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Synthesis and DPPH scavenging assay of reserpine analogues, computational studies and in silico docking studies in AChE and BChE responsible for Alzheimer's disease
Yar, Muhammad; Arshad, Muhammad; Farooq, Ariba; Gilani, Mazhar Amjad; Ayub, Khurshid; Ejaz, Asma; Kumar, Anupriya; Ninomiya, Ichiya.
  • Yar, Muhammad; COMSATS Institute of Information Technology. Interdisciplinary Research Centre in Biomedical Materials. Lahore. PK
  • Arshad, Muhammad; COMSATS Institute of Information Technology. Interdisciplinary Research Centre in Biomedical Materials. Lahore. PK
  • Farooq, Ariba; COMSATS Institute of Information Technology. Interdisciplinary Research Centre in Biomedical Materials. Lahore. PK
  • Gilani, Mazhar Amjad; COMSATS Institute of Information Technology. Interdisciplinary Research Centre in Biomedical Materials. Lahore. PK
  • Ayub, Khurshid; COMSATS Institute of Information Technology. Interdisciplinary Research Centre in Biomedical Materials. Lahore. PK
  • Ejaz, Asma; COMSATS Institute of Information Technology. Interdisciplinary Research Centre in Biomedical Materials. Lahore. PK
  • Kumar, Anupriya; COMSATS Institute of Information Technology. Interdisciplinary Research Centre in Biomedical Materials. Lahore. PK
  • Ninomiya, Ichiya; COMSATS Institute of Information Technology. Interdisciplinary Research Centre in Biomedical Materials. Lahore. PK
Braz. j. pharm. sci ; 51(1): 53-61, Jan-Mar/2015. tab, graf
Article Dans Anglais | LILACS | ID: lil-751357
ABSTRACT
Alzheimer's disease (AD) is a fast growing neurodegenerative disorder of the central nervous system and anti-oxidants can be used to help suppress the oxidative stress caused by the free radicals that are responsible for AD. A series of selected synthetic indole derivatives were biologically evaluated to identify potent new antioxidants. Most of the evaluated compounds showed significant to modest antioxidant properties (IC50 value 399.07 140.0±50 µM). Density Functional Theory (DFT) studies were carried out on the compounds and their corresponding free radicals. Differences in the energy of the parent compounds and their corresponding free radicals provided a good justification for the trend found in their IC50 values. In silico, docking of compounds into the proteins acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), which are well known for contributing in AD disease, was also performed to predict anti-AD potential.
RESUMO
A doença de Alzheimer (DA) é uma doença neurodegenerativado sistema nervoso central, em rápido crescimento, e antioxidantes ajudam a suprimir o estresse oxidativo causado por radicais livres, responsávies pela DA. Avaliou-se, biologicamente, série de derivados sintéticos de indol selecionados para identificar novos antioxidantes. A maioria dos compostos avaliados apresentou de significativa a boa propriedade antioxidante (valor de IC50 399,07140.0 ± 50 µM). Eftuaram-se estudos de Teoria do Funcional de Densidade (DFT) com os compostos e os seus correspondentes radicais livres. As diferenças de energia entre os compostos protótipos e os radicais livres correspondentes proporcionaram boa justificativa para a tendência encontrada nos seus valores de IC50. O ancoramento in silico dos compostos com a acetilcolinesterase (AChE) e com a butirilcolinesterase (BChE), que contribuem para a DA, foi, também, realizado para prever o seu potencial anti-DA.
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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Acetylcholinesterase / Butyrylcholine esterase / Maladie d'Alzheimer langue: Anglais Texte intégral: Braz. j. pharm. sci Année: 2015 Type: Article / descriptif de projet Pays d'affiliation: Pakistan Institution/Pays d'affiliation: COMSATS Institute of Information Technology/PK

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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Acetylcholinesterase / Butyrylcholine esterase / Maladie d'Alzheimer langue: Anglais Texte intégral: Braz. j. pharm. sci Année: 2015 Type: Article / descriptif de projet Pays d'affiliation: Pakistan Institution/Pays d'affiliation: COMSATS Institute of Information Technology/PK