OSU-2S
CAS No. 1351056-65-9
OSU-2S ( OSU 2S )
产品货号. M11419 CAS No. 1351056-65-9
一种非免疫抑制性 FTY720 类似物,PKCδ 激活剂,具有更高的抗增殖效力。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 100MG | 获取报价 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称OSU-2S
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述一种非免疫抑制性 FTY720 类似物,PKCδ 激活剂,具有更高的抗增殖效力。
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产品描述A non-immunosuppressive FTY720 analogue, PKCδ activator with higher antiproliferative potency with IC50 of 2.4, 2.4, and 3.5 uM in Huh7, Hep3B, and PLC5 cells, respectively; exhibited higher in vitro antiproliferative efficacy relative to FTY720 against HCC cells without cytotoxicity in normal hepatocytes, although devoid of S1P1 receptor activity; induces caspase-dependent apoptosis through ROS-dependent PKCδ activation in HCC tumor cells.
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体外实验Cell Proliferation AssayCell Line:Hep3B, Huh7, PLC-5, HepG2 cells Concentration:0-10 μM Incubation Time:48 h Result:Showed anti-proliferative effects with IC50s of 2.53, 2.41, 3.96, 1.84 μM for Hep3B, Huh7, PLC-5, HepG2 cells, respectively.Western Blot Analysis Cell Line:Hep3B cells Concentration:1.25, 2.5 μM combinated with sorafenib (2.5, 5 μM)Incubation Time:48 h Result:Decreased the expression of ERK1/2 phosphorylation, increased the expression of PKCδ (38 kDa) when sorafenib/OSU-2S combination.
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体内实验Animal Model:CD2F1 mice (Hep3B tumor xenograft models)Dosage:5, 10 mg/kg Administration:I.p.; once daily for 42 days Result:Exhibited a higher tumor-suppressive potency, achieving 80% reduction in bioluminescence at the end of treatment.
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同义词OSU 2S
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通路Angiogenesis
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靶点PKC
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受体PKC
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研究领域——
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适应症——
化学信息
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CAS Number1351056-65-9
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分子量335.532
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分子式C21H37NO2
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纯度>98% (HPLC)
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溶解度——
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SMILESCCC[C@@](CCC1=CC=C(OCCCCCC(C)C)C=C1)(N)CO.[H]Cl
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化学全称(S)-2-amino-2-(4-[(6-methylheptyl)-oxy]phenethyl)pentan-1-ol
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Omar HA, et al. Hepatology. 2011 Jun;53(6):1943-58.
2. Mani R, et al. Leukemia. 2015 Feb;29(2):346-55.
3. Mani R, et al. Exp Hematol. 2015 Sep;43(9):770-4.e2.
4. Omar HA, et al. Front Pharmacol. 2016 Nov 30;7:463. eCollection 2016.
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