化合物ACHP Hydrochloride T10237
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Product IntroductionBioactivity英文名: ACHP Hydrochloride描述: ACHP Hydrochloride (IKK-2 Inhibitor VIII) 是选择性的IKK-β抑制剂 (IC50=5
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Product Introduction
Bioactivity
英文名: ACHP Hydrochloride
描述: ACHP Hydrochloride (IKK-2 Inhibitor VIII) 是选择性的IKK-β抑制剂 (IC50=5.8 nM)。
细胞实验: HTLV-1-infected T-cell lines, ATL-35T, 81-66/45, MJ, and MT-2 cells, human ATL cell lines established from ATL patients, ATL-102, ED-40515(?) and TL-Om1 cells, and an HTLV-1-negative T-cell leukemia cell line Jurkat are used in this study. Approximately 1.5×10^4 cells are cultured in 96-well plates in triplicates at 37°C. Growth inhibitory effect of ACHP (0.01, 0.1, 1, 5, 10, 50 and 100 μM) is determined using MTT assay. Optical densities (OD) at 570 and 630?nm are measured with a multi-plate reader. Cell viability (%) is calculated [2].
动物实验: In vivo arachidonic acid-induced ear edema in mice: ear edema is induced by topical application of arachidonic acid (500 μg/ear). ACHP (0.3, 1 and 3 mg/kg, p.o.), Dexamethasone, and vehicle (10% cremophor in saline) are given po 60 min before the arachidonic acid application. Ear thickness is measured at 0, 1, 3, and 6 h after the arachidonic acid application [1].
体外活性: ACHP Hydrochloride展现出强效的IKK-β抑制作用（IC50：8.5 nM），以及显著的细胞内活性（IC50：40 nM，在A549细胞中）。ACHP对IKK-α具有适度抑制效果（IC50为250 nM），但对其他激酶如IKK3、Syk和MKK4则表现出良好的选择性（IC50>20,000 nM）。此化合物能抑制TNFα激活的HEK293细胞和PMA/钙离子载体激活的Jurkat T细胞中NF-κB依赖性报告基因的激活。然而在超过10μM的浓度下，ACHP未能抑制MRC-5细胞中PMA诱导的AP-1激活，也未能抑制Jurkat细胞中PMA/钙离子载体诱导的NF-κB依赖性报告基因转录。ACHP通过抑制活细胞中的IKK-β选择性干预NF-κB信号通路[1]。此化合物以剂量依赖方式抑制这些细胞的生长。Tax活跃细胞系对ACHP的敏感度高于Tax非活跃细胞系及Jurkat细胞（Tax活跃、非活跃细胞系或Jurkat细胞的IC50值分别为3.1±1.3μM、10.7±1.7μM和23.6μM），这表明Tax活跃细胞的生长更依赖NF-κB[2]。
体内活性: ACHP在小鼠和大鼠体内具有可口服和生物利用度，并在抗炎模型中显示出显著的体内活性（花生四烯酸引起的小鼠耳肿炎模型）。ACHP在水中具有合理的溶解度（在pH 7.4的等渗缓冲液中为0.12 mg/mL）和优秀的Caco-2透过性（Papp 62.3×10^-7 cm/s）。ACHP在大鼠中的良好生物利用度可能归因于其低清除率（0.33 L/h/kg）。在急性炎症模型中，ACHP以1 mg/kg的剂量依赖性方式表现出口服有效性[1]。
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 45 mg/mL (112.25 mM)
关键字: I kappa B kinase | IκB kinase | Inhibitor | ACHP | inhibit | IKK | ACHP Hydrochloride
相关产品: Bay 11-7085 | Kazinol U | Nyasol | TBK1/IKKε-IN-1 | WS6 | (Rac)-BAY-985 | 2-AMINO-5-PHENYL-THIOPHENE-3-CARBOXYLIC | NF-κB-IN-1 | Selinidin | TBK1/IKKε-IN-5
相关库: Anti-Breast Cancer Compound Library | Anti-Cancer Compound Library | NF-κB Signaling Compound Library | Bioactive Compounds Library Max | Anti-Ovarian Cancer Compound Library | Inhibitor Library | Kinase Inhibitor Library | Bioactive Compound Library
Bioactivity
英文名: ACHP Hydrochloride
描述: ACHP Hydrochloride (IKK-2 Inhibitor VIII) 是选择性的IKK-β抑制剂 (IC50=5.8 nM)。
细胞实验: HTLV-1-infected T-cell lines, ATL-35T, 81-66/45, MJ, and MT-2 cells, human ATL cell lines established from ATL patients, ATL-102, ED-40515(?) and TL-Om1 cells, and an HTLV-1-negative T-cell leukemia cell line Jurkat are used in this study. Approximately 1.5×10^4 cells are cultured in 96-well plates in triplicates at 37°C. Growth inhibitory effect of ACHP (0.01, 0.1, 1, 5, 10, 50 and 100 μM) is determined using MTT assay. Optical densities (OD) at 570 and 630?nm are measured with a multi-plate reader. Cell viability (%) is calculated [2].
