生物信息学
体内
植物化学
糖苷
肽
生物化学
化学
药理学
生物
立体化学
生物技术
基因
作者
Esraa M. Mohamed,Abeer H. Elmaidomy,Rania Alaaeldin,Faisal Alsenani,Faisal H. Altemani,Naseh A. Algehainy,Mohammad Alanazi,Alaa Bagalagel,Abdulhamid Althagafi,Mahmoud A. Elrehany,Usama Ramadan Abdelmohsen
出处
期刊:Metabolites
[Multidisciplinary Digital Publishing Institute]
日期:2023-06-07
卷期号:13 (6): 732-732
被引量:5
标识
DOI:10.3390/metabo13060732
摘要
Tamarindus indica Linn (tamarind, F. Leguminosae) is one of the most widely consumed edible fruits in the world. Phytochemical investigation of tamarind pulp n-butanol fraction yielded one new (+)-pinitol glycoside compound 1 (25% w/w), and 1D, 2D NMR, and HRESIMS investigation were used to confirm the new compound's structure. (+)-Pinitol glycoside showed anti-Alzheimer potential that was confirmed in prophylactic and treatment groups by decreasing time for the T-maze test; decreased TAO, brain and serum AChE, MDA, tau protein levels, and β amyloid peptide protein levels; and increasing GPX, SOD levels, and in vivo regression of the neurodegenerative features of Alzheimer's dementia in an aluminum-intoxicated rat model. The reported molecular targets for human Alzheimer's disease were then used in a network pharmacology investigation to examine their complex interactions and identify the key targets in the disease pathogenesis. An in silico-based analysis (molecular docking, binding free energy calculation (ΔGBinding), and molecular dynamics simulation) was performed to identify the potential targets for compound 1. The findings of this study may lead to the development of dietary supplements for the treatment of Alzheimer's disease.
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