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Results 1 - 10 of 387 > >>
EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
(+)-camphor + NADPH + O2
-
?
-
?
(+)-camphor + NADPH + O2
-
?
-
?
(+)-dihydrocarvone + NADPH + O2
-
?
-
?
(+)-dihydrocarvone + NADPH + O2
-
?
-
?
(1aS,4aS,8aS)-8a-methylhexahydronaphthalene-1,6-dione + NADPH + O2
Wieland–Miescher ketone, no activity with the (1aR,4aR,8aR)-stereoisomer, stereoselective formation of the cis-(5aR,9aS)-isomer
(5aR,9aS)-9a-methylhexahydrobenzo[b]oxepine-2,7-dione + NADP+ + H2O
-
?
(1aS,4aS,8aS)-8a-methylhexahydronaphthalene-1,6-dione + NADPH + O2
Wieland–Miescher ketone, no activity with the (1aR,4aR,8aR)-stereoisomer, stereoselective formation of the cis-(5aR,9aS)-isomer
(5aR,9aS)-9a-methylhexahydrobenzo[b]oxepine-2,7-dione + NADP+ + H2O
-
?
(1R)-bicyclo[2.2.1]heptane-2,5-dione + NADPH + O2
74.4% of the activity with cyclohexanone
? + NADP+ + H2O
-
?
(2R)-2-ethylcyclohexanone + NADPH + H+ + O2
92% conversion, 30% enantiomeric excess, (-)-product
(7S)-7-ethyloxepan-2-one + NADP+ + H2O
-
?
(2R,6S)-2,6-dimethylcyclohexanone + NADPH + H+ + O2
-
cis-3, 7-dimethyl-2-oxepanone + NADP+ + H2O
-
?
(2R,6S)-2,6-dimethylcyclohexanone + NADPH + O2 + H+
-
(3R,7S)-3,7-dimethyloxepan-2-one + NADP+ + H2O
90% conversion at 20 h, 99% enantiomeric excess
?
Results 1 - 10 of 387 > >>