Other

Samsung Electronics Co., Ltd.

Dongkook Pharmaceutical Co., Ltd.

Korea Institute of Science and Technology

Neocl Co., Ltd.

Jung Hyuck Cho

Kyung Rok Kim

Wan Soo Kim

Chang Hyun Oh

Yong Jun Kim

Ki Hong Nam

Chang H Oh

Kie H Nam

The present invention provides a composition of long-term constant-concentration aqueous chlorine dioxide solution including dissolved chlorine dioxide, a decomposition inhibitor for dissolved chlorine dioxide, and a pH modifier, and a method for preparing the same.

Composition for providing room temperature long-term constant-concentration chlorine dioxide solution in aqueous medium and preparation method thereof

A scanner module and an image scanning apparatus employing the same include a light source to generate light, a light guide member to guide the light toward an object, a sensor configured to detect the light reflected by the object, at least one reflecting mirror to reflect the light reflected by the object to the sensor, and a focusing lens to focus the reflected light redirected by the at least one reflecting mirror on the sensor. The light guiding member includes an incident surface to receive the light, a reflective surface to reflect the light received through the incident surface, a plurality of guide surfaces to guide the light received through the incident surface, and an exit surface to allow light reflected by the reflective surface to exit. An interval between reflective linear elements increases from a center of the light guide member towards the incident surface.

Scanner module and image scanning apparatus employing the same

Novel oxazolidinone derivatives with a difluorophenyl moiety, represented by Chemical Formula 1, pharmaceutically acceptable salts thereof, a preparation method thereof, and a pharmaceutical composition containing the same as an active ingredient are provided. Exhibiting potent inhibitory activity against Gram-positive bacteria includingand Coagulase negative staphylococci and resistant bacteria including vancomycin-resistant enterococci (VRE), the pharmaceutical composition is useful as an antibiotic 

Oxazolidinone derivative with difluorophenyl moiety, pharmaceutically acceptable salt thereof, preparation method thereof and antibiotic composition containing the same as an active ingredient

Disclosed are a scanner module and an image scanning apparatus employing the same. The scanner module includes a light source generating light to be irradiated onto an object and a light guide member extending in correspondence with a width of the object to be scanned. The light guide member has a reflective surface for reflecting the light generated from the light source, an exit surface for radiating the light, which is reflected from the reflective surface, toward the object, and a plurality of guide surfaces each guiding the light toward the exit surface by reflecting the light reflected from the reflective surface deviates from the exit surface. The light is effectively guided to be output from the exit surface without substantial light loss.

Disclosed are a scanner module and an image scanning apparatus employing the same. The scanner module includes a light source generating light to be irradiated onto an object and a light guide member extending in correspondence with a width of the object. The light guide member has a reflective surface defined by a plurality of reflective grooves, some of which arranged to be non-parallel with other ones. Light is effectively diffused and/or scattered in the width direction of the light guide member by the reflective grooves, allowing a uniform light distribution across the scanning width.

The present invention relates to new 1-.beta.-methyl-2-thiolic carbapenem derivatives represented by the following general formula (I) and producing method thereof. ##STR1## The above-mentioned compound is very stable against DHP-1 enzyme due to effective shielding of carbapenem ring structually and is highly effective in both gram-positive and gram-negative microorganism, especially has a remarkable effect on the Pseudomonas aeruginosa known as a disease germ having strong resistance.

1-.beta.-methyl-2-thiolic carbapenem derivatives

This invention relates to the process for producing ortho-isopropylated phenol derivatives having following general formula (VIII). ##STR1## (in the above formula, R.sub.1 is a hydrogen or a low alkyl group of C.sub.1 -C.sub.4) A process for producing ortho-isopropylated phenol derivatives (VIII) of the present invention is characterized by obtaining position isomer desired by means of Claisen rearrangement of phenyl allyl ether without catalyst in atmosphere, and then obtaining only one isomer by oxidation and reduction of the above-obtained position isomer. According to the present invention, ortho-alkylated phenol derivatives (VIII) having high purity at low temperature and low pressure can be prepared without producing a by-product and requirement of the complicated separation procedure.

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Seoul, South Korea

Jung Hyuck Cho