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- Title
Effect of substituents on benzenesulfonyl motif of 4-phenyl-1-arylsulfonylimidazolidinones for their cytotoxicity.
- Authors
Lee, Hui-Soon; Park, Kyung-Lae; Choi, Sang-Un; Lee, Chong-Ock; Jung, Sang-Hun
- Abstract
To explore the effect of substituents on phenyl motif on sulfonyl function of novel anticancer 4-phenyl-1-benzenesulfonylimidazolidinones ( 1), electron donating or withdrawing substituents were introduced at 3 or 4-position and the analogs were tested agaist human lung (A549) and colon (HCT-15) cancer cell lines. Quantitative structure activity relationship of the 4-substituted series shows that only STERIMOL L values are well correlated. The increment of substituent's volume enhances the activity against both cell lines. The small substituent at 3-position additionally increases the activity. However naphthyl group in place of phenyl reduces the activity. Therefore the phenyl motif with sterically large substituent at 4-position and small substituent at 3-position may be important for their activity. Integration of these substituents' effects into the structural design led to discover the more potent analog, 4-phenyl-1-( N-acetylindoline-5-sulfonyl) imidazolidinone ( 1n).
- Publication
Archives of Pharmacal Research, 2000, Vol 23, Issue 6, p579
- ISSN
0253-6269
- Publication type
Article
- DOI
10.1007/BF02975244