Discovery of natural product anticancer agents from biodiverse organisms

被引:0
作者
Kinghorn, A. Douglas [1 ]
Chin, Young-Won [1 ]
Swanson, Steven M. [2 ]
机构
[1] Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA
[2] Univ Illinois, Coll Pharm, Dept Med Chem & Pharmacognosy, Chicago, IL 60612 USA
关键词
Natural product; terrestrial and marine organisms; potential anticancer agent; structural diversity; HISTONE DEACETYLASE INHIBITOR; 1ST TOTAL-SYNTHESIS; ANTINEOPLASTIC AGENTS; ROCAGLAMIDE DERIVATIVES; ANTITUMOR METABOLITES; STRUCTURE REVISION; SPIRUCHOSTATIN-B; PALMEROLIDE; DRUGS; SILVESTROL;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Since the early 1960s, small organic molecules derived naturally from microbes and plants have provided a number of useful cancer chemotherapeutic drugs. The search for naturally occurring lead compounds of this type has continued in recent years, with the constituents of marine fauna and flora as well as those of terrestrial microorganisms and plants being investigated for their anticancer activities. In the present short review, selected novel compounds that have been obtained from organisms of diverse biological origin, or their derivatives, are discussed in terms of their potential use as cancer chemotherapeutic agents. Such promising lead compounds tend to generate considerable interest among scientists such as synthetic organic chemists and biologists. Consequently, the supply of a given precious natural product sample may be enhanced, and it may be possible to determine a preliminary notion of structure-activity relationships and of its potential mechanism of action.
引用
收藏
页码:189 / 196
页数:8
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