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<< < Results 11 - 20 of 1625 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-flurbiprofen ethyl ester + H2O enantioselective reaction Bacillus cereus C71 (S)-flurbiprofen ethyl ester + (R)-flurbiprofen + ethanol - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-flurbiprofen ethyl ester + H2O enantioselective hydrolysis, kinetic resolution, overview Serratia marcescens (S)-flurbiprofen + ethanol - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-flurbiprofen ethyl ester + H2O high enantiomeric excess and conversion yield of 98% and 48%, respectively Serratia marcescens (S)-flurbiprofen + ethanol - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-flurbiprofen ethyl ester + H2O enantioselective hydrolysis, kinetic resolution, overview Serratia marcescens ES-2 (S)-flurbiprofen + ethanol - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-ibuprofen + 1-propanol purified enzyme in a mixture of 1-propanol-isooctane in a ratio of 3:1, the conversion of racemic ibuprofen reaches 46% with very high enantioselectivity for production of the (S)-enantiomer Penicillium expansum (S)-ibuprofen n-propyl ester + (R)-ibuprofen - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-ibuprofen + 1-propanol purified enzyme in a mixture of 1-propanol-isooctane in a ratio of 3:1, the conversion of racemic ibuprofen reaches 46% with very high enantioselectivity for production of the (S)-enantiomer Penicillium expansum PED-03 (S)-ibuprofen n-propyl ester + (R)-ibuprofen - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-mandelonitrile + vinyl acetate transesterification Alcaligenes sp. (S)-cyano(phenyl)methyl acetate + (R)-mandelonitrite - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-naproxen 2,2,2-trifluoroethyl thioester (R,S)-profen 2,2,2-trifluoroethyl thioester Carica papaya (S)-naproxen + 2,2,2-trifluorothioethanol + (R)-naproxen 2,2,2-trifluoroethyl thioester - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R,S)-[4-[4a,6b(E)]]-6-[4,4-bis(4-fluorophenyl)-3-(1-methyl-1H-tetrazol-5-yl)-1,3-butadienyl]-tetrahydro-4-hydroxy-2H-pyran-2-one + isopropenyl acetate - Burkholderia cepacia (R)-(+)-[4-[4a,6b(E)]]-6-[4,4-bis(4-fluorophenyl)-3-(1-methyl-1H-tetrazol-5-yl)-1,3-butadienyl]-tetrahydro-4-hydroxy-2H-pyran-2-one + (S)-(-)-[4-[4a,6b(E)]]-6-[4,4-bis(4-fluorophenyl)-3-(1-methyl-1H-tetrazol-5-yl)-1,3-butadienyl]-tetrahydro-4-acetyloxy-2H-pyran-2-one + prop-1-en-2-ol - ?
Show all pathways known for 3.1.1.3Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.3(R/S)-ibuprofen methoxyethyl ester + H2O - Candida cyclindraceae (R)-ibuprofen methoxyethyl ester + (S)-ibuprofen + 2-methoxyethanol - ?
<< < Results 11 - 20 of 1625 > >>