Anthraquinones and stilbenes from the roots and rhizomes of Rhubarb

Journal of Asian Natural Products Research

Volumn 13, Issue 11, 2011, Pages 1036-1041

  Chen, Wen Hao ^a   Chen, Juan ^a   Shi, Yan Ping ^a  

^a LANZHOU INSTITUTE OF CHEMICAL PHYSICS   (China)

Author keywords

Anthraquinones; DPPH assay; Rheum hotaoense; Rhubarb; Stilbenes

Indexed keywords

1,1 DIPHENYL 2 PICRYLHYDRAZYL; ALOE EMODIN; ALOE EMODIN 8 O BETA DEXTRO (6' GALLOYL)GLUCOPYRANOSIDE; ALOE EMODIN 8 O BETA DEXTRO GLUCOPYRANOSIDE; ANTHRAQUINONE DERIVATIVE; CHRYSOPHANIC ACID; CHRYSOPHANOL 1 O BETA DEXTRO GLUCOPYRANOSIDE; CHRYSOPHANOL 8 O BETA DEXTRO (6' GALLOYL)GLUCOPYRANOSIDE; CHRYSOPHANOL 8 O BETA DEXTRO GLUCOPYRANOSIDE; DESOXYRHAPONTICIN; DESOXYRHAPONTIGENIN; EMODIN; FREE RADICAL; GALLIC ACID; GLUCOSIDE; PHYSCION; PICEATANNOL 3 O BETA DEXTRO GLUCOPYRANOSIDE; PYROGALLOL; QUERCETIN; RHAPONTIGENIN; RHAPONTIN; RHEIN; RHEIN 8 O BETA DEXTRO (6' GALLOYL)GLUCOPYRANOSIDE; SCAVENGER; STILBENE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIOXIDANT ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG ACTIVITY; DRUG ISOLATION; DRUG POTENCY; DRUG STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR SINGLE QUANTUM COHERENCE; PLANT ROOT; PROTON NUCLEAR MAGNETIC RESONANCE; RHEUM HOTAOENSE; RHIZOME; RHUBARB; STRUCTURE ANALYSIS;

ANTHRAQUINONES; BIPHENYL COMPOUNDS; DRUGS, CHINESE HERBAL; FREE RADICAL SCAVENGERS; GLUCOSIDES; PICRATES; PLANT ROOTS; PLANTS, MEDICINAL; RHEUM; RHIZOME; STILBENES;

ALOE; RHEUM HOTAOENSE; RHEUM X HYBRIDUM;

EID: 84862940984     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10286020.2011.613828     Document Type: Article

References (11)

1. China Pharmacopoeia Committee, China Pharmacopoeia, part 1 (Chemical Industry Press, Beijing, 2010), p. 22.
2. P.G. Xiao, L.Y. He, and L.W. Wang, J. Ethnopharmacol. 10, 275 (1984).
3. H. Matsuda, T. Morikawa, I. Toguchida, J.Y. Park, S. Harima, and M. Yoshikawa, Bioorg. Med. Chem. 9, 41 (2001).
4. H. Matsuda, S. Tewtrakul, T. Morikawa, and M. Yoshikaw, Bioorg. Med. Chem. 12, 4871 (2004).
5. M. Ye, J. Han, H.B. Chen, J.H. Zheng, and D.A. Guo, J. Am. Soc. Mass. Spectrom. 18, 82 (2007).
6. X.R. Cui, M. Tsukada, N. Suzuki, T. Shimamura, L. Gao, J. Koyanagi, F. Komada, and S. Saito, Eur. J. Med. Chem. 43, 1206 (2008).
7. T.M. Ngoc, P.T.H. Minh, T.M. Hung, P.T. Thuong, I. Lee, B.S. Min, and K. Bae, Arch. Pharm. Res. 31, 598 (2008).
8. J.L. Li, A.Q. Wang, J.S. Li, W.Y. He, and M. Kong, Chin. Tradit. Herb. Drugs 31, 321 (2000).
9. J.L. Li, A.Q. Wang, J.S. Li, W.Y. He, and M. Kong, Chin. Tradit. Herb. Drugs 29, 721 (1998).
10. H. Okabe, K. Matsuo, and I. Nishioka, Chem. Pharm. Bull. 21, 1254 (1973).
11. C.H. Chen, C.Y. Shaw, C.C. Chen, and Y.C. Tsai, J. Nat. Prod. 65, 740 (2002).