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发现新型嘧啶硼酸类小分子作为 VCP/p97 抑制剂。

Discovery of novel pyrimidine molecules containing boronic acid as VCP/p97 Inhibitors.

机构信息

National and Local Joint Engineering Research Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University, No. 1 Wenyuan Road, Nanjing 210023, PR China.

College of Life Science, Nanjing Normal University, No. 1 Wenyuan Road, Nanjing 210037, PR China.

出版信息

Bioorg Med Chem. 2021 May 15;38:116114. doi: 10.1016/j.bmc.2021.116114. Epub 2021 Mar 23.

Abstract

Valine-containing protein (VCP) is a member of the adenosine triphosphate family involved in a variety of cellular activities. VCP/p97 is capable of maintaining protein homeostasis and mediating the degradation of misfolded polypeptides by the ubiquitin-proteasome system (UPS). In this manuscript, a series of novel p97 inhibitors with pyrimidine as core structure were designed, synthesized and biologically evaluated. Based on the enzymatic results, a detailed structure-activity relationship discussion of the synthesized compounds was carried out. Furthermore, cellular activities of the compounds with enzymatic potency of less than 200 nM were investigated by using A549 and RPMI8226 cell lines. Among the screened inhibitors, compound 17 (IC, 54.7 nM) showed good enzymatic activity. Investigation of cellular activities with non-small cell lung cancer A549 and multiple myeloma (MM) RPMI8226 further confirmed the potency of 17 with the IC values of 2.80 μM and 0.86 μM, respectively. Compound 17 is now being developed as a candidate. Finally, docking studies were carried out to explore the possible binding mode between the active inhibitor 17 and p97.

摘要

富含缬氨酸的蛋白(VCP)是一种参与多种细胞活动的三磷酸腺苷家族成员。VCP/p97 能够维持蛋白质的内稳态,并通过泛素-蛋白酶体系统(UPS)介导错误折叠多肽的降解。在本手稿中,设计、合成并对一系列以嘧啶为核心结构的新型 p97 抑制剂进行了生物评估。基于酶学结果,对合成化合物进行了详细的构效关系讨论。此外,通过 A549 和 RPMI8226 细胞系,对具有低于 200 nM 酶效价的化合物的细胞活性进行了研究。在所筛选的抑制剂中,化合物 17(IC54.7 nM)表现出良好的酶活性。用非小细胞肺癌 A549 和多发性骨髓瘤(MM)RPMI8226 进行细胞活性研究进一步证实了 17 的效力,其 IC50 值分别为 2.80 μM 和 0.86 μM。化合物 17 目前正在开发中。最后,进行了对接研究以探索活性抑制剂 17 与 p97 之间可能的结合模式。

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