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3-hydroxy-3-phenylpentanamide

货号 T50100Cas号 131802-69-2 一键复制产品信息纯度: 98.42%
Rating icon 很棒

3-hydroxy-3-phenylpentanamide 是一种手性化合物,属于β-羟基酰胺类。在神经病学中,它已被证明对缺血性脑损伤和脑出血具有神经保护作用。在精神病学中,它被研究为焦虑、抑郁和成瘾的潜在治疗方法。在肿瘤学中,它已被证明通过诱导细胞凋亡和抑制肿瘤生长而具有抗肿瘤活性。

3-hydroxy-3-phenylpentanamide

一键复制产品信息
Rating icon 很棒

纯度: 98.42%

货号 T50100Cas号 131802-69-2

3-hydroxy-3-phenylpentanamide 是一种手性化合物,属于β-羟基酰胺类。在神经病学中,它已被证明对缺血性脑损伤和脑出血具有神经保护作用。在精神病学中,它被研究为焦虑、抑郁和成瘾的潜在治疗方法。在肿瘤学中,它已被证明通过诱导细胞凋亡和抑制肿瘤生长而具有抗肿瘤活性。

3-hydroxy-3-phenylpentanamide
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规格价格库存数量
1 mg
¥ 833
现货
5 mg
¥ 1,930
现货
10 mg
¥ 2,830
现货
25 mg
¥ 4,480
现货
50 mg
¥ 5,920
现货
100 mg
¥ 8,100
现货
200 mg
¥ 10,900
现货
1 mL x 10 mM (in DMSO)
¥ 1,470
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选择批次:
纯度: 98.42%
颜色: 白色
性状: Solid
资源下载: COA LCMS HNMR产品操作手册

产品介绍


3-hydroxy-3-phenylpentanamide AI Summary
3-hydroxy-3-phenylpentanamide exhibits diverse bioactivities, with notable antiviral properties demonstrated by its ability to inhibit SARS-CoV-2 induced cytotoxicity in Caco-2 cells (inhibitory effect of 29.94% at 10 µM after 48 hours) and VERO-6 cells (inhibition of -0.1% at 10 µM after 48 hours exposure to 0.01 MOI SARS-CoV-2 virus). Furthermore, the compound inhibits the SARS-CoV-2 3CL-Pro protease with an inhibition percentage of 15.81% at 20 µM, suggesting potential as a protease inhibitor. In antibacterial assays, 3-hydroxy-3-phenylpentanamide shows inhibition rates against Pseudomonas aeruginosa ATCC 27853 (1.83%) and Acinetobacter baumannii ATCC 19606 (11.78%), but has a negative inhibition rate against Pseudomonas aeruginosa PAO397 (-9.36%). Additionally, the compound exhibits bioactivity against Mycobacterium tuberculosis and minor inhibition of an enzyme related to Toxoplasma. It also shows varying inhibition on the human HDAC6 enzyme with 21.65% inhibition on a commercial peptide substrate and -6.56% on a custom peptide substrate..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
3-hydroxy-3-phenylpentanamide is a chiral compound belonging to the class of beta-hydroxyamides. In neurology, it has been shown to have neuroprotective effects against ischemic brain injury and cerebral hemorrhage. In psychiatry, it has been studied as a potential treatment for anxiety, depression and addiction. In oncology, it has been shown to have antitumor activity by inducing apoptosis and inhibiting tumor growth.
化学信息
分子量193.24
分子式C11H15NO2
CAS No.131802-69-2
SmilesC(CC(N)=O)(CC)(O)C1=CC=CC=C1
密度1.13g/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.

实际储存温度请以COA为准

溶解度信息
DMSO: 50 mg/mL (258.75 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM5.1749 mL25.8746 mL51.7491 mL258.7456 mL
5 mM1.0350 mL5.1749 mL10.3498 mL51.7491 mL
10 mM0.5175 mL2.5875 mL5.1749 mL25.8746 mL
20 mM0.2587 mL1.2937 mL2.5875 mL12.9373 mL
50 mM0.1035 mL0.5175 mL1.0350 mL5.1749 mL
100 mM0.0517 mL0.2587 mL0.5175 mL2.5875 mL
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。

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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