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基于药物化学方法的天然产物衍生化疗药物的发现和开发。

Discovery and development of natural product-derived chemotherapeutic agents based on a medicinal chemistry approach.

机构信息

Natural Products Research Laboratories, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina 27599-7568, USA.

出版信息

J Nat Prod. 2010 Mar 26;73(3):500-16. doi: 10.1021/np900821e.

Abstract

Medicinal plants have long been an excellent source of pharmaceutical agents. Accordingly, the long-term objectives of the author's research program are to discover and design new chemotherapeutic agents based on plant-derived compound leads by using a medicinal chemistry approach, which is a combination of chemistry and biology. Different examples of promising bioactive natural products and their synthetic analogues, including sesquiterpene lactones, quassinoids, naphthoquinones, phenylquinolones, dithiophenediones, neo-tanshinlactone, tylophorine, suksdorfin, DCK, and DCP, will be presented with respect to their discovery and preclinical development as potential clinical trial candidates. Research approaches include bioactivity- or mechanism of action-directed isolation and characterization of active compounds, rational drug design-based modification and analogue synthesis, and structure-activity relationship and mechanism of action studies. Current clinical trial agents discovered by the Natural Products Research Laboratories, University of North Carolina, include bevirimat (dimethyl succinyl betulinic acid), which is now in phase IIb trials for treating AIDS. Bevirimat is also the first in a new class of HIV drug candidates called "maturation inhibitors". In addition, an etoposide analogue, GL-331, progressed to anticancer phase II clinical trials, and the curcumin analogue JC-9 is in phase II clinical trials for treating acne and in development for trials against prostate cancer. The discovery and development of these clinical trial candidates will also be discussed.

摘要

药用植物长期以来一直是药物制剂的重要来源。因此,作者的研究计划的长期目标是通过采用化学与生物学相结合的药物化学方法,基于植物来源的化合物先导物来发现和设计新的化疗药物。本文将介绍一些有前途的生物活性天然产物及其合成类似物的例子,包括倍半萜内酯、苦木内酯、萘醌、苯并醌、二噻吩二酮、新丹参内酯、延胡索乙素、水黄皮素、DCK 和 DCP,就其作为潜在的临床试验候选药物的发现和临床前开发进行讨论。研究方法包括基于活性或作用机制的活性化合物的分离和鉴定、基于合理药物设计的修饰和类似物合成,以及构效关系和作用机制研究。北卡罗来纳大学天然产物研究实验室发现的目前处于临床试验阶段的药物包括比福马(二甲基琥珀酰桦木酸),它目前正在进行治疗艾滋病的 IIb 期临床试验。比福马也是被称为“成熟抑制剂”的新型 HIV 候选药物中的第一种。此外,依托泊苷类似物 GL-331 已进入抗癌 II 期临床试验,姜黄素类似物 JC-9 也正在进行治疗痤疮的 II 期临床试验,并正在开发用于治疗前列腺癌的临床试验。这些临床试验候选药物的发现和开发也将进行讨论。

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