目錄:MedChemExpress LLC>>生化試劑>> (2-Chloropyridin-4-yl)methanamine hydrochloride |
CAS | 916210-98-5 | 純度 | 98.70% |
---|---|---|---|
分子量 | 179.05 | 分子式 | C?H?Cl?N? |
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 100 mg |
貨號 | HY-101771A | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 916210-98-5
產(chǎn)品活性:(2-Chloropyridin-4-yl)methanamine hydrochloride is a selective LOXL2 inhibitor with an IC50 of 126 nM.
研究領(lǐng)域:Neuronal Signaling
作用靶點(diǎn):Monoamine Oxidase
In Vitro: (2-Chloropyridin-4-yl)methanamine hydrochloride is shown to be selective for LOXL2 over LOX and three other amine oxidases (MAO-A, MAO-B and SSAO). In the human whole blood LOXL2 assay, (2-Chloropyridin-4-yl)methanamine hydrochloride has an IC50 of 1.45 µM compared to 126 nM in the absence of blood proteins. (2-Chloropyridin-4-yl)methanamine hydrochloride shows a 31-fold selectivity for LOXL2+BSA (IC50=190 nM) over LOX+BSA (IC50=5.91 µM). Against a panel of non-LTQ-containing AO enzymes (MAO-A, MAO-B and SSAO), LOXL2-IN-1 is found to be inactive at 30 µM. (2-Chloropyridin-4-yl)methanamine hydrochloride is profiled for the inhibition of three different CYP enzymes (CYPs 3A4, 2C9 and 2D6) and in each case the IC50 is more than 30 µM.
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