Abstract: A multi-way earphone may include: a housing having a space therein; a first sound unit housed in the space of the housing, and configured to convert an electrical signal into a sound; and a second sound unit disposed in a vertical direction from the first sound unit, and configured to output a different range of sound from the sound outputted from the first sound unit. The housing may form a first transmission path through which the sound outputted from the first sound unit is transmitted to the outside along the inner circumferential surface of the housing, and the second sound unit may include a unit cap forming a second transmission path through which the sound outputted from the second sound unit is outputted while being separated from the sound passing through the first transmission path. The stereo performance of the multi-way earphone can be improved to provide a sound with a 3D effect to a listener.

Abstract: An information processing apparatus, an information processing apparatus system and a control method of an information processing apparatus are provided. The information processing apparatus includes a network unit which receives user recognition information having time data from an external device; and a processor which outputs a user recognition signal corresponding to the time data if a current time reaches a time corresponding to the time data.

Abstract: A display apparatus includes a display; a communication part which receives an image signal and information corresponding to a first image to be displayed on an external display apparatus and transmits a control signal to adjust the first image; an image processing part which performs image processing to display an image on the display; and a controller which controls the image processing part and the communication part to display the information corresponding to the first image on the display and to transmit the control signal to adjust the first image.

Abstract: An information processing apparatus, an information processing apparatus system and a control method of an information processing apparatus are provided. The information processing apparatus includes a network unit which receives user recognition information having time data from an external device; and a processor which outputs a user recognition signal corresponding to the time data if a current time reaches a time corresponding to the time data.

Abstract: In a broadcasting signal output apparatus and a method, an OSD processing unit produces a display-lock message if a display of contents is not permitted. A control unit determines whether the decoded video signal includes a copy protection signal for preventing the video signal from being reproduced, and if so, the control unit requests and receives a certification signal from the display device to determine whether the video signal can be transmitted to the display device through the video output terminal. The control unit then determines whether the certification signal corresponds with the reproduction preventing signal, and if it does not, prevents the decoded video and audio signal from being outputted, and controls the OSD processing unit so that the display-lock message is output to the display device (e.g., screen), so that the user knows when the currently received broadcasting signal is not displayed due to copy protection signal.

Abstract: The present invention relates to a portable computer having a base and a display panel coupled by a hinge structure. The base has a bottom and a top housing. The bottom housing has bottom bosses with holes extending upwardly. A circuit board has holes aligned with the bottom housing holes. The top housing also has holes aligned with the bottom housing. A top housing is coupled to the circuit board and the bottom housing. A display panel incorporating a display screen is attached pivotally to the top housing with a hinge assembly. The hinge assembly has holes aligned with the holes of the bottom housing. A pair of caps are coupled to the top housing to cover the hinge assembly. Each cap has a boss with a hole aligned with the hole of the bottom. A screw is inserted from outside the bottom housing and through the circuit board, the top housing, the hinge assembly, and finally coupling with the cap boss. A single set of screws attach the base portions and pivotally attaches the display panel with the base.

Abstract: The present invention includes novel compounds of formula ##STR1## where A, B, D, and E are selected from the group consisting of carbon, nitrogen and sulfur, R.sup.99 is selected from the group consisting of sulfur, SO, SO.sub.2, NH, N-alkyl, oxygen, C.dbd.C (cis or trans), and C.tbd.C, and R.sup.12 is NR.sup.13 R.sup.14, ##STR2## The invention also includes the pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel compounds of formula ##STR1## where R.sup.99 is selected from the group consisting of sulfur, SO, SO.sub.2, NH, N-alkyl, oxygen, C.dbd.C (cis or trans), and C.tbd.C, and R.sup.12 is ##STR2## The invention also includes the pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel compounds of formula ##STR1## where G, H, J, L and M are carbon or nitrogen, R.sup.99 is selected from the group consisting of sulfur, SO, SO.sub.2, NH, N-alkyl, oxygen, C.dbd.C (cis or trans), and C.tbd.C, and R.sup.12 is NR.sup.13 R.sup.14, ##STR2## The invention also includes the pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel compounds of formula where A, B, D, and E are selected from the group consisting of carbon, nitrogen and sulfur, R.sup.99 is selected from the group consisting of sulfur, SO, S0.sub.2, NH, N-alkyl, oxygen, C.dbd.C (cis or trans), and C.tbd.C, and R.sup.12 is NR.sup.13 R.sup.14, ##STR1## The invention also includes the pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel compounds of formula ##STR1## where G, H, J, L and M are carbon or nitrogen, R.sup.99 is selected from the group consisting of sulfur, SO, SO.sub.2, NH, N-alkyl, oxygen, C.tbd.C (cis or trans), and C.tbd.C, and R.sup.12 is NR.sup.13 R.sup.14, ##STR2## The invention also includes the pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel (7R)-7-(acylamino)-3-(arylthio)-3-cephem-4-carboxylic acids or their pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounde of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes (7R)-7-(acylamino)-3-(substituted-pyridinyl)-3-cephem-4-carboxylic acids or their pharmacologically acceptable salts which exhibit antibiotic activity against methicillin-resistant bacteria and are therefore useful as antibacterial agents.

Abstract: The present invention includes novel (7R)-7-(acylamino)-3-(arylthio)-3-cephem-4-carboxylic acids or their pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel (7R)-7-(acylamino)-3-(arylthio)-3-cephem-4-carboxylic acids or their pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel (7R)-7-(acylamino)-3-(arylthio)-3-cephem-4-carboxylic acids or their pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel (7R)-7-(acylamino)-3-(arylthio)-3-cephem-4-carboxylic acids or their pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: The present invention includes novel (7R)-7-(acylamino)-3-(arylthio)-3-cephem-4-carboxylic acids or their pharmacologically acceptable salts which exhibit antibiotic activity against a wide spectrum of organisms including organisms which are resistant to .beta.-lactam antibiotics and are useful as antibacterial agents. The invention also relates to novel intermediates useful for making the novel compounds of the present invention and to novel methods for producing the novel compounds and intermediate compounds.

Abstract: 5-Aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates of the formula ##STR1## are prepared from 2-aroylpyrroles. Hydrolysis and mono-decarboxylation of these compounds affords ketorolac and related compounds.

Abstract: 5-Aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates of the formula ##STR1## are prepared from 2-aroylpyrroles. Hydrolysis and mono-decarboxylation of these compounds affords ketorolac and related compounds.