Artigo em revista científica Q1
Chemical patterns of proteasome inhibitors: lessons learned from two decades of drug design
Romina A. Guedes (Guedes, R. A.); Natália Aniceto (Aniceto, N. ); Andrade, M. A. P. (Andrade, M. A. P.); J. A. R. Salvador (Salvador, J. A. R.); Rita C. Guedes (Guedes, R. C.);
Título Revista
International Journal of Molecular Sciences
Ano (publicação definitiva)
2019
Língua
Inglês
País
Suíça
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Abstract/Resumo
Drug discovery now faces a new challenge, where the availability of experimental data is no longer the limiting step, and instead, making sense of the data has gained a new level of importance, propelled by the extensive incorporation of cheminformatics and bioinformatics methodologies into the drug discovery and development pipeline. These enable, for example, the inference of structure-activity relationships that can be useful in the discovery of new drug candidates. One of the therapeutic applications that could benefit from this type of data mining is proteasome inhibition, given that multiple compounds have been designed and tested for the last 20 years, and this collection of data is yet to be subjected to such type of assessment. This study presents a retrospective overview of two decades of proteasome inhibitors development (680 compounds), in order to gather what could be learned from them and apply this knowledge to any future drug discovery on this subject. Our analysis focused on how different chemical descriptors coupled with statistical tools can be used to extract interesting patterns of activity. Multiple instances of the structure-activity relationship were observed in this dataset, either for isolated molecular descriptors (e.g., molecular refractivity and topological polar surface area) as well as scaffold similarity or chemical space overlap. Building a decision tree allowed the identification of two meaningful decision rules that describe the chemical parameters associated with high activity. Additionally, a characterization of the prevalence of key functional groups gives insight into global patterns followed in drug discovery projects, and highlights some systematically underexplored parts of the chemical space. The various chemical patterns identified provided useful insight that can be applied in future drug discovery projects, and give an overview of what has been done so far.
Agradecimentos/Acknowledgements
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Palavras-chave
Proteasome,Proteasome inhibitors,Molecular descriptors,Fingerprints,Chemical space,Decision tree,Structure-activity relationship
  • Ciências da Computação e da Informação - Ciências Naturais
  • Ciências Químicas - Ciências Naturais
  • Ciências Biológicas - Ciências Naturais
  • Engenharia Química - Engenharia e Tecnologia
  • Medicina Clínica - Ciências Médicas
  • Outras Ciências Médicas - Ciências Médicas
Registos de financiamentos
Referência de financiamento Entidade Financiadora
LISBOA-01-0145-FEDER-016405 (SAICTPAC/0019/2015) Comissão Europeia
CENTRO-01-0247-FEDER-003269 Comissão Europeia
UID/DTP/04138/2019 Fundação para a Ciência e a Tecnologia
SFRH/BD/104441/2014 Fundação para a Ciência e a Tecnologia
PTDC/QEQ-MED/7042/2014 Fundação para a Ciência e a Tecnologia
UID/MULTI/0446/2013 Fundação para a Ciência e a Tecnologia