动物实验: In vivo arachidonic acid-induced ear edema in mice: ear edema is induced by topical application of arachidonic acid (500 μg/ear). ACHP (0.3, 1 and 3 mg/kg, p.o.), Dexamethasone, and vehicle (10% cremophor in saline) are given po 60 min before the arachidonic acid application. Ear thickness is measured at 0, 1, 3, and 6 h after the arachidonic acid application [1].
体外活性: ACHP Hydrochloride展现出强效的IKK-β抑制作用（IC50：8.5 nM），以及显著的细胞内活性（IC50：40 nM，在A549细胞中）。ACHP对IKK-α具有适度抑制效果（IC50为250 nM），但对其他激酶如IKK3、Syk和MKK4则表现出良好的选择性（IC50>20,000 nM）。此化合物能抑制TNFα激活的HEK293细胞和PMA/钙离子载体激活的Jurkat T细胞中NF-κB依赖性报告基因的激活。然而在超过10μM的浓度下，ACHP未能抑制MRC-5细胞中PMA诱导的AP-1激活，也未能抑制Jurkat细胞中PMA/钙离子载体诱导的NF-κB依赖性报告基因转录。ACHP通过抑制活细胞中的IKK-β选择性干预NF-κB信号通路[1]。此化合物以剂量依赖方式抑制这些细胞的生长。Tax活跃细胞系对ACHP的敏感度高于Tax非活跃细胞系及Jurkat细胞（Tax活跃、非活跃细胞系或Jurkat细胞的IC50值分别为3.1±1.3μM、10.7±1.7μM和23.6μM），这表明Tax活跃细胞的生长更依赖NF-κB[2]。
体内活性: ACHP在小鼠和大鼠体内具有可口服和生物利用度，并在抗炎模型中显示出显著的体内活性（花生四烯酸引起的小鼠耳肿炎模型）。ACHP在水中具有合理的溶解度（在pH 7.4的等渗缓冲液中为0.12 mg/mL）和优秀的Caco-2透过性（Papp 62.3×10^-7 cm/s）。ACHP在大鼠中的良好生物利用度可能归因于其低清除率（0.33 L/h/kg）。在急性炎症模型中，ACHP以1 mg/kg的剂量依赖性方式表现出口服有效性[1]。
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 45 mg/mL (112.25 mM)
关键字: I kappa B kinase | IκB kinase | Inhibitor | ACHP | inhibit | IKK | ACHP Hydrochloride
相关产品: Bay 11-7085 | Kazinol U | Nyasol | TBK1/IKKε-IN-1 | WS6 | (Rac)-BAY-985 | 2-AMINO-5-PHENYL-THIOPHENE-3-CARBOXYLIC | NF-κB-IN-1 | Selinidin | TBK1/IKKε-IN-5
相关库: Anti-Breast Cancer Compound Library | Anti-Cancer Compound Library | NF-κB Signaling Compound Library | Bioactive Compounds Library Max | Anti-Ovarian Cancer Compound Library | Inhibitor Library | Kinase Inhibitor Library | Bioactive Compound Library
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