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AS8351

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纯度: 99.72%

货号 T4100Cas号 796-42-9

别名 NSC51355, AS-8351, AS 8351

AS8351 (NSC51355) 是一种组蛋白去甲基化酶抑制剂,可以诱导人胎儿肺成纤维细胞重编程为功能性心肌细胞。

AS8351
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AS8351

一键复制产品信息
Rating icon 很棒

纯度: 99.72%

货号 T4100 别名 NSC51355, AS-8351, AS 8351Cas号 796-42-9

AS8351 (NSC51355) 是一种组蛋白去甲基化酶抑制剂,可以诱导人胎儿肺成纤维细胞重编程为功能性心肌细胞。

规格价格库存数量
2 mg
¥ 258
现货
5 mg
¥ 396
现货
10 mg
¥ 567
现货
25 mg
¥ 1,120
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50 mg
¥ 1,980
现货
100 mg
¥ 3,730
现货
200 mg
¥ 5,330
现货
500 mg
¥ 7,880
现货
1 mL x 10 mM (in DMSO)
¥ 455
现货
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纯度: 99.72%
颜色: 黄色
性状: Solid
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产品介绍


AS8351 AI Summary
AS8351 exhibits a broad spectrum of bioactivities. Notably, it shows significant antiproliferative activity against human SK-N-MC cells, with reported IC50 values ranging from 300.0 nM to 2530.0 nM across different studies. In an MTT assay conducted over 72 hours, the IC50 values commonly observed are approximately 710.0 nM and 1300.0 nM. Additionally, AS8351 inhibits iron uptake from transferrin in SK-N-MC cells, demonstrating an inhibition rate of up to 9% at 50 µM, and induces intracellular iron mobilization with an activity level of up to 44.0%. Despite its diverse activities, the compound exhibits weak inhibitory effects against HIV1 reverse transcriptase ribonuclease H, with IC50 values greater than 100,000.0 nM. AS8351 also demonstrates antimicrobial activity against various bacteria and fungi, cytotoxicity against several human cell lines, and antiviral activity against a range of viruses. Additionally, it shows bioactivity as an inhibitor of the interaction between human Flag-tagged LEDGF and His6-tagged HIV1 integrase with an IC50 of 6000.0 nM, but does not affect HIV1 integrase's strand transfer or 3'-processing activities significantly. Lastly, it exhibits antimalarial activity against Plasmodium falciparum 7G8, with an IC50 of 42.2 nM..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
AS8351 (NSC51355) is a histone demethylase inhibitor. It has been used in combination with CHIR99021, A 83-01, BIX01294, SC-1, Y-27632, OAC2, SU 16f, and JNJ-10198409 to induce reprogramming of human fetal lung fibroblasts into functional cardiomyocytes.
别名NSC51355, AS-8351, AS 8351
化学信息
分子量291.3
分子式C17H13N3O2
CAS No.796-42-9
SmilesNN(\C=C1/C(=O)C=Cc2ccccc12)C(=O)c1ccncc1
密度1.364g/cm3
储存&溶解度
存储In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 37.59 mg/mL (129.04 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.87 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.4329 mL17.1644 mL34.3289 mL171.6444 mL
5 mM0.6866 mL3.4329 mL6.8658 mL34.3289 mL
10 mM0.3433 mL1.7164 mL3.4329 mL17.1644 mL
20 mM0.1716 mL0.8582 mL1.7164 mL8.5822 mL
50 mM0.0687 mL0.3433 mL0.6866 mL3.4329 mL
100 mM0.0343 mL0.1716 mL0.3433 mL1.7164 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

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 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / 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 100 μL DMSO ( 母液浓度为 20 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:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 混匀澄清
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
方案所需的各类助溶剂如: DMSOPEG300PEG400Tween 80SBE-β-CD玉米油等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 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。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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