Cytotoxic cholestane-Type and ergostane-Type steroids from the aerial parts of Euphorbia altotibetic

Steroids

Volumn 78, Issue 1, 2013, Pages 38-43

  Zhang, Bei Bei ^a   Han, Xue Lian ^a   Jiang, Qian ^a   Liao, Zhi Xin ^a   Wang, Heng Shan ^b  

^a SOUTHEAST UNIVERSITY   (China)

^b GUANGXI NORMAL UNIVERSITY   (China)

Author keywords

Cytotoxic activity; Euphorbia altotibetic PAULS; Euphorbieceae; HeLa cell; Hep G2 cell; Steroids

Indexed keywords

5ALPHA METHOXY ERGOSTA 7,9,22 TRIEN 3BETA OL BETA DEXTRO GLUCOSIDE; 6BETA METHOXY ERGOSTA 7,9,22 TRIEN 3BETA OL BETA DEXTRO GLUCOSIDE; ANTINEOPLASTIC AGENT; CHOLEST 5 EN 1ALPHA,3BETA,4ALPHA TRIOL; CHOLEST 5 EN 1BETA,4BETA DIOL; CHOLEST 5 EN 2BETA,4BETA DIOL; ERGOSTA 7,9,22 TRIEN 3BETA OL BETA DEXTRO GLUCOSIDE; EUPHORBIA ALTOTIBETIC EXTRACT; EUPHORBIA EXTRACT; STEROID; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CELL STRAIN HEPG2; CONTROLLED STUDY; DRUG ISOLATION; DRUG SCREENING; DRUG STRUCTURE; EUPHORBIA; EUPHORBIA ALTOTIBETIC; FEMALE; HELA CELL; HUMAN; HUMAN CELL; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

ANTINEOPLASTIC AGENTS, PHYTOGENIC; CELL SURVIVAL; CHOLESTANES; ERGOSTEROL; EUPHORBIA; HELA CELLS; HEP G2 CELLS; HUMANS; INHIBITORY CONCENTRATION 50; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; PLANT COMPONENTS, AERIAL; PLANT EXTRACTS;

EUPHORBIA;

EID: 84869863766     PISSN: 0039128X     EISSN: 18785867     Source Type: Journal    
DOI: 10.1016/j.steroids.2012.10.011     Document Type: Article

References (10)

1. Y.C. Yang Handbook of Tibetan Medicnine 1991 Qinghai People's Press Xining
2. L. Pan, X.F. Zhang, Y. Deng, H. Wang, D.G. Wu, and X.D. Luo Chemical constituents from the whole plant of Euphorbia altotibetic Helv. Chim. Acta 86 2003 2525 2532
3. J. Chen, C.F. Zhang, and M. Zhang Chemical constituents from aerial parts of Fallopia convolvulus Zhongguo Zhong Yao Za Zhi 35 2010 3165 3167
4. Q. Chen, L.J. Wu, J. Wang, and H. Li Studies on the chemical constituents of Lophatherum gracile Brongn J. Shenyang. Pharm. Univ. 19 2002 23 24
5. T. Kato, and Y. Morita C-Glycosyflavones with acetyl substitution from Rumex acetosa Chem. Pharm. Bull. 38 1990 2277 2280
6. Z.X. Liao, B.L. Hu, L.J. Ji, S.F. Fan, J.Y. Ding, and H.F. Sun Study on chemical constituents of Swertia verticillifolia Acta Bot. Sin. 33 1991 968 970
7. J.H. Lu, Y.Y. Zhao, L. Qiao, Y.O. Fang, and Q.A. Huang Studies on chemical constituents from Buddleja lindleyana Zhongguo Zhong Yao Za Zhi 26 2001 43 45
8. L. Fang, H.F. Guo, and H.X. Lou Three new bibenzyl derivatives from the Chinese Liverwort Marchantia polymorpha L Helv. Chim. Acta 90 2007 748 752
9. A. Rivera, O.L. Benavides, and J. Rios-Motta 22E)-Ergosta-6,22-diene- 3β,5α,8α-Triol: a new polyhydroxysterol isolated from Lentinus edodes (Shiitake Nat. Prod. Res. 23 2009 293 330
10. L. Hua, W.Y. Qi, S.H. Hussain, K. Gao, and M. Arfan Highly oxygenated stigmastane-Type steroids from the aerial parts of Vernonia anthelmintica Willd Steroids 77 2012 811 818