陈一心, 虞佩琳, 李英, 嵇汝运. 青蒿素类似物的研究 Ⅶ.双(二氢青蒿素)醚和双(二氢脱氧青蒿素)醚类化合物的合成J. 药学学报, 1985, 20(6): 470-473.
引用本文: 陈一心, 虞佩琳, 李英, 嵇汝运. 青蒿素类似物的研究 Ⅶ.双(二氢青蒿素)醚和双(二氢脱氧青蒿素)醚类化合物的合成J. 药学学报, 1985, 20(6): 470-473.
CHEN Yi-Xin, YU Pei-Lin, LI Ying , JI Ru-Yun, . STUDIES ON ANALOGS OF QINGHAOSU Ⅶ.THE SYNTHESIS OF ETHERS OF BIS(DIHYDROQINGHAOSU) AND BIS(DIHYDRODEOXYOINGHAOSU)J. Acta Pharmaceutica Sinica, 1985, 20(6): 470-473.
Citation: CHEN Yi-Xin, YU Pei-Lin, LI Ying , JI Ru-Yun, . STUDIES ON ANALOGS OF QINGHAOSU Ⅶ.THE SYNTHESIS OF ETHERS OF BIS(DIHYDROQINGHAOSU) AND BIS(DIHYDRODEOXYOINGHAOSU)J. Acta Pharmaceutica Sinica, 1985, 20(6): 470-473.

青蒿素类似物的研究 Ⅶ.双(二氢青蒿素)醚和双(二氢脱氧青蒿素)醚类化合物的合成

STUDIES ON ANALOGS OF QINGHAOSU Ⅶ.THE SYNTHESIS OF ETHERS OF BIS(DIHYDROQINGHAOSU) AND BIS(DIHYDRODEOXYOINGHAOSU)

  • Abstract: Some ethers, of bis(dihydroqinghaosu) Ⅲ and bis(dihydrodeoxyqinghaosu) Ⅳ were prepared in order to study the structure-activity relationships and to search for new antimalarials. Compounds Ⅲ were sythesized by condensation of glycol with two moles of dihydroqinghaosu using boron trifluoride etherate as catalyst. Compounds Ⅳ were prepared from ethers of bis (dihydroqinghaosu) by reduction with zinc and acetic acid.The bis-ethers were evaluated against chloroquine-resistant strain of plasmodium berghei in mice. Compounds Ⅲ were less potent than methyl-dihydroqinghaosu (Ⅰ) and compounds Ⅳ were inactive.

     

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