Imine reductases (IREDs) are NADPH-dependent enzymes with significant biocatalytic potential for the synthesis of primary, secondary, and tertiary chiral amines. Their applications include the reduction of cyclic imines and the reductive amination of prochiral ketones. In this study, twenty-nine novel IREDs were revealed through genome mining. Imine reductase activities were screened at pH 7 and 9 and in presence of either NADPH or NAD
Reductive Aminases (RedAms) catalyze the asymmetric reductive amination of ketones with primary amin...
Reductive amination is one of the most important methods for the synthesis of chiral amines. Here we...
Meyer T, Zumbrägel N, Geerds C, Gröger H, Niemann H. Structural Characterization of an S-enantiosele...
The imine reductase AoIRED from Amycolatopsis orientalis (Uniprot R4SNK4) catalyzes the NADPH-depend...
Current abiotic synthetic methods of obtaining chiral amines often involve conditions that are not c...
Imine reductases (IREDs) offer biocatalytic routes to chiral amines and have a natural preference fo...
The synthesis of chiral molecules by asymmetric hydrogenation applying rhodium and ruthenium-based m...
The synthesis of secondary and tertiary amines through the reductive amination of carbonyl compounds...
Imine reductases (IREDs) have emerged as a valuable new set of biocatalysts for the asymmetric synth...
Chiral amines have proven to be powerful building blocks for defining new pharmaceutical and agroche...
Biocatalytic imine reduction has been a topic of intense research by the artificial metalloenzyme co...
Chiral amine diastereomers are ubiquitous in pharmaceuticals and agrochemicals(1), yet their prepara...
Imine Reductases (IREDs) catalyze the asymmetric reduction of cyclic imines, but also in some cases ...
We report the exploration of the evolutionary relationship between imine reductases (IREDs) and othe...
Chiral amine moieties are widely distributed in bioactive natural products and pharmaceutical ingred...
Reductive Aminases (RedAms) catalyze the asymmetric reductive amination of ketones with primary amin...
Reductive amination is one of the most important methods for the synthesis of chiral amines. Here we...
Meyer T, Zumbrägel N, Geerds C, Gröger H, Niemann H. Structural Characterization of an S-enantiosele...
The imine reductase AoIRED from Amycolatopsis orientalis (Uniprot R4SNK4) catalyzes the NADPH-depend...
Current abiotic synthetic methods of obtaining chiral amines often involve conditions that are not c...
Imine reductases (IREDs) offer biocatalytic routes to chiral amines and have a natural preference fo...
The synthesis of chiral molecules by asymmetric hydrogenation applying rhodium and ruthenium-based m...
The synthesis of secondary and tertiary amines through the reductive amination of carbonyl compounds...
Imine reductases (IREDs) have emerged as a valuable new set of biocatalysts for the asymmetric synth...
Chiral amines have proven to be powerful building blocks for defining new pharmaceutical and agroche...
Biocatalytic imine reduction has been a topic of intense research by the artificial metalloenzyme co...
Chiral amine diastereomers are ubiquitous in pharmaceuticals and agrochemicals(1), yet their prepara...
Imine Reductases (IREDs) catalyze the asymmetric reduction of cyclic imines, but also in some cases ...
We report the exploration of the evolutionary relationship between imine reductases (IREDs) and othe...
Chiral amine moieties are widely distributed in bioactive natural products and pharmaceutical ingred...
Reductive Aminases (RedAms) catalyze the asymmetric reductive amination of ketones with primary amin...
Reductive amination is one of the most important methods for the synthesis of chiral amines. Here we...
Meyer T, Zumbrägel N, Geerds C, Gröger H, Niemann H. Structural Characterization of an S-enantiosele...