Abstract: A method, a device, and a non-transitory storage medium are described in which a multi-operator anchor service is provided. A multi-operator anchor device may provide a centralized user plane anchor for traffic of end devices associated with multiple networks and operators. The multi-operator anchor device may provide virtual routing and forwarding to isolate traffic among the networks and operators. The multi-operator anchor device may provide a charging service for traffic and a handover service based on end device mobility.

Abstract: An auxiliary hydraulic manifold for connecting different implements to a work vehicle for hydraulic control may include a housing, a plurality of vehicle-side ports in the housing including a first vehicle-side port, and a plurality of implement-side ports in the housing including a first implement-side port fluidly coupled to the first vehicle-side port and a second implement-side port fluidly coupled to the first vehicle-side port. A number of the plurality of implement-side ports is greater than a number of the plurality of vehicle-side ports. Additionally, the auxiliary hydraulic manifold may include a pilot-operated check valve fluidly coupled between the first vehicle-side port and the first implement-side port.

Abstract: A method, a device, and a non-transitory storage medium are described in which a multi-operator anchor service is provided. A multi-operator anchor device may provide a centralized user plane anchor for traffic of end devices associated with multiple networks and operators. The multi-operator anchor device may provide virtual routing and forwarding to isolate traffic among the networks and operators. The multi-operator anchor device may provide a charging service for traffic and a handover service based on end device mobility.

Abstract: The present application is directed towards systems and methods for providing audience interaction with a broadcast media program. A producer, utilizing an intuitive interface provided by a computing device can request audience input by providing polls or questions, which may be transmitted to a plurality of remote computing devices of the audience. An audience member may record a brief audio or video file, of up to a predetermined length, in response to a question via an application executed by their remote computing device. The application may transmit the recorded file to the computing device of the producer, who may review the recorded file and delete it, post it to a website, or download it for playback on air. Accordingly, the resulting system provides the ease, efficiency, and safety of asynchronous communication systems, while allowing audience members to hear their own comments and own voices on air.

Abstract: Selected bis-amino acid hydroxyethylamino sulfonamide compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease. The present invention relates to such retroviral protease inhibitors and, more particularly, relates to selected novel compounds, compositions, and methods for inhibiting retroviral proteases, such as human immunodeficiency virus (HIV) protease, prophylactically preventing retroviral infection or the spread of a retrovirus, and treatment of a retroviral infection.

Abstract: N-heterocyclic moiety containing hydroxyethylamino compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease.

Abstract: ?- and ?-amino acid hydroxyethylamino sulfonamide compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease.

Abstract: A class of pyrazole derivatives is described for use in treating p38 kinase medicated disorders. Compounds of particular interest are defined by Formula IA wherein R1, R2, R3 and R4 are as described in the specification.

Abstract: Selected bis-amino acid hydroxyethylamino sulfonamide compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease. The present invention relates to such retroviral protease inhibitors and, more particularly, relates to selected novel compounds, compositions, and methods for inhibiting retroviral proteases, such as human inmmunodeficiency virus (HIV) protease, prophylactically preventing retroviral infection or the spread of a retrovirus, and treatment of a retroviral infection.

Abstract: Selected heterocyclecarbonyl amino acid hydroxyethylamino sulfonamide compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease. The present invention relates to such retroviral protease inhibitors and, more particularly, relates to selected novel compounds, compositions, and methods for inhibiting retroviral proteases, such as human immunodeficiency virus (HIV) protease, prophylactically preventing retroviral infection or the spread of a retrovirus, and treatment of a retroviral infection.

Abstract: Selected sulfonylalkanoylamino hydroxyethylamine sulfonamide compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease. The present invention relates to such retroviral protease inhibitors and, more particularly, relates to selected novel compounds, composition and method for inhibiting retroviral proteases, such as human immunodeficiency virus (HIV) protease, prophylactically preventing retroviral infection or the spread of a retrovirus, and treatment of a retroviral infection.

Abstract: Selected amino acid hydroxyethylamino sulfonamide compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease. The present invention relates to such retroviral protease inhibitors and, more particularly, relates to selected novel compounds, composition and method for inhibiting retroviral proteases, such as human immunodeficiency virus (HIV) protease, prophylactically preventing retroviral infection or the spread of a retrovirus, and treatment of a retroviral infection.

Abstract: N-heterocyclic moiety containing hydroxyethylamine compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease.

Abstract: ?- and ?-amino acid hydroxyethylamino sulfonyl urea derivative compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease.

Abstract: Succinoylamino hydroxyethylamino sulfonyl urea derivatives of the formula: wherein R1-R6, R7, R7?, R8, R30-R34, X?, Y, Y?, t, x, and n are as defined herein, are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease.

Abstract: ?- and ?-amino acid hydroxyethylamino sulfonamide compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease.

Abstract: Certain Alpha- and Beta-amino acid hydroxyethylamino sulfamic acid derivatives represented by the following formula are useful as retroviral protease inhibitors:

Abstract: The present invention relates to substituted pyrazolyl derivatives, compositions comprising such, intermediates, methods of making substituted pyrazolyl derivatives, and methods for treating cancer, inflammation, and inflammation-associated disorders, such as arthritis.