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Fig. 1 | Journal of Cheminformatics

Fig. 1

From: Reconstruction of lossless molecular representations from fingerprints

Fig. 1

The normalized molecular weight distribution of our training dataset along with several drug and natural product libraries such as KEGG DRUG Database, DRUGBANK and Universal Natural Product Database (UNPD). The training dataset consisted of five million small- and medium-sized molecules of approximately 50 heavy atoms or less that maximally represent available drug-like chemical space

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