SIRT7 inhibitor 97491
目录号: PL11305 纯度: ≥98%
CAS No. :1807758-81-1
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中文名称
SIRT7 inhibitor 97491
中文别名
N1-(5-(4-氯苯基)恶唑-2-基)苯-1,3-二胺
英文名称
SIRT7 inhibitor 97491
英文别名
SIRT7 inhibitor 97491;N1-(5-(4-Chlorophenyl)oxazol-2-yl)benzene-1,3-diamine
Cas No.
1807758-81-1
分子式
C15H12ClN3O
分子量
285.73
包装储存
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
产品详情
SIRT7 inhibitor 97491 是一种有效的 SIRT7 抑制剂,IC50 为 325 nM,SIRT7 inhibitor 97491 降低 SIRT7 去乙酰化酶活性,这种作用存在剂量依赖性。SIRT7 inhibitor 97491 通过在 K373/382 处进行乙酰化来提高 p53 的稳定性,从而防止肿瘤进展。SIRT7 inhibitor 97491 通过
生物活性
SIRT7 inhibitor 97491, a potent SIRT7 inhibitor with an IC 50 of 325 nM, reduces deacetylase activity of SIRT7 in a dose-dependent manner. SIRT7 inhibitor 97491 prevents tumor progression by increasing p53 stability through acetylation at K373/382. SIRT7 inhibitor 97491 promotes apoptosis through caspase pathway..
性状
Solid
IC50 & Target[1][2]
SIRT7 325 nM (IC50)
体外研究(In Vitro)
SIRT7 inhibitor 97491 (1-10 μM) reduces cell growth in MES-SA cells, without causing cytotoxicity in HEK293 cells. has not independently confirmed the accuracy of these methods. They are for reference only.Cell Proliferation Assay
体内研究(In Vivo)
SIRT7 inhibitor 97491 (2 mg/kg; intraperitoneally injected; for 3 weeks, except on weekends) inhibits tumor growth in xenograft mice. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: B
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Ji-Hye Kim, et al. Identification of a Novel SIRT7 Inhibitor as Anticancer Drug Candidate. Biochem Biophys Res Commun. 2019 Jan 8;508(2):451-457.
溶解度数据
In Vitro: DMSO : 500 mg/mL (1749.90 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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