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AOH1160

目录号 : GC68448

AOH1160 是一种有效的可口服的小分子增殖细胞核抗原 (PCNA) 抑制剂,干扰 DNA 复制,阻断同源重组介导的 DNA 修复,导致细胞周期停滞并诱导细胞凋亡。 AOH1160 选择性杀死多种类型的癌细胞 (平均 GI50=330 nM),不会对广泛的非恶性细胞造成显着毒性。

AOH1160 Chemical Structure

Cas No.:2089314-57-6

规格 价格 库存 购买数量
5mg
¥540.00
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10mg
¥900.00
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25mg
¥1,800.00
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50mg
¥2,700.00
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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

IC50: PCNA[1]

AOH1160 is a potent, first-in-class, orally available small molecule proliferating cell nuclear antigen (PCNA) inhibitor, interferes with DNA replication, blocks homologous recombination-mediated DNA repair, causes cell-cycle arrest and induces Apoptosis. AOH1160 selectively kills many types of cancer cells (mean GI50=330 nM) without causing significant toxicity to a broad range of nonmalignant cells[1].

[1]. Gu L, et al. The Anticancer Activity of a First-in-class Small-molecule Targeting PCNA. Clin Cancer Res. 2018 Dec 1;24(23):6053-6065.

Chemical Properties

Cas No. 2089314-57-6 SDF Download SDF
分子式 C25H20N2O3 分子量 396.44
溶解度 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.5224 mL 12.6122 mL 25.2245 mL
5 mM 0.5045 mL 2.5224 mL 5.0449 mL
10 mM 0.2522 mL 1.2612 mL 2.5224 mL
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Research Update

The Anticancer Activity of a First-in-class Small-molecule Targeting PCNA

Clin Cancer Res 2018 Dec 1;24(23):6053-6065.PMID:29967249DOI:PMC6279569

Purpose: Proliferating cell nuclear antigen (PCNA) plays an essential role in regulating DNA synthesis and repair and is indispensable to cancer cell growth and survival. We previously reported a novel cancer associated PCNA isoform (dubbed caPCNA), which was ubiquitously expressed in a broad range of cancer cells and tumor tissues, but not significantly in nonmalignant cells. We found the L126-Y133 region of caPCNA is structurally altered and more accessible to protein-protein interaction. A cell-permeable peptide harboring the L126-Y133 sequence blocked PCNA interaction in cancer cells and selectively kills cancer cells and xenograft tumors. On the basis of these findings, we sought small molecules targeting this peptide region as potential broad-spectrum anticancer agents. Experimental design: By computer modeling and medicinal chemistry targeting a surface pocket partly delineated by the L126-Y133 region of PCNA, we identified a potent PCNA inhibitor (AOH1160) and characterized its therapeutic properties and potential toxicity. Results: AOH1160 selectively kills many types of cancer cells at below micromolar concentrations without causing significant toxicity to a broad range of nonmalignant cells. Mechanistically, AOH1160 interferes with DNA replication, blocks homologous recombination-mediated DNA repair, and causes cell-cycle arrest. It induces apoptosis in cancer cells and sensitizes them to cisplatin treatment. AOH1160 is orally available to animals and suppresses tumor growth in a dosage form compatible to clinical applications. Importantly, it does not cause significant toxicity at 2.5 times of an effective dose. Conclusions: These results demonstrated the favorable therapeutic properties and the potential of AOH1160 as a broad-spectrum therapeutic agent for cancer treatment.