A new anthraquinone and two new tetrahydroanthraquinones from the roots of Prismatomeris connata

Helvetica Chimica Acta

Volumn 94, Issue 10, 2011, Pages 1843-1849

  Feng, Shi Xiu ^a,b   Hao, Jing ^a   Chen, Tao ^b   Qiu, Samuel X ^a  

^a SOUTH CHINA INSTITUTE OF BOTANY   (China)

^b INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

Author keywords

Anthraquinones; Cytotoxic activity; Prismatomeris connata

Indexed keywords

ANTHRAQUINONES; CYTOTOXIC ACTIVITIES; HUMAN CANCER CELLS; OH GROUP; PRISMATOMERIS CONNATA; SPECTROSCOPIC DATA; TEST CELL;

AROMATIC COMPOUNDS; CELL CULTURE; CYTOTOXICITY;

KETONES;

1 METHOXY 2 METHYLANTHRAQUINONE; 1,2,3 TRIMETHOXY 7 METHYLANTHRAQUINONE; 1,3 DIHYDROXY 2 (HYDROXYMETHYL) 9,10 ANTHRAQUINONE; 1,3 DIHYDROXY 5,6 DIMETHOXY 2 METHYL 9,10 ANTHRAQUINONE; 1,3 DIHYDROXY 5,6 DIMETHOXY 2- METHOXYMETHYL) 9,10 ANTHRAQUINONE; 2 METHOXYANTHRAQUINONE; 2 METHYLANTHRAQUINONE; 3 HYDROXY 1 METHOXY 2 METHYL 9,10 ANTHRAQUINONE; 3 HYDROXY 1,5,6 TRIMETHOXY 2 METHYL 9,10 ANTHRAQUINONE; 4 HYDROXY 1,2,3 TRIMETHOXY 6 METHYLANTHRACENE 9,10 DIONE; 6 METHOXYIBERICIN; [7], 1,3 DIHYDROXY 2 METHYL ANTHRAQUINONE; ALIZARIN 1 METHYL ETHER; ANTHRAQUINONE DERIVATIVE; ANTINEOPLASTIC AGENT; IBERICIN; LUCIDIN OMEGA METHYL ETHER; PRISCONNATANONE A; PRISCONNATANONE B; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CANCER CELL CULTURE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; HUMAN; HUMAN CELL; IC 50; NONHUMAN; NUCLEAR OVERHAUSER EFFECT; PLANT ROOT; PRIORITY JOURNAL; PRISMATOMERIS CONNATA; PROTON NUCLEAR MAGNETIC RESONANCE; RUBIACEAE; STRUCTURE ANALYSIS;

EID: 80055011550     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201100108     Document Type: Article

References (15)

1. J. T. Johansson, Opera Bot. 1987, 94, 5.
2. Y.-Z. Ruan, J. Syst. Evol. 1988, 26, 443.
3. 'Compendium of Chinese Traditional Herbal Drugs', People's Health Press, Beijing, 1992, Vol. 2, p. 772.
4. C. Y. Zhou, J. G. Deng, J. Guangxi Tradit. Chin. Med. Univ. 2006, 9, 90.
5. K. Krohn, D. Gehle, S. K. Dey, N. Nahar, M. Mosihuzzaman, N. Sultana, M. H. Sohrab, P. J. Stephens, J.-J. Pan, F. Sasse, J. Nat. Prod. 2007, 70, 1339.
6. J. S. Jiang, Z. M. Feng, P. C. Zhang, China J. Chin. Mater. Med. 2005, 30, 1751.
7. Z.-M. Feng, J.-S. Jiang, Y.-H. Wang, P.-C. Zhang, Chem. Pharm. Bull. 2005, 53, 1330.
8. A. A. El-Gamal, K. Tankeya, H. Itokawa, A. F. Halim, M. M. Amer, A. S. Hassan-Elrady, S. A. Awad, Phytochemistry 1995, 40, 245.
9. D. J. Tu, Z. H. Pang, N. J. Bi, Acta Pharm. Sin. 1981, 16, 631.
10. A. R. Burnett, R. H. Thomson, Phytochemistry 1968, 7, 1421.
11. V. V. S. Murti, T. R. Seshadri, S. Sivakumaran, Phytochemistry 1972, 11, 1524.
12. D. A. Benson, I. Karsch-Mizrachi, D. J. Lipman, J. Ostell, B. A. Rapp, D. L. Wheeler, Nucleic Acids Res. 2000, 28, 15.
13. P. Tuntiwachwuttikul, Y. Butsuri, P. Sukkoet, U. Prawat, W. C. Taylor, Nat. Prod. Res. 2008, 22, 962.
14. R. Suemitsu, Y. Yamada, T. Sano, K. Yamashita, Agric. Biol. Chem. 1984, 48, 2383.
15. T. Mosmann, J. Immunol. Methods 1983, 65, 55.