GND1, VC4, VC5, VC6, VC7, GND) of the multi-cell protection integrated circuit module are connected to the positive and negative poles of corresponding cells. The output terminals (co, do) of the multi-cell protection integrated circuit module are connected to the interior signal input terminals (Dco, Ddo) of the expansion connection module. The expansion signal input terminals (exterior.co, exterior.do) of the expansion connection module are connected to expansion signal output terminals (Co?, Do?) of an expansion connection module in a multi-cell protection chip adjacent to this multi-cell protection chip.

Abstract: Voltage balance circuit for dual cell rechargeable battery having a balancing circuit coupled to an integrated control circuit. The balancing circuit can be configured to charge and discharge current during a voltage balancing process allowing a higher charged cell to discharge or dissipate excess capacity to a lower charged cell. The integrated control circuit, having a plurality of modules, can be configured to output balancing directional and timing control signals for signaling the activation and deactivation of the voltage balancing process.

Abstract: Novel compounds of Formula (1) and esters, salts, and physiologically functional derivatives thereof are disclosed. Methods for preparing and using the compounds are also disclosed. Many of these compounds are selective activators of PPAR alpha. The compounds are particularly useful for treating obesity.

Abstract: The present invention provides a library of compounds, each comprised of a common aminobenzenedicarboxylic acid core structure (scaffold) that serves as a template for synthesizing approximately 10.sup.1 -10.sup.6 compounds which are analogs of the scaffold. The library is employed to study ligand binding by biological receptors, such as enzymes, G-protein coupled receptors and membrane channels. For example, certain individual compounds within the library selectively bind and inhibit the action of trypsin-like serine proteases. The present invention also relates to combinatorial synthetic methods for making such libraries of compounds. Additionally, the present invention relates to novel scaffold-modified solid supports, particularly scaffold-modified polymer resins and methods for preparing said resins.