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CA-5f

CA-5f

产品编号 T5181   CAS 1370032-19-1

CA-5f 是晚期巨自噬/自噬抑制剂,通过抑制自噬体-溶酶体融合起作用。它能够增加监控自噬的标记物 LC3B-II 和 SQSTM1 蛋白水平,促进 ROS 的产生,具有抗肿瘤活性。

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CA-5f Chemical Structure
CA-5f, CAS 1370032-19-1
规格 价格/CNY 货期 数量
1 mg ¥ 346 现货
5 mg ¥ 913 现货
10 mg ¥ 1,490 现货
25 mg ¥ 3,160 现货
50 mg ¥ 4,660 现货
100 mg ¥ 6,650 现货
1 mL * 10 mM (in DMSO) ¥ 969 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
Doxorubicin hydrochloride限时半价
产品目录号及名称: CA-5f (T5181)
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纯度: 99.83%
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生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 CA-5f is a potent late-stage macroautophagy/autophagy inhibitor via inhibiting autophagosome-lysosome fusion.
体外活性 Treatment of human umbilical vein endothelial cells (HUVECs) with CA-5f for 1 h suppressed the levels of cytoskeletal proteins and membrane traffic proteins. CA-5f exhibited strong cytotoxicity against A549 NSCLC cells, but low cytotoxicity to normal HUVECs, by increasing mitochondrial-derived reactive oxygen species (ROS) production.
体内活性 CA-5f effectively suppressed the growth of A549 lung cancer xenograft as a single agent with an excellent tolerance in vivo. Results from western blot, immunofluorescence, and TdT-mediated dUTP nick end labeling (TUNEL) assays showed that CA-5f inhibited autophagic flux, induced apoptosis, and did not affect the level of CTSB (cathepsin B) and CTSD (cathepsin D) in vivo, which were consistent with the in vitro data.
细胞实验 A549 cells or HUVECs were seeded into 100-mm culture dishes. When cells reached 80% confluency, they were exposed to DMSO or CA-5f for 6 h or 24 h. Then the cells were fixed, dehydrated, embedded, sectioned, and stained as previously described. Finally, the ultrathin sections of these samples were observed under a JEM-1230 transmission electron microscopy.
动物实验 Four-week-old BALB/c nude mice were purchased from Beijing Vital River Laboratory Animal Technology Co., Lt and kept in specific pathogen-free conditions at the Experimental Animal Center in the Institute of Medicine in Zhengzhou University. Nude mice underwent subcutaneous injection of A549 cells (1 × 10^6) at the right scapula. 8 days after A549 cell implantation, mice exhibited palpable tumors, then they were randomly divided into 2 groups (each group n = 5). CA-5f was injected via caudal vein every 2 days for up to 30 days. DMSO was used as a control. From the initial injection, the tumor size was measured every 2 days. Tumor volumes were calculated as tumor length × (square of width)/2. At the end of the experiment, all mice were sacrificed and the tumors were resected immediately and photographed. The weight of each tumor was measured.
分子量 388.46
分子式 C24H24N2O3
CAS No. 1370032-19-1

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 55 mg/mL (141.58 mM)

H2O: Insoluble

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.5743 mL 12.8713 mL 25.7427 mL 64.3567 mL
5 mM 0.5149 mL 2.5743 mL 5.1485 mL 12.8713 mL
10 mM 0.2574 mL 1.2871 mL 2.5743 mL 6.4357 mL
20 mM 0.1287 mL 0.6436 mL 1.2871 mL 3.2178 mL
50 mM 0.0515 mL 0.2574 mL 0.5149 mL 1.2871 mL
100 mM 0.0257 mL 0.1287 mL 0.2574 mL 0.6436 mL

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TargetMol Library Books参考文献

1. Zhang L, et al. Identification of compound CA-5f as a novel late-stage autophagy inhibitor with potent anti-tumor effect against non-small cell lung cancer. Autophagy. 2019 Mar;15(3):391-406.
MPI-0479605 Decursin Diclofenac diethylamine Liensinine ZINC69391 Sinomenine Devimistat KEA1-97

相关化合物库

该产品包含在如下化合物库中:
抑制剂库 抗癌活性化合物库 抗衰老化合物库 细胞凋亡化合物库 已知活性化合物库 自噬库 抗癌化合物库 经典已知活性库

TargetMol Calculator剂量换算

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TargetMol Calculator 体内实验配液计算器

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。

第一步:请输入动物实验的基本信息
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第二步:请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
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技术支持

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。

Keywords

CA-5f 1370032-19-1 Apoptosis Autophagy inhibit Inhibitor CA 5f CA5f inhibitor

 

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