Abstract: The invention provides novel substituted heterocyclic rings represented by Formula I, or a pharmaceutically acceptable salt, solvate, polymorph, ester, tautomer or prodrug thereof, and a composition comprising these compounds. The compounds provided can be used as inhibitors of RIPK1 and the therapeutic methods.

Abstract: Disclosed are a neural network acceleration system and an operating method of the same. The neural network acceleration system includes a first memory module that generates a first reduced embedding segment through a tensor operation, based on a first segment of a first embedding and a second segment of a second embedding, a second memory module that generates a second reduced embedding segment through the tensor operation, based on a third segment of the first embedding and a fourth segment of the second embedding, and a processor that processes a reduced embedding including the first reduced embedding segment and the second reduced embedding segment, based on a neural network algorithm.

Abstract: A computing system includes a host processor, a plurality of accelerators that communicate with the host processor based on a communication interface, and a plurality of memory nodes that are connected with the plurality of accelerators through an interconnection network. A first data link is established between a first accelerator of the plurality of accelerators and a first memory node of the plurality of memory nodes, and a second data link is established between the first accelerator and a second memory node of the plurality of memory nodes.

Abstract: Described herein is a method for the attachment of proteins to any solid support with control over the orientation of the attachment. The method is extremely efficient, not requiring the previous purification of the protein to be attached, and can be activated by UV-light. Spatially addressable arrays of multiple protein components can be generated by using standard photolithographic techniques.

Abstract: Described herein is a method for the attachment of proteins to any solid support with control over the orientation of the attachment. The method is extremely efficient, not requiring the previous purification of the protein to be attached, and can be activated by UV-light. Spatially addressable arrays of multiple protein components can be generated by using standard photolithographic techniques.

Abstract: Described herein is a method for the attachment of proteins to any solid support with control over the orientation of the attachment. The method is extremely efficient, not requiring the previous purification of the protein to be attached, and can be activated by UV-light. Spatially addressable arrays of multiple protein components can be generated by using standard photolithographic techniques.

Abstract: Described herein is a method for the attachment of proteins to any solid support with control over the orientation of the attachment. The method is extremely efficient, not requiring the previous purification of the protein to be attached, and can be activated by UV-light. Spatially addressable arrays of multiple protein components can be generated by using standard photolithographic techniques.

Abstract: Disclosed herein is an improved method for the attachment of proteins to any solid support with control over the orientation of the attachment. The method is extremely efficient, not requiring the previous purification of the protein to be attached, and can be activated by UV-light. Spatially addressable arrays of multiple protein components can be generated by using standard photolithographic techniques.