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JAK3-IN-9
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。
JAK3-IN-9图片
CAS NO:1430095-30-9
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
JAK3-IN-9 是一种具有口服活性的JAK3抑制剂,其IC50值为1.7 nM。JAK3-IN-9 对JAK3具有高度选择性。JAK3-IN-9 低毒并且具有较高的口服生物利用度。JAK3-IN-9 显示良好的抗关节炎活性,可用于自身免疫疾病的研究。
生物活性

JAK3-IN-9 is an orally activeJAK3inhibitor withIC50value of 1.7 nM. JAK3-IN-9 is highly selective to theJAK3signal path. JAK3-IN-9 is lowly toxic with high oral bioavailability, shows goodanti-arthritisactivity. JAK3-IN-9 can be used inautoimmunedisease research[1].

IC50& Target

JAK3

1.7 nM (IC50)

体外研究
(In Vitro)

JAK3-IN-9 (compound 11i) shows high selective inhibition of JAK3 withIC50value of 1.7 nM[1].

Cell Viability Assay

Cell Line:PBMCs[1]
Concentration:1 μM
Incubation Time:30 min
Result:Showed preferential inhibition of JAK3[1].
体内研究
(In Vivo)

JAK3-IN-9 (compound 11i) (Female Lewis rats; 3, 10 and 30 mg/kg; Oral gavage once daily for 20 days) can selectively inhibit JAK3 cytokine signaling in the primary cells[1].
JAK3-IN-9 (Male DBA1j of 8 to 12-weeks old mice; 1mg/kg, Intravenous injection, Single administration) shows high AUC of 2104 μg/ml, extends t1/2to 2.56 h and good oral bioavailability of 48%[1].
JAK3-IN-9 (30 mg/kg; Oral gavage once daily for 20 days) suppress paw swelling in a dose-dependent manner withED50value of 10 mg/kg[1].

Animal Model:Male DBA1j (8 to 12-weeks old) mice; Female Lewis rats[1].
Dosage:1, 3, 10 and 30 mg/kg
Administration:I.V, Single administration; IG, once daily for 20 days.
Result:Showedanti-arthritisactivity in the CIA mice model[1].
分子量

393.46

Formula

C17H23N5O4S

CAS 号

1430095-30-9

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.