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Insilico Analysis and Docking of Tacrine and Donepezil Derivatives Targeting Histamine-N-Methyltransferase and Acetyl Cholinesterase Protein Respectively for Alzheimer's Disease


Affiliations
1 Dept. of Pharmaceutical Chemistry, JNTU-OTRI, Anantapur. Andhra Pradesh, India
2 Dept. of Pharmaceutical Analysis, JNTU-OTRI, Anantapur. Andhra Pradesh, India
3 Dept. of Pharmaceutics, PRRM College of Pharmacy, Andhra Pradesh, India
4 Dept. of Pharmacology, Royal College of Pharmacy and Health Sciences, Berhampur, Odisha, India
     

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Alzheimer's disease is characterized by loss of neurons and synapses in the cerebral cortex and certain sub cortical regions. The earliest observable symptoms are often mistakenly thought to be 'age-related' concerns, or manifestations of stress. As the disease advances, symptoms include confusion, irritability and aggression, long-term memory loss. Two drugs specifically approved for treating Alzheimer's disease were Tacrine and Donezepil. Tacrine mainly inhibit the histamine-N-methyltransferase protein which block the histamine transmission. Donepezil inhibit the acetyl cholinesterase which degrades the acetylcholine transmitter. In this study, computational methods are used to design novel tacrine and donepezil derivatives and evaluated them for interaction with the Histamine-N-methyltransferase protein and acetyl cholinesterase protein respectively through insilico analysis by using Hyperchem 8.0, Gold 3.01 docking software. The result of the docking studies shows that ligands of T3 and D3 with R - CH2CH3 are having highest binding affinity.

Keywords

Alzheimer's Disease, Acetyl Cholinesterase, Histamine-N-Methyltransferase Protein, Molecular Docking, Docking Interactions
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  • Insilico Analysis and Docking of Tacrine and Donepezil Derivatives Targeting Histamine-N-Methyltransferase and Acetyl Cholinesterase Protein Respectively for Alzheimer's Disease

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Authors

M. Sravani
Dept. of Pharmaceutical Chemistry, JNTU-OTRI, Anantapur. Andhra Pradesh, India
P. Sai Lakshmi
Dept. of Pharmaceutical Chemistry, JNTU-OTRI, Anantapur. Andhra Pradesh, India
K. Amuktha Reddy
Dept. of Pharmaceutical Analysis, JNTU-OTRI, Anantapur. Andhra Pradesh, India
N Naga Deepthi
Dept. of Pharmaceutics, PRRM College of Pharmacy, Andhra Pradesh, India
Uday Sasi Kiran Kantheti
Dept. of Pharmacology, Royal College of Pharmacy and Health Sciences, Berhampur, Odisha, India

Abstract


Alzheimer's disease is characterized by loss of neurons and synapses in the cerebral cortex and certain sub cortical regions. The earliest observable symptoms are often mistakenly thought to be 'age-related' concerns, or manifestations of stress. As the disease advances, symptoms include confusion, irritability and aggression, long-term memory loss. Two drugs specifically approved for treating Alzheimer's disease were Tacrine and Donezepil. Tacrine mainly inhibit the histamine-N-methyltransferase protein which block the histamine transmission. Donepezil inhibit the acetyl cholinesterase which degrades the acetylcholine transmitter. In this study, computational methods are used to design novel tacrine and donepezil derivatives and evaluated them for interaction with the Histamine-N-methyltransferase protein and acetyl cholinesterase protein respectively through insilico analysis by using Hyperchem 8.0, Gold 3.01 docking software. The result of the docking studies shows that ligands of T3 and D3 with R - CH2CH3 are having highest binding affinity.

Keywords


Alzheimer's Disease, Acetyl Cholinesterase, Histamine-N-Methyltransferase Protein, Molecular Docking, Docking Interactions

References