• Proceedings of the Korean Information Science Society Conference
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• 2001.10c
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• pp.520-522
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• 2001

본 논문에서 제시하는 시스템은 MPEG-4로 부호화된 비디오/오디오에 대해서 MPEG-4 파일 포맷에 맞는 MPEG-4 파일 생성 포맷터이다. 본 논문에서 설계하고 구현된 파일 포맷터는 전처리 부분, 부호화기 파일 포맷터로 구성된 저작도구의 모듈로서 존재한다. 따라서 본 논문에서는 저작도구에서 사용될 MPEG-4 파일 포맷터의 구조 및 기능에 대해서 선명하고, 포맷터의 세부 설계 사항을 기술한다. 본 논문에서 MPEG-4 파일 포맷터의 기능은 비디오/오디오 인코더로부터 출력되는 비디오/오디오 데이터를 MPEG-4 파일 포맷의 형식에 맞는 MPEG-4 파일을 생성하는 것이다. 생성된 파일은 비디오/오디오 각각에 대한 정보와 생성된 비디오/오디오를 처리할 디코더에 대한 정보를 제공한다. 표준 상의 MPEG-4 시스템에서의 동기화 정보를 파일 포맷상의 비디오/오디오 데이터에 제공하여 , 스트리밍 서비스을 제공하는 서버쪽에서의 동기화 과정과 먹싱을 배제할 수 있게 한다. 비디오/오디오 인코더로부터 생성되는 다양만 종류의 비디오/오디오 데이터를 효율적으로 포맷팅하여 다양한 범위의 응용에서 사용될 수 있게 하며, 차기에 계위화 부호화를 효율적으로 적용시키기 위해 파일 포맷팅을 수행하게 된다.

• Journal of Microbiology and Biotechnology
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• v.8 no.1
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• pp.96-100
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• 1998

Pseudomonas sp. S-47 degraded 4-chlorobenzoate (4CBA) to 4-chlorocatechol (4CC) that was subsequently ring-cleaved to form 5-chloro-2-hydroxymuconic semialdehyde. These intermediate compounds were identified by GC-mass spectrometry and UV-visible spectrophotometry. 5-chloro-2-hydroxymuconic acid converted from 5-chloro-2- hydroxymuconic semialdehyde (5C-2HMS) was dechlorinated to produce 2-hydroxypenta-2,4-dienoic acid (2HP-2,4DA) by the strain. These results indicate that Pseudomonas sp. S-47 degrades 4CBA to 2HP-2,4DA via a novel pathway including the meta-cleavage of 4CC and dechlorination of 5C-2HMS.

• YAKHAK HOEJI
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• v.34 no.2
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• pp.133-138
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• 1990

The reaction of 2-aminobenzamide with phthalic acid anhydride In dioxane produced a bicyclic product 2,8-dioxoisoindole(1,2,a) quinazoline (I) in addition to hydrolysis product 2(2-Carboxyphenyl)-1,2-2H-quinazoline-4-one (II). The yields were 64% and 30% respectively. On the other hand, the same reaction in DMF afforded compound (I) and 2(2N-dimethyl carbamyl phenyl)-1,4-2H-quinazoline-4-one (III) in 30% and 60% yield respectively. The compound III was also obtained by the reaction of compound II with dimethylamine. However the reaction of 2-aminobenzamide with neat succinic acid anhydride gave only bicyclic product 2,8-oxopyrrolidine (2,1,a)-1,4-2H-quinazoline (IV) in 93%.

• Journal of the Korean Ceramic Society
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• v.37 no.6
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• pp.552-558
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• 2000

LiMn2O4 thin fiolm cathodes for Li-ion secondary battery were fabricated by r.f. magnetron sputtering technique. As-deposited films were amorphous. A spinel structure could not be obtained LiMn2O4 films by in-situ thermal annealing. After post thermal annealing over $700^{\circ}C$ in oxygen atmosphere, LiMn2O4 films prepared above 100 W r.f. power could be crystallized into a spinel structure. The electrochemical property of the LiMn2O4 film cathodes was tested in a Li/1 M LiClO4 in PC/LiMn2O4 cell. From cyclic voltammetry at scan rate of 2mV/sec of 2.5~4.5V, LiMn2O4 electrode prepared by post annealing at 75$0^{\circ}C$ showed good initial capacity. LiMn2O4 electrode prepared by post annealing at 80$0^{\circ}C$ showed the best crycling performance.

