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Image Search Results
Journal: Computational toxicology (Amsterdam, Netherlands)
Article Title: A systematic evaluation of analogs and automated read-across prediction of estrogenicity: A case study using hindered phenols
doi: 10.1016/j.comtox.2017.09.001
Figure Lengend Snippet: Each phenol was decomposed to extract the basic phenol scaffold to identify different substitution positions and R-groups using a KNIME workflow. The decomposition resulted in 12 distinct substituent positions, which included conjoined and bridging rings. R2, R3, R4, and R6 were the most commonly occupied substituent positions.
Article Snippet: A
Techniques: