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HDAC6-IN-49(Compound 3)作为HDAC的抑制剂,针对HDAC6与HDAC1的IC50值分别为0.012 μM和0.735 μM。此化合物还能够抑制MAO-B、胆碱酯酶 (ChE)、组胺受体 (H3R)以及血清素6受体 (5-HT6R)。在生物学应用方面,HDAC6-IN-49对SH-SY5Y细胞展示出神经保护效果,并在果蝇的帕金森病模型与C. elegans的阿尔茨海默病模型中改善了认知功能与运动能力。
HDAC6-IN-49(Compound 3)作为HDAC的抑制剂,针对HDAC6与HDAC1的IC50值分别为0.012 μM和0.735 μM。此化合物还能够抑制MAO-B、胆碱酯酶 (ChE)、组胺受体 (H3R)以及血清素6受体 (5-HT6R)。在生物学应用方面,HDAC6-IN-49对SH-SY5Y细胞展示出神经保护效果,并在果蝇的帕金森病模型与C. elegans的阿尔茨海默病模型中改善了认知功能与运动能力。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | HDAC6-IN-49 (Compound 3) is an inhibitor of HDAC, with IC50 values of 0.012 and 0.735 µM against HDAC6 and HDAC1, respectively. Additionally, it inhibits MAO-B, cholinesterase (ChE), histamine receptor (H3R), and serotonin 6 receptor (5-HT6R). HDAC6-IN-49 exhibits neuroprotective effects in SH-SY5Y cells and enhances cognitive functions and motor abilities in fruit fly models of Parkinson's disease and C. elegans models of Alzheimer's disease. |
靶点活性 | HDAC6:0.012 μM, HDAC1:0.735 μM |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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