Carbazole moiety is an important scaffold with a variety of biological applications, for example, antioxidative stress. Our previous synthesized carbazoles were screened for their neuroprotective properties against two individual oxidative stresses. Some of the new carbazole derivatives were observed with modest to good neuroprotective effects on neuronal cells HT22 against cell injury induced by glutamate or homocysteic acid (HCA). Substituents introduced to the carbazole ring system play crucial roles in their biological activities. In particular, a bulky group favors the neuroprotective activity of the compounds. One of the new compounds, 6, showed the best neuroprotective effects, which might result from its anti-oxidative activity with a GSH-independent mechanism. These findings might provide an alternative strategy for the development of novel carbazole derivatives for the treatment of CNS diseases such as Alzheimer’s disease.
|Autori interni:||RAPPOSELLI, SIMONA|
|Autori:||Zhu D.; Chen M.; Li M.; Luo B.; Zhao Y.; Huang P.; Xue F.; Rapposelli S.; Pi R.; Wen S.|
|Titolo:||Discovery of novel N-substituted carbazoles as neuroprotective agents with potent anti-oxidative activity|
|Anno del prodotto:||2013|
|Digital Object Identifier (DOI):||10.1016/j.ejmech.2013.07.029|
|Appare nelle tipologie:||1.1 Articolo in rivista|