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OTS514

    级别和纯度:
  • 10mM in DMSO
  • CAS编号: 1338540-63-8
  • 分子式: C21H20N2O2S
  • 分子量: 364.46
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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
O656432-1ml
1ml 期货 Stock Image

基本描述

规格或纯度 10mM in DMSO
英文名称 OTS514
生化机理 OTS514 是一种强效 TOPK 抑制剂,其 IC 50 为 2.6 nM。OTS514 能强烈抑制 TOPK 阳性癌细胞的生长。OTS514 可诱导细胞周期停滞和细胞凋亡。
储存温度 -80℃储存
运输条件 超低温冰袋运输
产品介绍


OTS514 is a highly potent TOPK inhibitor with an IC 50 of 2.6 nM. OTS514 strongly suppresses the growth of TOPK-positive cancer cells OTS514 induces cell cycle arrest and apoptosis .

In Vitro

OTS514 (1.5625-100 nM) induces cell cycle arrest and apoptosis at nanomolar concentrations in a series of human myeloma cell lines (HMCL) and prevents outgrowth of a putative CD138 + stem cell population from multiple myeloma (MM) patient-derived peripheral blood mononuclear cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: Human myeloma cell lines (MM1.S, MM1.R, RPMI 8226, 8226Dox40, KMS34, KMS34CFZ, KMS11, JJN3, LP-1, NCI H929, U266B1) Concentration: 1.5625, 3.125, 6.25, 12.5, 25, 50, and 100 nM Incubation Time: 72 hours Result: IC 50 values ranged from 11.6 to 29.4 nM in parental cell lines, indicating a potent inhibitory effect. Only the RPMI 8226-Dox40 cell line, which overexpresses the multi-drug resistance transporter gene ABCB1, is resistant.

In Vivo

OTS514 (1-5 mg/kg; once a day for 2 weeks; intravenous administration) induces tumor regression in a xenograft model of A549 cells (TOPK-positive lung cancer cells) . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Female BALB/cSLC-nu/nu mice bearing a xenograft model of A549 cells Dosage: 1, 2.5, and 5 mg/kg Administration: Intravenously treated; once every day for 2 weeks Result: Resulted in tumor growth inhibition (TGI) of 5.7, 43.3, and 65.3% on day 15, respectively, without any body weight loss.

IC50& Target:IC50: 2.6 nM (TOPK)

关联靶点(人)

PBK Tchem 淋巴因子激活杀伤T细胞来源的蛋白激酶(Lymphokine-activated killer T-cell-originated protein kinase) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
NEK1 Tchem 丝氨酸/苏氨酸蛋白激酶 Nek1(Serine/threonine-protein kinase Nek1) (2 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

分子类型 小分子
Isomeric SMILES CC1=CC(=C(C2=C1NC(=O)C3=C2C=CS3)C4=CC=C(C=C4)[C@@H](C)CN)O
PubChem CID 67448836
分子量 364.46

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