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从红淡比(Litsea rubescens)和山鸡椒(Litsea pedunculata)中提取的新型细胞毒性查耳酮。

Novel cytotoxic chalcones from Litsea rubescens and Litsea pedunculata.

机构信息

Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091, PR China.

出版信息

Bioorg Med Chem Lett. 2011 Dec 15;21(24):7431-3. doi: 10.1016/j.bmcl.2011.10.003. Epub 2011 Oct 8.

Abstract

Two novel flavonoids with chalcone skeleton, together with seven known flavonoids, were isolated from the stem barks of Litsea rubescens and Litsea pedunculata. The structures of the new compounds were elucidated on the basis of spectral methods including IR, UV, 1D and 2D NMR. The new chalcones were found to contain the rare epoxy or ethylidenedioxy group. This is the first report on the presence of chalcone in the plant genus Litsea. The cytotoxic potential of two new chalcones was evaluated in vitro against three human tumor cell lines. Both new chalcones displayed potent cytotoxic activities against myeloid leukaemia (HL-60) and epidermoid carcinoma (A431) cell lines and more active than cisplatin (DDP). Interestingly, compound 1 exhibited cytotoxic activity against HL-60 with IC(50) value 2.1-fold more sensitive to DDP.

摘要

从红毛树和山鸡椒的茎皮中分离得到两种具有查尔酮骨架的新黄酮类化合物,以及七种已知的黄酮类化合物。根据包括 IR、UV、1D 和 2D NMR 在内的光谱方法阐明了新化合物的结构。新查尔酮含有罕见的环氧或亚乙基二氧基。这是首次在山鸡椒属植物中发现查尔酮。体外评估了两种新查尔酮对三种人肿瘤细胞系的细胞毒性潜力。两种新查尔酮对髓性白血病 (HL-60) 和表皮样癌 (A431) 细胞系均显示出很强的细胞毒性活性,比顺铂 (DDP) 更有效。有趣的是,化合物 1 对 HL-60 的细胞毒性活性具有更高的敏感性,IC(50) 值比 DDP 低 2.1 倍。

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