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hBChE-IN-4(compound 40)作为一种hCA激活剂和BChE抑制剂,显示出对多种hCA亚型的高效活性,其KA值对应hCA I、hCA II、hCA IV、hCA VB以及hCA VII分别为266、76.9、918、893和98.0 nM。此外,该化合物在抑制eeAChE和eqBChE方面同样表现出色,IC50值分别仅为72.1和4.2 nM。值得注意的是,hBChE-IN-4无显示出细胞毒性,且被认为具有促进认知功能的有效作用。因其在神经退行性疾病和其他神经精神疾病研究中的潜在应用价值,hBChE-IN-4备受关注。
hBChE-IN-4(compound 40)作为一种hCA激活剂和BChE抑制剂,显示出对多种hCA亚型的高效活性,其KA值对应hCA I、hCA II、hCA IV、hCA VB以及hCA VII分别为266、76.9、918、893和98.0 nM。此外,该化合物在抑制eeAChE和eqBChE方面同样表现出色,IC50值分别仅为72.1和4.2 nM。值得注意的是,hBChE-IN-4无显示出细胞毒性,且被认为具有促进认知功能的有效作用。因其在神经退行性疾病和其他神经精神疾病研究中的潜在应用价值,hBChE-IN-4备受关注。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | hBChE-IN-4 (compound 40) serves as an effective activator for hCA and an inhibitor for BChE. It demonstrates affinity for various hCA subtypes with affinity constants (KA) of 266 nM for hCA I, 76.9 nM for hCA II, 918 nM for hCA IV, 893 nM for hCA VB, and 98.0 nM for hCA VII. Inhibition concentrations (IC50) for eeAChE and eqBChE are recorded at 72.1 nM and 4.2 nM, respectively. hBChE-IN-4 is non-cytotoxic and has demonstrated potential cognitive enhancement effects. It holds potential for research in neurodegenerative and other neuropsychiatric disorders. |
靶点活性 | EeAChE:72.1 nM, eqBChE:4.2 nM, CA I (human):266 nM (Ka), CA II (human):76.9 nM (Ka), CA VB (human):893 nM (Ka), CA IV (human):918 nM (Ka), CA VII (human):98.0 nM (Ka) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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