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S2157

    
≥98%

源叶(MedMol)
V47326 一键复制产品信息
2262488-39-9
C23H28ClF2N3O2
451.94
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V47326-1mg
≥98%

¥2190.00

货期:3-5天 - - - -
V47326-5mg
≥98%

¥5390.00

货期:3-5天 - - - -
V47326-10mg
≥98%

¥8630.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: S2157, a N-alkylated tranylcypromine (TCP) derivative, is a potent lysine-specific demethylase 1 (LSD1) inhibitor. S2157 increases H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. S2157 induces apoptosis in TCP-resistant T-cell acute lymphoblastic leukemia (T-ALL) cells by repressing transcription of the NOTCH3 and TAL1 genes. S2157 efficiently pass through the blood-brain barrier and can almost completely eradicate CNS leukemia in mice transplanted with T-ALL cells.
体外研究: S2157 (50 mg/kg; IP; 3 times a week; for 28 days) causes the size of subcutaneous tumors reduced to less than 20% of that in the untreated control[1].
S2157 (50 mg/kg; IP) has a T1/2 of 0.88 hours, a Cmax of 4.33 μM and an AUC of 5.75 μM•h[1].
S2157 (30 mg/kg or 50 mg/kg; twice a week for 3 weeks) almost completely suppressed the growth of MOLT4 cells in most but not all NOD/SCID mice with MOLT4 cells. S2157 eradicates CNS leukemia in murine xenotransplanted models[1].
体内研究: S2157 is particularly effective for T-ALL cell lines with the IC50 values between 1.1 µM for human T-ALL cell lines CEM and 6.8 µM for MOLT4.
S2157 (4-20 µM; 72 hours) modestly inhibits mitogen-activated normal T-lymphocytes.
S2157 (4-8 µM; 24 hours) induces apoptosis and down-regulates the expression of NOTCH3 and TAL1 proteins in T-cell acute lymphoblastic leukemia (T-ALL) cells.
保存条件: 2-8°C, 干燥
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.213 ml 11.063 ml 22.127 ml
5 mM 0.443 ml 2.213 ml 4.425 ml
10 mM 0.221 ml 1.106 ml 2.213 ml
50 mM 0.044 ml 0.221 ml 0.443 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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