GNA002|1385035-79-9|-陌孚医药/Medlife

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GNA002

目录号: PL15024 纯度: ≥98%

CAS No. :1385035-79-9

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中文名称	GNA002
英文名称	GNA002
英文别名	(Z)-4-[(1R,2R,13R,15S)-7-[(2E)-3,7-Dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methyl;GNA002
Cas No.	1385035-79-9
分子式	C₄₂H₅₅NO₈
分子量	701.89
包装储存	-20°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

产品详情	GNA002 是一种有效，选择性的，共价 EZH2 抑制剂，对 EZH2 的 IC₅₀ 为1.1 μM。GNA002 可以特异性，共价结合 EZH2-SET 结构域内的 Cys668，通过 Hsp70 相互作用蛋白 (CHIP) 介导的泛素化的 COOH 末端引发 EZH2 降解。GNA002 有效降低 EZH2 介导的 H3K27 三甲基化，重新激活 polycomb 阻遏复合物 2 (PRC2) 沉默的肿瘤抑制基因。
生物活性	GNA002 is a highly potent, specific and covalent EZH2 (Enhancer of zeste homolog 2) inhibitor with an IC 50 of 1.1 μM. GNA002 can specifically and covalently bind to Cys668 within the EZH2-SET domain, triggering EZH2 degradation through COOH terminus of Hsp70-interacting protein (CHIP)-mediated ubiquitination. GNA002 efficiently reduces EZH2-mediated H3K27 trimethylation, reactivates polycomb repressor complex 2 (PRC2)-silenced tumor suppressor genes.
性状	Oil
IC50 & Target[1][2]	EZH2 1.1 μM (IC50)
体外研究(In Vitro)	GNA002 (10 μM; 72 hours) clearly inhibits the proliferation of numerous cancer cell lines with IC50s of 0.070 μM and 0.103 μM for MV4-11 and RS4-11. GNA002 (2 μM; 24 hours) demonstrates an elevated capacity to induce cell death in human cancer cells. GNA002 (0.1-4 μM; 48 hours) efficiently reduces EZH2-mediated H3K27 trimethylation in Cal-27 head and neck cancer cells. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)	GNA002 (oral administration; 100 mg/kg; daily) significantly decreases the volumes of Cal-27-derived tumors and reduces H3K27Me3 levels in tumor tissues. GNA002 also significantly suppresses the in vivo tumor growth derived from the xenografted A549 lung cancer cells, Daudi and Pfeiffer cells. GNA002 inhibits the aberrant oncogenic functions of EZH2, thus inhibiting tumor growth in vivo, at least in the xenograft experimental model. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件	Room temperature in continental US; may vary elsewhere.
储存方式	-20°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
参考文献	[1]. Wang X, et al. A covalently bound inhibitor triggers EZH2 degradation through CHIP-mediated ubiquitination. EMBO J. 2017 May, 36(9):1243-1260.

溶解度数据	In Vitro: DMSO : 25 mg/mL (35.62 mM; Need ultrasonic)配制储备液

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1：一般建议：溶解度为Medlife测试数据，可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解，请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异，仅做参考，具体以实验方案为准。

2：储存条件：粉末-20°C一般情况可以保存3年，溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异，请细致阅读产品信息，并辅助参考相关文献描述。

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