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• W3033251065 abstract "Human ether-a-go-go-related gene (hERG) potassium channel blockage by small molecules may cause severe cardiac side effects. Thus, it is crucial to screen compounds for activity on the hERG channels early in the drug discovery process. In this study, we collected 5299 hERG inhibitors with diverse chemical structures from a number of sources. Based on this dataset, we evaluated different machine learning (ML) and deep learning (DL) algorithms using various integer and binary type fingerprints. A training set of 3991 compounds was used to develop quantitative structure–activity relationship (QSAR) models. The performance of the developed models was evaluated using a test set of 998 compounds. Models were further validated using external set 1 (263 compounds) and external set 2 (47 compounds). Overall, models with integer type fingerprints showed better performance than models with no fingerprints, converted binary type fingerprints or original binary type fingerprints. Comparison of ML and DL algorithms revealed that integer type fingerprints are suitable for ML, whereas binary type fingerprints are suitable for DL. The outcomes of this study indicate that the rational selection of fingerprints is important for hERG blocker prediction." @default.
• W3033251065 created "2020-06-12" @default.
• W3033251065 creator A5021200477 @default.
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• W3033251065 date "2020-06-04" @default.
• W3033251065 modified "2023-10-16" @default.
• W3033251065 title "The Study on the hERG Blocker Prediction Using Chemical Fingerprint Analysis" @default.
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• W3033251065 doi "https://doi.org/10.3390/molecules25112615" @default.
• W3033251065 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7321128" @default.
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