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. 2003 Sep 22;100(20):11741–11746. doi: 10.1073/pnas.2032621100

Fig. 1.

Fig. 1.

LC-MS analysis of the product formed from E1 on exposure to •OH generated by the Fenton reaction. (a) Extracted ion-current chromatogram (m/z 287); mass spectra are from the major LC peak at tR = 1.3 min; (b) full-scan APCI-MS; (c) MS/MS (MS2) product-ion scan from the molecular ion m/z 287 isolated as the precursor; and (d)MS3 product-ion scan of m/z 269 (the major product ion of the MS2, c). Fragmentation pattern and tR are identical to those of a synthetic 10β-hydroxyestra-1,4-dien-3,17-dione (E1-quinol).