Proceedings of the PSK Conference (대한약학회:학술대회논문집)
- 2003.10b
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- Pages.188.3-189
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- 2003
Synthesis of Novel 3-(H or aralkyl)-1-phenyl-5-(p-H or halo)phenyl-2-thiohydantoins as Selective COX-2 Inhibitors
- Park, Hae-Sun (College of Pharmacy, Dongduk Women's University) ;
- Kim, Nan-Young (College of Pharmacy, Dongduk Women's University) ;
- Choi, Hee-Jeon (College of Pharmacy, Dongduk Women's University) ;
- Park, Eun-Hee (College of Pharmacy, Dongduk Women's University) ;
- park, Myung-Sook (College of Pharmacy, Dongduk Women's University) ;
- Lee, Myung-Sook (College of Pharmacy, Dongduk Women's University) ;
- Shin, Hea-Soon (College of Pharmacy, Dongduk Women's University) ;
- Kwon, Soon-Kyoung (College of Pharmacy, Dongduk Women's University)
- Published : 2003.10.01
Abstract
Nonsteriodal antiinflammatory drugs(NSAIDs) are widely used to treat pain, fever, and inflammatory conditions including osteoarthritis. But chronic patients suffer from gastrointestinal 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-l accompanied with side effects in the stomach and kidney. Therefore, in this study, we designed a new 2-thiohydantoin derivatives as selective COX-2 inhibitors is that the 5-membered heterocycle ring is substituted with two aryl groups. (omitted)
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