CAS NO: | 2227149-22-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | DS18561882 is a highly potent, isozyme-selectivemethylenetetrahydrofolate dehydrogenase2 (MTHFD2)inhibitor with anIC50value of 0.0063 μM. DS18561882 also has inhibitory effect on MTHFD1 (IC50=0.57 μM). DS18561882 exhibits a good oral pharmacokinetic profile[1]. | ||||||||||||||||
IC50& Target | IC50: 0.0063 μM (MTHFD2); 0.57 μM (MTHFD1)[1] | ||||||||||||||||
体外研究 (In Vitro) | DS18561882 (0-150 nM) gives the lowestGI50value (140 nM) against the MDA-MB-231 cell line[1]. | ||||||||||||||||
体内研究 (In Vivo) | DS18561882 (oral administration; 30, 100 or 300 mg/kg; twice daily) inhibits tumor growth inhibition with a dose-dependent manner, the tumor is completely inhibited (TGI: 67%) at the dose of 300 mg/kg in mice[1].DS18561882 (oral administration; 10, 30, 100, or 300 mg/kg) has a good oral pharmacokinetic profile, including ACU (64.6, 264, 726 μg.h/ml ); Cmax(11.4, 56.5, 90.1 μg/ml); t1/2(2.21, 2.16, 2.32 hours) for 30 mg/kg; 100mg/kg; 200 mg/kg, respectively[1].DS18561882 is suspended in a 0.5% (w/v) methyl cellulose 400 solution in this article[1].
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分子量 | 608.63 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C28H31F3N4O6S | ||||||||||||||||
CAS 号 | 2227149-22-4 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, stored under nitrogen *In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 150 mg/mL(246.46 mM;Need ultrasonic) 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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