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IRAK4-IN-19
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
IRAK4-IN-19图片
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
IRAK4-IN-19 是一种有效的白介素 1 受体相关激酶 4 (IRAK4)抑制剂,IC50为 4.3 nM。IRAK4-IN-19 可抑制 THP 和 DC 细胞中 LPS 诱导的 IL23 产生,阻止关节炎模型大鼠的关节炎发展。IRAK4-IN-19 可用于关节炎疾病的研究。
生物活性

IRAK4-IN-19 is a potentinterleukin-1 receptor-associated kinase 4 (IRAK4)inhibitor with anIC50value of 4.3 nM. IRAK4-IN-19 can inhibit LPS-induced IL23 production in THP and DC cells, and stop arthritis development in arthritis rats. IRAK4-IN-19 can be used for researching arthritis disease[1].

IC50& Target[1]

IRAK4

4.3 nM (IC50)

体外研究
(In Vitro)

IRAK4-IN-19 (compound 39) has inhibitory activity against LPS-induced IL23 in THP and DC with IC50s of 0.23 and 0.22 μM, respectively[1].

体内研究
(In Vivo)

IRAK4-IN-19 (30 mg/kg; twice daily for 21 days) completely stops arthritis development in arthritis rats at 30 mg/kg[1].
IRAK4-IN-19 (1 mg/kg for IV, 5 mg/kg for PO, single dosage) exhibits a favorable pharmacokinetics profile[1].
IRAK4-IN-19 (5, 15, 45 and 75 mg/kg) exhibits good efficacy in an acute mouse model for the IL-1β induced IL-6 expression, with 64% inhibition at 75 mg/kg dose, 37% inhibition at 45 mg/kg dose, 16% inhibition at 15 mg/kg dose and 9% inhibition at 5 mg/kg[1].

Animal Model:Rats[1]
Dosage:30 mg/kg
Administration:twice daily for 21 days
Result:Completely stopped arthritis development in arthritis rats at 30 mg/kg.
Animal Model:Rats[1]
Dosage:1 mg/kg, 5 mg/kg
Administration:IV and PO, single dosage
Result:Exhibited a favorable pharmacokinetics profile with a clearance of 6 mL/min/kg and oral bioavailability of 43%.
分子量

492.52

Formula

C25H26F2N8O

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.