期刊文献+

Identification and Synthesis of Impurities in Pinocembrin A New Drug for the Treatment of Ischemic Stroke

Identification and Synthesis of Impurities in Pinocembrin A New Drug for the Treatment of Ischemic Stroke
原文传递
导出
摘要 Four minor impurities in pinocembrin (1)--a new drug to treat ischemic stroke, were analysed and identified by means of HPLC-UV-MS analysis, spectroscopic evidences and chemical synthetic methods. Their chemical struc- tures were identified as 5,7-dihydroxy-2-phenyl-4H-l-benzopyran-4-one (2), 3-phenyl-l-(2,4,6-trihydroxyphenyl)- 1-propanone (3), 5,%dihydroxy-2-cyclohexyl-4H-l-benzopyran-4-one (4), and 2,3-dihydro-5,7-dihydroxy-2- cyclohexyl-4H-l-benzopyran-4-one (5), respectively. All of the impurities were side products of excessive hydro- genation of the target product I or the starting material 2 in the course of synthesis, and 5 was a new compound. Four minor impurities in pinocembrin (1)--a new drug to treat ischemic stroke, were analysed and identified by means of HPLC-UV-MS analysis, spectroscopic evidences and chemical synthetic methods. Their chemical struc- tures were identified as 5,7-dihydroxy-2-phenyl-4H-l-benzopyran-4-one (2), 3-phenyl-l-(2,4,6-trihydroxyphenyl)- 1-propanone (3), 5,%dihydroxy-2-cyclohexyl-4H-l-benzopyran-4-one (4), and 2,3-dihydro-5,7-dihydroxy-2- cyclohexyl-4H-l-benzopyran-4-one (5), respectively. All of the impurities were side products of excessive hydro- genation of the target product I or the starting material 2 in the course of synthesis, and 5 was a new compound.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2012年第6期1315-1319,共5页 中国化学(英文版)
关键词 PINOCEMBRIN IMPURITY ischemic stroke side product synthesis pinocembrin, impurity, ischemic stroke, side product, synthesis
  • 相关文献

参考文献13

  • 1Ju, S. H.; Liu, A. L.; Cai, L. Q.; Zhu, L.; Lu, S. J. J. Chin. Trad. Chin. Med. Inform. 2009, 1, 54.
  • 2Gree, A. R.; Shuaib, A. DrugDiseov. Today 2006, 11,681.
  • 3Li, Y. P.; Liu, Y. P. Adv. Cardiovasc. Dis. 2007, 28, 954.
  • 4Hyun, K.; Pedro, L. R.; Jaime, A. C.; Yong, K. P.; William, H. B.; Antimicrob. Agents Chemother. 2002, 46, 1302.
  • 5Kbushbaktova, Z. A.; Yusupova, S. M.; Zamaraeva, M. V.; Tadzhi- baeva, E. T.; Syrov, V. N.; Batirov, E. K.; Yuldashev, M. P. Chem. Nat. Compd. 1996, 32, 338.
  • 6Jung, J. H.; Pummangura, S.; Chaichantipyuth, C.; Patarapanich, C.; Mclaughin, J. L. Phytochemistry 1990, 29, 1667.
  • 7Tepy, U.; Arjun, H. B.; Yasuhiro, T.; Kiyoshi, M.; Katsumichi, M.; Shigetoshi, K. J. Nat. Prod. 2002, 65, 673.
  • 8Zhu, X. M.; Fang, L. H.; Li, Y. J.; Du, G. H. Vascul. Pharmacol. 2007, 46, 160.
  • 9Duan, Y. B.; Qi, Y.; Ji, Z.; Fang, G.; Cheng, Y. H.; Wu, S. Chin. J. Med. Chem. 2006, 16, 342.
  • 10Tanka, H.;lchino, K.; Ito, K. Phytochemistry 1984, 23, 1198.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部