
OTS-964
CAS No. 1338545-07-5
OTS-964 ( OTS964 )
产品货号. M11360 CAS No. 1338545-07-5
OTS-964 是 OTS514 的二甲基化衍生物,是有效的选择性 TOPK 抑制剂,IC50 为 28 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥437 | 有现货 |
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5MG | ¥689 | 有现货 |
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10MG | ¥1021 | 有现货 |
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25MG | ¥1677 | 有现货 |
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50MG | ¥2989 | 有现货 |
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100MG | ¥4447 | 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 |
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生物学信息
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产品名称OTS-964
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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OTS-964 是 OTS514 的二甲基化衍生物,是有效的选择性 TOPK 抑制剂,IC50 为 28 nM。
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产品描述OTS-964 is a dimethylated derivative of OTS514 and potent, selective TOPK inhibitor with IC50 of 28 nM, exhibits excellent in vivo efficacy with liposomal formulation; inhibits the growth of TOPK-positive cells with low IC50 values (A549 IC50=31 nM), decreases autophosphorylation of TOPK (Thr9), as well as phosphorylation of histone H3 (Ser10), in both T47D and LU-99 cells; the liposomal OTS964 causes complete regression of tumors without any detectable toxicity in the xenograft models.
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体外实验OTS964 hydrochloride (10 nM; 48 hours) suppresses cancer cell proliferation. OTS964 hydrochloride (10 nM; 48 hours) increases cancer cell death. OTS964 (0.1-2 μM; 24 and 48 hours) increases the expression of LC3-II and decreases the expression of P62, both in a dose-dependent manner. Cell Proliferation Assay Cell Line:LU-99 cells.Concentration:10 nM Incubation Time:48 hours Result:Suppressed cancer cell proliferation.Apoptosis Analysis Cell Line:LU-99 cells Concentration:10 nM Incubation Time:48 hoursResult:Increased cancer cell death.Western Blot AnalysisCell Line:Hs683 cells, H4 cells Concentration:0.1, 1, 2 μM Incubation Time:24 and 48 hours Result:Increased the expression of LC3-II and decreased the expression of P62, both in a dose-dependent manner.
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体内实验OTS964 hydrochloride (intravenously; 40 mg/kg on days 1, 4, 8, 11, 15, and 18) makes tumors shrinking even after the treatment and finally revealing complete regression. OTS964 hydrochloride (oral administration; 50 or 100 mg/kg/day for 2 weeks) ultimately achieves complete tumor regression. Animal Model:Nude mice bearing LU-99 lung cancer cells Dosage:40 mg/kg Administration:Intravenously; on days 1, 4, 8, 11, 15, and 18 Result:The tumors continued shrinking even after the treatment and finally revealed complete regression. Animal Model:Nude mice bearing LU-99 lung cancer cellsDosage:50 or 100 mg/kg Administration:Oral administration; once every day for 2 weeks Result:Achieved complete tumor regression.
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同义词OTS964
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通路MAPK/ERK Signaling
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靶点MEK
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受体TOPK
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研究领域Cancer
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适应症——
化学信息
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CAS Number1338545-07-5
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分子量428.9748
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分子式C23H25ClN2O2S
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纯度>98% (HPLC)
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溶解度10 mM in DMSO
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SMILESCC1=CC(=C(C2=C1NC(=O)C3=C2C=CS3)C4=CC=C(C=C4)C(C)CN(C)C)O.Cl
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化学全称Thieno[2,3-c]quinolin-4(5H)-one, 9-[4-[(1R)-2-(dimethylamino)-1-methylethyl]phenyl]-8-hydroxy-6-methyl-, hydrochloride (1:1)
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. Matsuo Y, et al. Sci Transl Med. 2014 Oct 22;6(259):259ra145.
2. Ikeda Y, et al. Clin Cancer Res. 2016 Dec 15;22(24):6110-6117.
3. Pirovano G, et al. Br J Cancer. 2017 Aug 8;117(4):503-512.
4. Sugimori M, et al. Oncotarget. 2017 Dec 9;9(3):3043-3059.
产品手册




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