Action Mechanisms of Chinese Herbal Compound at the Molecular Level

Authors: Yan, Lu; Lao, Yong-Min; Jiang, Jian-Guo

Source: Letters in Drug Design & Discovery, Volume 6, Number 5, July 2009 , pp. 397-402(6)

Publisher: Bentham Science Publishers

Buy & download fulltext article:

OR

Price: $63.10 plus tax (Refund Policy)

Abstract:

As an important part of traditional Chinese medicine (TCM), Chinese Herbal Compound (CHC) is paid more and more attention nowadays. The elucidation of CHC action mechanisms becomes the key problem of how to further develop the TCM and find new novel drugs. Compound prescription is a complex system originating in China that accumulated enormous effective experiences in the thousands of years of its practice. It is very difficult to explain the effectiveness of CHC just using traditional pharmacological methods due to its extremely complex composition, uncertain action mechanism, and too many acting targets. The rapid development of molecular biology and genetics makes it possible to study the mechanism of TCM compounds at the cellular and molecular level. In the past, research of CHC on the organism level has achieved remarkable results. This paper reviews some progresses on the relevant action mechanisms of CHC at molecular level. Recent studies have shown that CHC may play an important role on interfering cell signal transduction pathways, such as apoptosis in tumor cells and regulating the expression of disease-related genes. Further studies should be conducted on its active components by detecting the disease-related genes and drug responsive genes through biochip technology.

Keywords: Chinese herbal compound; Traditional Chinese medicine; Molecular biology; Cell; Gene; Proteomics

Document Type: Research article

Publication date: 2009-07-01

More about this publication?
  • Letters in Drug Design & Discovery publishes original letters on all areas of rational drug design and discovery including medicinal chemistry, in-silico drug design, combinatorial chemistry, high-throughput screening, drug targets, and structure-activity relationships. The emphasis will be on publishing quality papers very rapidly. Letters will be processed rapidly by taking full advantage of Internet technology for both the submission and review of manuscripts. The journal is essential reading to all pharmaceutical scientists involved in research in drug design and discovery.
Related content

Tools

Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content

Text size:

A | A | A | A
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages. print icon Print this page