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. 2016 Jun 23;291(33):17143–17164. doi: 10.1074/jbc.M116.732966

FIGURE 10.

FIGURE 10.

Reaction products formed from 17α-hydroxyprogesterone and 17α-hydroxypregnenolone in P450 17A1 reactions supported by various factors. Retention times (tR) and integration units are indicated on the chromatograms. A–C, 17α-hydroxyprogesterone; D–F, 17α-hydroxypregnenolone. A and D, NADPH-P450 reductase, cytochrome b5, and NADPH; B and E, H2O2 (10 mm) (with cytochrome b5); C and F, iodosylbenzene (PhI=O, 300 μm) (with cytochrome b5). In these studies the Δ5 products (formed from 17α-hydroxypregnenolone) were oxidized to Δ4 products to facilitate LC-UV analysis.