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The winding road of the uvaretin class of natural products: from total synthesis to bioactive agent discovery

机译:Uvaretin类自然产品的绕线道路:从总合成到生物活性剂发现

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Herein, we disclose the development of a synthetic route to gain access to the uvaretin class of chalcone natural products. In this, the construction of a small library was achieved, and the collection was evaluated for cytotoxicity and other biological properties. Uvaretin (1) was accessed via a seven-step route in an overall yield of 15.1%. Within this route, the unsaturated enone variant of uvaretin (2), also a natural product, was accessed in a 16.7% yield over six steps. This route provides a nearly three-fold increase in yields of 1 and 2 in comparison to the previous synthetic route accessing them in 5.8% and 3.0% overall yields, respectively. Evaluation of 1 and 2 revealed IC_(50) values between 2.0 and 5.1 μM in the cancerous cell lines HeLa, U937, A549, and MIA PaCa-2. Screening of the whole chalcone library set led to the discovery of over 30 compounds, within six cancerous cell lines, possessing single digit μM IC_(50) activity as sole agents. Furthermore, multiple library members were found to possess promising potentiating properties with known chemotherapeutic agents.
机译:在此,我们公开了一种综合途径的开发,以获得对乌瓦替汀类的硫酮天然产物的途径。在此,实现了小文库的构建,并评估了细胞毒性和其他生物学性质的收集。通过七步途径进入Uvaretin(1)的总收益率为15.1%。在该途径内,Uvaretin(2)的不饱和酶变体,也是一种天然产物,得到16.7%的产量超过六步。与先前的合成路线分别以5.8%和3.0%的总收益率相比,该途径为1和2的产量增加了几乎三倍的产量增加。评价1和2显示癌细胞系Hela,U937,A549和MIA Paca-2中2.0和5.1μm之间的IC_(50)值。整个Chalcode图书馆的筛选导致在六种癌细胞系中发现超过30种化合物,具有单位数μmIC_(50)活性作为唯一剂。此外,发现多种文库成员具有具有已知化学治疗剂的有前增强性能的有前途的增强性能。

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