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Cefpiramide acid

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纯度: 97.40%

货号 T0138Cas号 70797-11-4

别名 头孢匹胺, Cefpiramidum, Cefpiramido

Cefpiramide acid (Cefpiramidum) 是第三代头孢菌素类抗生素。

Cefpiramide acid
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Cefpiramide acid

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Rating icon 很棒

纯度: 97.40%

货号 T0138 别名 头孢匹胺, Cefpiramidum, CefpiramidoCas号 70797-11-4

Cefpiramide acid (Cefpiramidum) 是第三代头孢菌素类抗生素。

规格价格库存数量
5 mg
¥ 192
现货
10 mg
¥ 336
现货
25 mg
¥ 664
现货
50 mg
¥ 1,064
现货
100 mg
¥ 1,383
现货
200 mg
¥ 1,952
现货
1 mL x 10 mM (in DMSO)
¥ 294
现货
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产品介绍


生物活性
产品描述
Cefpiramide acid (Cefpiramidum) is a third-generation cephalosporin antibiotic.
别名头孢匹胺, Cefpiramidum, Cefpiramido
化学信息
分子量612.64
分子式C25H24N8O7S2
CAS No.70797-11-4
Smiles[H][C@]12SCC(CSc3nnnn3C)=C(N1C(=O)[C@H]2NC(=O)[C@H](NC(=O)c1cnc(C)cc1O)c1ccc(O)cc1)C(O)=O
密度1.75 g/cm3 (Predicted)
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: 27.5 mg/mL (44.89 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM1.6323 mL8.1614 mL16.3228 mL81.6140 mL
5 mM0.3265 mL1.6323 mL3.2646 mL16.3228 mL
10 mM0.1632 mL0.8161 mL1.6323 mL8.1614 mL
20 mM0.0816 mL0.4081 mL0.8161 mL4.0807 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:
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

对于不同动物的给药剂量换算,您也可以参考 更多

TargetMol AI Summary
Cefpiramide acid is a multi-functional compound exhibiting diverse bioactivities across several contexts. It shows species-dependent pharmacokinetics with varying volumes of distribution and clearance rates; notably, it has a lower volume of distribution and clearance in humans and monkeys compared to rats and dogs. As a potent inhibitor of the vitamin D receptor (VDR) with a potency of 39810.7 nM, Cefpiramide acid also demonstrates significant delayed death inhibition of the malarial parasite plastid, exhibiting a potency of 13459.1 nM after 96 hours. The compound demonstrates moderate liver toxicity with hepatotoxic effects observed in clinical trials, manifesting as acute and cytolytic liver toxicity without indications of severe hepatitis or chronic liver disease. In addition, Cefpiramide acid possesses potent antibacterial properties, particularly against tolC-deficient Escherichia coli (MIC of 0.5 ug.mL-1) and demonstrates activity against wild-type Staphylococcus aureus with a MIC of 32.0 ug.mL-1, which increases in the presence of human serum albumin (HSA). Bioactivity studies also indicate its involvement in hepatic drug metabolism, excretion, and clearance processes in human, dog, and rat models. Notably, the compound has a low fraction unbound in human plasma (0.09%) compared to dog plasma (0.6%), highlighting differences in binding affinity or bioavailability across species. While showing moderate inhibition of cell viability in Vero E6 cells infected with SARS-CoV-2, its antiviral activity against the SARS-CoV-2 USA-WA1/2020 strain is below the hit threshold. Furthermore, Cefpiramide acid exhibits inhibition of the human HDAC6 enzyme, with differing inhibition percentages depending on the assay substrate used. Overall, Cefpiramide acid showcases a range of bioactivities from antibacterial and antiviral properties to liver toxicity and enzyme inhibition, dependent on the context and specific biological system evaluated..
Note: Summary generated by AI, AI may be wrong some times, we do not provide any medical advice and only sell our product to accredited institution, Please cross-check with other sources, data source: chembl
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