CAS NO: | 1334493-07-0 |
生物活性 | BP-1-102 is an orally available, small-molecule inhibitor of transcription factorStat3, with anIC50of 6.8 μM. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | BP-1-102 binds Stat3 with an affinity KDof 504 nM. BP-1-102 inhibits Stat3 DNA-binding activityin vitro, with an IC50value of 6.8±0.8 μM. It blocks Stat3-phospho-tyrosine peptide interactions and Stat3 activation at 4-6.8 μM, and selectively inhibits growth, survival, migration, and invasion of Stat3-dependent tumor cells. BP-1-102-mediated inhibition of aberrantly active Stat3 in tumor cells suppresses the expression of c-Myc, Cyclin D1, Bcl-xL, Survivin, VEGF, and Krüppel-like factor 8[1]. | ||||||||||||||||
体内研究 (In Vivo) | Mice therapeutically given BP-1-102, an orally bioavailable compound targeting STAT3/NF-kB activation and cross-talk, exhibit reduced colon tumorigenesis and diminished expression of STAT3/NF-kB-activating cytokines in the neoplastic areas[2]. BP-1-102 is orally bioavailable and that the agent accumulates in tumor tissues at levels sufficient to inhibit aberrantly active Stat3 functions and inhibit tumor growth[1]. | ||||||||||||||||
分子量 | 626.59 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C29H27F5N2O6S | ||||||||||||||||
CAS 号 | 1334493-07-0 | ||||||||||||||||
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 : ≥ 33 mg/mL(52.67 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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