Name | SD-6 |
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Description | SD-6 is an orally active inhibitor of hAChE and hBChE with IC50 values of 0.907 µM and 1.579 µM, respectively. SD-6 has excellent blood-brain barrier (BBB) permeability and no neurotoxicity, which can be used for research on Alzheimer's disease[1]. |
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Related Catalog | |
Target |
hAChE:0.907 μM (IC50) hBCHE:1.579 μM (IC50) |
In Vitro | SD-6 (5-80 µM;24 h) 在 SH-SY5Y 细胞中具有神经保护作用[1]。 Cell Viability Assay[1] Cell Line: SH-SY5Y cells. Concentration: 5, 10, 20, 40 or 80 µM. Incubation Time: 24 h. Result: Exhibited toxicity to differentiated SH-SY5Y cell lines and has a protective effect on undifferentiated SH-SY5Y cell lines. |
In Vivo | SD-6 (100、300 和 500 mg/kg;口服;单剂量) 对未怀孕的雌性 Wistar 大鼠没有毒性作用[1]。 SD-6 (2.5、5 和 10 mg/kg;口服;一天 3 次,持续 7 天) 改善了东莨菪碱 (HY-N0296) 诱导的雄性 Wistar 大鼠认知和记忆缺陷[1]。 SD-6 (2.5、5 和 10 mg/kg;口服;单剂量) 显著改善了大鼠中东莨菪碱诱导的异常,促进生化指标正常化[1]。 Animal Model: 10–11 weeks nonpregnant female Wistar rats (220–280 g)[1]. Dosage: 100, 300 and 500 mg/kg. Administration: Oral gavage; single dose. Result: Showed safety and tolerability. Animal Model: 10–11 weeks male Wistar rats (220–280 g)[1]. Dosage: 2.5、5、10 mg/kg. Administration: Oral gavage; 3 times a day for 7 days or single dose. Result: Had the function of repairing cognitive and memory deficits. Reduced the level of AChE and malonaldehyde (MDA), increased the level of acetylcholine, superoxide dismutase (SOD), glutathione (GSH) and catalase. |
References |
Molecular Formula | C20H22N4OS |
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Molecular Weight | 366.48 |