
ACHP Hydrochloride
CAS No. 406209-26-5
ACHP Hydrochloride ( IKK-2 Inhibitor VIII )
产品货号. M24367 CAS No. 406209-26-5
ACHP Hydrochronide (IKK-2 Inhibitor VIII) 是一种高效、选择性 IKK-β 抑制剂 (IC50: 8.5 nM)。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1450 | 有现货 |
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10MG | ¥2373 | 有现货 |
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25MG | ¥3953 | 有现货 |
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50MG | ¥5630 | 有现货 |
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100MG | ¥8060 | 有现货 |
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500MG | ¥16119 | 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ACHP Hydrochloride
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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ACHP Hydrochronide (IKK-2 Inhibitor VIII) 是一种高效、选择性 IKK-β 抑制剂 (IC50: 8.5 nM)。
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产品描述ACHP Hydrochloride (IKK-2 Inhibitor VIII) is a highly potent and selective IKK-β inhibitor (IC50: 8.5 nM).
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体外实验ACHP Hydrochloride (Compound 4j) exhibits potent IKK-β inhibitory (IC50: 8.5 nM) and cellular activities (IC50=40 nM, in A549 cells). ACHP moderately inhibits IKK-α with an IC50 of 250 nM but exhibits good selectivity towards other kinases, such as IKK3, Syk and MKK4 (IC50>20,000 nM). Moreover, ACHP demonstrates quite potent activity in various cellular assays. ACHP inhibits NF-κB-dependent reporter gene activation in TNFα-activated HEK293 cells and PMA/calcium ionophore-activated Jurkat T cells. ACHP fails to inhibit PMA-induced AP-1 activation in MRC-5 cells and PMA/calcium ionophore induced NF-κB dependent reporter gene transcription in Jurkat cells even at concentrations exceeding 10 μM. ACHP selectively interferes with the NF-κB signaling cascade by inhibition of IKK-β in living cells. ACHP inhibits the growth of these cells in a dose-dependent manner. Tax-active cell lines are more susceptible to ACHP than Tax-inactive cell lines and Jurkat (IC50 values in Tax-active cell lines, Tax-inactive cell lines or Jurkat are 3.1±1.3?μM, 10.7±1.7?μM and 23.6?μM, respectively), suggesting that the growth of Tax-active cells depends on NF-κB more than Tax-inactive cells.
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体内实验ACHP (Compound 4j) is orally bioavailable in mice and rats and demonstrates significant in vivo activity in anti-inflammatory models (arachidonic acid-induced mouse ear edema model). ACHP has reasonable aqueous solubility (0.12 mg/mL in pH 7.4 isotonic buffer) and excellent Caco-2 permeability (Papp 62.3×10-7 cm/s), and demonstrates orally bioavailability in mice (BA: 16%) and rats (BA: 60%). The favourable bioavailability of ACHP in rats is likely due to its low clearance (0.33 L/h/kg). In an acute inflammation model, ACHP exhibits oral efficacy at 1 mg/kg in a dose-dependent manner.
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同义词IKK-2 Inhibitor VIII
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通路Others
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靶点Other Targets
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受体IKKα|IKKβ
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研究领域——
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适应症——
化学信息
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CAS Number406209-26-5
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分子量400.9
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分子式C21H25ClN4O2
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纯度>98% (HPLC)
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溶解度DMSO:45 mg/mL (112.25 mM; Need ultrasonic)
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SMILESN#CC1=C(C=C(N=C1N)C2=C(C=CC=C2OCC3CC3)O)C4CCNCC4.[H]Cl
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化学全称——
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.Murata T, et al. Synthesis and structure-activity relationships of novel IKK-beta inhibitors. Part 3: Orally active anti-inflammatory agents. Bioorg Med Chem Lett. 2004 Aug 2;14(15):4019-22.