• Biomedical Science Letters
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• v.12 no.4
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• pp.343-348
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• 2006

Drosophila Sog and vertebrate Noggin play important roles during development. They function as antagonists against BMP4 signaling and induce neural ectoderm during embryogenesis. They are also engaged in appendage formation by inhibiting BMP4 signaling during late development. To understand further functions of Sog, Supersog, which is a more potent form of Sog, and Noggin BMP4 antagonists during development, I performed the molecular genetic analysis using Drosophila embryogenesis and wing formation as assay systems. In cellular blastoderm embryos, Sog inhibited Dpp signaling, Drosophila BMP4 signaling, whereas Supersog or Noggin did not block Dpp signaling. During wing formation, Sog inhibited Sax type I receptor of Dpp signaling whereas Noggin inhibited Tkv type I receptor of Dpp signaling. However, Supersog inhibited both Sax and Tkv type I receptors. These results suggest that functions of BMP4 antagonists are developmental stage dependent and indicate that each BMP4 antagonist inhibits BMP4 signaling by blocking different BMP4 receptors.

• Proceedings of the Korean Society of Applied Pharmacology
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• 1993.04a
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• pp.122-122
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• 1993

살균, 정균, 살진균, 정진균등의 효능이 있는 나프토퀴논꼴 화합물인 6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2,2-dimethylnaphtho [1,2] pyran(1)과 그의 유도체인 9-methoxy-6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2, 2-dimethylnaphtho [1,2] pyran(2), 8,9-dimethoxy-6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2, 2-dimethylnaph-the [1,2] pyran(3), 9-bromomethyl-6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2, 2-dimethyl-naphtho [1,2] pyran(4)와 8, 9-methylenedioxy-6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2, 2-dimethylnaphtho [1,2] pyran(5)을 손쉽게 구할 수 있는 benzene, anisole, 1, 2-di-methoxybenzene, bromomethylbenzene, 1, 3-benzodioxole등을 원료로 하여 합성하는 것이 본 연구의 목적이다.

• Journal of the Korean Chemical Society
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• v.46 no.4
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• pp.393-397
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• 2002

• Environmental Analysis Health and Toxicology
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• v.21 no.1 s.52
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• pp.87-92
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• 2006

This study was done to investigate the protective effect of novel 9-amino-1, 2, 3, 4-tetrahydroacridine derivatives on the hepatoprotective effect intoxicated rats induced by carbon tetrachloride ($CCl_4$). A series of currently derivatives of 9-amino-1, 2, 3, 4-tetrahydroacridine have been prepared through the alkly substitution or the ring expansion for the treatment of the Alzheimer's disease. The activities of aminotransferase (aspartate and alanine) and contents of alkaline phosphatase, triglyceride and glutathione S-transferase in 9-amino-1, 2, 3, 4-tetrahydroacridine derivatives pretreated rats were significantly decreased compared to the only carbon tetrachloride treated rats but the contents of cholesterol were increased compared to the only $CCl_4$ treated rats. The result indicated that 9-amino-1, 2, 3, 4-tetrahydroacridine derivatives showed hepatoprotective effect in $CCl_4$ treated rats.

• Korean Journal of Crystallography
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• v.8 no.2
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• pp.124-126
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• 1997

The comples of [Ni(L)](ClO4)2 (L:3,5,10,12-tetramethyl-1,4,8,12-tetraazacyclotetradecane), C14H32Cl2N4NiO8, has a NiN4 square planar geometry and adopts a thermodynamically most stable trans-III conformation.

• Journal of the Korean Chemical Society
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• v.40 no.4
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• pp.249-253
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• 1996

The synthesis of new 5-benzyl-4-cyanomethyl-2-methylpyrimidine derivatives (5) containing chloro, methoxy, ethoxy, phenoxy and anilino groups at 6-position on the pyrimidine ring were prepared from 5-benzyl-4-chloro-2-methylpyrimidine derivatives (3) and tert-butylcyanoacetate. The derivatives of 5-benzyl-4-chloro-2-methylpyrimidine (3) containing chloro, methoxy, ethoxy, isopropoxy, phenoxy and anilino groups at 6-position on the pyrimidine ring were prepared from 5-benzyl-4,6-dichloro-2-methylpyrimidine (2).