Synthesis and neuroprotective activity of resveratrol-3-n-butylphthalide hybrids / 药学学报
Acta Pharmaceutica Sinica
; (12): 1461-1469, 2019.
Article
in Chinese
| WPRIM (Western Pacific)
| ID: wpr-780248
Responsible library:
WPRO
ABSTRACT
6-Bromo-3-n-butylphthalide was obtained by nitration, reduction and diazotization from carboxybenzaldehyde. Twenty hybrids from substituted styrene and 6-bromo-3-n-butylphthalide were synthesized and the structure was confirmed by 1H NMR, 13C NMR and ESI-MS. All compounds were evaluated for neuroprotective activity against OGD/R-induced neurotoxicity in rat cortical neurons by MTT assay. The mechanism of neuroprotection was investigated by Western blot analyses. The results indicated that most of these compounds had a potent neuroprotective activity (All animal experiments were approved by the Experimental Animal Ethics Committee of Anhui University of Chinese Medicine), especially 10h and 10i showed significant effects, which may play a neuroprotective role by activating the PI3K/Akt signaling pathway.
Full text:
Available
Database:
WPRIM (Western Pacific)
Aspects:
Ethical aspects
Language:
Chinese
Journal:
Acta Pharmaceutica Sinica
Year:
2019
Document type:
Article