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Results 1 - 10 of 55 > >>
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EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 1.1.1.423(-)-(1R,2S)-ephedrine + NAD+ - Arthrobacter sp. TS-15 (S)-2-methylamino-1-phenylpropan-1-one + NADH + H+ - ?
Display the reaction diagram Show all sequences 1.1.1.4234-chlorobenzil + NADH + H+ 10.2% of the activity as compared to 1-phenyl-1,2-propanedione. The (R)-enantiomer is formed with 58% enantiomeric excess Arthrobacter sp. TS-15 ? + NAD+ - ?
Display the reaction diagram Show all sequences 1.1.1.423isatin + NADH + H+ 12.25% of the activity as compared to 1-phenyl-1,2-propanedione. The (R)-enantiomer is formed with 52% enantiomeric excess Arthrobacter sp. TS-15 (3R)-3-hydroxy-1,3-dihydro-2H-indol-2-one + NAD+ - ?
Display the reaction diagram Show all sequences 1.1.1.4232-chloro-1-phenyl-1-propanone + NADH + H+ 12.5% of the activity as compared to 1-phenyl-1,2-propanedione Arthrobacter sp. TS-15 2-chloro-1-phenyl-1-propan-1-ol + NAD+ - ?
Display the reaction diagram Show all sequences 1.1.1.4232-chloroacetophenone + NADH + H+ 13.6% of the activity as compared to 1-phenyl-1,2-propanedione. The (R)-enantiomer is formed with 98% enantiomeric excess Arthrobacter sp. TS-15 (1R)-2-chloro-1-phenylethan-1-ol + NAD+ - ?
Display the reaction diagram Show all sequences 1.1.1.4232-bromoacetophenone + NADH + H+ 14.8% of the activity as compared to 1-phenyl-1,2-propanedione. The (R)-enantiomer is formed with 85% enantiomeric excess Arthrobacter sp. TS-15 (1R)-2-bromo-1-phenylethan-1-ol + NAD+ - ?
Display the reaction diagram Show all sequences 1.1.1.423phenylglyoxal + NADH + H+ 18.9% of the activity as compared to 1-phenyl-1,2-propanedione. The (R)-enantiomer is formed with 99% enantiomeric excess Arthrobacter sp. TS-15 (2R)-hydroxy(phenyl)acetaldehyde + NAD+ - ?
Display the reaction diagram Show all sequences 1.1.1.4231-phenyl-1-propanone + NADH + H+ 2.4% of the activity as compared to 1-phenyl-1,2-propanedione. The (R)-enantiomer is formed with 99% enantiomeric excess Arthrobacter sp. TS-15 (1R)-1-phenylpropan-1-ol + NAD+ - ?
Display the reaction diagram Show all sequences 1.1.1.423(4-chlorophenyl)-2-pyridinylmethanone + NADH + H+ 2.7% of the activity as compared to 1-phenyl-1,2-propanedione. The (R)-enantiomer is formed with 70% enantiomeric excess Arthrobacter sp. TS-15 (R)-(4-chlorophenyl)(pyridin-2-yl)methanol + NAD+ - ?
Display the reaction diagram Show all sequences 1.1.1.4232,2'-furil + NADH + H+ 20% of the activity as compared to 1-phenyl-1,2-propanedione. The (R)-enantiomer is formed with 99% enantiomeric excess Arthrobacter sp. TS-15 (2R)-1,2-di(furan-2-yl)-2-hydroxyethan-1-one + NAD+ - ?
Results 1 - 10 of 55 > >>
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