CAS NO: | 1427058-33-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | E6130 is an orally active and highly selectiveCX3CR1modulator, that may be effective for treatment of inflammatory bowel disease. | ||||||||||||||||
IC50& Target | CX3CR1[1] | ||||||||||||||||
体外研究 (In Vitro) | E6130 is an orally active and highly selective CX3CR1 modulator, inhibits the fractalkine-induced chemotaxis of human peripheral blood natural killer cells (IC50, 4.9 nM), and down-regulates CX3CR1 on the cell surface of CD56+NK cells with an EC50value of 5.2 nM. E6130 also shows agonistic activity via CX3CR1 with respect to GTPγS binding (EC50= 133 nM) and β-arrestin recruitment (EC50= 2.4 μM) in CX3CR1-expressing CHO-K1 membrane but show no antagonistic activity[1]. | ||||||||||||||||
体内研究 (In Vivo) | E6130 (10 or 30 mg/kg, p.o.) reduces several inflammatory bowel disease-related parameters in a murine CD4+CD45RBhighT-cell-transfer colitis model and a murine oxazolone-induced colitis model[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 556.06 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C28H37ClF3N3O3 | ||||||||||||||||
CAS 号 | 1427058-33-0 | ||||||||||||||||
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 : ≥ 250 mg/mL(449.59 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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