
JAK3-IN-1
CAS No. 1805787-93-2
JAK3-IN-1 ( JAK3-IN-1 | JAK3IN1 | JAK3 IN 1 | JAK3IN-1 | JAK3-IN1 )
产品货号. M12759 CAS No. 1805787-93-2
JAK3-IN-1 是一种有效的选择性 JAK3 抑制剂,IC50 为 4.8 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1847 | 有现货 |
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50MG | ¥8068 | 有现货 |
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100MG | ¥11259 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称JAK3-IN-1
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述JAK3-IN-1 是一种有效的选择性 JAK3 抑制剂,IC50 为 4.8 nM。
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产品描述JAK3-IN-1 is a potent and selective JAK3 inhibitor with IC50 of 4.8 nM; displays >150 fold selectivity versus JAK1 and JAK2; exhibits decent pharmacokinetic properties and is suitable for use in vivo.
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体外实验JAK3-IN-1(Compound 9; 0-5 μM; 3 hours; BMDMs cells) treatment completely inhibits IL-4 induced p-STAT6 at a concentration of 500 nM and only partially inhibits IFNβ-induced p-STAT1 at a concentration of 5.0 μM.JAK3-IN-1(Compound 9) most potently inhibits JAK3 and identified fms-related tyrosine kinase 3 (FLT3) and several tyrosine protein kinase (TEC)-family kinases as being potential off-targets. Enzymatic assays using the Z’-lyte or LanthaScreen formats confirmed enzymatic inhibition of FLT3 (IC50 = 13 nM), TTK protein kinase (TTK, IC50 = 49 nM), BLK proto-oncogene (BLK, IC50 = 157 nM) and tyrosine protein kinase TXK (TXK, IC50 = 36 nM). JAK3-IN-1 shows very low inhibition scores for other JAKs and wild-type (WT) EGFR, which is consistent with the over 180-fold higher IC50s against EGFRWT andTYK2 (IC50s =409 nM,> 10000 respectively). JAK3-IN-1 possesses over 165-fold higher IC50s for BTK or ITK (IC50s = 794 and 1070 nM respectively).JAK3-IN-1(Compound 9) selectively inhibits the proliferation of JAK3-dependent Ba/F3 cells (IC50 = 69 nM) relative to other JAK-dependent Ba/F3 cells, for which there was no antiproliferative effect at concentrations below 3.0 μM. TWestern Blot Analysis Cell Line:BMDMs cells Concentration:0 μM, 0.1 μM, 0.5 μM, 1 μM, 5 μM Incubation Time:3 hours Result:Completely inhibited IL-4 induced p-STAT6 at a concentration of 500 nM and only partially inhibited IFNβ-induced p-STAT1 at a concentration of 5.0 μM.
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体内实验JAK3-IN-1(Compound 9) shows reasonable pharmacokinetic properties, with moderate T1/2 of 1.4 h, area under the curve (AUC) value of 795 ng*hr/mL following a 10 mg/Kg oral dose and good oral bioavailability of 66%. After oral administration with JAK3-IN-1(Compound 9) (75 mpk, QD) for 8 days, the numbers of B or T lymphocytes in the tumor-bearing lungs and spleens of treated mice is not affected, however, the number of NK cells is reduced.
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同义词JAK3-IN-1 | JAK3IN1 | JAK3 IN 1 | JAK3IN-1 | JAK3-IN1
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通路Angiogenesis
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靶点JAK
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受体JAK
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研究领域Cancer
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适应症——
化学信息
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CAS Number1805787-93-2
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分子量508.0151
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分子式C26H30ClN7O2
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纯度>98% (HPLC)
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溶解度DMSO: ≥ 47 mg/mL
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SMILESC=CC(NC1=CC=CC(CNC2=NC(NC3=CC=C(N4CCN(C)CC4)C=C3OC)=NC=C2Cl)=C1)=O
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化学全称2-Propenamide, N-[3-[[[5-chloro-2-[[2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]amino]methyl]phenyl]-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Tan L, et al. J Med Chem. 2015 Aug 27;58(16):6589-606.