LT-630
LT-630 is a HDAC6 inhibitor. LT-630 ameliorates liver injury by reducing oxidative damage.
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。
- 分子式: C19H17FN4O3
- 分子量:368.36
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
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HDAC6 |
LT-630 (2-8 nM, 3 h and 24 h) inhibits Acetaminophen (HY-66005)-induced cell damage, reduces the increased oxidative stress and apoptosis in AML-12 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:AML-12 cells
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Concentration:2-8 nM
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Incubation Time:3 h and 24 h
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Result:Reduced the increased ratio of bax/bcl-2 and the levels of cleaved caspase3 and cyt-c.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:male C57BL/6J mice (16–20 g, 6-week-old)[1]
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Dosage:10-40 mg/kg befor APAP (350 mg/kg, i.p.)
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Administration:tail vein injection
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Result:Enhanced the release of GSH, SOD and NADPH.
Reduced apoptosis, the bax/bcl-2 ratio, and the levels of cleaved caspase3 and cyt-c in APAP.
化学情報
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分子量 368.36
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分子式 C19H17FN4O3
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SMILES
O=C(NO)C1=CC=C(CN2N=C(C(NC3=CC(F)=CC=C3)=O)C=C2C)C=C1
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)