Cefotaxime (sodium salt)
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 1mL(10 mM in DMSO) | ¥454.00 | 现货 | |
| 1g | ¥436.00 | 现货 | |
| 5g | ¥690.00 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
MIC: <0.1 μg/ml for S. pneumoniae
Cefotaxime is a cephalosporin antibiotic.
The cephalosporins, a class of β-lactam antibiotics originally derived from the fungus Acremonium, are indicated for the prophylaxis and treatment of infections caused by bacteria susceptible to this particular form of antibiotic.
In vitro: Previous studies found that the in-vitro activity of cefotaxime against Staphylococcus au reus has ranged from 0.8 g to 8 μg/ml with 50% of isolates inhibited by 2 μg/ml and 90% by 4 μg/ml. Moreover, it was found that methicillin resistant S. aureus were resistant to cefotaxime with MIC values above 64 μg/ml. The cefotaxime MICs against S. pneumoniae were found to be below 0.1 μg/ml, with 90% inhibited by 0.04 μg/ml. Cefotaxime has also been shown to have excellent activity against Haemophilus injluenzae, such as β-lactamase-containing strains [1].
In vivo: An in-vivo study with the mouse model of Vibrio vulnificus infection was conducted to evaluate the efficacies of therapy with minocycline or cefotaxime alone and in combination. Results indicated that combination therapy with cefotaxime and minocycline was distinctly more advantageous than therapy with the single antibiotic regimen for the treatment of severe Vibrio vulnificus infections [2].
Clinical trial: A clinical trial was conducted to test the efficacy and safety of cefotaxime in the therapy of community-and hospital-acquired pneumonias. The results suggested that cefotaxime would be an affective and well-tolerated antimicrobial agent for the treatment of pneumonia becuause of susceptible organisms [3].
References:
[1] Neu HC. The in vitro activity, human pharmacology, and clinical effectiveness of new beta-lactam antibiotics. Annu Rev Pharmacol Toxicol. 1982;22:599-642.
[2] Chuang YC, Ko WC, Wang ST, Liu JW, Kuo CF, Wu JJ, Huang KY. Minocycline and cefotaxime in the treatment of experimental murine Vibrio vulnificus infection. Antimicrob Agents Chemother. 1998 Jun;42(6):1319-22.
[3] Schleupner CJ, Engle JC. Clinical evaluation of cefotaxime for therapy of lower respiratory tract infections. Antimicrob Agents Chemother. 1982 Feb;21(2):327-33.
产品性质
| 物理外观 | Solid |
| CAS号 | 64485-93-4 |
| 分子式 | C16H16N5O7S2·Na |
| 分子量 | 477.5 |
| 小分子别名 | Cefotaxime sodium |
| 化学名称 | (6R)-3-[(acetyloxy)methyl]-7R-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, monosodium salt |
| 溶解度 | ≥18.8 mg/mL in DMSO |
| SMILES | CC(OCC(CS[C@@H]1[C@@H]2NC(/C(\c3c[s]c(N)n3)=N\OC)=O)=C(C([O-])=O)N1C2=O)=O.[Na+] |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | 头孢噻肟钠(Cefotaxim)是一种对β-内酰胺酶稳定的头孢菌素,也是第三代头孢菌素抗生素,对多种革兰氏阳性和革兰氏阴性菌具有广谱抗生素活性。 |



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