RSS-Feed abonnieren
DOI: 10.1055/s-2008-1034361
© Georg Thieme Verlag KG Stuttgart · New York
Chemical Constituents from the Stem Bark of Trewia nudiflora L. and their Antioxidant Activities
Publikationsverlauf
Received: February 8, 2007
Revised: January 16, 2008
Accepted: February 22, 2008
Publikationsdatum:
26. März 2008 (online)
Abstract
Three new compounds, namely, (+)-dihydrodehydrodiconiferyl alcohol 4-O-β-(6″-O-galloyl)-glucopyranoside (1), 4,4′-O-dimethylellagic acid 3-(2″-O-acetyl)-α-rhamnopyranoside (2), and ethyl O-β-(6′-galloyl)-glucopyranoside (3), together with eleven known ones, were isolated from the stem bark of Trewia nudiflora. Their structures were elucidated by means of 1D, 2 D NMR and HR-MS analyses. The antioxidant activities of these compounds were evaluated with the DPPH radical-scavenging assay. Compound 1 showed significant antioxidant activity. In addition, compounds 1, 2 and 3 rescued the H2O2-induced PC12 cell death at 0.4 μM in the MTT assay.
Key words
Trewia nudiflora - Euphorbiaceae - stem bark - antioxidant activities
- Supporting Information for this article is available online at
- Supporting Information .
References
- 1 Li B J, Wan C, Xu X K, Yue X F, Sheng Z M, Han J X. et al . Maytansinoids from the seeds of Trewia nudiflora. . Acta Bot Yunn. 1991; 13 432-9
- 2 Powell R G, Weisleder D, Smith C R. Novel maytansinoid tumor inhibitors from Trewia nudiflora: trewiasine, dehydrotrewiasine and demethyltrewiasine. J Org Chem. 1981; 46 4398-403
- 3 Powell R G, Weisleder D, Smith C R, Kozlowski J, Rohwedder W K. Treflorine, trenudine, and N-methyltrenudone: novel maytansinoid tumor inhibitors containing two fused macrocyclic rings. J Am Chem Soc. 1982; 104 4929-34
- 4 Zhao P J, Shen Y M. Neo-lignans in the seed crusts of Trewia nudiflora. . Chin Chem Lett. 2004; 15 921-4
- 5 Kang Q J, Zhao P J, He H P, Shen Y M. Cardenolides and cardiac aglycone from the stem bark of Trewia nudiflora. . Helv Chim Acta. 2005; 88 2781-7
- 6 Du Z Z, He H P, Wu B, Shen Y M, Hao X J. Chemical constituents from the pericarp of Trewia nudiflora. . Helv Chim Acta. 2004; 87 758-63
- 7 Lennart N L, Thomas P, Olof T. Dilignol glycosides from needles of Picea abies. . Phytochemistry. 1981; 20 1967-9
- 8 Lynn D G, Chen R H, Manning K S, Wood H N. The structural characterization of endogenous factors from Vinca rosea crown gall tumors that promote cell division of tobacco cells. Proc Natl Acad Sci USA. 1987; 84 615-9
- 9 Ito A, Chai H B, Lee D, Kardono L BS, Riswan S, Farnsworth N R. et al . Ellagic acid derivatives and cytotoxic cucurbitacins from Elaeocarpus mastersii. . Phytochemistry. 2002; 61 171-4
- 10 Yue J M, Lin Z W, Wang D Z, Sun H D. A sesquiterpene and other constituents from Erigeron breviscapus. Phytochemistry. 1994; 36 717-9
- 11 Yang X W, Zhao P J, Ma Y L, Xiao H T, Zuo Y Q, He H P. et al . Mixed lignan-neolignans from Tarenna attenuata. . J Nat Prod. 2007; 70 521-5
Dr. Yuemao Shen
State Key Laboratory of Phytochemistry and Plant Resources in West China
Kunming Institute of Botany
Chinese Academy of Sciences
Kunming 650204
People’s Republic of China
Telefon: +86-871-522-3111
Fax: +86-871-515-0227
eMail: yshen@xmu.edu.cn
- www.thieme-connect.de/ejournals/toc/plantamedica