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Discovering active compounds from mixture of natural products
ORIGINAL ARTICLE
Discovering active compounds from mixture of natural products
by data mining approach
Yi Wang ? Yecheng Jin ? Chenguang Zhou ?
Haibin Qu ? Yiyu Cheng
Received: 8 August 2007 / Accepted: 19 February 2008 / Published online: 5 March 2008
International Federation for Medical and Biological Engineering 2008
Abstract Traditionally, active compounds were discov-
ered from natural products by repeated isolation and
bioassays, which can be highly time consuming. Here, we
have developed a data mining approach using the casual
discovery algorithm to identify active compounds from
mixtures by investigating the correlation between their
chemical composition and bioactivity in the mixtures. The
efficacy of our algorithm was validated by the cytotoxic
effect of Panax ginseng extracts on MCF-7 cells and
compared with previous reports. It was demonstrated that
our method could successfully pick out active compounds
from a mixture in the absence of separation processes. It is
expected that the presented algorithm can possibly accel-
erate the process of discovering new drugs.
Keywords Quantitative composition–activity
relationship Causality Bioassay-guided isolation
Drug discovery Traditional chinese medicine
1 Introduction
Natural products like alkaloids and terpenes from medical
plants and some bacteria, steroids from marine animals,
macromolecular products have been important sources for
drug discovery [9]. It has been reported that over 70% of
new anti-cancer drugs are isolated from natural products or
from synthetic molecules with naturally occurring molec-
ular scaffolds [16]. Plant extracts that are traditionally used
in China and India for memory-enhancing, as nerve tonics,
anxiolytic, anti-inflammatory and immunopotentiation,
have recently been screened for new leads of psychother-
apeutic compounds using bioassay-guided screening [10,
11, 23]. Since, natural occurring compounds contain more
chemical diversity than synthetic compound libraries, th
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