CAS NO: | 1423715-09-6 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | SP2509 is a potent and selective antagonist oflysine specific demethylase 1 (LSD1)with anIC50of 13 nM[1]. | ||||||||||||||||
IC50& Target | IC50: 13 nM (LSD1)[1] | ||||||||||||||||
体外研究 (In Vitro) | SP2509 (250, 500, 1000 nM) inhibits LSD1 activity, depletes colony growth and induces apoptosis and cell death of cultured human acute myeloid leukemia cells, and increases H3K4Me3 on the promoters of p57 Kip, KLF4, and p21 and induces mRNA expression of p57Kip, KLF4 and p21 in AML cells. SP2509 (250, 1000 nM) induces features of morphologic differentiation of cultured and primary AML cells. Besides, SP2509 in combination with PS exerts synergistic lethal activity against cultured and primary AML cells[1]. SP2509 does not destabilize the CoREST-LSD1 interaction, and has no major destabilizing effect on the CRC. SP2509 (1 or 10 μM) induces cell death, but there are no morphological changes at a low concertation of 0.1 μM. SP2509 likewise interferes with the viability of medulloblastoma cells[2]. | ||||||||||||||||
体内研究 (In Vivo) | Treatment with SP2509 (25 mg/kg) and/or PS (5 mg/kg) significantly enhances PS-mediated loss of viability of CD34+primary AML cells and improves the survival of mice bearing AML xenografts and primagrafts[2]. | ||||||||||||||||
分子量 | 437.90 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C19H20ClN3O5S | ||||||||||||||||
CAS 号 | 1423715-09-6 | ||||||||||||||||
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) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : ≥ 33 mg/mL(75.36 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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