SBE13 Hydrochloride

目录号: PL04364 纯度: ≥98%
SBE13 Hydrochloride 是一种有效的,选择性的 Plk1 抑制剂,IC50 值为 200 pM,对 Plk2 (IC50>66 μM) 或 Plk3 (IC50=875 nM) 的作用较弱。
CAS No. :1052532-15-6
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PL04364-10mg 10mg ¥388.00 请登录
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PL04364-1 mL x 10 mM (in DMSO) ¥248.00 请登录
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中文名称
SBE13 Hydrochloride
中文别名
4-咪唑-1苯乙酮;N-[[4-[(6-氯-3-吡啶基)甲氧基]-3-甲氧基苯基]甲基]-3,4-二甲氧基苯乙胺盐酸盐;SBE 13 HCl 抑制剂;SBE 13盐酸盐;SBE13 (Hydrochloride)
英文名称
SBE13 Hydrochloride
英文别名
SBE 13 hydrochloride;N-[[4-[(6-chloropyridin-3-yl)methoxy]-3-methoxyphenyl]methyl]-2-(3,4-dimethoxyphenyl)ethanamine,hydrochloride;SBE 13 HCl;SBE-13 Hydrochloride;SBE-13 HCl;N-(4-((6-Chloro-3-pyridinyl)methoxy)-3-methoxybenzyl)-N-(2-(3,4-dimethoxyphenyl)ethyl)amine;N-(4-((6-chloropyridin-3-yl)Methoxy)-3-Methoxybenzyl)-2-(3,4-diMethoxyphenyl)ethanaMine hydrochloride;N-[[4-[(6-Chloro-3-pyridinyl)methoxy]-3-methoxyphenyl]methyl]-3,4-dimethoxy-benzeneethanamine hydrochloride;SBE13 (Hydrochloride);SBE13 hydrochloride;N-[[4-[(6-Chloro-3-pyridinyl)methoxy]-3-methoxyphenyl]methyl]-3,4-dimethoxybenzeneethanamine hydrochloride;MLS000538104;SBE13 HCl;C24H27ClN2O4.ClH;AOB6814;BCP23836;4031AH;s7720;SMR000161652;AK340937;SBE 13 hydrochloride, >=98% (HPLC);B5857;A14426;N-{4-[(6-chloro-;N-(4-((6-Chloro-3-pyridinyl)methoxy)-3-methoxybenzyl)-N-(2-(3,4-dimethoxyphenyl)ethyl)amine; N-[[4-[(6-Chloro-3-pyridinyl)methoxy]-3-methoxyphenyl]methyl]-3,4-dimethoxy-benzeneethanamine hydrochloride
Cas No.
1052532-15-6
分子式
C24H28Cl2N2O4
分子量
479.40
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
详情描述
SBE13 Hydrochloride 是一种有效的,选择性的 Plk1 抑制剂,IC50 值为 200 pM,对 Plk2 (IC50>66 μM) 或 Plk3 (IC50=875 nM) 的作用较弱。
产品详情
SBE13 Hydrochloride 是一种有效的,选择性的 Plk1 抑制剂,IC50 值为 200 pM,对 Plk2 (IC50>66 μM) 或 Plk3 (IC50=875 nM) 的作用较弱。
生物活性
SBE13 Hydrochloride is a potent and selective Plk1 inhibitor, with an IC 50 of 200 pM; SBE13 Hydrochloride poorly inhibits Plk2 (IC 50 >66?μM) or Plk3 (IC 50 =875?nM).
性状
Solid
IC50 & Target[1][2]
PLK1 200 pM (IC50) PLK3 875 nM (IC50
体外研究(In Vitro)
SBE13 significantly reduce cell proliferation and induce apoptosis in HeLa cells, with an EC50 of 18?μM. SBE13 (1-100 μM) shows no effect on Caspase 3/7 activity in NIH-3T3 cells. SBE13 (66 and 100 μM) does not change morphology after treatment of primary cells. SBE13 (10 and 100 μM) reduces pRb staining in primary cells, and this indicates a G0/G1 arrest. SBE13 (66 and 100 μM) increases levels of cyclin B1, phospho histone H3, Wee1, Emi1 and securin, and results in cleavage of Cdc27 in HeLa cells. SBE13 (10 and 100 μM) also induces apoptosis of HeLa cells. 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
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Keppner S, et al. Identification and validation of a potent type II inhibitor of inactive polo-like kinase 1. ChemMedChem. 2009 Nov;4(11):1806-9.
[2]. Keppner S, et al. Fate of primary cells at the G?/S boundary after polo-like kinase 1 inhibition by SBE13. Cell Cycle. 2011 Feb 15;10(4):708-20. Epub 2011 Feb 15.
溶解度数据
In Vitro: DMSO : ≥ 100 mg/mL (208.59 mM)H2O : 5 mg/mL (10.43 mM; Need ultrasonic)
搜索质检报告(COA)
[1]. Keppner S, et al. Identification and validation of a potent type II inhibitor of inactive polo-like kinase 1. ChemMedChem. 2009 Nov;4(11):1806-9.
[2]. Keppner S, et al. Fate of primary cells at the G?/S boundary after polo-like kinase 1 inhibition by SBE13. Cell Cycle. 2011 Feb 15;10(4):708-20. Epub 2011 Feb 15.

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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