Cefradine

製品コードS4671 バッチS467101

印刷

化学情報

 Chemical Structure Synonyms Cephradine, Sefril, Anspor, Cephradin, Velosef Storage
(From the date of receipt)
3 years -20°C powder
1 years -80°C in solvent
化学式

C16H19N3O4S

分子量 349.4 CAS No. 38821-53-3
Solubility (25°C)* 体外 Water 10 mg/mL (28.62 mM)
DMSO Insoluble
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 Cefradine (Cephradine, Sefril, Anspor, Velosef) is a semi-synthetic cephalosporin antibiotic.
in vivo Cephradine has a low order of acute, subacute, and chronic oral toxicity, and acute and subacute parenteral toxicity. After daily intravenous doses of cephradine has been given to monkeys for 2 weeks, these animals show no signs of nephrotoxicity. Cephradine does not induce any teratogenic changes in the offspring of either mice or rats. The route of administration has been a determinant in the choice of a cephalosporin antibiotic. It is a distinct therapeutic advantage that a single cephalosporin antibiotic, cephradine, may be used in both oral and parenteral preparations[2].

プロトコル(参考用のみ)

細胞アッセイ 細胞株 CHO/hPEPT1 cells
濃度 1 mg/mL
反応時間 10, 20, 30, 45, 60, 90 min
実験の流れ

Cells Are seeded in six-well culture plates (9.6 cm2, growth area) at a density of 105 cells/cm2. At 2 days postseeding, the medium is removed and cells are washed twice with pH 6.0 uptake buffer. Independent studies are performed for each drug solution at 1 mg/mL made in pH 6.0 uptake buffer. At each time point (10, 20, 30, 45, 60, 90 min), drug solution is removed and cells are washed three times with ice-cold pH 6.0 uptake buffer. One milliliter of Milli-Q water is added to each well and incubated for 30 min at 25 °C. Cells are harvested and sonicated for 1-2 min. ZnSO4 solution (8%, 200 mL) is added to the cell lysate, vortexed rigorously, and centrifuged for 5 min at 3000 rpm. After filtration of the supernatant through a membrane filter (0.45 mm), samples are analyzed by HPLC.

動物実験 動物モデル Charles River CD Sprague-Dawley rats
投薬量 100, 300, or 1,000 mg/kg
投与方法 p.o.

参考

  • https://pubmed.ncbi.nlm.nih.gov/10052994/
  • https://pubmed.ncbi.nlm.nih.gov/4790617/

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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