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Merck
  • Ligustrazine derivatives. Part 3: Design, synthesis and evaluation of novel acylpiperazinyl derivatives as potential cerebrocardiac vascular agents.

Ligustrazine derivatives. Part 3: Design, synthesis and evaluation of novel acylpiperazinyl derivatives as potential cerebrocardiac vascular agents.

Bioorganic & medicinal chemistry (2009-03-31)
Xian-Chao Cheng, Xin-Yong Liu, Wen-Fang Xu, Xiu-Li Guo, Ning Zhang, Yu-Ning Song
摘要

A series of novel acylpiperazinyl Ligustrazine derivatives was designed, synthesized, and their protective effects on damaged ECV-304 cells and antiplatelet aggregation activities were evaluated. The results showed that compound E33 displayed most potential protective effects on the ECV-304 cells damaged by hydrogen peroxide, and compound E1 was found to be the most active antiplatelet aggregation agent. Structure-activity relationships were briefly discussed.

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Sigma-Aldrich
2,3,5,6-四甲基吡嗪, natural, ≥98%, FG
Sigma-Aldrich
2,3,5,6-四甲基吡嗪, 98%
Sigma-Aldrich
2,3,5,6-四甲基吡嗪, ≥98%, FG