CAS NO: | 919486-40-1 |
生物活性 | AS1517499 is a potent and brain-permeableSTAT6phosphorylation inhibitor with anIC50of 21 nM. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | AS1517499 shows potent STAT6 inhibition with an IC50value of 21 nM, and also inhibits IL-4-induced Th2 differentiation of mouse spleen T cells with an IC50value of 2.3 nM and without influencing T-helper cell 1 (Th1) differentiation induced by IL-12. AS1517499 selectively inhibits Th2 differentiation without affecting Th1 differentiation[1]. In cultured human BSM cells, IL-13 (100 ng/mL) causes a phosphorylation of STAT6 and an up-regulation of RhoA, a monomeric GTPase responsible for Ca2+sensitization of smooth muscle contraction: both events are inhibited by co-incubation with AS1517499 (100 nM)[2]. | ||||||||||||||||
体内研究 (In Vivo) | In BALB/c mice that are actively sensitized and repeatedly challenged with ovalbumin antigen, an increased IL-13 level in bronchoalveolar lavage fluids and a phosphorylation of STAT6 in bronchial tissues are observed after the last antigen challenge. These mice have an augmented BSM contractility to acetylcholine together with an up-regulation of RhoA in bronchial tissues. Intraperitoneal injections of AS1517499 (10 mg/kg) 1 hour before each ovalbumin exposure inhibits both the antigen-induced up-regulation of RhoA and BSM hyperresponsiveness, almost completely[2]. | ||||||||||||||||
分子量 | 397.86 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H20ClN5O2 | ||||||||||||||||
CAS 号 | 919486-40-1 | ||||||||||||||||
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 : ≥ 35 mg/mL(87.97 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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