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. 2024 Sep 16;16(12):1989–1998. doi: 10.1038/s41557-024-01603-z

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Extended Data Fig. 6 — a, HPLC chromatogram showing the formation of 5,7-dibromo-indole-3-carbaldehyde (10) product in addition to the native 5,7-dibromo indole-3-carbonitrile (8) product. The retention time of the aldehyde shunt product formed in the AetD-catalysed reaction matches with that of an authentic standard. b, The observed mass of 5,7-dibromo-indole-3-carbaldehyde product in negative ionization mode.