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作为信号转导和转录激活因子3(STAT3)抑制剂的先导化合物的鉴定:设计、合成与生物活性

Identification of Lead Compounds as Inhibitors of STAT3: Design, Synthesis and Bioactivity.

作者信息

Botta Antonio, Sirignano Esther, Popolo Ada, Saturnino Carmela, Terracciano Stefania, Foglia Antonio, Sinicropi Maria Stefania, Longo Pasquale, Di Micco Simone

机构信息

Dipartimento di Farmacia, Università degli Studi di Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, Salerno, Italy phone/fax: +39 089969176 (S. D. M.); +39 089969769 (C. S.); +39 089969602 (fax).

Dipartimento di Chimica e Biologia, Università degli Studi di Salerno Via Giovanni Paolo II 132, 84084 Fisciano, Salerno, Italy.

出版信息

Mol Inform. 2015 Oct;34(10):689-97. doi: 10.1002/minf.201500043. Epub 2015 Jul 1.

Abstract

STAT3 belongs to the signal transducers and activators of transcription (STAT) family. It has been demonstrated that STAT3 is constitutively activated in many tumors, playing a role in carcinogenesis and tumor progression. For this reason, it has being considered a potential target for cancer therapy. In this context, we have designed, synthesized and evaluated 1,4-dimethyl-carbazole derivatives, targeting the STAT3 protein. Moreover, MTT assay performed on A375 and HeLa, showed significant antiproliferative activity of some of synthesized compounds (3-5). The same compounds (3-5) considerably reduced STAT3 expression, as demonstrated by Western blot analysis. Our multidisciplinary approach shows that 1,4-dimethyl-carbazoles are potential building blocks to develop more affinity ligands of STAT3.

摘要

信号转导与转录激活因子3(STAT3)属于信号转导与转录激活因子(STAT)家族。已有研究表明,STAT3在许多肿瘤中持续激活,在肿瘤发生和进展中发挥作用。因此,它被认为是癌症治疗的一个潜在靶点。在此背景下,我们设计、合成并评估了针对STAT3蛋白的1,4 - 二甲基咔唑衍生物。此外,对A375和HeLa细胞进行的MTT试验表明,一些合成化合物(3 - 5)具有显著的抗增殖活性。蛋白质印迹分析表明,相同的化合物(3 - 5)能显著降低STAT3的表达。我们的多学科研究方法表明,1,4 - 二甲基咔唑是开发更多STAT3亲和配体的潜在基础材料。

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