Synthesis and SAR Studies for the Inhibition of TNF-$\alpha$ Production. Part 2. 2-[3-(Cyclopenthloxy)4-Methoxyphenyl]-Substituted-1-Isoindolinone Derivatives

  • Park, Joon-Seok (Institute of Bioscience & Biotechnology Daewoong Pharm. Co., Ltd.) ;
  • Moon, Seong-Cheol (Institute of Bioscience & Biotechnology Daewoong Pharm. Co., Ltd.) ;
  • Baik, Kyung-Up (Institute of Bioscience & Biotechnology Daewoong Pharm. Co., Ltd.) ;
  • Cho, Jae-Youl (Institute of Bioscience & Biotechnology Daewoong Pharm. Co., Ltd.) ;
  • Yoo, Eun-Sook (Institute of Bioscience & Biotechnology Daewoong Pharm. Co., Ltd.) ;
  • Byun, Young-Seok (Institute of Bioscience & Biotechnology Daewoong Pharm. Co., Ltd.) ;
  • Park, Myung-Hwan (Institute of Bioscience & Biotechnology Daewoong Pharm. Co., Ltd.)
  • Published : 2002.04.01

Abstract

This study describes the synthesis and in vitro evaluation of 2-[3- (Cyclopenthloxy) 4-Methoxyphenyl] - Substituted-1-Isoindolinone derivatives substituted on benzene moiety of isoindoline ring for the inhibition of $TNF-{\alpha}$ production. From this study, we have found the 6-C position on isoindolinone ring is an optimal derivatization site. Among the compounds synthesized, 6-ammo-2-[3-(cyclopentyloxy)-4-methoxyphenyl]-1-isoindolinone (6) was the most potent in inhibitory activity of $TNF-{\alpha}$ production in LPS-stimulated RAW264.7 cells.

Keywords

References

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