Powder: -20°C for 3 years | In solvent: -80°C for 1 year
FT709 is a selective and potent inhibitor of USP9X (IC50: 82 nM). Among others, USP9X is associated with centrosome function, EGF receptor degradation, chromosome alignment during mitosis, chemosensitization and circadian rhythms.
パッケージサイズ | 在庫状況 | 単価(税別) |
---|---|---|
1 mg | 約 35 days | ¥ 45,500 |
5 mg | 約 35 days | ¥ 204,500 |
10 mg | 約 35 days | ¥ 363,000 |
説明 | FT709 is a selective and potent inhibitor of USP9X (IC50: 82 nM). Among others, USP9X is associated with centrosome function, EGF receptor degradation, chromosome alignment during mitosis, chemosensitization and circadian rhythms. |
分子量 | 498.51 |
分子式 | C23H22N4O7S |
CAS No. | 2413991-74-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
You can also refer to dose conversion for different animals. 詳細
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FT709 2413991-74-7 Inhibitor inhibitor inhibit