CAS NO: | 1799753-84-6 |
生物活性 | BAY-876 is an orally active and selectiveglucose transporter 1 (GLUT1)inhibitor with anIC50of 2 nM. BAY-876 is >130-fold more selective forGLUT1thanGLUT2,GLUT3, andGLUT4[1]. BAY-876 is also a potent blocker of glycolytic metabolism and ovariancancergrowth[2]. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | BAY-876 (25-75 nM; 24 and 72 hours) has the growth-inhibitory effect and leads to a dose-dependent decrease in numbers of SKOV-3 and OVCAR-3 cells[2]. Cell Proliferation Assay[2]
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体内研究 (In Vivo) | BAY-876 (oral administration; 1.5-4.5 mg/kg/day for 28 days) causes a clear dose-dependent inhibition of tumorigenicity in mice[2].
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分子量 | 496.42 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C24H16F4N6O2 | ||||||||||||||||
CAS 号 | 1799753-84-6 | ||||||||||||||||
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 : ≥ 100 mg/mL(201.44 mM) Methanol : 1 mg/mL(2.01 mM;ultrasonic and warming and heat to 60℃) *"≥" means soluble, but saturation unknown. 配制储备液
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