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Microbes CUR61414hydrochloridein which CYP17 expression was induced as explained above were utilised to examine their power to metabolize radiolabeled progesterone and squalene. 3H-Progesterone was incubated withCT-1 bacteria CT 1alongside one another and substrate declineCUR61414 was firm by TLC separation. Figure 9C demonstrates that, as envision
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