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Results 1 - 10 of 11 > >>
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EC Number Natural Substrates Commentary (Nat. Sub.)
Display the reaction diagram Show all sequences 1.14.99.1411-deoxycorticosterone + AH2 + O2 -
Display the reaction diagram Show all sequences 1.14.99.1411-deoxycortisol + AH2 + O2 -
Display the reaction diagram Show all sequences 1.14.99.1416alpha,17-epoxyprogesterone + AH2 + O2 -
Display the reaction diagram Show all sequences 1.14.99.1417alpha-hydroxyprogesterone + AH2 + O2 -
Display the reaction diagram Show all sequences 1.14.99.14more the enzyme is capable of converting useful pharmaceutical targets such as 3-oxo-DELTA4-steroids (e.g., testosterone, 11-deoxycorticosterone, androstenedione, and progesterone) mainly into their 15beta-hydroxy homologues. In addition, the enzyme hydroxylates progesterone to a minor extent at the 11alpha-, 9alpha-, and 6beta-positions
Display the reaction diagram Show all sequences 1.14.99.14progesterone + AH2 + O2 -
Display the reaction diagram Show all sequences 1.14.99.14progesterone + NADPH + O2 -
Display the reaction diagram Show all sequences 1.14.99.14progesterone + NADPH + O2 activity dependent upon NADPH and O2
Display the reaction diagram Show all sequences 1.14.99.14progesterone + NADPH + O2 multicomponent monooxygenase system
Display the reaction diagram Show all sequences 1.14.99.14progesterone + NADPH + O2 necessary step in the synthesis of cortico-steroid hormones
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