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Journal of Medicinal Chemistry|July 15, 2020
The Most Common Functional Groups in Bioactive Molecules and How Their Popularity Has Evolved over TimePeter Ertl, Eva Altmann, Jeffrey M McKennaBioorganic & Medicinal Chemistry|February 11, 2023
The most common linkers in bioactive molecules and their bioisosteric replacement networkPeter Ertl, Eva Altmann, Sophie RacineEuropean Journal of Medicinal Chemistry|September 24, 2025
Ring systems in medicinal chemistry: A cheminformatics analysis of ring popularity in drug discovery over timePeter Ertl, Eva Altmann, Rainer WilckenEuropean Journal of Medicinal Chemistry|May 31, 2022
Ring replacement recommender: Ring modifications for improving biological activityPeter Ertl, Eva Altmann, Sophie Racine, et al.Bioorganic & Medicinal Chemistry|July 8, 2023
Which boronic acids are used most frequently for synthesis of bioactive molecules?Peter Ertl, Eva Altmann, Sophie Racine, et al.Journal of Chemical Information and Computer Sciences|March 26, 2003
Cheminformatics analysis of organic substituents: identification of the most common substituents, calculation of substituent properties, and automatic identification of drug-like bioisosteric groupsPeter ErtlBioorganic & Medicinal Chemistry|March 23, 2012
Database of bioactive ring systems with calculated properties and its use in bioisosteric design and scaffold hoppingPeter ErtlJournal of Chemical Information and Modeling|August 27, 2021
Magic Rings: Navigation in the Ring Chemical Space Guided by the Bioactive RingsPeter ErtlJournal of Cheminformatics|January 12, 2021
Craig plot 2.0: an interactive navigation in the substituent bioisosteric spacePeter ErtlJournal of Chemical Information and Modeling|May 22, 2014
Intuitive ordering of scaffolds and scaffold similarity searching using scaffold keysPeter ErtlPageof 23