C28 sterols with a cyclopentane ring at C-22 and 26 from cape gooseberry (berries of Physalis pubeacens L.)

Journal of Asian Natural Products Research

Volumn 12, Issue 9, 2010, Pages 752-759

  Xu, Qiong Ming ^a   Liu, Yan Li ^a   Feng, Yu Lin ^b   Li, Xiao Ran ^a   Yang, Shi Lin ^a,b  

^a SOOCHOW UNIVERSITY   (China)

^b JIANGXI UNIVERSITY OF TRADITIONAL CHINESE MEDICINE   (China)

Author keywords

alkesterol A; alkesterol B; C28 sterols; cytotoxic activities; Physalis pubeacens L

Indexed keywords

ALKESTEROL A; ALKESTEROL B; CYCLOPENTANE; PHYSALIS PUBEACENS EXTRACT; PLANT EXTRACT; SITOSTEROL; STEROL DERIVATIVE; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; HERBACEOUS AGENT; PHYTOSTEROL;

ARTICLE; CHEMICAL REACTION; CIRCULAR DICHROISM; CONCENTRATION RESPONSE; CONTROLLED STUDY; CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; GOOSEBERRY; HUMAN; HUMAN TISSUE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; BLACK CURRANT; CELL STRAIN HL 60; CHEMICAL STRUCTURE; CHEMISTRY; DRUG SCREENING; FRUIT; HELA CELL; ISOLATION AND PURIFICATION; NUCLEAR MAGNETIC RESONANCE;

PHYSALIS; PHYSALIS PERUVIANA;

ANTINEOPLASTIC AGENTS, PHYTOGENIC; DRUG SCREENING ASSAYS, ANTITUMOR; DRUGS, CHINESE HERBAL; FRUIT; HELA CELLS; HL-60 CELLS; HUMANS; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PHYTOSTEROLS; RIBES;

EID: 77956621668     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10286020.2010.497657     Document Type: Article

References (10)

1. Editorial Committee of Flora of China, Flora of China, Sec. A (Science Press, Beijing, China, 1975), Vol. 67, pp. 58-59.
2. Editorial Committee of Chinese Pharmacopeia, Pharmacopeia of the Peoples Republic of China, Sec. A (Chemical Industry Press, Beijing, China, 2005), p. 250.
3. S.J. Wu, J.Y. Tsai, S.P. Chang, D.L. Lin, S.S. Wang, S.N. Huang, and L.T. Ng, J. Ethnopharmacol. 108, 407 (2006).
4. B. Makino, J. Ohya, H. Yamamura, S. Araki, Y. Butsugan, and M. Kawai, Pharmazie 57, 70 (2002).
5. W. Huang, K.P. Xu, F.S. Li, S.H. Yuan, Z.K. Li, P.S. Xu, and G.S. Tan, Chin. J. Org. Chem. 29, 1564 (2009).
6. C. Duque, A. Bernal, R. Correa, M. Morisaki, and N. Ikekawa, Chem. Pharm. Bull. 31, 366 (1983).
7. J.B. Chang, R.F. Chen, Q. Wang, P. Liu, X.P. Pan, and D.Q. Yu, Acta Chem. Sin. 58, 554 (2000).
8. G. Piancatellig and A. Scettri, Synthesis 9, 116 (1977).
9. A. Liu, Z.Z. Liu, Z.M. Zou, S.Z. Chen, L.Z. Xu, and S.L. Yang, Tetrahedron 60, 3689 (2004).
10. M.B. Hansen, S.E. Nielsen, and K. Berg, J. Immunol. Methods 119, 203 (1989).