@article {6, title = {New triterpenoids from Kadsura heteroclita and their cytotoxic activity.}, journal = {Planta medica}, volume = {72}, year = {2006}, pages = {450{\textendash}457}, author = {Wang, Wei and Liu, Jinzhi and Han, Jian and Xu, Zhengren and Liu, Rongxia and Liu, Peng and Ma, X and Guan, S and Guo, D} } @article {5, title = {A coumarin lignanoid from the stems of Kadsura heteroclita.}, journal = {Bioorg Med Chem Lett}, volume = {25}, year = {2015}, month = {2015 Apr 1}, pages = {1506-8}, abstract = {

Coumarinlignan (1), possessing a unique coumarin-containing lignan skeleton, was isolated from the stems of Kadsura heteroclita. Its structure and absolute configuration were determined by spectroscopic techniques, especially 2D NMR and X-ray crystallographic data analyses. The proposed biosynthetic pathway is discussed. This new compound showed good anti-HBV activity against HBeAg and HBsAg, and moderate anti-fibrotic and neuroprotective activities.

}, issn = {1464-3405}, doi = {10.1016/j.bmcl.2015.02.022}, author = {Su, Wei and Zhao, Jianping and Yang, Min and Yan, Hui-Wen and Pang, Tao and Chen, Sheng-Huang and Huang, Hui-Yong and Zhang, Shui-Han and Ma, Xiao-Chi and Guo, De-An and Khan, Ikhlas A and Wang, Wei} } @article {4, title = {Triterpenes from Kadsura coccinea.}, journal = {J Tradit Complement Med}, volume = {2}, year = {2012}, month = {2012 Apr}, pages = {154-7}, abstract = {

In vitro anti-allergic screening of medicinal herbal extracts revealed that the 80\% acetone extract of the rhizome of Kadsura coccinea inhibited nitric oxide (NO) production in a lipopolysaccharide (LPS) and recombinant mouse interferon-\γ (IFN-\γ) activated murine macrophage like cell line, RAW264.7. Further fractionation of the EtOAc extract led to the isolation of one new 3,4-seco-lanostane type triterpene named kadsuracoccin acid A (1) together with two known triterpenes anwuweizonic acid (2) and neokadsuranic acid B (3). Compounds 1-3 did not exhibit any inhibitory activities for NO production and IFN-\γ activation.

}, issn = {2225-4110}, author = {Li, Hai-Xia and Fan, Jie and Hu, Wen and Wang, Chao and Kitanaka, Susumu and Li, He-Ran} } @article {3, title = {Two new triterpenoid acids from Kadsura coccinea.}, journal = {Arch Pharm Res}, volume = {33}, year = {2010}, month = {2010 Dec}, pages = {1933-6}, abstract = {

An investigation of EtOAc extracts of Kadsura coccinea (Lem.) A. C. Smith, has led to the isolation of two new compounds characterized as 3-hydroxy-12-hydroxyl coccinic acid (1) and 3-hydroxy-neokadsuranic acid A (2). Their structures were established by 1D and 2D NMR techniques and mass spectroscopy. Antiproliferative effects of the isolated compounds were evaluated against four human tumor cell lines (A549, HCT116, HL-60 and HepG2), and it was found that compound 1 exhibited antiproliferative effects with IC(50) values ranging from 3.01 to 18.08 \μg/mL.

}, keywords = {Antineoplastic Agents, Phytogenic, Cell Line, Tumor, Cell Proliferation, HCT116 Cells, Hep G2 Cells, HL-60 Cells, Humans, Kadsura, Magnetic Resonance Spectroscopy, Plant Extracts, Plant Roots, Triterpenes}, issn = {0253-6269}, doi = {10.1007/s12272-010-1207-0}, author = {Song, Yan and Zhao, Qing-Jie and Jin, Yong-Sheng and Feng, Chuan-Wei and Chen, Hai-Sheng} } @article {2, title = {A new description of Kadsura ananosma Kerr (Schisandraceae)}, journal = {Thai Forest Bull., Bot}, year = {1999}, pages = {31{\textendash}35}, author = {Trisonthi, CHUSIE and Trisonthi, P} } @article {1, title = {Monograph of Kadsura (Schisandraceae)}, journal = {Systematic botany monographs}, year = {1998}, pages = {1{\textendash}106}, author = {Saunders, Richard MK} }