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Abafungin

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纯度: 98.11%

货号 T21448Cas号 129639-79-8

别名 阿巴芬净, UNII-11DI31LWXF, Bay w 6341

Abafungin (Bay w 6341) 是抗真菌药物,可抑制由 sterol-C-24-methyltransferase 催化的固醇侧链 C-24位点的甲基转移。

Abafungin
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Abafungin

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Rating icon 很棒

纯度: 98.11%

货号 T21448 别名 阿巴芬净, UNII-11DI31LWXF, Bay w 6341Cas号 129639-79-8

Abafungin (Bay w 6341) 是抗真菌药物,可抑制由 sterol-C-24-methyltransferase 催化的固醇侧链 C-24位点的甲基转移。

规格价格库存数量
1 mg
¥ 188
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5 mg
¥ 397
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10 mg
¥ 653
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25 mg
¥ 1,120
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50 mg
¥ 1,660
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100 mg
¥ 2,380
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200 mg
¥ 3,380
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产品介绍


Abafungin AI Summary
Abafungin exhibits significant antiviral and antifungal activities. It shows potent inhibition of SARS-CoV-2 induced cytotoxicity in Caco-2 cells at 10 μM concentration with an inhibition rate of 92.89% after 48 hours, and a lesser inhibition rate of -0.22% in VERO-6 cells under similar conditions. The compound also moderately inhibits the SARS-CoV-2 3CL-Pro protease with 9.394% inhibition at 20 μM, observed through a FRET assay. For antifungal properties, Abafungin demonstrates activity against Candida albicans with a MIC of 312.5 nM and against Aspergillus fumigatus ATCC 204305 with a MIC value of 2.0 μg/mL. It also shows efficacy against pan-azole resistant Aspergillus fumigatus SR47013 with similar MIC values. However, it does not exhibit antifungal activity against Cryptococcus neoformans, nor does it show antibacterial activity as evidenced by MIC values greater than 20000.0 nM against several bacterial strains. In addition, Abafungin exhibits inhibition of human HDAC6 activity, with 38.23% inhibition using a commercial peptide substrate. It has low hemolytic activity on human red blood cells (HC10 > 20.0 μM) and no cytotoxicity against HEK293 cells (CC50 > 20000.0 nM). The compound shows metabolic stability in human liver microsomes (64.0%) but much lower stability in rat liver microsomes at 0.5 μM. Pharmacokinetic data indicate an unbound fraction of less than 0.001 in Sprague-Dawley rats, a clearance rate of 51.4 mL.min-1.kg-1, and a volume of distribution at steady state of 4.92 L.kg-1..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Abafungin (Bay w 6341) is an antifungal agent with a broad-spectrum.
别名阿巴芬净, UNII-11DI31LWXF, Bay w 6341
化学信息
分子量378.49
分子式C21H22N4OS
CAS No.129639-79-8
SmilesCc1ccc(Oc2ccccc2-c2csc(NC3=NCCCN3)n2)c(C)c1
密度1.28g/cm3
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: 3.79 mg/mL (10.01 mM), Sonication is recommended.
H2O: Insoluble
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM2.6421 mL13.2104 mL26.4208 mL132.1039 mL
5 mM0.5284 mL2.6421 mL5.2842 mL26.4208 mL
10 mM0.2642 mL1.3210 mL2.6421 mL13.2104 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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