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Merck
  • Synthesis and biological evaluation of rhodanine derivatives as PRL-3 inhibitors.

Synthesis and biological evaluation of rhodanine derivatives as PRL-3 inhibitors.

Bioorganic & medicinal chemistry letters (2006-03-15)
Jin Hee Ahn, Seung Jun Kim, Woul Seong Park, Sung Yun Cho, Jae Du Ha, Sung Soo Kim, Seung Kyu Kang, Dae Gwin Jeong, Suk-Kyeong Jung, Sang-Hyeup Lee, Hwan Mook Kim, Song Kyu Park, Ki Ho Lee, Chang Woo Lee, Seong Eon Ryu, Joong-Kwon Choi
摘要

A series of rhodanine derivatives was synthesized and evaluated for their ability to inhibit PRL-3. Benzylidene rhodanine derivative showed good biological activity, while compound 5e was the most active in this series exhibiting an IC50 value of 0.9 microM in vitro and showed a reduced invasion in cell-based assay.

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Sigma-Aldrich
FPT 抑制剂I,1 X 1MG, ≥98% (HPLC), solid