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使用基于3D配体的虚拟筛选发现对伯基特淋巴瘤细胞具有选择性细胞毒性的新型小分子化合物。

Discovery of novel small-molecule compounds with selective cytotoxicity for Burkitt's lymphoma cells using 3D ligand-based virtual screening.

作者信息

Gobec Martina, Sosič Izidor, Brus Boris, Obreza Aleš, Gobec Stanislav, Mlinarič-Raščan Irena

机构信息

University of Ljubljana, Faculty of Pharmacy, Aškerčeva cesta 7, Ljubljana 1000, Slovenia.

出版信息

Molecules. 2014 Nov 19;19(11):19209-19. doi: 10.3390/molecules191119209.

Abstract

We describe a ligand-based approach towards compounds with more specific targeting for Burkitt's lymphoma. Using three-dimensional ligand-based similarity searches and a previously described hit compound, we have identified six compounds that are chemically different but with similar spatial conformations. Biological evaluation revealed that one compound has better growth inhibition and improved selectivity towards Burkitt's lymphoma cells than the query compound. However, initial mechanism-of-action studies show a different target profile in comparison with the previous hit compound, which does not involve the inhibition of the proteasome or the NFκB pathway. The data from this study provide a solid basis for further efforts in the search for selective agents against Burkitt's lymphoma.

摘要

我们描述了一种基于配体的方法,用于寻找对伯基特淋巴瘤具有更特异性靶向作用的化合物。利用基于三维配体的相似性搜索和一种先前描述的活性化合物,我们鉴定出了六种化学结构不同但空间构象相似的化合物。生物学评估显示,其中一种化合物对伯基特淋巴瘤细胞具有比查询化合物更好的生长抑制作用和更高的选择性。然而,初步的作用机制研究表明,与先前的活性化合物相比,其靶点谱不同,不涉及蛋白酶体或NFκB通路的抑制。这项研究的数据为进一步寻找针对伯基特淋巴瘤的选择性药物提供了坚实的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25ae/6270761/d90dfcbed9fa/molecules-19-19209-g001.jpg

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