Proceedings of the PSK Conference (대한약학회:학술대회논문집)
- 2002.10a
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- Pages.343.1-343.1
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- 2002
Synthesis of selective COX-2 inhibitors: Novel 1.5-diarylhydantoins via cyclization of methyl $\alpha$ -aminoacetates with aralkyl isocyanate
- Choi, Hee-Jeon (College of Pharmacy. DukSung Women′s University) ;
- Park, Hae-Sun (College of Pharmacy. DukSung Women′s Universi) ;
- Park, Myoung-Sook (College of Pharmacy. DukSung Women′s University) ;
- Kwon, Soon-Kyoung (College of Pharmacy. DukSung Women′s University)
- Published : 2002.10.01
Abstract
Nonsteroidal antiinflammatory drugs(NSAIDs) are widely used to treat pain. fever and inflammatory condition. But chronic-disease patients suffer from gastro-intestinal disturbances such as discomfort. nausea. peptic ulcer and severe bleeding because NSAIDs inhibit not only COX-2 associated with anti-inflammatory activity but also COX-1 associated with adverse gastro-intestinal effects. On the basis of this fact. specific COX-2 inhibitors such as celecoxib and rofecoxib are introduced in the drug market. (omitted)
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