Natural Products as Sources of New Drugs over the Period 1981−2002

天然产物 自然(考古学) 药物发现 产品(数学) 计算机科学 细分 天然产物研究 组合化学 计算生物学 化学 生化工程 立体化学 数学 生物信息学 生物 工程类 生物活性 土木工程 古生物学 生药学 体外 生物化学 几何学
作者
David Newman,Gordon M. Cragg,Kenneth M. Snader
出处
期刊:Journal of Natural Products [American Chemical Society]
卷期号:66 (7): 1022-1037 被引量:3006
标识
DOI:10.1021/np030096l
摘要

This review is an updated and expanded version of a paper that was published in this journal in 1997. The time frame has been extended in both directions to include the 22 years from 1981 to 2002, and a new secondary subdivision related to the natural product source but applied to formally synthetic compounds has been introduced, using the concept of a "natural product mimic" or "NM" to join the original primary divisions. From the data presented, the utility of natural products as sources of novel structures, but not necessarily the final drug entity, is still alive and well. Thus, in the area of cancer, the percentage of small molecule, new chemical entities that are nonsynthetic has remained at 62% averaged over the whole time frame. In other areas, the influence of natural product structures is quite marked, particularly in the antihypertensive area, where of the 74 formally synthetic drugs, 48 can be traced to natural product structures/mimics. Similarly, with the 10 antimigraine drugs, seven are based on the serotonin molecule or derivatives thereof. Finally, although combinatorial techniques have succeeded as methods of optimizing structures and have, in fact, been used in the optimization of a number of recently approved agents, we have not been able to identify a de novo combinatorial compound approved as a drug in this time frame.
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