López Silvia N, Ramallo I Ayelen, Sierra Manuel Gonzalez, Zacchino Susana A, Furlan Ricardo L E
Farmacognosia, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario. Suipacha 531, S2002LRK Rosario, Argentina.
Proc Natl Acad Sci U S A. 2007 Jan 9;104(2):441-4. doi: 10.1073/pnas.0608438104. Epub 2006 Dec 27.
The access to libraries of molecules with interesting biomolecular properties is a limiting step in the drug discovery process. By virtue of a long molecular evolution process, natural products are recognized as biologically validated starting points in structural space for library development. We introduce here a strategy to generate natural product-like libraries. A semisynthetic mixture of compounds was produced by diversification of a natural product extract through the chemical transformation of common chemical functionalities in natural products into chemical functionalities rarely found in nature. The resulting mixture showed antifungal activity against Candida albicans, whereas the starting extract did not show such activity. Bioguided fractionation led to the isolation of a previously undescribed active semisynthetic pyrazole. The result illustrates how biological activity can be generated by designed chemical diversification of a natural product mixture, and represents the proof of principle of an alternative strategy for producing natural product-like libraries from natural products libraries.
获取具有有趣生物分子特性的分子库是药物发现过程中的一个限制步骤。由于漫长的分子进化过程,天然产物被认为是用于库开发的结构空间中经过生物学验证的起始点。我们在此介绍一种生成类天然产物库的策略。通过将天然产物中常见的化学官能团化学转化为自然界中罕见的化学官能团,对天然产物提取物进行多样化处理,从而产生了一种半合成化合物混合物。所得混合物对白色念珠菌显示出抗真菌活性,而起始提取物则没有这种活性。生物导向分馏导致分离出一种先前未描述的活性半合成吡唑。该结果说明了如何通过对天然产物混合物进行设计化学多样化来产生生物活性,并代表了从天然产物库生产类天然产物库的替代策略的原理证明。