Cefsulodin (sodium salt)
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 250mg | ¥890.00 | 现货 | |
| 500mg | ¥1578.00 | 现货 | |
| 1g | ¥2100.00 | 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
Cefsulodin, formerly named as SCE-129, is a cephalosporin with a spectrum of antibacterial activity against Staphylococcus aureus, Pseudomonas aeruginosa, and most other gram-positive cocci [1]. Cefsulodin shows little activity against other species of Acinetobacter spp., Pseudomonas, or members of the Enterobacteriaceae [1]. Cefsulodin is a β-lactam antibiotic that involved in lysing actively-growing E. coli by specifically binding to the intermembrane proteins, penicillin-binding proteins 1a and b, whose transglycosylase and transpeptidase activities are involved in cell elongation and septation [2].
Cefsulodin was active against P. aeruginos. Cefsulodin was active against penicillinase-producing strains of S. aureus. The MICs of cefsulodin for Pseudomonas aeruginosa and its mutants Pseudomonas aeruginosa PAO4089 were 0·78 and 12· mg/l [3]. Cefsulodin was active in minimum inhibitory concentrations (MICs) of 0.5 to 64 μg/ml. Cefsulodin was active against P. diminuta, P. maltophilia, P. paucimobilis, and P. pseudoalcaligenes with MICs of 1-32 μg/ml. Cefsulodin was not hydrolyzed by the β-lactamase induced in P. aeruginosa by growth in the presence of benzylpenicillin and was a poor substrate for β-lactamases from Enterobacter cloacae and Proteus morganii [4].
References:
[1] Barry A L, Jones R N, Thornsberry C. Cefsulodin: antibacterial activity and tentative interpretive zone standards for the disk susceptibility test[J]. Antimicrobial agents and chemotherapy, 1981, 20(4): 525-529.
[2] Jacoby G H, Young K D. Cell cycle-independent lysis of Escherichia coli by cefsulodin, an inhibitor of penicillin-binding proteins 1a and 1b[J]. Journal of bacteriology, 1991, 173(1): 1-5.
[3] Bryan L E, Kwan S, Godfrey A J. Resistance of Pseudomonas aeruginosa mutants with altered control of chromosomal beta-lactamase to piperacillin, ceftazidime, and cefsulodin[J]. Antimicrobial agents and chemotherapy, 1984, 25(3): 382-384.
[4] King A, Shannon K, Phillips I. In vitro antibacterial activity and susceptibility of cefsulodin, an antipseudomonal cephalosporin, to beta-lactamases[J]. Antimicrobial agents and chemotherapy, 1980, 17(2): 165-169.
产品性质
| 物理外观 | Solid |
| CAS号 | 52152-93-9 |
| 分子式 | C22H19N4O8S2·Na |
| 分子量 | 554.5 |
| 小分子别名 | Cefsulodin sodium |
| 化学名称 | 4-(aminocarbonyl)-1-[[(6R,7R)-2-carboxy-8-oxo-7-[[(2R)-2-phenyl-2-sulfoacetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-pyridinium inner salt, monosodium salt |
| 溶解度 | ≥22.75 mg/mL in DMSO with gentle warming; insoluble in EtOH; ≥49.3 mg/mL in H2O |
| SMILES | O=C(N[C@H]1[C@@]2([H])SCC(C[N+]3=CC=C(C(N)=O)C=C3)=C(C([O-])=O)N2C1=O)[C@@H](C4=CC=CC=C4)S(=O)(O[Na])=O |
| 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 | 头孢磺啶钠盐水合物是一种 β 内酰胺类抗生素。 |



沪公网安备 31011002003500