CAS NO: | 2234285-81-3 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | IDH1 Inhibitor1 is a potent, orally bioavailable, brain-penetrant and selective mutantIDH1inhibitor withIC50s of 0.021 μM, 0.045 μM, and 2.52 μM forIDH1R132H,IDH1R132C, andIDH1WT, respectively[1]. Anticancer activity[1]. | ||||||||||||||||
IC50& Target | IC50: 0.021 μM (IDH1R132H), 0.045 μM (IDH1R132C), and 2.52 μM (IDH1WT)[1] | ||||||||||||||||
体外研究 (In Vitro) | IDH1 Inhibitor 1 (Compound 19) inhibits cellular HCT116-IDH1R132H/+with an IC50of 0.039 μM[1]. | ||||||||||||||||
体内研究 (In Vivo) | IDH1 Inhibitor 1 (Compound 19) inhibits 2-hydroxyglutarate (2-HG) production in a preclinical xenograft tumor model. IDH1 Inhibitor 1 is also profiled in a patient-derived IDH1 mutant HCT116-IDH1R132H/+mechanistic xenograft tumor model in mice to evaluate in vivo inhibition of 2-HG production. IDH1 Inhibitor 1, dosed orally at 150 mg/kg, inhibits new 2-HG production[1]. | ||||||||||||||||
分子量 | 450.39 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H18F4N6O2 | ||||||||||||||||
CAS 号 | 2234285-81-3 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : ≥ 100 mg/mL(222.03 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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