In silico development of new acetylcholinesterase inhibitors

Abstract

In this work, we made use of fragment-based drug design (FBDD) and de novo design to obtain more powerful acetylcholinesterase (AChE) inhibitors. AChE is associated with Alzheimer’s disease (AD). It was found that the cholinergic pathways in the cerebral cortex are compromised in AD and the accompanying cholinergic deficiency contributes to the cognitive deterioration of AD patients. In the FBDD approach, fragments are docked into the active site of the protein. As fragments are molecular groups with a low number of atoms, it is possible to study their interaction with localized amino acids. Once the interactions are measured, the fragments are organized by affinity and then linked together to form new molecules with a high degree of interaction with the active site. In the other approach, we used the de novo design technique starting from reference drugs used in the AD treatment. These drugs were broken into fragments (seeds). In the growing strategy, fragments were added to each seed, growing new molecules. In the linking strategy, two or more separated seeds were linked with different fragments. Both strategies combined produced a library of more than 2 million compounds. This library was filtered using absorption, distribution, metabolism, and excretion properties. The resulting library with around six thousand compounds was filtered again. In this case, structures with Tanimoto coefficients >.85 were discarded. The final library with 1500 compounds was submitted to docking studies. As a result, 10 compounds with better interaction energy than the reference drugs were obtained.

Keywords:

• acetylcholinesterase
• Alzheimer disease
• de novo design
• fragment docking
• molecular dynamics

Acknowledgments

BAV and ALFA acknowledge grant from PIBICT/FAPEMIG program. Portion of the results presented here were developed using the computational resources in CENAPAD- SP (Centro Nacional de Processamento de Alto Desempenho em Sao Paulo) grant UNICAMP/FINEP-MCT and in CENAPAD-UFC (Centro Nacional de Processamento de Alto Desempenho da Universidade Federal do Ceará).

Notes

1. https://www.alz.co.uk/research/world-report

2. http://www.fda.gov/