Powder: -20°C for 3 years | In solvent: -80°C for 1 year
GSK3186899 is an inhibitor of Cdc2-related kinase 12 with an EC50 of 1.4 μM for L. donovani.
パッケージサイズ | 在庫状況 | 単価(税別) |
---|---|---|
1 mg | 在庫あり | ¥ 68,500 |
5 mg | 在庫あり | ¥ 148,500 |
10 mg | 在庫あり | ¥ 226,500 |
25 mg | 在庫あり | ¥ 337,500 |
50 mg | 在庫あり | ¥ 457,000 |
100 mg | 在庫あり | ¥ 615,000 |
説明 | GSK3186899 is an inhibitor of Cdc2-related kinase 12 with an EC50 of 1.4 μM for L. donovani. |
In vitro | GSK3186899 is active in cidal axenic amastigote assay with an EC50 value of 0.1 μM. GSK3186899 shows good selectivity against mammalian THP-1 host cells (EC50 value > 50 μM). GSK3186899 exhibits a less than 10-fold variation in potency against a panel of Leishmania-derived lines. GSK3186899 is more active using human peripheral blood mononuclear cells as the host cells[1]. |
In vivo | In the mouse model of infection, GSK3186899 (25 mg/kg; orally) reduces parasite levels by 99%. The efficacy of treatment is dependent on dose, frequency, and duration (10 days better than 5). There are no notable adverse effects in a rat seven-day repeat-dose oral toxicity study with respect to clinical chemistry and histopathology at all doses tested[1]. |
別名 | 3,3,3-trifluoro-N-[4-[[3-[(2R)-2-methylmorpholin-4-yl]-1H-pyrazolo[3,4-d]pyrimidin-6-yl]amino]cyclohexyl]propane-1-sulfonamide, DDD-853651 |
分子量 | 491.53 |
分子式 | C19H28F3N7O3S |
CAS No. | 1972617-87-0 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 200 mg/mL (406.89 mM), Sonication is recommended.
You can also refer to dose conversion for different animals. 詳細
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GSK3186899 1972617-87-0 Microbiology/Virology Parasite GSK 3186899 DDD 853651 3,3,3-trifluoro-N-[4-[[3-[(2R)-2-methylmorpholin-4-yl]-1H-pyrazolo[3,4-d]pyrimidin-6-yl]amino]cyclohexyl]propane-1-sulfonamide GSK-3186899 DDD-853651 DDD853651 Inhibitor inhibitor inhibit