• Proceedings of the Korean Society of Applied Pharmacology
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• 2003.04a
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• pp.113-130
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• 2003

1. We have established a model system to study sodium chloride, an environmental factor, induced gene regulations. 2. ${\alpha}$ENaC, cox-2, and c-fos genes are regulated by sodium chloride at mRNA level as well as at protein level. 3. Regulation of ${\alpha}$ENaC requires syntheses of new protein(s). 4. COX-2 may have a important role for homeostasis in hypertonic situation.

• Proceedings of the Korean Ceranic Society Conference
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• 2000.10a
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• pp.70.1-70
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• 2000

• Macromolecular Research
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• v.14 no.6
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• pp.668-672
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• 2006

• Proceedings of the Korean Society of Tribologists and Lubrication Engineers Conference
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• 1999.11a
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• pp.247-256
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• 1999

This paper describes the results of analysis, syntheses and Roll Stability of various Di-urea greases. Di-urea greases were synthesized by reaction of 4,4'-Methylenebis(phenyl isocyanate) and various amines, such as cyclohexylamine, octylamine, stearylamine and p-toluidine with base oil at 80-180 $^{\circ}C$. The synthesized di-urea greases were analyzed by FT-R spectroscopy. The Roll Stability of synthesized di-urea greases was evaluated.

• Macromolecular Research
• /
• v.15 no.7
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• pp.595-600
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• 2007

• YAKHAK HOEJI
• /
• v.8 no.2
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• pp.45-47
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• 1964

Two new orotic acid derivatives orotyl-DL-alanine and orotyl-L-tyrosine were synthesized. They were obtained as high melting crystalline masses by condensing DL-alanine and L-tyrosine each with orotyl chloride in aqueous sodium hydroxide solution, followed by acidifying the reaction mixture.

• Archives of Pharmacal Research
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• v.26 no.12
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• pp.990-996
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• 2003

A novel carboacyclic nucleoside analogue, 9-[2-bromo-4-hydroxy-3-hydroxymethyl-2-butenyl] adenine, and its derivatives were designed and synthesized as open-chain analogues of neplanocin A. The syntheses were accomplished via the coupling of adenine or pyrimidine bases to the key intermediate allylic bromide 7. The bromide 7 was prepared from epichlorohydrin in a seven step process in a 54% overall yield. The synthesized compounds were evaluated for their antiviral activity against the polio virus, HSV and HIV.

• Bulletin of the Korean Chemical Society
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• v.29 no.11
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• pp.2277-2280
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• 2008

• Bulletin of the Korean Chemical Society
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• v.34 no.11
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• pp.3499-3502
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• 2013

• Journal of the Korean Chemical Society
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• v.35 no.3
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• pp.262-267
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• 1991

Bromo-acivicin derivative(17) and its homologs(15,16,8) were synthesized by 1,3-dipolar cycloaddition of vinyl glycine derivative(13) and allylglycine derivatives(9,12), respectively, with bromonitrile oxide(5).