エチオナミド
Based on 5 publication(s) in Google Scholar
Ethionamide (2-ethylthioisonicotinamide) is a second-line anti-tuberculosis antibiotic with antibacterial effect and oral activity.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 99.98%
- CAS 番号: 536-33-4
- 分子式: C8H10N2S
- 分子量:166.25
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保管条件:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
MedChemExpress(MCE)の使用を引用している文献 Ethionamide
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生物活性
Ethionamide strongly inhibits mycolic acid synthesis in BCG strain Mycobacterium bovis cells. For M. tuberculosis Canetti, Mycobacterium sp. strain CR21, and ATCC 23366, the MIC values are 0.5, 3, and 60 μg/ml, respectively[2].
Ethionamide (60 μg/ml, 0-120 min) concurrently increases unsaturated mycolic acids and decreases oxygenated mycolic acids in M. aurum ATCC 23366[2].
Ethionamide's S-oxidation is primarily catalyzed by FMOs, particularly in the liver and lung[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:M.aurum ATCC 23366
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Concentration:60 μg/ml
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Incubation Time:0, 20, 40, 60, 80, 100, 120 min
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Result:Unsaturated mycolic acid increases, oxygenated mycolic acid decreases.
Pharmacokinetic parameters of ethionamide in mice[4]
| Sex | Tmax (h) | Cmax (μg/mL) |
| Male | 1 | 15.1±34.4 |
| Femal | 1±0.5 | 15.1±14.8 |