Natural product scores and fingerprints extracted from artificial neural networks
收藏DataCite Commons2026-02-19 更新2026-05-07 收录
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https://datastore.uni-muenster.de/doi/10.17879/2vs7c-1h637
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资源简介:
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 evalu-
ated the ability of neural networks to generate fingerprints more appropriate for use with natural prod-
ucts. 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 nat-
ural product-specific neural fingerprint outperforms traditional as well as natural product-specific finger-
prints 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 gen-
erated, which are publicly available together with the code to create the fingerprints and the novel nat-
ural product likeness score.
提供机构:
University of Münster
创建时间:
2026-02-09



