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新型 2-[(苄基氨基)甲基]吡咯烷-3,4-二醇衍生物作为 α-甘露糖苷酶抑制剂及对血液系统和实体瘤的抗肿瘤活性。

Novel 2-[(benzylamino)methyl]pyrrolidine-3,4-diol derivatives as alpha-mannosidase inhibitors and with antitumor activities against hematological and solid malignancies.

机构信息

Laboratory of Glycochemistry and Asymmetric Synthesis (LGSA), Ecole Polytechnique Fédérale de Lausanne (EPFL), Batochime, CH-1015 Lausanne, Switzerland.

出版信息

Bioorg Med Chem. 2010 May 1;18(9):3320-34. doi: 10.1016/j.bmc.2010.03.009. Epub 2010 Mar 9.

Abstract

Novel alpha-mannosidase inhibitors of the type (2R,3R,4S)-2-({[(1R)-2-hydroxy-1-arylethyl]amino}methyl)pyrrolidine-3,4-diol have been prepared and assayed for their anticancer activities. Compound 30 with the aryl group=4-trifluoromethylbiphenyl inhibits the proliferation of primary cells and cell lines of different origins, irrespective of Bcl-2 expression levels, inducing a G2/Mcell cycle arrest and by modification of genes involved in cell cycle progression and survival.

摘要

新型α-甘露糖苷酶抑制剂为(2R,3R,4S)-2-{[(1R)-2-羟基-1-芳基乙基]氨基}甲基吡咯烷-3,4-二醇,已对其抗癌活性进行了检测。具有芳基=4-三氟甲基联苯的化合物 30 可抑制不同来源的原代细胞和细胞系的增殖,而与 Bcl-2 表达水平无关,诱导 G2/M 细胞周期停滞,并通过改变参与细胞周期进程和存活的基因来实现。

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