a Dipartimento di Biotecnologie , Chimica e Farmacia, Università di Siena , Siena , Italy.
Expert Opin Ther Pat. 2016;26(4):529-35. doi: 10.1517/13543776.2016.1132309. Epub 2016 Feb 16.
In recent years, the involvement of the Hedgehog (Hh) signaling pathway in various human diseases and dysfunctions has been clearly demonstrated. Smoothened (Smo), one of the upstream signal transducers, has been the most druggable target of the Hh pathway. However, the emergence of resistance to Smo inhibitors and the identification of Smo-independent activation of the Hh pathway led to the need to find new chemical entities able to interfere with downstream components, such as Gli. For this purpose, two different computational approaches have been applied to a small-sized library of natural compounds. As a result, an isoflavone derivative that showed ability to inhibit both Smo and Gli1 has been identified; namely, Glabrescione B. A new synthetic approach has been planned for this compound and its derivatives. Biological evaluation demonstrated the mechanism of action and showed a promising preclinical profile.
近年来,Hedgehog(Hh)信号通路在各种人类疾病和功能障碍中的作用已得到明确证实。Smo( smoothened)是上游信号转导物之一,是 Hh 通路最具成药性的靶标。然而,对 Smo 抑制剂的耐药性的出现以及 Hh 通路的 Smo 非依赖性激活的鉴定,导致需要寻找新的化学实体来干扰下游成分,如 Gli。为此,我们应用了两种不同的计算方法对一个小型天然化合物库进行了研究。结果,鉴定出一种具有抑制 Smo 和 Gli1 能力的异黄酮衍生物,即 Glabrescione B。我们计划为该化合物及其衍生物设计新的合成方法。生物学评估证实了其作用机制,并显示出有前景的临床前特征。