3α-Aminocholestane (Synonyms: 3α-氨基胆甾烷)
目录号: PL09593 纯度: ≥98.0%
CAS No. :2206-20-4
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中文名称
3α-Aminocholestane
中文别名
3-Α-氨基胆甾烷(3AC);二-Μ-氯代双[2-[(二甲基氨基)甲基]-4,6-二甲氧基苯基-C,N]二钯(II);5alpha-胆甾烷-3alpha-胺;3α-氨基胆甾烷
英文名称
3α-Aminocholestane
英文别名
Cholestan-3-amine, (3α,5α)-;3α-Aminocholestane;3alpha-Aminocholestane;3AC;Cholestan-3alpha-amine;3 alpha-aminocholestane;GTPL9564
Cas No.
2206-20-4
分子式
C27H49N
分子量
387.68
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
3α-Aminocholestane 是含有选择性 SH2 结构域的肌醇-5'-磷酸酶 1 (SHIP1) 的抑制剂,其 IC50 值约为 2.5 μM。
生物活性
3α-Aminocholestane is a selective SH2 domain-containing inositol-5′-phosphatase 1 (SHIP1) inhibitor with an IC 50 of ~2.5 μM.
性状
Solid
IC50 & Target[1][2]
IC50: 2.5 μM (SHIP1)
体外研究(In Vitro)
OPM2 cell viability is effectively reduced by 3α-Aminocholestane (3AC) treatment. RPMI8226 and U266 cells show significantly less sensitivity to 3α-Aminocholestane treatment when compare with OPM2 cells, although viability is decreased significantly at concentrations of ≥12.5 μM. Treatment with 3α-Aminocholestane for 36 h severely reduces the percentage of cells in the S phase, which is accompanied by an increase of cells in the G2/M phase. In contrast, in the less proliferative RPMI8226 and U266 cells, cell cycle progression is blocked in the G0/G1 phase upon 3α-Aminocholestane treatment, in conjunction with a reduced percentage of cells undergoing the S phase. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
It is found that 3α-Aminocholestane (3AC) results in reduced multiple myeloma (MM) growth in vivo, as determined by quantitation of free human Igλ light chain in the plasma after OPM2 challenge. In addition, reduced numbers of circulating OPM2 cells, as determined by human HLA-ABC staining, is observed in peripheral blood from 3α-Aminocholestane-treated mice compare with vehicle controls. Most importantly, 3α-Aminocholestane treatment results in significantly enhanced survival of mice after tumor challenge. In 3α-Aminocholestane-treated mice that resist treatment, it is found that MM tumors exhibit an upregulation of SHIP2, reminiscent of in vitro treatment of OPM2 cells and suggesting that SHIP1 inhibition may select for tumor cells with increased SHIP2 expression. has not independently confirmed the accu
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Chen Z, et al. Signalling thresholds and negative B-cell selection in acute lymphoblastic leukaemia. Nature. 2015 May 21;521(7552):357-61.
[2]. Gwenny M Fuhler, et al. Therapeutic Potential of SH2 Domain-Containing Inositol-5′-Phosphatase 1 (SHIP1) and SHIP2 Inhibition in Cancer. Mol Med. 2012 Feb 10;18:65-75.
溶解度数据
In Vitro: Ethanol : 50 mg/mL (128.97 mM; Need ultrasonic)DMSO : < 1 mg/mL (insoluble or slightly soluble)配制储备液
搜索质检报告(COA)

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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