42528-76-7Relevant academic research and scientific papers
Evaluation of Cytotoxic Properties of N,N'-bis[(1-aryl-3-heteroaryl)propylidene]-hydrazine dihydrochlorides
Kucukoglu,Gul,Sakagami
, p. 784 - 787 (2020/11/23)
N,N'-bis[(1-aryl-3-heteroaryl)propylidene]hydrazine dihydrochlorides, P1, P4 – P8, and R1 – R7, were assayed against human oral squamous cell carcinoma (HSC-2, HSC-3, HSC-4), human promyelocytic leukemia cell line (HL-60), and human normal oral cells (HGF
Design, synthesis and evaluation of tacrine based acetylcholinesterase inhibitors
Shen, Yanhong,Yu, Youzhu,Lv, Huichao,Feng, Liping,Zhang, Guoqiang
scheme or table, p. 341 - 345 (2011/10/18)
A series of tacrine based cholinesterase inhibitors was designed, synthesized and assayed for their biological activity. Among them, five compounds inhibited acetylcholinesterase in micromolar range and most of the compounds demonstrated much better selectivity for AChE than reference compound tacrine.
2-Phenoxy-indan-1-one derivatives as acetylcholinesterase inhibitors: A study on the importance of modifications at the side chain on the activity
Shen, Yanhong,Sheng, Rong,Zhang, Jing,He, Qiaojun,Yang, Bo,Hu, Yongzhou
, p. 7646 - 7653 (2008/12/23)
As a part of our project aimed at developing new agents of potential application in AD, a new series of 2-phenoxy-indan-1-one derivatives which possess alkylamine side chain were designed, synthesized, and evaluated for their inhibitory activity against AChE and BuChE. Most of the compounds were found to inhibit AChE in the nanomolar range. The optimum inhibitor 3g exhibited 34-fold increase in AChE inhibition than donepezil and displayed neuroprotective effect against H2O2-induced cell death.
