store at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
LTX315 acetate (Oncopore acetate) 是一种具有强抗癌活性的溶瘤肽,MRC-5 的 IC50 值分别为 34.3 µM、A20 和 AT84 分别为 8.3 µM 和 11 µM。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 655 | 现货 | ||
2 mg | ¥ 957 | 现货 | ||
5 mg | ¥ 1,310 | 现货 | ||
10 mg | ¥ 2,290 | 现货 | ||
25 mg | ¥ 3,890 | 现货 | ||
50 mg | ¥ 5,560 | 现货 | ||
100 mg | ¥ 7,790 | 现货 |
产品描述 | LTX315 acetate (Oncopore acetate) is an oncolytic peptide with potent anticancer activity, with IC50 values of 34.3 µM for MRC-5, 8.3 µM for A20, and 11 µM for AT84, respectively. |
靶点活性 | A20:8.3 µM, AT84:11 µM, MRC5:34.3 µM |
体外活性 | LTX315 acetate induces rapid killing of cancer cells. LTX315 acetate is equally potent against drug-resistant cancer cells, non-toxic to erythrocytes, shows high plasma protein binding, and can be rapidly degraded to non-toxic metabolites. The oncolytic activity of LTX315 acetate results from direct lysis of the plasma membrane and permeabilization of the mitochondrial membrane, resulting in cell death due to necrosis and release of tumor antigens. Treatment of cancer cells with LTX315 acetate results in the release of several danger signals (DAMPs) that are associated with immunogenic cell death and stimulation of adaptive immune responses[1]. |
体内活性 | Intratumoral administration of LTX315 acetate resulted in tumor necrosis and immune cell infiltration into the tumor parenchyma, followed by complete tumor regression in most animals. LTX-315 induces the release of risk-associated molecular patterning molecules, such as high mobility group box-1 proteins, in vitro, followed by upregulation of pro-inflammatory cytokines such as interleukin (IL) 1β, IL6, and IL18 in vivo. Animals cured by LTX315 acetate treatment were protected from rechallenging with live intradermal and intravenous B16 tumor cells [2]. |
别名 | LTX315醋酸盐, KKWWKKW-Dip-K-NH2 acetate, Oncopore acetate, Ruxotemitide acetate, LTX315 acetate(1345407-05-7, Free base) |
分子量 | 1499.84 |
分子式 | C80H110N18O11 |
store at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
LTX315 acetate Others Ruxotemitide Acetate LTX315醋酸盐 LTX-315 acetate KKWWKKW-Dip-K-NH2 acetate Oncopore acetate LTX-315 Acetate Ruxotemitide acetate LTX315 acetate(1345407-05-7, Free base) LTX 315 Acetate KKWWKKW-Dip-K-NH2 Acetate Oncopore Acetate LTX315 Acetate Inhibitor inhibitor inhibit