Natural product scores and fingerprints extracted from artificial neural networks

Due to their desirable properties, natural products are an important ligand class for medicinal chemists. However, due to their structural distinctiveness, traditional cheminformatic approaches, like ligand-based virtual screening, often perform worse for natural products. Based on our recent work,...

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Main Authors: Janosch Menke, Joana Massa, Oliver Koch
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Computational and Structural Biotechnology Journal
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2001037021003226
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spelling doaj-f08a6de9c6c64dd49c9c562a7aa4d9f52021-09-15T04:21:03ZengElsevierComputational and Structural Biotechnology Journal2001-03702021-01-011945934602Natural product scores and fingerprints extracted from artificial neural networksJanosch Menke0Joana Massa1Oliver Koch2Institute of Pharmaceutical and Medicinal Chemistry, Westfälische Wilhelms-Universität Münster, Corrensstraße 48, 48149 Münster, GermanyInstitute of Pharmaceutical and Medicinal Chemistry, Westfälische Wilhelms-Universität Münster, Corrensstraße 48, 48149 Münster, GermanyInstitute of Pharmaceutical and Medicinal Chemistry, Westfälische Wilhelms-Universität Münster, Corrensstraße 48, 48149 Münster, Germany; Center for Multiscale Theory and Computation, Westfälische Wilhelms-Universität Münster, Corrensstraße 48, 48149 Münster, Germany; Corresponding author.Due to their desirable properties, natural products are an important ligand class for medicinal chemists. However, due to their structural distinctiveness, traditional cheminformatic approaches, like ligand-based virtual screening, often perform worse for natural products. Based on our recent work, we evaluated the ability of neural networks to generate fingerprints more appropriate for use with natural products. A manually curated dataset of natural products and synthetic decoys was used to train a multi-layer perceptron network and an autoencoder-like network. In-depth analysis showed that the extracted natural product-specific neural fingerprint outperforms traditional as well as natural product-specific fingerprints on three datasets. Further, we explored how the activations from the output layer of a network can work as a novel natural product likeness score. Overall, two natural product-specific datasets were generated, which are publicly available together with the code to create the fingerprints and the novel natural product likeness score.http://www.sciencedirect.com/science/article/pii/S2001037021003226Natural productsNeural fingerprintsSimilarity searchVirtual screeningNatural product likeness scoreNeural networks
collection DOAJ
language English
format Article
sources DOAJ
author Janosch Menke
Joana Massa
Oliver Koch
spellingShingle Janosch Menke
Joana Massa
Oliver Koch
Natural product scores and fingerprints extracted from artificial neural networks
Computational and Structural Biotechnology Journal
Natural products
Neural fingerprints
Similarity search
Virtual screening
Natural product likeness score
Neural networks
author_facet Janosch Menke
Joana Massa
Oliver Koch
author_sort Janosch Menke
title Natural product scores and fingerprints extracted from artificial neural networks
title_short Natural product scores and fingerprints extracted from artificial neural networks
title_full Natural product scores and fingerprints extracted from artificial neural networks
title_fullStr Natural product scores and fingerprints extracted from artificial neural networks
title_full_unstemmed Natural product scores and fingerprints extracted from artificial neural networks
title_sort natural product scores and fingerprints extracted from artificial neural networks
publisher Elsevier
series Computational and Structural Biotechnology Journal
issn 2001-0370
publishDate 2021-01-01
description Due to their desirable properties, natural products are an important ligand class for medicinal chemists. However, due to their structural distinctiveness, traditional cheminformatic approaches, like ligand-based virtual screening, often perform worse for natural products. Based on our recent work, we evaluated the ability of neural networks to generate fingerprints more appropriate for use with natural products. A manually curated dataset of natural products and synthetic decoys was used to train a multi-layer perceptron network and an autoencoder-like network. In-depth analysis showed that the extracted natural product-specific neural fingerprint outperforms traditional as well as natural product-specific fingerprints on three datasets. Further, we explored how the activations from the output layer of a network can work as a novel natural product likeness score. Overall, two natural product-specific datasets were generated, which are publicly available together with the code to create the fingerprints and the novel natural product likeness score.
topic Natural products
Neural fingerprints
Similarity search
Virtual screening
Natural product likeness score
Neural networks
url http://www.sciencedirect.com/science/article/pii/S2001037021003226
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