CAS NO: | 1884222-74-5 |
生物活性 | SBP-7455 is a potent, high affinity and orally active dualULK1/ULK2autophagy inhibitorwithIC50s of 13 nM and 476 nM in the ADP-Glo assays, respectively. SBP-7455 potently inhibitsULK1/2enzymatic activity and can be used for triple-negative breastcancer(TNBC) research[1]. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | SBP-7455 (compound 26; 72 h) treatment inhibits cell growth with an IC50of 0.3 μM for MDA-MB-468 cells. SBP-7455 inhibits starvation-induced autophagic flux in TNBC cells that are dependent on autophagy for survival[1]. | ||||||||||||||||
体内研究 (In Vivo) | A single dose of SBP-7455 (compound 26) (30 mg/kg) is orally administered to mice. The Tmaxfor SBP-7455 is approximately 1 h, the Cmaxis 990 nM and the T1/2is 1.7 h. The plasma concentration of SBP-7455 remains above the ULK1 IC50for almost 4 h after oral dosing[1]. | ||||||||||||||||
分子量 | 354.33 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C16H17F3N4O2 | ||||||||||||||||
CAS 号 | 1884222-74-5 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 125 mg/mL(352.78 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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