CAS NO: | 675103-36-3 |
生物活性 | BAY-678 is an orally bioavailable, highly potent, selective and cell-permeable inhibitor of human neutrophilelastase(HNE), with anIC50of 20 nM. BAY-678 is also nominated as a chemical probe to the public via the Structural Genomics Consortium (SGC). | ||||||||||||||||
IC50& Target | IC50: 20 nM (HNE)[1]. | ||||||||||||||||
体外研究 (In Vitro) | BAY-678 is an orally bioavailable, highly potent, selective and cell-permeable inhibitor of human neutrophil elastase (HNE), with an IC50of 20 nM. The Ki value of BAY-678 for MNE is 700 nM. BAY-678 is the 4th generation inhibitor of HNE[1]. BAY-678 is also nominated as a chemical probe to the public via the Structural Genomics Consortium (SGC)[2]. BAY-678 has more than 2,000-fold selectivity in a panel of 21 serine proteases[3]. | ||||||||||||||||
体内研究 (In Vivo) | BAY-678 (17) reveals significant efficacy in preclinical models of ALI and lung emphysema, demonstrating their anti-inflammatory and anti-remodeling mode of action. Additionally, BAY-678 (17) has shown significant beneficial pulmonary hemodynamic and vascular effects in models of PAH in rats and mice[2]. | ||||||||||||||||
分子量 | 400.35 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H15F3N4O2 | ||||||||||||||||
CAS 号 | 675103-36-3 | ||||||||||||||||
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 : ≥ 100 mg/mL(249.78 mM) Ethanol : ≥ 4.76 mg/mL(11.89 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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