Cefadroxil (hydrate)
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 1mL(10 mM in DMSO) | ¥454.00 | 现货 | |
| 250mg | ¥1040.00 | 现货 | |
| 500mg | ¥1973.00 | 现货 | |
| 1g | ¥3498.00 | 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
Cefadroxil is a new semisynthetic cephalosporin with a broad antibacterial spectrum and a high chemotherapeutic potential [1].
In vitro: The inhibitory activity of this compound was similar to that of cephalexin and cephradine when tested against 602 clinical isolates on Mueller-Hinton medium. In the oral treatment of experimental infections of mice, cefadroxil was more effective than cephalexin against Streptococcus pyogenes, and comparably effective against Streptococcus pneumoniae, Staphylococcus aureus, and several gram-negative species [1].
In vivo: In mice, oral administration of cefadroxil at doses ranging from 25 to 100 mg/kg attained peak concentrations in the blood. Higher peak levels were noted with cefadroxil than with cephalexin at a dose of 200 mg/kg [1].
Clinical trials: A single daily dose of cefadroxil appeared to be as effective in the treatment of patients with A β-hemolytic streptococcal (GABHS) pharyngitis [2].
References:
[1] Buck R E, Price K E. Cefadroxil, a new broad-spectrum cephalosporin[J]. Antimicrobial agents and chemotherapy, 1977, 11(2): 324-330.
[2] Gerber M A, Randolph M F, Chanatry J, et al. Once daily therapy for streptococcal pharyngitis with cefadroxil[J]. The Journal of pediatrics, 1986, 109(3): 531-537.
产品性质
| CAS号 | 66592-87-8 |
| 分子式 | C16H17N3O5S·H2O |
| 分子量 | 381.4 |
| 小分子别名 | Cefadroxil hydrate |
| 化学名称 | (6R,7R)-7-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, monohydrate |
| 溶解度 | insoluble in EtOH; insoluble in H2O; ≥5.8 mg/mL in DMSO with gentle warming |
| SMILES | CC(CS[C@@H]1[C@@H]2NC([C@@H](c(cc3)ccc3O)N)=O)=C(C(O)=O)N1C2=O.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 | 头孢羟氨苄一水合物(BL-S 578 一水合物)是一种口服活性第一代头孢菌素,具有广谱抗菌活性。头孢羟氨苄一水合物(BL-S 578 一水合物)还是肽转运体 PEPT1 和 PEPT2 的底物。 |



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