New tigliane-type diterpenoids from Euphorbia aellenii Rech. f. with immunomodulatory activity

被引:0
|
作者
Ghanadian, M. [1 ]
Ayatollahi, A. M. [2 ]
Mesaik, M. A. [3 ]
Afsharypour, S. [4 ,5 ]
Abdalla, O. M. [3 ]
Kobarfard, F. [6 ]
机构
[1] Isfahan Univ Med Sci, Isfahan Pharmaceut Sci Res Ctr, Esfahan, Iran
[2] Shahid Beheshti Univ Med Sci, Shahid Beheshti Phytochem Res Ctr, Tehran, Iran
[3] Univ Karachi, Int Ctr Chem & Biol Sci, Panjwani Ctr Mol Med & Drug Res, Karachi 75270, Pakistan
[4] Isfahan Univ Med Sci, Isfahan Pharmaceut Sci Res Ctr, Dept Pharmacognosy, Esfahan, Iran
[5] Isfahan Univ Med Sci, Isfahan Pharmaceut Sci Res Ctr, Sch Pharm & Pharmaceut Sci, Esfahan, Iran
[6] Shahid Beheshti Univ Med Sci, Sch Pharm, Med Chem, Tehran, Iran
关键词
Euphorbia aellenii; Immunomodulatory activity; Tigliane-type diterpenoid; Phorbol diterpene;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The cytotoxic chloroform fraction of Euphorbia aellenii Rech. F. (Euphorbiaceae) afforded two new phorbol diterpenoids: 4-deoxy-4 alpha-phorbol-12-(2,3-dimethyl) butyrate-13-isobutyrate and 17-hydroxy-4-deoxy-4 alpha-phorbol-12-(2,3-dimethyl) butyrate-13-isobutyrate. Their structures were elucidated by NMR and other spectroscopic methods. The immunomodulating potentials of the isolated compounds were tested using standard proliferation and chemiluminescence assays. Compound 2 showed moderate inhibitory activity against both T-cell proliferation and reactive oxygen species (ROS) production in whole blood with IC50 of 14.0 +/- 0.57 and 44.1 +/- 3.8 mu g/ml, respectively, while compound 1 was relatively inactive with IC50 >50 mu g/mL for T-cell proliferation, and >100 mu g/mL for ROS.
引用
收藏
页码:35 / 41
页数:7
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