Article
Cytotoxicity and DNA topoisomerase inhibitory activity of constituents isolated from the fruits of Evodia officinalis.
College of Pharmacy, Yeungnam University, Gyongsan 712-749, Korea.
Archives of Pharmacal Research (impact factor:
1.59).
08/2006;
29(7):541-7.
Source: PubMed
-
Citations (0)
- Cited In (1)
-
Article: Evodiamine: a novel anti-cancer alkaloid from Evodia rutaecarpa.
[show abstract] [hide abstract]
ABSTRACT: Traditional Chinese herbs are regarded as a new and promising source of potential anti-cancer remedies and new chemotherapy adjuvants to enhance the efficacy of chemotherapy and/or to ameliorate its side effects. Extensive investigations have been undertaken both in the experimental and clinical studies over the years to augment the efficacy of chemotherapy. Evodia rutaecarpa is a very popular multi-purpose herb traditionally used in China for the treatment of headaches, abdominal pain, postpartum hemorrhage, dysentery and amenorrhea. The major constituents of Evodia rutaecarpa are evodiamine and rutaecarpine. Growing evidence demonstrates that evodiamine possesses anti-cancer activities both in vitro and in vivo by inhibiting proliferation, invasion and metastasis, inducing apoptosis of a variety of tumor cell lines. This review is aimed to summarize the recent researches on evodiamine focusing on anti-cancer activity and to highlight molecular mechanisms during the past ten years.Molecules 02/2009; 14(5):1852-9. · 2.39 Impact Factor
Data provided are for informational purposes only. Although carefully collected, accuracy cannot be guaranteed.
The impact factor represents a rough estimation of the journal's impact factor and does not reflect the actual
current impact factor.
Publisher conditions are provided by RoMEO. Differing provisions from the publisher's actual policy or licence
agreement may be applicable.
Keywords
20 microM
5-7 exhibited moderate cytotoxicities
96% inhibition
Compound 8
compounds
cultured human colon carcinoma
flavanoid glucosides
human breast carcinoma
human hepatoblastoma
MCF-7
strong inhibitory effects