张蕾磊, 薛海, 李莉, 陆小凡, 陈志伟, 刘刚. (±)-F18对映异构体的HPLC手性分离、绝对构型确定以及抗HIV-1活性研究J. 药学学报, 2015,50(6): 733-737.
引用本文: 张蕾磊, 薛海, 李莉, 陆小凡, 陈志伟, 刘刚. (±)-F18对映异构体的HPLC手性分离、绝对构型确定以及抗HIV-1活性研究J. 药学学报, 2015,50(6): 733-737.
ZHANG Lei-lei, XUE Hai, LI Li, LU Xiao-fan, CHEN Zhi-wei, LIU Gang. HPLC enantioseparation, absolute configuration determination and anti-HIV-1 activity of (±)-F18 enantiomersJ. Acta Pharmaceutica Sinica, 2015,50(6): 733-737.
Citation: ZHANG Lei-lei, XUE Hai, LI Li, LU Xiao-fan, CHEN Zhi-wei, LIU Gang. HPLC enantioseparation, absolute configuration determination and anti-HIV-1 activity of (±)-F18 enantiomersJ. Acta Pharmaceutica Sinica, 2015,50(6): 733-737.

(±)-F18对映异构体的HPLC手性分离、绝对构型确定以及抗HIV-1活性研究

HPLC enantioseparation, absolute configuration determination and anti-HIV-1 activity of (±)-F18 enantiomers

  • 摘要: 消旋 (±)-F18 (10-chloromethyl-11-demethyl-12-oxo-calanolide A) 是对天然产物 (+)-calanolide A进行结构优化得到的四环香豆素类非核苷类逆转录酶抑制剂.本文建立了高效液相色谱法手性分离 (±)-F18对映异构体的方法, 并制备得到两个光学异构体 (R)-F18和 (S)-F18.应用电子圆二色谱技术和量化计算方法确定了二者光学异构体的绝对构型.抗HIV-1活性筛选表明, (S)-F18和 (R)-F18对17个NNRTI耐药病毒株有相似的耐药谱, 但二者的抗病毒活性有显著的区别.其中 (R)-F18对野生型病毒株、K101E和P225H耐药株抗病毒活性较 (S)-F18高近10倍.

     

    Abstract: Racemic (±)-F18 (10-chloromethyl-11-demethyl-12-oxo-calanolide A), an analog of nature product (+)-calanolide A, is a new anti-HIV-1 nonnucleoside reverse transcript inhibitor (NNRTI). A successful enantioseparation of (±)-F18 offering (R)-F18 and (S)-F18 was achieved by a chiral stationary phase prepared HPLC. Their absolute configurations were determined by measurement of their electronic circular dichroisms combined with modern quantum-chemical calculations. Further investigation revealed that (R)-F18 and (S)-F18 shared a similar anti-HIV activities, however, (R)-F18 was more potent than (S)-F18 against wild-type virus, K101E mutation and P225H mutation pseudoviruses.

     

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