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SARS-CoV-2-IN-14

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纯度: 99.78%

货号 T60538Cas号 22203-98-1

别名 3',5-Dichlorosalicylanilide

SARS-CoV-2-IN-14 是一种有效的、可口服的 SARS-CoV-2 抑制剂(IC50 :0.39 μM),是一种氯硝柳胺类似物。SARS-CoV-2-IN-14在人血浆和肝 S9 酶测定中比氯硝柳胺稳定性更强。SARS-CoV-2-IN-14以口服的方式给药可以提高其生物利用度和半衰期。

SARS-CoV-2-IN-14
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SARS-CoV-2-IN-14

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Rating icon 很棒

纯度: 99.78%

货号 T60538 别名 3',5-DichlorosalicylanilideCas号 22203-98-1

SARS-CoV-2-IN-14 是一种有效的、可口服的 SARS-CoV-2 抑制剂(IC50 :0.39 μM),是一种氯硝柳胺类似物。SARS-CoV-2-IN-14在人血浆和肝 S9 酶测定中比氯硝柳胺稳定性更强。SARS-CoV-2-IN-14以口服的方式给药可以提高其生物利用度和半衰期。

规格价格库存数量
1 mg
¥ 108
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5 mg
¥ 221
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10 mg
¥ 359
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25 mg
¥ 648
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50 mg
¥ 978
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100 mg
¥ 1,450
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200 mg
¥ 2,150
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1 mL x 10 mM (in DMSO)
¥ 226
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产品介绍


SARS-CoV-2-IN-14 AI Summary
SARS-CoV-2-IN-14 exhibits a range of bioactivities, including significant antimycobacterial effects, antiviral properties, and inhibition of specific biochemical pathways and receptors. It shows activity against various Mycobacterium strains, such as Mycobacterium tuberculosis, Mycobacterium avium, and Mycobacterium kansasii, with MIC values ranging from 4000.0 nM to 16000.0 nM. In HEK293 cells, it inhibits the Wnt/beta-catenin pathway with an IC50 of 1650.0 nM. Moreover, it reduces the activity of Cryptosporidium hominis TS-DHFR enzyme by 54% at 500 uM. In terms of receptor antagonism, SARS-CoV-2-IN-14 inhibits ATP-induced calcium influx at the human P2X1 receptor (P2X2/P2X1 chimera) with an IC50 of 75.6 nM and 64.0% inhibition at 10 uM pre-incubation, and shows moderate inhibition at the P2X4 receptor with an IC50 of 135.0 nM. It does not significantly affect P2X2, P2X3, or P2X7 receptors, with IC50 values above 10000.0 nM. The compound demonstrates antiviral activity against SARS-CoV-2 in African Green monkey Vero cells with an IC50 of 390.0 nM and cytotoxicity in Vero E6 cells with a CC50 of 2460.0 nM, giving a selectivity ratio of 6.3. It has a permeability of 8.6 x 10^-6 cm/s, low water solubility (<1.0 ug/mL), 71.0% stability in human plasma, and 33.0% metabolic stability in human liver microsomes. Additionally, it exhibits cytotoxicity against Vero E6 cells preincubated for 2 hours, followed by SARS-CoV-2 addition, with a CC50 of 100000.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
SARS-CoV-2-IN-14 is a potent and oral inhibitor of SARS-CoV-2 (IC50:0.39 μM), which is an analogue of niclosamide. SARS-CoV-2-IN-14 was more stable than niclosamide in the determination of human plasma and liver S9 enzyme. Oral administration of SARS-CoV-2-IN-14 can improve its bioavailability and half-life.
靶点活性
SARS-CoV-2:0.39 μM
别名3',5-Dichlorosalicylanilide
化学信息
分子量282.12
分子式C13H9Cl2NO2
CAS No.22203-98-1
SmilesC(NC1=CC(Cl)=CC=C1)(=O)C2=C(O)C=CC(Cl)=C2
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 9 mg/mL (31.9 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.5446 mL17.7230 mL35.4459 mL177.2295 mL
5 mM0.7089 mL3.5446 mL7.0892 mL35.4459 mL
10 mM0.3545 mL1.7723 mL3.5446 mL17.7230 mL
20 mM0.1772 mL0.8861 mL1.7723 mL8.8615 mL

计算器

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  • 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:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 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:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 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: DMSOPEG300 / PEG400Tween 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

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