
OTS-167
CAS No. 1431697-89-0
OTS-167 ( OTSSP-167 )
产品货号. M11833 CAS No. 1431697-89-0
OTS-167 (OTSSP-167) 是一种高效、选择性的 MELK 抑制剂,IC50 为 0.41 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥381 | 有现货 |
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5MG | ¥648 | 有现货 |
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10MG | ¥988 | 有现货 |
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25MG | ¥1596 | 有现货 |
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50MG | ¥2406 | 有现货 |
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100MG | ¥3686 | 有现货 |
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500MG | ¥7995 | 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-167
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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-167 (OTSSP-167) 是一种高效、选择性的 MELK 抑制剂,IC50 为 0.41 nM。
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产品描述OTS-167 (OTSSP-167)?is a highly potent and selective MELK inhibitor with IC50 of 0.41 nM; shows anti-proliferative activity for A549, T47D, DU4475, and 22Rv1 cancer cells with IC50 of 6.7, 4.3, 2.3, and 6.0 nM, respectively; inhibits the phosphorylation of PSMA1 and DBNL, two novel MELK substrates and are important for stem-cell characteristics and invasiveness; shows robust tumor growth inhibition (TGI) in xenograft models; orally active.Blood Cancer Phase 2 Clinical(In Vitro):OTSSP167 inhibits the growth of A549 (lung), T47D (breast), DU4475 (breast), 22Rv1 (prostate) and HT1197 (bladder) cancer cells with IC50 values of 6.7, 4.3, 2.3, 6.0 and 97 nM, respectively. OTSSP167 can abrogate the mitotic checkpoint, disrupt MCC and MCC-APC/C interaction in MCF7 cells. OTSSP167 causes GFP-MELK localization to cell cortex in prometaphase cells. OTSSP167 is a MELK selective inhibitor, exhibits a strong in vitro activity, conferring an IC50 of 0.41 nM.(In Vivo):OTSSP167 (20 mg/kg, i.v.) results in tumor growth inhibition (TGI) of 73% in xenograft mouse model; OTSSP167 (1, 5, and 10 mg/kg, p.o.) reveals TGI of 51, 91, and 108%, respectively. OTSSP167 (20 mg/kg, p.o.) shows no tumor growth suppressive effect on PC-14 xenografts.
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体外实验OTSSP167 inhibits the growth of A549 (lung), T47D (breast), DU4475 (breast), 22Rv1 (prostate) and HT1197 (bladder) cancer cells with IC50 values of 6.7, 4.3, 2.3, 6.0 and 97 nM, respectively. OTSSP167 can abrogate the mitotic checkpoint, disrupt MCC and MCC-APC/C interaction in MCF7 cells. OTSSP167 causes GFP-MELK localization to cell cortex in prometaphase cells. OTSSP167 is a MELK selective inhibitor, exhibits a strong in vitro activity, conferring an IC50 of 0.41 nM.
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体内实验OTSSP167 (20 mg/kg, i.v.) results in tumor growth inhibition (TGI) of 73% in xenograft mouse model; OTSSP167 (1, 5, and 10 mg/kg, p.o.) reveals TGI of 51, 91, and 108%, respectively. OTSSP167 (20 mg/kg, p.o.) shows no tumor growth suppressive effect on PC-14 xenografts.
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同义词OTSSP-167
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通路PI3K/Akt/mTOR signaling
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靶点MELK
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受体MELK
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研究领域Cancer
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适应症Blood cancer
化学信息
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CAS Number1431697-89-0
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分子量487.4214
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分子式C25H28Cl2N4O2
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纯度>98% (HPLC)
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溶解度10 mM in DMSO
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SMILESCN(C)CC1CCC(CC1)NC1=C2NC(C=CC2=NC=C1C(C)=O)=C1C=C(Cl)C(=O)C(Cl)=C1
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化学全称1-(6-(3,5-dichloro-4-hydroxyphenyl)-4-(((1r,4r)-4-((dimethylamino)methyl)cyclohexyl)amino)-1,5-naphthyridin-3-yl)ethanone
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. Chung S, et al. Oncotarget. 2012 Dec;3(12):1629-40.
2. Alachkar H, et al. Oncotarget. 2014 Dec 15;5(23):12371-82.
3. Stefka AT, et al. Blood Cancer J. 2016 Aug 19;6(8):e460.