CAS NO: | 1816294-67-3 |
生物活性 | SR-4370 is an inhibitor ofHDAC, withIC50s of 0.13 μM, 0.58 μM, 0.006 μM, 2.3 μM, and 3.4 μM forHDAC1,HDAC2,HDAC3,HDAC8, andHDAC6, respectively. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | SR-4370 is an inhibitor of HDAC, with IC50s of 0.13 μM, 0.58 μM, 0.006 μM, 2.3 μM, and 3.4 μM for HDAC1, HDAC2, HDAC3, HDAC8, and HDAC6, respectively. SR-4370 is cytotoxic to the breast cancer cells (MDA-MB-231), with an IC50of 12.6 μM[1]. | ||||||||||||||||
分子量 | 304.33 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H18F2N2O | ||||||||||||||||
CAS 号 | 1816294-67-3 | ||||||||||||||||
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 : ≥ 150 mg/mL(492.89 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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